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Psychoneuroimmunoendocrinology: clinical implications

Abstract

Psychoneuroimmunoendocrinology, which was first described in 1936, is the study of the interactions between the psyche, neural and endocrine functions and immune responses. The aim of psychoneuroimmunoendocrinology is to apply medical knowledge to the treatment of different allergic, immune, autoimmune, rheumatic, neoplastic, endocrine, cardiovascular and dental pathologies, among other disorders. Epigenetic factors and major stresses from different types of stimuli acting through distinct pathways and neurotransmitters are highly involved in altering the psychoneuroimmunoendocrine axis, resulting in the emergence of disease. The main purpose of this report is to expand the understanding of psychoneuroimmunoendocrinology and to demonstrate the importance of the above-mentioned interactions in the etiology of multiple pathologies. In this review, a search of the medical literature using PubMed (free access search engine for the Medline database of the National Library of Medicine of the United States) over the years 1936 to 2016 was conducted, and descriptive and experimental studies and reviews of the scientific literature were included.

Background

Each field of medicine has a defined scope; however, interactions between systems covered by different fields exist. A link between findings from psychiatry, neurology, immunology and endocrinology has been noted for many years. From the functional, anatomical and physiological perspectives, the correlation between the central nervous system (CNS) and the endocrine system is complex and involves several actors, such as cytokines, receptors and neurotransmitters. The immune system is connected to the endocrine and neural systems via a number of pathways that integrate the functions of the hypothalamus, pituitary glands, adrenal glands, thyroid glands, gonads and autonomic nervous system. Major clinical implications and a vast amount of pathologies are related to the relationships between the systems covered by the science of psychoneuroimmunoendocrinology.

Many studies have described the negative effects of stress on health. Ader and Cohen in 1975 studied the effects of stress on the immune system. These previous findings are currently accepted, and a new area of study focusing on inflammation, autoimmunity and secondary hypersensitivity to stress has been developed.

Neuroimmunophysiologists have found that stress, anxiety and depression not only affect the protective function of the immune system but also alter its regulatory function.

Socioeconomic status as well as chronic illnesses such as autoimmune and rheumatic diseases, asthma, allergic rhinitis, atopic dermatitis, urticaria, cardiovascular disease, hypertension and diabetes mellitus affect mood by generating stress, anxiety and depression, all of which negatively influence immune system function and regulation. For example, asthma was historically referred to as “nervous asthma” in relation to living with a histrionic mother, and atopic dermatitis was referred to as “neurodermatitis.”

This review seeks to gather knowledge and the main clinical implications from the field of psychoneuroimmunoendocrinology.

Psychoneuroimmunoendocrinology

Psychoneuroimmunoendocrinology is the study of the interaction between the psyche, neural function, endocrine function and immune responses. These systems can interact through two pathways: changes in neural and endocrine functions that alter immune responses or stimulation of immune responses that modify the functionality of the endocrine system and the CNS. Behavioral processes are able to initiate both pathways, which leads to altered behavior in an individual [1]. Interactions between these various systems regulate a variety of physiological processes, and their normal interaction helps to reduce the vulnerability of individuals to certain diseases [2, 3]. One aim of psychoneuroimmunoendocrinology is to apply medical knowledge to different psychological disorders (e.g., depression), neurological conditions (e.g., dementia), immune disorders (e.g., autoimmune diseases) and neoplastic diseases [4].

Background and origin of psychoneuroimmunoendocrinology

The theory of “general adaptation syndrome” proposed in 1936 relates stress with cortico-adrenal secretion and accounts for the protective effects of adrenal extracts on stress [5]. Subsequently, Solomon et al., introduced a “speculative theory”, later known as psychoimmunology, and following the introduction of this theory, Ader and Cohen published their work on classical conditioning of immune functions entitled “Behavioral conditioning of immunosuppression”, in which they proposed a functional link between the immune system and the nervous system such that the immune response generates cytokines that stimulate the CNS [6, 7]. This stimulation of the brain activates the hypothalamic-pituitary-adrenal axis, which in turn suppresses the immune response through the secretion of glucocorticoids [8]. Accumulating evidence since 1980 has established the mechanism by which thoughts, emotions and behavior modulate and mediate endocrine and immune functions [7].

Pathophysiology of the psychoneuroendocrine axis

The presence of cellular receptors in the nervous, endocrine and immune systems allows the reception of information from other systems via chemical messengers. Under normal conditions, these three systems interact to establish a homeostatic balance [4, 9] that promotes adequate health and prepares the body for constant struggle against various diseases. The loss of this balance represents an interruption in the processes of interaction among these four systems, resulting in the onset of symptoms that characterize a pathogenic state. Many factors, such as heredity, environment, personality traits, emotions and lifestyles, influence these interactions. Whether the stress generated by psychiatric disorders such as depression and anxiety, behavior disorders, daily hassles, and changes in the environment helps or impairs the control of chronic inflammatory diseases remains under debate. It is common to observe people who thrive in environments or situations of high stress as well as people whose health is negatively affected by such stress [7].

Although no specific atopic personality profile has been established, growing knowledge of the nervous system supports new findings concerning the interaction between neuroimmunological and epigenetic factors. The skin and nervous system share a common origin: the ectoderm. Any factor that plays a neurological role can be observed in keratinocytes, fibroblasts, wandering or resident cells (mast cells, Langerhans cells), or stem or transient cells (lymphocytes, neutrophils and monocytes) of the skin. Thus, primitive defense responses such as inflammation and stress may modulate endocrine, dermatological and neurological responses [9, 10].

Stress modulates the immune response through the psychoneuroimmunoendocrine pathway and the hypothalamic-pituitary-adrenal axis [11] via the release of cortisol, norepinephrine, epinephrine and interferon-gamma (IFN-γ) by T lymphocytes. Increased levels of proinflammatory cytokines such as IFN-γ (T helper cell type 1 (Th1) cytokine) and a rapid but tissue-damaging cellular immune response constitute the immune system response [12]. Cortisol and catecholamines decrease the production of tumor necrosis factor-alpha (TNF-α) by antigen-presenting cells and promote Th2 responses via the release of interleukin (IL)10, IL13 and IL4 [13]. This process permits the immune system to halt acute responses but also favors allergic diseases [14, 15]. It has recently been found that epigenetic factors encourage the development of inadequate stress responses, paving the way for a chronic stress response instead of an acute stress response [10, 16, 17].

Table 1 shows a summary of different studies providing scientific relevance regarding the effect of stress on the immune system.

Table 1 Relevant studies about the influence of psychological stress on the immune system

Stress and the psychoneuroimmunoendocrine axis

In 1936, the concept of general adaptation syndrome and its phases of alarm, resistance and exhaustion in response to an aggression were first proposed [5]. Currently, consensus continues to be sought concerning the definition of stress, for which terms such as homeostatic imbalance, a discrepancy between expectations and perceptions of the environment, and allostasis are used. Allostasis is the ability to maintain a stable internal environment despite the influence of external elements, i.e., adaptation. Adaptation is not achieved when the response is ineffective or inadequate or when exposure to the agent that induces the response is prolonged, resulting in allostatic load, which is defined as wear and tear from the under- or overactivity of allostatic systems [18]. Allostatic load is increased by an overreaction of the adaptive mechanisms capable of generating a disease, transforming a protective mechanism that maintains systemic homeostasis when faced with an aggression into a highly pathogenic mechanism with a prolonged effect. Stress is defined as a real or interpreted threat to the physiological or psychological integrity of an individual that results in specific, physiological or behavioral responses seeking to restore homeostasis and whose chronicity is potentially pathogenic [19]. Castrillón et al. defined psychological stress as a pathophysiological process that occurs when an individual is faced with environmental demands that exceed his or her resources, inducing a response that involves physiological and cognitive activation of the body (CNS, endocrine system and immune system) in order to quickly and forcefully meet the demands of the situation. Therefore, the response to psychological stress is systemic in nature and has several metabolic consequences, such as increased steroid synthesis and a state of chronic inflammation [1]. The response of the body to stress involves the participation of different homeostatic regulatory systems, causing functional alterations that lead to chronic stress, which forms the basis for the development of cardiovascular, metabolic, immunologic, allergic, oncologic and psychiatric disease. An individual’s response to stress is provoked by genetic and psychological factors, which explains the large interindividual variability in the response to similar stimuli [18]. Different stressors cause distinct responses through the activation of specific neuroendocrine systems [19].

The following points are taken into account when explaining pathophysiological stress: first, the emotional, behavioral and physiological components of a stress reaction are controlled by corticotropin-releasing hormone; second, the intensity and duration of the reaction of the hypothalamic-pituitary-adrenal axis to stress are modulated by the release of glucocorticoids from the hippocampus, which is very sensitive to hippocampal neuronal activity and glucocorticoid insufficiency, and variation in the effectiveness of the brake system for hypothalamic-pituitary-adrenal axis activity likely accounts for interindividual differences in stress responses; and third, through a combination of cytokines and glucocorticoids, the reciprocal interactions between the immune system and the CNS constitute another regulatory element, and altered function of these interactions can be the origin of a pathology [20]. Chronic stress produces alterations in hippocampal neurons, resulting in memory problems. Similarly, chronic stress can suppress immune system defenses and produce a range of psychophysiological symptoms such as adrenal fatigue caused by reduced cortisol levels. Emotional distress has a direct influence on inflammatory processes due to the chronic upregulation of proinflammatory cytokines, which are direct causes of respiratory allergies, rheumatoid arthritis, fibromyalgia, obesity, metabolic syndrome, type 2 diabetes, cancer and cardiovascular diseases. In addition, depression, insomnia, and chronic fatigue syndrome are caused by a reduction in cortisol levels [21]. Such diseases are the result of a continuous process of multidirectional interactions among the frontal lobe of the brain (which perceives stress), the autonomic nervous system, the endocrine system and the immune system [18]. A better understanding of the molecular actions of cortisol in the processes of memory and learning or in sleep disorders such as insomnia would facilitate progress in the prevention and both pharmacological and psychological treatment of stress disorders for those who are predisposed to such conditions [22]. Figure 1 shows the impact of stress on the psychoneuroimmunoendocrine axis.

Fig. 1
figure 1

Stress and psychoneuroimmunoendocrinology axis. ANS: autonomic nervous system; HPA: hypothalamic-pituitary-adrenal; IL-6: interleukin 6; RAA: renin-angiotensin-aldosterone

Relationship of epigenetic factors with psychoneuroimmunoendocrine factors

Epigenetics is the study of all non-genetic factors that interfere in the determination of ontogeny or in the development of an organism from fertilization to senescence. Such factors are involved in the heritable regulation of gene expression via methylation, acetylation and phosphorylation of DNA rather than alteration of the nucleotide sequence. The concept of epigenetics was coined by Conrad Waddington in 1953 and gained importance after the human genome project in 2003 [23, 24]. Living in urban areas, resulting in greater exposure to chemicals, reduced green spaces, and the consequent limited presence of flora, fauna and microbial life, is associated with immune dysfunction in humans. Reduced contact with nature and environmental microbiota appears to be related to a range of diseases including allergy and type 1 diabetes [25, 26]. Alterations in intestinal flora influence the development of not only asthma and allergies but also other chronic and recurring inflammatory disorders, such as type 1 diabetes, inflammatory bowel disease, obesity, and even psychiatric disorders [27]. Epigenetics has transformed our understanding of the impact of the environment on our genes and health, which in turn will potentially streamline many lines of research in psychoneuroimmunology seeking to explain how environmental cues are transduced into the genome [28, 29]. In turn, the psychosocial environment can substantially change behavior and alter nervous, endocrine and immune functions.

Allergic diseases and the psychoneuroimmunoendocrine axis

A close relationship between allergic diseases and psychoneuroimmunoendocrinology exists [10, 30]. Stress negatively impacts patient quality of life, leading to development of depression, anxiety and unhealthy lifestyles along with secondary problems such as overweight and obesity, which negatively impact the control of atopic diseases [6]. Studies support this association and urge further investigation. A study of adolescents in the United States documented that atopic diseases such as asthma, allergic rhinitis and atopic dermatitis correlate with increased risk of anxiety and depression and that this risk is further increased when asthma and allergic rhinitis are concomitantly present [31]. Further research found that depressive disorders are common in individuals with asthma but that there is no correlation between the severity of asthma and the severity of depression [32]. The quality of life of adolescent patients with atopic dermatitis and underlying psychiatric disorders was also assessed: a high prevalence of anxiety and depression was found in these individuals. Studies have shown a link between quality of life and sleep loss and depression induced by atopic dermatitis [33]. Recently, the association between allergic rhinitis and psychiatric diseases such as depression and anxiety has been determined. In nine out of 11 studies, there was an association between allergic rhinitis and anxiety, and in ten out of 12 studies, there was an association of depressive disorder with allergic rhinitis [34]. Patients with attention deficit/hyperactivity disorder have a higher incidence of asthma, allergic rhinitis and atopic dermatitis than the general population. Children with atopic diseases are exposed to higher levels of inflammatory cytokines that are released due to an allergic response, and these cytokines can cross the blood–brain barrier and activate neuroimmunological mechanisms involved in emotions and behavior. Furthermore, activation in regions of the prefrontal cortex, potentially due to exaggerated and sustained release of inflammatory mediators, has been found. Another possible hypothesis explaining the relationship between these two diseases is based on the finding that allergic rhinitis is often associated with sleep disturbance, which may cause symptoms of daytime fatigue, inattention, irritability and impulsivity, which are in turn components of clinical attention deficit/hyperactivity disorder and its associated pathologies [35]. Urticaria occurs frequently in patients with psychiatric problems and emotional distress. Staubach P et al., found that 48 percent of patients with chronic spontaneous urticaria have at least one mental disorder; anxiety was the primary associated pathology, but depression and somatization disorders were also found [33, 36].

There is a relationship between obesity and allergic diseases. Adipokines, which are fat proteins that function as cytokines, chemokines and cytokine receptors have an important role in that relationship. At present, most studies on obesity, allergic diseases and asthma are based on the inflammatory and metabolic roles of leptin and adiponectin. Adiponectin is an anti-inflammatory protein that inhibits IL6, the transcription factor NFκB and TNF-α and that increases the concentration of IL1 and IL10. Adiponectin levels are decreased in obese people due to necrosis of fat tissue resulting from hypoxia, which causes infiltration of polymorphonuclear cells and macrophages that secrete IL6 and TNF-α and inhibit the synthesis of adiponectin [37]. Lectin is a proinflammatory protein that promotes the release of IL6 and TNF-α, decreases the activity of regulatory T cells, promotes Th1 lymphocyte activity and increases the levels of IFN-γ [38, 39].

There is a strong positive association between asthma incidence and lectin levels in prepubescent males and postmenopausal women. Obesity reduces progesterone levels in women, which lowers the levels of β2 adrenergic receptors, decreasing the relaxation of muscle in the respiratory tract [40]. The concentrations of both total and specific IgE in children and adolescents with allergic symptoms are higher among those who are overweight or obese [41].

Vitamin D deficiency is more common in the obese population, in whom there is an inverse relationship between serum vitamin D levels and the degree of obesity. Vitamin D has also been shown to skew T cells toward a less inflammatory state. For instance, 1,25(OH)2D3 decreases T cell-mediated IFN-γ production while increasing IL4 production [42, 43]. Both the generation and immunosuppressive capacity of Foxp3 + CD4+ regulatory T cells are increased by 1,25(OH)2D3 [44]. Moreover, recent studies showed that production of the inflammatory cytokine IL17 by T cells is prevented by 1,25(OH)2D3 [43, 45]. In line with these results, other groups have documented that the development of Th17 cells is negatively modulated by 1,25(OH)2D3 [46]. Production of IL21, IL22 and IL17 is also inhibited by physiologically relevant doses of 1,25(OH)2D3 in Th17-skewed T cells; this evidence suggests that principal changes in transcription are driven by the vitamin D receptor-transcription factor complex [43].

At the same time, vitamin D deficiency is associated with a decrease in immune cell proliferation as well as synthesis of cytokines, including IL1, IL2, IL6 and IL12, TNF-α and IFN-γ. These cytokines, which are upregulated in patients with obesity and metabolic syndrome, decrease the serum concentrations of vitamin D. Thus, it has been presumed that in overweight patients, as the amount of visceral adipose tissue increases, the kidnapping of vitamin D by adipose tissue increases. Secondarily, it is proposed that vitamin D deficiency or insufficiency is responsible for insulin resistance and thereby promotes metabolic syndrome [47]. Vitamin D deficiency has been associated with increased airway hyperresponsiveness, decreased lung function, reduced asthma control, and resistance to steroids [48]. A recently conducted study of treated asthmatic children showed that 84.2% of children with asthma had low levels of vitamin D. In that study, overweight was an important risk factor for vitamin D deficiency and insufficiency [49]. Another study found that vitamin D deficiency is associated with an increased risk of severe asthma in asthmatic adults (odds ratio [OR], 5.04; 95% confidence interval [CI]: 1.23 to 20.72; p = 0.02) and that high levels of vitamin D are related to a lower risk of hospitalization or emergency department visitation in the past year (OR, 0.90; 95% CI, 0.84 to 0.98; p = 0.04) [50]. Obesity and overweight have also been associated with increased residual capacity and increased risk of asthma. It has been observed that children with asthma are at an increased risk of exacerbations as well as uncontrolled asthma [51, 52]. It has also been shown that there is an association between low vitamin D levels, physical inactivity and high BMI [53]. Alternatively, vitamin D may reduce asthma severity and improve asthma control [54].

The psychoneuroimmunoendocrine axis and its relationship to other relevant diseases

Based on the pathophysiological mechanisms described above, the psychoneuroimmunoendocrine axis has been related to neuropsychiatric diseases such as depression [4, 55,56,57] and schizophrenia [56, 58,59,60,61], metabolic syndrome [62, 63], rheumatologic and autoimmune diseases [64,65,66,67,68,69,70,71,72], irritable bowel syndrome [73, 74], periodontal disease [75, 76] and neoplastic diseases [62, 77], and these relationships warrant significant attention. Psychoneuroimmunology represents the challenge of health professionals to achieve multidisciplinary management of each of these pathologies.

Psychoneuroimmunology and the naturalistic model

We propose a new medical model that has been described to be based on the concept of holistic medicine, in which biological, psychological, social and environmental aspects of the health-disease process are taken into account in the recommendation of a revised lifestyle. Through allostasis, the autonomic nervous system, the hypothalamic-pituitary-adrenal axis, the cardiovascular system, the immune system, the endocrine system and metabolism protect the body by preparing these systems to address both internal and external stress. This concept of allostasis complements the concept of stress. Allostasis represents the active adaptation process involving the production of mediators such as adrenal steroids, catecholamines, cytokines, neurotransmitters and other factors. After suffering chronic stress, adaptation responses or allostatic responses are initiated in the body. Inadequate or excessive responses following repeated stressful situations lead to allostatic load, which is the “price paid by the organism” for being forced to adapt to psychosocial or physical adversity. Thus, allostatic load constitutes the cumulative wear and tear resulting from chronic hyperactivity as an adaptation to the constant demands of life. The response to stress is physical, mental and behavioral and depends on basic personality as well as social, cultural, environmental and genetic factors. A new medical paradigm of health promotion and disease prevention is very important, as this paradigm supports lifestyle changes that increase resilience to stress and augment immune system defenses [78].

Psychoneuroimmunology, education and stress management strategies

Health education must consider the need to educate people regarding their potential and shortcomings in assuming their own identity. Another contribution of health education is to orient people regarding the management of emotions in order to facilitate the appropriate channeling and expression of emotions, which is a form of disease prevention and, consequently, a reflection of health and wellbeing.

The discipline of health education has the major challenge of establishing principles and methodologies that enable people to learn healthy practices and lifestyles so as to enhance their capacity for resilience. In addition, health education seeks to develop and promote the process of addressing struggles or mishaps of life and of resisting, overcoming and transforming adversity in order to emerge strengthened or even renewed. The development of fundamental strategies for the prevention of disease and the recovery of health through health education interventions results in positive adaptation in contexts of great adversity. In addition, health education interventions should help people learn to take measures that enhance their ability to combat disease and that properly harmonize and balance mind-body function. Health promotion strategies should be directed toward prevention and resolution of health problems and toward improving quality of life [79].

As mentioned above, lifestyle changes that increase resilience to stress and enhance immune system defenses are indispensable. Adequate daily rest; a diet that decreases oxidative stress, including daily consumption of fruits, vegetables, legumes, essential fatty acids and trace elements; and physical exercises that activate the immune system, such as breathing exercises that increase breathing capacity, and elimination of cigarette, drug and alcohol use are among the lifestyle changes to be considered. In addition, focusing on psychological aspects such as tracing life goals, being flexible, maintaining harmonious communication with others, having a consistent attitude in life, optimism and proper management of emotions, can also help with stress management [80].

Diet appears to play an important role in stress management. Relations of multivitamins and minerals with stress have been described: the main identified antistress drugs contain vitamins E, B1, B2, B3, B5, B6, B12, and C, folic acid and the minerals zinc and iron [81]. Omega-3 fatty acids are very important for the functioning of the human brain. Poor intake of these acids induces several alterations in neurotransmission that can cause diverse psychiatric disorders, including schizophrenia and major depression. It has been observed that patients with psychiatric disorders who use fatty acid supplements exhibit a significant improvement in their symptoms. In addition, omega-3 fatty acids have been shown to be useful in decreasing antisocial behavior, hostility and aggressiveness in patients who are exposed to a psychologically stressful environment. Therefore, supplements containing omega-3 fatty acids can reduce such behaviors [82].

Exercise can be an effective stress management strategy and should be recommended for addressing acute, episodic acute, and chronic stress. One advantage of incorporating exercise with other stress management techniques is the psychological and physical beneficial effects of exercise. However, it is important to remember that exercise is only one component of a stress management program. Even though exercise may be effective in helping a person feel calmer, this change will not resolve the main triggers of chronic stress. It may be necessary to refer people suffering from chronic stress to professionals who can help them cope with their stressors [83]. Research on exercise and stress has typically focused on aerobic exercise. For instance, it has been reported that patients feel calmer after 20 to 30 min of aerobic exercise and that the calming effect of exercise can last for several hours afterwards. Recently, there has been an increase in the amount of research examining the role of body-mind types of exercise, such as yoga and Tai Chi in reducing stress. Nevertheless, there is limited research on the role of resistance exercise in managing stress [83]. Studies of humans and animal models have shown that being physically active improves the ability of the body to handle stress due to changes in hormonal responses and that exercise results in actions of brain neurotransmitters, such as dopamine and serotonin, that affect the body, state of mind and behavior. Additionally, exercise may serve as a time away or release from stressors. In a study of women attending a university who reported that studying was their main stressor, performing a constant exercise activity without performing a study activity and resting while exercising had a greater calming effect than quiet rest [84]. Recent publications on yoga or Tai Chi indicate that these types of mental exercise can be effective in reducing stress. Authors have suggested that the results should be viewed with caution because the quality of the studies varied [85, 86]. The decrease in stress reported in one review was similar to or greater than the reduction in other types of commonly used stress management strategies [87]. Lack of time is the limitation to performing exercise most commonly expressed by individuals. Lack of motivation, tiredness, and poor sleep and eating habits are additional factors associated with stress that can negatively affect compliance with an exercise regime [88].

Acupuncture may be effective in the treatment of chronic stress symptoms [89]. The main investigative findings concerning the effects of acupuncture on stress are outlined in Table 2.

Table 2 Acupuncture as a stress management strategy: randomized controlled trials

Mindfulness, a new therapeutic model proposed for the management of chronic stress, consists of an individual’s awareness of and attention to his or her symptoms of emotional distress experienced under chronic stress. This strategy facilitates therapies and enables the modifications necessary to improve lifestyle. This intervention is practiced by Manolete S. Moscoso at the University of South Florida. The purpose of this therapeutic intervention program is to instruct the individual in the relaxation response, reduce the level of chronic stress and change patterns of self-destructive behavior, obtaining an immune and neuroendocrine benefit that promotes the restoration of health and helps control the symptoms caused by medical treatments, which allows patients experiencing severe depression to counter the recurrence of this disease. Mindfulness allows focus and consciousness in the body through breathing, in the mind through thought, and the environment through the senses. The belief of “living on the run” from stress and emotional pain through daily life experiences contributes to fear, tension, anxiety, worry, anger and hostility. When behavior is modified in response to the difficulties of life and when it is understood that pain and pleasure are genuinely human experiences, an individual can achieve an adequate level of acceptance and peace [18, 62].

Conclusions

Diseases are the result of an alteration at the bio-psycho-social level that can indicate lifestyle changes that should be made in addition to appropriate medical management and treatment. Emotions and stress significantly affect health and one’s susceptibility to a pathology, as well as one’s ability to recover from an illness. Psychoneuroimmunology should provide knowledge about the biological dynamics of conventional and alternative medicines for fighting disease. The psychoneuroimmunological axis comprises several disease-producing mechanisms in which different disciplines of medicine interact, implying the need for an integrative approach. The science of psychoneuroimmunology must go hand in hand with health education and the promotion of healthy lifestyles in order to attain patient health.

Abbreviations

CNS:

Central nervous system

CPR:

C-reactive protein

IFN-γ:

Interferon-gamma

IL:

Interleukin

NK:

Natural killer

TNF-α:

Tumor necrosis factor-alpha

References

  1. Castrillón E. Estrés académico y sus manifestaciones inmunológicas: La evidencia de la psico-neuroendocrino-inmunología. Salut Sci Spiritus. 2015;I(1):16–28.

    Google Scholar 

  2. De González T. Psiconeuroinmunoendocrinología, emociones y enfermedad. Una revisión.S. MedULA. 2009;18(2):155.

    Google Scholar 

  3. Intebi A. The psychoneuroimmunoendocrinology and its importance in modern medicine. Rev Méd-Cient “Luz Vida”. 2012;3(1):71–2.

    Google Scholar 

  4. Nemeroff C. Psychoneuroimmunoendocrinology: The biological basis of mind-body physiology and pathophysiology. Depress Anxiety. 2013;30(4):285–7. doi:10.1002/da.22110.

    Article  PubMed  Google Scholar 

  5. Szabo S, Tache Y, Somogyi A. The legacy of Hans Selye and the origins of stress research: a retrospective 75 years after his landmark brief “letter” to the editor of nature. Stress. 2012;15(5):472–8. doi:10.3109/10253890.2012.710919.

    Article  CAS  PubMed  Google Scholar 

  6. Marshall J. The adverse effects of psychological stress on immunoregulatory balance: applications to human inflammatory diseases. Immunol Allergy Clin North Am. 2011:1–8. doi:10.1016/j.iac.2010.09.013.

  7. Ochoa J. Psiconeuroendocrinología un modelo integrador y explicativo del estrés laboral. Univ San Buenaventura – Cali Fac Psicol Santiago Cali. 2014.

  8. Besedovsky H, Sorkin E. Network of immune-neuroendocrine interactions. Clin Exp Immunol. 1977;27(1):1–12.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Pittman Q. A Neuro-Endocrine-Immune Symphony. J Neuroendocrinol. 2011;23(12):1296–7. doi:10.1111/j.1365-2826.2011.02176.x.

    Article  PubMed  Google Scholar 

  10. Liezmann C, Klapp B, Peters E. Stress, atopy and allergy: A re-evaluation from a psychoneuroimmunologic persepective. Dermatoendocrinol. 2011;3(1):37–40. doi:10.4161/derm.3.1.14618.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Marshall G. Neuroendocrine mechanisms of immune dysregulation: applications to allergy and asthma. Ann Allergy Asthma Immunol. 2004;93(2 Suppl 1):S11–7.

    Article  PubMed  Google Scholar 

  12. Buske-Kirschbaum, A. et al. Endocrine stress responses in TH1-mediated chronic inflammatory skin disease (psoriasis vulgaris)—do they parallel stress-induced endocrine changes in TH2-mediated inflammatory dermatoses (atopic dermatitis)?. Psychoneuroendocrinology. 2006;31(4)439–46.

  13. Marshall G, Agarwal S. Stress, immune regulation, and immunity: applications for asthma. Allergy Asthma Proc. 2000;21(4):241–6.

    Article  PubMed  Google Scholar 

  14. Elenkov I, Chrousos G. Stress hormones, proinflammatory and antiinflammatory cytokines, and autoimmunity. Ann N Y Acad Sci. 2002;966(1):290–303.

    Article  CAS  PubMed  Google Scholar 

  15. Dave N, Xiang L, Rehm K, et al. Stress and Allergic Diseases. Immunol Allergy Clin North Am. 2011;31(1):55–68. doi:10.1016/j.iac.2010.09.009.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Branchi I, Francia N, Alleva E. Epigenetic control of neurobehavioural plasticity: the role of neurotrophins. Behav Pharmacol. 2004;15(5–6):353–62.

    Article  CAS  PubMed  Google Scholar 

  17. Weaver IC, Cervoni N, Champagne FA, D’Alessio AC, Sharma S, Seckl JR, Dymov S, Szyf M, Meaney MJ. Epigenetic programming by maternal behavior. Nat Neurosci. 2004;7(8):847–54.

    Article  CAS  PubMed  Google Scholar 

  18. Moscoso M. El estrés crónico y la Terapia Cognitiva Centrada en Mindfulness: Una nueva dimensión en psiconeuroinmunología. Persona. 2015;13:11–29.

    Google Scholar 

  19. Plá J, Rodríguez J. Aspectos psicológicos de las enfermedades cardiovasculares. Editorial Acción Médica. Sociedad Española de Cardiología; 2006.

  20. Duval F, González F. Neurobiología del estrés Neurobiology of stress. Rev Chil Neuro Psiquiat. 2010;48(4):307–18. doi:10.4067/S0717-92272010000500006.

    Article  Google Scholar 

  21. Ogłodek E, Szota A, Just M, et al. The role of the neuroendocrine and immune systems in the pathogenesis of depression. Pharmacol Reports. 2014;66(5):776–81. doi:10.1016/j.pharep.2014.04.009.

    Article  CAS  Google Scholar 

  22. Cortés C. Estrés y cortisol: implicaciones en la memoria y el sueño, Elem 82. 2011. p. 33–8.

    Google Scholar 

  23. Haahtela T, Holgate S, Pawankar R, et al. The biodiversity hypothesis and allergic disease: world allergy organization position statement. World Allergy Organ J. 2013;6(1):3. doi:10.1186/1939-4551-6-3.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Prescott S, Saffery R. The role of epigenetic dysregulation in the epidemic of allergic disease. Clin Epigenetics. 2011;2(2):223–32. doi:10.1007/s13148-011-0028-4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Akdis M, Akdis C. Therapeutic manipulation of immune tolerance in allergic disease. Nat Rev Drug Discov. 2009;8(8):645–60. doi:10.1038/nrd2653.

    Article  CAS  PubMed  Google Scholar 

  26. Chatenoud L, You S, Okada H, et al. 99th Dahlem Conference on Infection, Inflammation and Chronic Inflammatory Disorders: Immune therapies of type 1 diabetes: New opportunities based on the hygiene hypothesis. Clin Exp Immunol. 2010;160:106–12. doi:10.1111/j.1365-2249.2010.04125.x.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Bienenstock J. Psycho-neuroimmunology and the intestinal microbiota: clinical observations and basic mechanisms. Clin Exp Immunol. 2010;160:85–91.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Feinberg A. Epigenetics at the epicenter of modern medicine. JAMA. 2008;299(11):1345–50. doi:10.1001/jama.299.11.1345.

    Article  CAS  PubMed  Google Scholar 

  29. Mathews H, Janusek L. Epigenetics and psychoneuroimmunology: Mechanisms and models. Brain Behav Immun. 2011;25(1):25–39. doi:10.1016/j.bbi.2010.08.009.

    Article  PubMed  Google Scholar 

  30. Lee M, Son B, Park Y, et al. The relationship between psychosocial stress and allergic disease among children and adolescents in Gwangyang Bay, Korea. J Prev Med Public Heal. 2012;45(6):374–80. doi:10.3961/jpmph.2012.45.6.374.

    Article  Google Scholar 

  31. Slattery M, Essex M. Specificity in the association of anxiety, depression, and atopic disorders in a community sample of adolescents. J Psychiatr Res. 2011;45(6):788–95. doi:10.1016/j.jpsychires.2010.11.003.

    Article  PubMed  Google Scholar 

  32. Kumar P, Misra S, Kundu S, et al. Asthma diagnosis and treatment-1024. Prevalence of depression among asthma patients and effects of asthma control on severity of depression. World Allergy Organ J. 2013;6:23.

    Article  Google Scholar 

  33. Staubach P, Dechene M, Metz M, et al. High prevalence of mental disorders and emotional distress in patients with chronic spontaneous urticaria. Acta Derm Venereol. 2011;91(5):557–61. doi:10.2340/00015555-1109.

    Article  PubMed  Google Scholar 

  34. Sansone R, Sansone L. Allergic rhinitis: Relationships with anxiety and mood syndromes. Innov Clin Neurosci. 2011;8(7):12–7. doi:10.1007/978-0-387-49979-6_21.

    Google Scholar 

  35. Treviño C, Juárez M, González S, et al. Association between attentiondeficit/hyperactivity disorder and allergic rhinitis: a review: a review. Arch Med. 2015;11(1):9.

    Google Scholar 

  36. Ozkan M, Oflaz S, Kocaman N, et al. Psychiatric morbidity and quality of life in patients with chronic idiopathic urticaria. Ann Allergy Asthma Immunol. 2007;99(1):29–33. doi:10.1016/S10811206(10)60617-5.

    Article  PubMed  Google Scholar 

  37. Luo X, Xiang J, Dong X, et al. Association between obesity and atopic disorders in Chinese adults: an individually matched case–control study. BMC Public Health. 2013;13:12. doi:10.1186/1471-2458-13-12.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Cojocaru M, Cojocaru I, Silosi I, Rogoz S. Role of leptin in autoimmune diseases. Maedica (Buchar). 2013;8:68.

    Google Scholar 

  39. Matarese G. Leptin and the immune system: how nutritional status influences the immune response. Eur Cytokine Netw. 2000;11(1):7–14.

    CAS  PubMed  Google Scholar 

  40. Sood A. Sex differences: implications for the obesity-asthma association. Exerc Sport Sci Rev. 2011;39(1):48–56. doi:10.1097/JES.0b013e318201f0c4.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Visness C, London S, Daniels J et al. Association of obesity with IgE levels and allergy symptoms in children and adolescents: Results from the National Health and Nutrition Examination Survey 2005–2006. J Allergy Clin Immunol. 2009;123(5). doi:10.1016/j.jaci.2008.12.1126.

  42. Mahon B, Wittke A, Weaver V, et al. The targets of vitamin D depend on the differentiation and activation status of CD4 positive T cells. J Cell Biochem. 2003;89(5):922–32.

    Article  CAS  PubMed  Google Scholar 

  43. Weeres M, Robien K, Ahn Y, et al. The Effects of 1,25 Dihydroxyvitamin D3 (1,25(OH)2D3) on In Vitro Human Natural Killer Cell Development From Hematopoietic Stem Cells. J Immunol. 2014;193(7):3456–62. doi:10.4049/jimmunol.1400698.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Dimeloe S, Nanzer A, Ryanna K, et al. Regulatory T cells, inflammation and the allergic response-The role of glucocorticoids and Vitamin D. J Steroid Biochem Mol Biol. 2010;120(2–3):86–95.

    Article  CAS  PubMed  Google Scholar 

  45. Colin E, Asmawidjaja P, van Hamburg J, et al. 1,25-dihydroxyvitamin D3 modulates Th17 polarization and interleukin-22 expression by memory T cells from patients with early rheumatoid arthritis. Arthritis Rheum. 2010;62(1):132–42.

    Article  CAS  PubMed  Google Scholar 

  46. Ikeda U, Wakita D, Ohkuri T, et al. α,25-Dihydroxyvitamin D3 and all-trans retinoic acid synergistically inhibit the differentiation and expansion of Th17 cells. Immunol Lett. 2010;134(1):7–16.

    Article  CAS  PubMed  Google Scholar 

  47. García M, Luna L, Akaki J, et al. Hipovitaminosis D y resistencia a la insulina en obesidad. Med Int Mex. 2012;28(1):21–31.

    Google Scholar 

  48. Sandhu M, Casale T. The role of vitamin D in asthma. Ann Allergy Asthma Immunol. 2010;105(3):191–2. doi:10.1016/j.anai.2010.01.013. 217.

    Article  CAS  PubMed  Google Scholar 

  49. Yong R. Niveles de 1.25 dihidroxivitamina D3 y su relación con el control del asma en niños de 6 a 12 años de edad. 2015.

    Google Scholar 

  50. Montero F, Sedó G, Ramos A. Vitamin d insufficiency and asthma severity in adults from costa rica. Allergy, Asthma Immunol Res. 2013;5(5):283–8. doi:10.4168/aair.2013.5.5.283.

    Article  CAS  Google Scholar 

  51. Melamed M, Kumar J. Low levels of 25-hydroxyvitamin D in the pediatric populations: prevalence and clinical outcomes. Ped Health. 2010;4(1):89–97.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Vázquez F, Morales J, Crodova J, et al. Association between obesity and asthma in preschool Mexican children. Sci World J. 2010;10:1339–46. doi:10.1100/tsw.2010.134.

    Article  Google Scholar 

  53. Thacher T, Clarke B. Vitamin D insufficiency. Mayo Clin Proc. 2011;86(1):50–60. doi:10.4065/mcp.2010.0567.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Brehm J, Celedón J, Soto M, et al. Serum Vitamin D Levels and Markers of Severity of Childhood Asthma in Costa Rica. Am J Respir Crit Care Med. 2009;179(9):765–71. doi:10.1164/rccm.200808-1361OC.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Castillo J, Barrera D, Pérez J, et al. Depresión y diabetes: de la epidemiología a la neurobiología. Rev Neurol. 2010;51(6):347–59.

    Google Scholar 

  56. Meyer U, Schwarz M, Müller N. Inflammatory processes in schizophrenia: A promising neuroimmunological target for the treatment of negative/cognitive symptoms and beyond. Pharmacol Ther. 2011;132(1):96–110. doi:10.1016/j.pharmthera.2011.06.003.

    Article  CAS  PubMed  Google Scholar 

  57. Marsiglia I. La psiconeuroinmunología: Nueva visión sobre la salud y la enfermedad. Gac Méd Caracas. 2009;117(3):183–95.

    Google Scholar 

  58. Benros M, Mortensen P, Eaton W. Autoimmune diseases and infections as risk factors for schizophrenia. Ann NY Acad Sci. 2012;1262(1):56–66. doi:10.1111/j.1749-6632.2012.06638.x.

    Article  PubMed  Google Scholar 

  59. Benros M, Nielsen P, Nordentoft M, et al. Autoimmune Diseases and Severe Infections as Risk Factors for Schizophrenia: A 30-Year Population-Based Register Study. Am J Psychiatry. 2011;168(12):1303–10. doi:10.1176/appi.ajp.2011.11030516.

    Article  PubMed  Google Scholar 

  60. Benros M, Waltoft B, Nordentoft M, et al. Autoimmune Diseases and Severe Infections as Risk Factors for Mood Disorders. JAMA Psychiatry. 2013;70(8):812. doi:10.1001/jamapsychiatry.2013.1111.

    Article  PubMed  Google Scholar 

  61. Robaina J, Contreras R, Morales E, et al. Niveles plasmáticos de triptófano en pacientes cubanos con esquizofrenia. Rev Biomed. 2014;25(3):111–8.

    Google Scholar 

  62. Moscoso M. El estudio científico del estrés crónico en neurociencias y psicooncología. Pers Rev la Fac Psicol. 2014;17:53–70.

    Google Scholar 

  63. Mazzotta V. Depresión y Síndrome metabólico. Rev Argentina Clínica Neuropsiquiátrica. 2011;16(4):396–424.

    Google Scholar 

  64. Deckx N, Lee W, Berneman Z, Cools N. Neuroendocrine immunoregulation in multiple sclerosis. Clin Dev Immunol. 2013;2013. doi:10.1155/2013/705232.

  65. Tzioufas A, Tsonis J, Moutsopoulos H. Neuroendocrine dysfunction in Sjogren’s syndrome. Neuroimmunomodulation. 2008;15(1):37–45. doi:10.1159/000135622.

    Article  CAS  PubMed  Google Scholar 

  66. Jara L. La interacción inmuno-neuro-endocrina en enfermedades reumáticas autoinmunes: un nuevo desafío para el reumatólogo. Reum Clin. 2011;7(2):85–7.

    Article  Google Scholar 

  67. Jara L, Navarro C, Medina G, et al. Immune-Neuroendocrine Interactions and Autoimmune Diseases. Clin Dev Immunol. 2006;13(2–4):109–23. doi:10.1080/17402520600877059.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Masi A, Aldag J, Jacobs J. Rheumatoid arthritis: Neuroendocrine immune integrated physiopathogenetic perspectives and therapy. Rheum Dis Clin North Am. 2005;31(1):131–60. doi:10.1016/j.rdc.2004.09.006.

    Article  PubMed  Google Scholar 

  69. Straub R, Bijlsma J, Masi A, et al. Role of neuroendocrine and neuroimmune mechanisms in chronic inflammatory rheumatic diseases-The 10-year update. Semin Arthritis Rheum. 2013;43(3):392–404. doi:10.1016/j.semarthrit.2013.04.008.

    Article  CAS  PubMed  Google Scholar 

  70. Jensen E, Untersmayr E. Gender-medicine aspects in allergology. Allergy Eur J Allergy Clin Immunol. 2008;63(5):610–5. doi:10.1111/j.1398-9995.2008.01645.x.

    Article  Google Scholar 

  71. Sánchez P, de Lamo M, Peiró G. Psicobioquimica (Estrés, Ansiedad y Depresión) en Fibromialgia. C Psicobioquímica. 2014;3:55–68.

    Google Scholar 

  72. Miniati A, Weng Z, Zhang B, et al. Neuro-immuno-endocrine processes in vitiligo pathogenesis. Int J Immunopathol Pharmacol. 2012;25(1):1–7.

    Article  CAS  PubMed  Google Scholar 

  73. Sebastián J, Sebastián B. Psychoneuroimmunology in irritable bowel syndrome. Gastroenterol y Hepatol. 2015;38(7):413–6. doi:10.1016/j.gastrohep.2015.01.005.

    Google Scholar 

  74. Ortiz M, Saz P, Sebastián J. Irritable bowel syndrome immune hypothesis. Part one: the role of lymphocytes and mast cells. Rev Esp Enferm Dig. 2010;102(11):637–47. doi:10.4321/S1130-01082010001100004.

    Google Scholar 

  75. Rettori E, De Laurentiis A, Dees W, et al. Host neuro- immuno-endocrine responses in periodontal disease. Curr Pharm Des. 2014;20(29):4749–59. doi:10.2174/1381612820666140130204043.

    Article  CAS  PubMed  Google Scholar 

  76. Feldman L, Goncalves L, Chacón G, et al. Relaciones entre estrés académico, apoyo social, salud mental y rendimiento académico en estudiantes universitarios venezolanos. Univ Psychol. 2008;7:739–52.

    Google Scholar 

  77. Gordon J. Neuro-immuno-endocrine considerations for cancer development and therapeutics. Semin Cancer Biol. 2008;18:149.

    Article  PubMed  Google Scholar 

  78. Rodríguez P, Rodríguez R. Psiconeuroinmunoendocrinología (PNIE), el Pensamiento Complejo y la Medicina Naturista. Med Natur. 2009;3(2):86–91.

    Google Scholar 

  79. Ortega M. La psiconeuroinmunología y la promoción de la salud. In: Universidad Nacional de Educación a Distancia (España). 2011.

    Google Scholar 

  80. Moscoso M. El estrés crónico y la Terapia Cognitiva Centrada en Mindfulness: Una nueva dimensión en psiconeuroinmunología. Persona: Universidad de Florida del Sur; 2010. p. 11–9.

    Google Scholar 

  81. Espinoza J, Cue M. Vitaminas y minerales contra el estrés. Rev Cubana Farm. 2001;35(1):74–8.

    Google Scholar 

  82. Tapia S, Alexis E. La suplementación con ácidos grasos omega-3 disminuye la agresividad, hostilidad y comportamiento antisocial. Rev Chil Nutr. 2005;32(2):95–101.

    Article  Google Scholar 

  83. Jackson E. Stress Relief: The Role of Exercise in Stress Management. ACSMs Health Fit J. 2013;17:14–9.

    Article  Google Scholar 

  84. Breus M, O’Connor P. Exercise-induced anxiolysis: a test of the “time out” hypothesis in high anxious females. Med Sci Sports Exerc. 1998;30(7):1107–12.

    Article  CAS  PubMed  Google Scholar 

  85. Gallego J, Aguilar J, Cangas J et al. Efecto de intervenciones mente/cuerpo sobre los niveles de ansiedad, estrés y depresión en futuros docentes de educación primaria: un estudio controlado. Revista de Psicodidáctica. 2016;21(1):87–101.

    Article  Google Scholar 

  86. Wang W, Zhang A, Rasmussen B, et al. The effect of Tai Chi on psychological well-being: a systematic review of randomized controlled trials. J Acupunct Meridian Stud. 2009;2(3):171–81.

    Article  PubMed  Google Scholar 

  87. Chong C, Tsunaka M, Tsang H, et al. Effects of yoga on stress management in healthy adults: a systematic review. Altern Ther Health Med. 2011;17(1):32–8.

    PubMed  Google Scholar 

  88. American Psychological Association Website. Washington (D.C.): American Psychological Association; [cited 2012 June 27]. Available from: http://www.apa.org. Accessed Oct 2015.

  89. Huang W, Howie J, Taylor A, et al. An investigation into the effectiveness of traditional Chinese acupuncture (TCA) for chronic stress in adults: a randomised controlled pilot study. Complement Ther Clin Pract. 2011;17(1):16–21. doi:10.1016/j.ctcp.2010.05.013. Epub 2010 Jun 19.

    Article  PubMed  Google Scholar 

  90. Ortega M. Educación para la salud en el ámbito laboral. Revista Española de Pedagogía. 2006;235:483–500.

    Google Scholar 

  91. Rosenthal S. 50 Ways to Prevent and Manage Stress. Cochin: McGraw Hill Contemporary Books; 2002.

    Google Scholar 

  92. Ray O. The revolutionary health science of psychoendoneuroimmunology: a new paradigm for understanding health and treating illness. Ann N Y Acad Sci. 2004;1032:35–51.

    Article  PubMed  Google Scholar 

  93. Sierra R, et al. Inmunología, estrés, depresión y cáncer. Psicooncología. 2006;3:35–48.

    Google Scholar 

  94. Sandín B. El estrés psicosocial: Conceptos y consecuencias clínicas. Madrid: Klinik; 2008.

    Google Scholar 

  95. McEwen B. Central effects of stress hormones in health and disease: Understanding the protective and damaging effects of stress and stress mediators. Eur J Pharmacol. 2008;583(2–3):174–85.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  96. Borysenko J, Borysenko M. Sobre la Psiconeuroinmunología: Cómo la mente influye sobre la salud y las enfermedades…y cómo hacer que esta influencia sea beneficiosa. Exec Health. 1983;19:1–12.

    Google Scholar 

  97. Gidron Y, Armon T, Gilutz H, Huleihel M. Psychological factors correlate meaning fully with percent-monocytes among acute coronary syndrome patients. Brain Behav Immun. 2003;17:310–5.

    Article  PubMed  Google Scholar 

  98. Ho W, Evans D, Douglas S. Substance P and Human Immuno deficiency Virus infection: Psychoneuroimmunology. CNS Spectr. 2002;7:867–74.

    Article  PubMed  Google Scholar 

  99. Monjan A, Collector M. Stress induced modulation of the inmune response. Science. 1977;196:307–8.

    Article  CAS  PubMed  Google Scholar 

  100. Fillion L, Belles M, Lemyre L, Roy R. Reliability of lymphocyte proliferation assays. Stress Med. 1994;10:43–8.

    Article  Google Scholar 

  101. Weiss J, Sundar S, Becquer K, Cierpial M. Behavioral and neural iInfluences on cellular immune responses: Effects of stress and interleukin-1. J Clin Psychiatry. 1989;50:43–53.

    PubMed  Google Scholar 

  102. Hucklebridge F, Clow A, Evans P. The relationship between salivary immunoglobulin A and cortisol: Neuroendocrine response to awakening and the diurnal cycle. Int J Psychophysiol. 1998;31:69–76.

    Article  CAS  PubMed  Google Scholar 

  103. Moynihan J, Ader R, Crota L, Schachtman T, Cohen N. The Effects of stress on the development of immunological memory following low-dose antigen priming in mice. Brain Behav Immun. 1990;4:1–2.

    Article  CAS  PubMed  Google Scholar 

  104. Croiset G, Heijnen C, Veldhuis H, De Wied R. Modulation of the immune response by emotional stress. Life Sci. 1987;40:775–82.

    Article  CAS  PubMed  Google Scholar 

  105. Shirinsky I, Shirinsky V. Social Stress Disorders and Immunity. Russ J Immunol. 2001;6:207–14.

    CAS  PubMed  Google Scholar 

  106. Belova T, Gorina N, Ivanitskaia W, Ishchenko A, Magaeva S. Structural bases of the induction of immune reactions in emotional stress. Bull Eksp Biol Med. 1988;106:191–5.

    CAS  Google Scholar 

  107. Churin A, Masnaya N, Borsuk O, Sherstoboev E. Reactions ofimmune system to immobilization stress in inbread mice of different strains. Bull Exp Biol Med. 2003;136:266–9.

    Article  CAS  PubMed  Google Scholar 

  108. De Groot J, Boersma W, Scholten J, Koolhaas J. Social stress in male mice impairs long-term antiviral immunity selectively in wounded subjects. Physiol Behav. 2002;75:277–85.

    Article  PubMed  Google Scholar 

  109. Guayerbas N, Catalan M, Víctor V, Miquel J, De la Fuente M. Relation of behavior and macrophage function to life span in a murine model of premature immunosenescense. Behav Brain Res. 2002;134:41–8.

    Article  PubMed  Google Scholar 

  110. Zelena D, Meryl Z, Foldes A, Kovacs K, Toth Z, Makara G. Role of hypothalamic inputs in maintaining pituitary-adrenal responsiveness in repeated restraint. Am J Physiol Endocrinol Metab. 2003;285:1110–7.

    Article  Google Scholar 

  111. Molina P. Noradrenergic inhibition of TNF upregulation in hemorrhagic shock. Neuroimmunomodulation. 2001;9:125–33.

    Article  CAS  PubMed  Google Scholar 

  112. Wonnacott K, Bonneau R. Effect of stress on memory cytotoxic T lymphocyte-mediated protection against herpes simplex virus Infection at mucosal sites. Brain Behav Immun. 2002;16:104–17.

    Article  CAS  PubMed  Google Scholar 

  113. Paltrinieri S, Panelli S, Comazzi S, Sartorelli F. Effect of 1–24 ACTH administration on sheep blood granulocyte functions. Vet Res. 2002;33:71–82.

    Article  CAS  PubMed  Google Scholar 

  114. Sánchez M, Cruz C. Roseta alogénica. Su aplicación en pacientes sometidos a estrés agudo. Rev Cubana Hematol Inmunol Hemoter. 1991;7:88–92.

    Google Scholar 

  115. Stowell J. Use and abuse of academic examinations in stress research. Psychosom Med. 2003;65:1055–7.

    Article  PubMed  Google Scholar 

  116. Matalka K. Neuroendocrine and cytokines-induced responses tominutes, hours and days of mental stress. Neuroendocrinol Lett. 2003;24:283–92.

    CAS  PubMed  Google Scholar 

  117. Anyanwu E, Campbell A, Jones J, Ehiri J, Akpan A. The neuro-logical significance of abnormal natural killer cell activity in chronic toxigenic mold exposures. Scientific World J. 2003;3:1128–37.

    Article  Google Scholar 

  118. Ho C, López J, Vuckovic S, Pyke C, Hockey R, Hart D. Surgical and physical stress increases circulating blood dendritic cell counts independently of monocyte counts. Blood. 2001;98:140–4.

    Article  CAS  PubMed  Google Scholar 

  119. Woiciechowsky C, Asadullah K, Nestler D, et al. Sympathetic activation triggers systemic interleukin-10 release in immunodepression induced by brain injury. Nat Med. 1998;4:768–9.

    Article  Google Scholar 

  120. Dhabhar F, McEwen B. Enhancing versus suppressive effects of stress hormones on skin immune function. Proc Natl Acad Sci. 1999;96:1059–66.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  121. Glaser R, Kiecolt-Glaser JK. Stress-induced immune dysfunction: implications for health. Nat Rev Immunol 2005;5:243–251.

  122. Levitina E. Membrane and immunological aspects of perinatal nervous system disorders in newborns. Klin Lab Diagn. 2001;12:36–7.

    Google Scholar 

  123. Ramos V, Rivero R, Piqueras J, et al. Psiconeuroinmunología: conexiones entre sistema nervioso y sistema inmune. Suma Psicológica. 2008;1(5):115–42.

    Google Scholar 

  124. Mohr D, Pelletier D. A temporal Framework for understanding the effects of the stressful life events on inflammation in patients with multiple sclerosis. Brain Behav Immun. 2006;20(1):27–36.

    Article  PubMed  Google Scholar 

  125. Selye H. A síndrome produced by diverse nocuos agents. Nature. 1936;138:32.

    Article  Google Scholar 

  126. Kay G, Tarcic N, Poltyrev T, Weinstock M. Prenatal stress depresses immune funtion in rats. Physiol Behav. 1998;63:397–402.

    Article  CAS  PubMed  Google Scholar 

  127. Spitzer C, Barnow S, Völzke H, et al. Association of posttraumatic stress disorder with low-grade elevation of C-reactive protein: Evidence from the general population. J Psychiatr Res. 2010;44:15–21. doi:10.1016/j.jpsychires.2009.06.002.

    Article  PubMed  Google Scholar 

  128. Gill J, Page G. Low levels of cortisol and sIgA, high levels of DHEA-S, and high stimulated levels of TNF-α and IL-6 women with PTSD. Brain Behav Immun. 2008;22(4):31. doi:10.1016/j.bbi.2008.04.101.

    Article  Google Scholar 

  129. Gola H, Engler H, Sommershof A, et al. Posttraumatic stress disorder is associated with an enhanced spontaneous production of pro-inflammatory cytokines by peripheral blood mononuclear cells. BMC Psychiatry. 2013;13(40):1–8. doi:10.1186/1471-244X-13-40.

    Google Scholar 

  130. Sutherland A, Alexander D, Hutchison J. Disturbance of pro-inflammatory cytokines in post-traumatic psychopathology. Cytokine. 2003;24:219–25.

    Article  CAS  PubMed  Google Scholar 

  131. von Kanel R, Hepp U, Kraemer B, et al. Evidence for low-grade systemic proinflammatory activity in patients with posttraumatic stress disorder. J Psychiatr Res. 2007;41(9):744–52. doi:10.1016/j.jpsychires.2006.06.009.

    Article  Google Scholar 

  132. von Kanel R, Hepp U, Traber R, et al. Measures of endothelial dysfunction in plasma of patients with posttraumatic stress disorder. Psychiatry Res. 2006;158:363–73. doi:10.1016/j.psychres.2006.12.003.

    Article  CAS  Google Scholar 

  133. Baker D, Ekhator N, Kasckow J. Plasma and cerebrospinal fluid interleukin-6 concentrations in posttraumatic stress disorder. Neuroimmunomodulation. 2001;9:209–17.

    Article  CAS  PubMed  Google Scholar 

  134. Maes M, Lin A, Delmeire L. Elevated serum Interleukin-6 (IL-6). And IL-6 receptor concentrations in posttraumatic stress disorder following accidental man-made traumatic events. Biol Psychiatry. 1999;45:833–9.

    Article  CAS  PubMed  Google Scholar 

  135. Newport D, Nemeroff C. Neurobiology of posttraumatic stress disorder. Curr Opin Neurobiol. 2000;10(2):211–8.

    Article  CAS  PubMed  Google Scholar 

  136. Katja G, Andelko V, Herman V, et al. Natural killer cell_cytotoxicity and lymphocyte perforin expression in veterans with posttraumatic stress disorder. Prog Neuro-Psychopharmacol Biol Psychiatry. 2010;34:597–604. doi:10.1016/j.pnpbp.2010.02.018.

    Article  CAS  Google Scholar 

  137. Pace T, Wingenfeld K, Schmidt I, et al. Increased peripheral NF-KB pathway activity in women with childhood abuse-related posttraumatic stress disorder. Brain Behav Immun. 2012;26:13–7. doi:10.1016/j.bbi.2011.07.232.

    Article  CAS  PubMed  Google Scholar 

  138. Cohen S, Miller G, Rabin B. Psychological stress and antibody response to immunization: a critical review of the human literatura. Psychosom Med. 2001;63(1):7–18.

    Article  CAS  PubMed  Google Scholar 

  139. Herbert T, Cohen S. Stress and immunity in humans: a meta-analytic review. Psychosom Med. 1993;55(4):364–79.

    Article  CAS  PubMed  Google Scholar 

  140. Montoro J, et al. Stress and allergy. J Investig Allergol Clin Immunol. 2009;19 Suppl 1:40–7.

    CAS  PubMed  Google Scholar 

  141. Wu Y, Yuan J, Feng X. Effect of acupuncture-assisted anesthesia on stress response during laparoscopic cholecystectomy in aged patients. Acupunct Moxibustion. 2011;31(2):155–7.

    CAS  Google Scholar 

  142. Kwong E, Yiu E. A preliminary study of the effect of acupuncture on emotional stress in female dysphonic speakers. J Voice. 2010;24(6):719–23. doi:10.1016/j.jvoice.2009.05.005. Epub 2010 Jan 18.

    Article  PubMed  Google Scholar 

  143. Middlekauff H, Hui K, Yu J. Acupuncture inhibits sympathetic activation during mental stress in advanced heart failure patients. J Card Fail. 2002;8(6):399–406.

    Article  PubMed  Google Scholar 

  144. Balk J, Catov J, Horn B, et al. The relationship between perceived stress, acupuncture, and pregnancy rates among IVF patients: a pilot study. Complement Ther Clin Pract. 2010;16(3):154–7. doi:10.1016/j.ctcp.2009.11.004.

    Article  PubMed  Google Scholar 

  145. Hui K, Marina O, Liu J, et al. Acupuncture, the Limbic System, and the Anticorrelated Networks of the Brain. Auton Neurosci. 2010;157:81–90.

    Article  PubMed  PubMed Central  Google Scholar 

  146. Erickson K, Voss M, Prakash R, et al. Exercise training increases size of hippocampus and improves memory. Proc Natl Acad Sci U S A. 2011;108(7):3017–22. doi:10.1073/pnas.1015950108.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  147. Kim H, Park H, Shim H, et al. The effects of acupuncture (PC6) on chronic mild stress-induced memory loss. Neurosci Lett. 2011;488(3):225–8. doi:10.1016/j.neulet.2010.09.080.

    Article  CAS  PubMed  Google Scholar 

  148. Park H, Kim H, Hahm D. Electroacupuncture to ST36 ameliorates behavioral and biochemical responses to restraint stress in rats. Neurol Res. 2010;32 Suppl 1:111–5. doi:10.1179/016164109X12537002794480.

    Article  PubMed  Google Scholar 

  149. Lee A, Fan L. Stimulation of the wrist acupuncture point P6 for preventing postoperative nausea and vomiting. Cochrane Database Syst Rev. 2009;2:CD003281. doi:10.1002/14651858.CD003281.pub3.

    Google Scholar 

  150. Cheng K. Neuroanatomical basis of acupuncture treatment for some common illnesses. Acupunct Med. 2009;27(2):61–4. doi:10.1136/aim.2009.000455.

    Article  PubMed  Google Scholar 

  151. Arranz L, Guayerbas N, Siboni L, et al. Effect of acupuncture treatment on the immune function impairment found in anxious women. Am J Chin Med. 2007;35(1):35–51.

    Article  PubMed  Google Scholar 

  152. Kavoussi B, Ross B. The neuroimmune basis of antiinflammatory acupuncture. Integr Cancer Ther. 2007;6(3):251–7.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

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Funding

This research did not receive any specific grant funding from any agency in the public, commercial, or not-for-profit sectors.

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A search of the medical literature using PubMed (free access search engine for the Medline database of the National Library of Medicine of the United States) including the years 1936 to 2016 was conducted for this review. Descriptive and experimental studies and reviews of the scientific literature were included.

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Correspondence to Sandra Nora González-Díaz.

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González-Díaz, S.N., Arias-Cruz, A., Elizondo-Villarreal, B. et al. Psychoneuroimmunoendocrinology: clinical implications. World Allergy Organ J 10, 19 (2017). https://doi.org/10.1186/s40413-017-0151-6

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