Abstract
Schizophrenia is a complex trait disorder with serious neurocognitive dysfunctions. As a neuropsychiatric disease with heterogeneous properties and various clinical manifestations, schizophrenia is influenced by many factors including gene–environment interactions and epigenetic elements. Among all of the factors, the immune system is especially important as demonstrated by the anti-inflammatory therapies. Chronic stress has been closely linked to immune responses that may enhance the levels of proinflammatory cytokines, a significant feature among schizophrenia patients. The dynamical interactions among the immune, endocrine, and nervous systems via cytokines, hormones, and neurotransmitters may be the essential mechanisms in schizophrenia with etiological implications. Neurotransmitters such as dopamine (DA) may have the key roles in bridging the interactions between the nervous and the immune systems. The functions of multiple elements in the hypothalamic–pituitary–adrenal–gonadal (HPAG) axis have been correlated to schizophrenia. The elucidation of these pathways is critical in psychoneuroimmunology (PNI) research as the common inflammatory networks may be involved in the pathological mechanisms of both depression and schizophrenia. Such understanding may contribute to patient stratification and the development of strategies in personalized, systems, and dynamical medicine.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Asevedo, E., Rizzo, L. B., Gadelha, A., Mansur, R. B., Ota, V. K., Berberian, A. A., et al. (2014). Peripheral interleukin-2 level is associated with negative symptoms and cognitive performance in schizophrenia. Physiology and Behavior, 129, 194–198.
Debnath, M., & Venkatasubramanian, G. (2013). Recent advances in psychoneuroimmunology relevant to schizophrenia therapeutics. Current Opinion in Psychiatry, 26, 433–439.
Dimitrov, D. H., Lee, S., Yantis, J., Valdez, C., Paredes, R. M., Braida, N., et al. (2013). Differential correlations between inflammatory cytokines and psychopathology in veterans with schizophrenia: Potential role for IL-17 pathway. Schizophrenia Research, 151, 29–35.
DPNI. (2016). The database of psychoneuroimmunology. Retrieved July 1, 2016, from http://pharmtao.com/health/psychoneuroimmunology-database/
Drzyzga, L., Obuchowicz, E., Marcinowska, A., & Herman, Z. S. (2006). Cytokines in schizophrenia and the effects of antipsychotic drugs. Brain, Behavior, and Immunity, 20, 532–545.
Emamian, E. S. (2012). AKT/GSK3 signaling pathway and schizophrenia. Frontiers in Molecular Neuroscience, 5, 33.
Enriquez-Barreto, L., & Morales, M. (2016). The PI3K signaling pathway as a pharmacological target in Autism related disorders and Schizophrenia. Molecular and Cellular Therapies, 4, 2.
Gadelha, A., Yonamine, C. M., Nering, M., Rizzo, L. B., Noto, C., Cogo-Moreira, H., et al. (2015). Angiotensin converting enzyme activity is positively associated with IL-17a levels in patients with schizophrenia. Psychiatry Research, 229, 702–707.
Guest, P. C., Schwarz, E., Krishnamurthy, D., Harris, L. W., Leweke, F. M., Rothermundt, M., et al. (2011). Altered levels of circulating insulin and other neuroendocrine hormones associated with the onset of schizophrenia. Psychoneuroendocrinology, 36, 1092–1096.
Miüller, N., & Schwarz, M. J. (2007). The immunological basis of glutamatergic disturbance in schizophrenia: Towards an integrated view. Journal of Neural Transmission. Supplementa, 72, 269–280.
Mizoguchi, Y., Kato, T. A., Horikawa, H., & Monji, A. (2014). Microglial intracellular Ca(2+) signaling as a target of antipsychotic actions for the treatment of schizophrenia. Frontiers in Cellular Neuroscience, 8, 370.
Moieni, M., Irwin, M. R., Jevtic, I., Breen, E. C., & Eisenberger, N. I. (2015). Inflammation impairs social cognitive processing: A randomized controlled trial of endotoxin. Brain, Behavior, and Immunity, 48, 132–138.
Müller, N., & Dursun, S. M. (2011). Schizophrenia genes, epigenetics and psychoneuroimmunology therapeutics: All make sense now? Journal of Psychopharmacology (Oxford), 25, 713–714.
Müller, N., & Schwarz, M. J. (2008). A psychoneuroimmunological perspective to Emil Kraepelins dichotomy: Schizophrenia and major depression as inflammatory CNS disorders. European Archives of Psychiatry and Clinical Neuroscience, 258(Suppl 2), 97–106.
Müller, N., Weidinger, E., Leitner, B., & Schwarz, M. J. (2015). The role of inflammation in schizophrenia. Frontiers in Neuroscience, 9, 372.
Nagano, T., Mizuno, M., Morita, K., & Nawa, H. (2015). Pathological implications of oxidative stress in patients and animal models with schizophrenia: The role of epidermal growth factor receptor signaling. Current Topics in Behavioral Neurosciences, 29, 429–446.
Pandya, C. D., Kutiyanawalla, A., & Pillai, A. (2013). BDNF-TrkB signaling and neuroprotection in schizophrenia. Asian Journal of Psychiatry, 6, 22–28.
Petitto, J. M., Meola, D., & Huang, Z. (2012). Interleukin-2 and the brain: Dissecting central versus peripheral contributions using unique mouse models. Methods in Molecular Biology, 934, 301–311.
Rolland, B., Deguil, J., Jardri, R., Cottencin, O., Thomas, P., & Bordet, R. (2013). Therapeutic prospects of PPARs in psychiatric disorders: A comprehensive review. Current Drug Targets, 14, 724–732.
Roussos, P., Katsel, P., Davis, K. L., Giakoumaki, S. G., Lencz, T., Malhotra, A. K., et al. (2013). Convergent findings for abnormalities of the NF-kB signaling pathway in schizophrenia. Neuropsychopharmacology, 38, 533–539.
Sarkar, C., Basu, B., Chakroborty, D., Dasgupta, P. S., & Basu, S. (2010). The immunoregulatory role of dopamine: An update. Brain, Behavior, and Immunity, 24, 525–528.
Singh, K. K. (2013). An emerging role for Wnt and GSK3 signaling pathways in schizophrenia. Clinical Genetics, 83, 511–517.
Sperner-Unterweger, B., & Fuchs, D. (2015). Schizophrenia and psychoneuroimmunology: An integrative view. Current Opinion in Psychiatry, 28, 201–206.
van Beveren, N. J. M., Schwarz, E., Noll, R., Guest, P. C., Meijer, C., de Haan, L., et al. (2014). Evidence for disturbed insulin and growth hormone signaling as potential risk factors in the development of schizophrenia. Translational Psychiatry, 4, e430.
Vetlugina, T. P., Lobacheva, O. A., Sergeeva, S. A., Nikitina, V. B., Nevidimova, T. I., & Semke, A. V. (2016). Adjunctive use of interferon γ inducer for treatment of patients with schizophrenia. Acta Neuropsychiatrica, 28, 149–156.
Wu, J. Q., Green, M. J., Gardiner, E. J., Tooney, P. A., Scott, R. J., Carr, V. J., et al. (2016). Altered neural signaling and immune pathways in peripheral blood mononuclear cells of schizophrenia patients with cognitive impairment: A transcriptome analysis. Brain, Behavior, and Immunity, 53, 194–206.
Yan, Q. (2014). From pharmacogenomics and systems biology to personalized care: A framework of systems and dynamical medicine. Methods in Molecular Biology, 1175, 3–17.
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2016 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Yan, Q. (2016). Psychoneuroimmunology of Schizophrenia. In: Psychoneuroimmunology. Springer, Cham. https://doi.org/10.1007/978-3-319-45111-4_7
Download citation
DOI: https://doi.org/10.1007/978-3-319-45111-4_7
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-45109-1
Online ISBN: 978-3-319-45111-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)