Sex hormones and immune system: a possible interplay in affective disorders? A systematic review.

Author(s):  
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Valeria Mondelli ◽  
Paola Dazzan ◽  
Carmine M. Pariante
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Vol 13 (4) ◽  
pp. 332-346 ◽  
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Mohammad Roufarshbaf ◽  
Sina Soheili ◽  
Farzaneh Payghambarzadeh ◽  
Mohsen Masjedi

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Ilya M Mukovozov ◽  
Lawrence E Hart

Planta Medica ◽  
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Vol 86 (11) ◽  
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Federico Visconti ◽  
Mara De Amici ◽  
Angelo Guglielmi ◽  
Costanza N. Colombo ◽  
...  

Author(s):  
Katarzyna Curzytek ◽  
Monika Leśkiewicz

AbstractSince affective disorders are considered to be underlain by the immune system malfunction, an important role in their pathophysiology is assigned to the proinflammatory mediators. Recently, chemokines, the group of chemotactic cytokines, have become a focus for basic and clinical scientists in the context of the development and treatment of brain diseases. Among them, chemokine CCL2 and its main receptor CCR2 have become candidate mediators of abnormal brain-immune system dialogue in depression. Besides the chemotactic activity, the CCL2-CCR2 axis is involved in various neurobiological processes, neurogenesis, neurotransmission, neuroinflammation, neurodegeneration, as well as neuroregeneration. Given the range of immunomodulatory possibilities that the CCL2-CCR2 pair can exert on the nervous system, its proinflammatory properties were initially thought to be a major contributor to the development of depressive disorders. However, further research suggests that the malfunctions of the nervous system are rather associated with impaired homeostatic properties manifested by the CCL2-CCR2 dyad dysfunctions. This review aims to present literature data on the action of the CCL2-CCR2 axis in the central nervous system under physiological and pathological conditions, as well as the contribution of this ligand-receptor system to the processes underlying affective disorders. Additionally, this article draws attention to the importance of the CCL2-CRR2 pathway as a potential pharmacological target with antidepressant potential.


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