Autoantibodies against Central Nervous System Antigens and the Serum Levels of IL-32 in Patients with Schizophrenia.

IF 2.2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Neuroimmunomodulation Pub Date : 2022-01-01 DOI:10.1159/000526425
Fatemeh Keshavarz, Marziyeh Soltani, Kobra Mokhtarian, Pezhman Beshkar, Jafar Majidi, Fatemeh Azadegan-Dehkordi, Maryam Anjomshoa, Nader Bagheri
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引用次数: 5

Abstract

Background: Schizophrenia is a disease of the nervous system, and immune system disorders can affect its pathogenesis. Activation of microglia, proinflammatory cytokines, disruption of the blood-brain barrier due to inflammation, activation of autoreactive B cells, and consequently the production of autoantibodies against system antigens are among the immune processes involved in neurological diseases. Interleukin-32 (IL-32) is a proinflammatory cytokine that is essential in activating innate and adaptive immune responses. This study aimed to measure the serum level of IL-32 as well as the frequency of autoantibody positivity against several nervous system antigens in patients with schizophrenia.

Material and methods: This study was conducted on 40 patients with schizophrenia and 40 healthy individuals in the control group. Serum IL-32 levels were measured by ELISA. The frequency of autoantibodies against Hu, Ri, Yo, Tr, CV2, amphiphysin, SOX1, Zic4, ITPR1, CARP, glutamic acid decarboxylase GAD, recoverin, titin, and ganglioside antigens was measured by the indirect immunofluorescence method.

Results: Serum IL-32 levels in patients with schizophrenia were significantly higher compared to the control group. The frequency of autoantibodies against GAD and RI antigens in patients with schizophrenia was significantly higher than in the control group. Autoantibodies were positive in 8 patients for GAD antigen and 5 patients for RI antigen. Autoantibodies were also positive in 2 patients for CV2, 1 patient for Hu, and 1 patient for CARP. Negative results were reported for other antigens.

Conclusion: Our findings suggest that elevated the serum IL-32 level and autoantibodies against GAD and RI antigens may be a reflection of immune system dysregulation in patients with schizophrenia.

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精神分裂症患者抗中枢神经系统抗原自身抗体与血清IL-32水平的关系
背景:精神分裂症是一种神经系统疾病,免疫系统紊乱可影响其发病机制。小胶质细胞、促炎细胞因子的激活、炎症引起的血脑屏障的破坏、自身反应性B细胞的激活,以及由此产生的针对系统抗原的自身抗体,都是涉及神经系统疾病的免疫过程。白细胞介素-32 (IL-32)是一种促炎细胞因子,在激活先天和适应性免疫反应中至关重要。本研究旨在测定精神分裂症患者血清IL-32水平以及几种神经系统抗原自身抗体阳性频率。材料与方法:本研究以40例精神分裂症患者和40例健康对照组为研究对象。ELISA法检测血清IL-32水平。采用间接免疫荧光法测定抗Hu、Ri、Yo、Tr、CV2、amphiphysin、SOX1、Zic4、ITPR1、CARP、谷氨酸脱羧酶GAD、recoverin、titin和神经节苷脂抗原的自身抗体频率。结果:精神分裂症患者血清IL-32水平明显高于对照组。精神分裂症患者抗GAD和RI抗原自身抗体的频率明显高于对照组。GAD抗原自身抗体阳性8例,RI抗原自身抗体阳性5例。2例CV2、1例Hu、1例CARP自身抗体阳性。其他抗原均呈阴性。结论:我们的研究结果提示,血清IL-32水平和抗GAD和RI抗原自身抗体的升高可能是精神分裂症患者免疫系统失调的一个反映。
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来源期刊
Neuroimmunomodulation
Neuroimmunomodulation 医学-免疫学
CiteScore
3.60
自引率
4.20%
发文量
35
审稿时长
>12 weeks
期刊介绍: The rapidly expanding area of research known as neuroimmunomodulation explores the way in which the nervous system interacts with the immune system via neural, hormonal, and paracrine actions. Encompassing both basic and clinical research, ''Neuroimmunomodulation'' reports on all aspects of these interactions. Basic investigations consider all neural and humoral networks from molecular genetics through cell regulation to integrative systems of the body. The journal also aims to clarify the basic mechanisms involved in the pathogenesis of the CNS pathology in AIDS patients and in various neurodegenerative diseases. Although primarily devoted to research articles, timely reviews are published on a regular basis.
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