A comparative study of human endogenous retrovirus HERV-E λ 4-1 activation in autoimmune pathology

I. Goldina, E. V. Markova
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Abstract

Considering the presence of immunomodulatory properties of human endogenous retroviruses, namely (i) the ability to activate the innate immune response by HERVs nucleic acids; (ii) the antigenicity of transcriptionally competent endogenous retroviruses envelope protein molecule, which causes polyclonal activation of lymphocytes; (iii) the absence of HERVs expression and protein production in the thymus during the immune tolerance formation, which allows us to consider these proteins as autoantigens or neoantigens, it seemed relevant to investigate the association of replication-competent human endogenous retrovirus HERV-E λ 4-1 with course of some of autoimmune diseases, such as multiple sclerosis, rheumatoid arthritis and systemic lupus erythematosus. The aim of this work was a comparative study of the human endogenous retrovirus HERV-E λ 4-1 activation frequency in blood mononuclear cells in multiple sclerosis, rheumatoid arthritis, systemic lupus erythematosus, as well as in chronic nervous system non-progressive diseases and the degenerative-dystrophic disease of the musculoskeletal system. The peripheral blood mononuclear cells were isolated by the venous blood centrifugation on Ficoll density gradient of 1.078 g/cm3. Expression of the HERV-E λ 4-1 envelope gene was detected by reverse transcriptase polymerase chain reaction. It was found that the HERV-E λ 4-1 envelope gene expression frequency in the chronic non-progressive diseases of nervous system, as well as in degenerative-dystrophic joint disease, is comparable to the expression frequency in conditionally healthy individuals. However, the HERV-E λ 4-1 envelope gene expression frequency in autoimmune diseases significantly exceeded that in conditionally healthy individuals and in non-inflammatory diseases. The maximum values of expression frequency were observed in active multiple sclerosis, significantly higher than in systemic lupus erythematosus and rheumatoid arthritis in the acute stage. Moreover, the expression frequency in the remission stage of multiple sclerosis was significantly lower than in the acute stage of the relapsing-remitted course, as well as in the progredient course. Estimation of HERV-E λ 4-1 envelope gene expression frequency at different severity levels of multiple sclerosis revealed its maximum rates at III and IV-V severity levels, both in relapsing-remitting and progressive course of multiple sclerosis. Thus, activation of the human endogenous retrovirus HERV-E λ 4-1 is associated with the course of autoimmune diseases, namely multiple sclerosis, rheumatoid arthritis, and systemic lupus erythematosus; it positively correlates with the activity and severity of multiple sclerosis.
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人内源性逆转录病毒HERV-E λ 4-1在自身免疫病理中的激活比较研究
考虑到人内源性逆转录病毒存在免疫调节特性,即(i)通过herv核酸激活先天免疫反应的能力;(ii)转录能力强的内源性逆转录病毒包膜蛋白分子的抗原性,导致淋巴细胞的多克隆活化;(iii)在免疫耐受形成过程中胸腺中缺乏herv的表达和蛋白产生,这使得我们可以将这些蛋白视为自身抗原或新抗原,因此研究具有复制能力的人内源性逆转录病毒HERV-E λ 4-1与一些自身免疫性疾病(如多发性硬化症、类风湿性关节炎和系统性红斑狼疮)病程的相关性似乎是相关的。这项工作的目的是比较研究人类内源性逆转录病毒HERV-E λ 4-1在多发性硬化症、类风湿性关节炎、系统性红斑狼疮以及慢性神经系统非进行性疾病和肌肉骨骼系统退行性营养不良疾病的血液单核细胞中的激活频率。静脉血在1.078 g/cm3的Ficoll密度梯度下离心分离外周血单个核细胞。逆转录聚合酶链式反应检测HERV-E λ 4-1包膜基因的表达。我们发现HERV-E λ 4-1包膜基因在慢性非进行性神经系统疾病以及退行性营养不良关节疾病中的表达频率与条件健康个体的表达频率相当。然而,HERV-E λ 4-1包膜基因在自身免疫性疾病中的表达频率明显高于条件健康个体和非炎症性疾病。在活动性多发性硬化症中表达频率最高,明显高于急性期系统性红斑狼疮和类风湿关节炎。多发性硬化症缓解期的表达频率明显低于复发缓解期的急性期和进展期的表达频率。对不同严重程度的多发性硬化症患者HERV-E λ 4-1包膜基因表达频率的估计显示,在多发性硬化症复发缓解期和进展期,HERV-E λ 4-1包膜基因在III和IV-V严重程度时的表达频率最高。因此,人内源性逆转录病毒HERV-E λ 4-1的激活与自身免疫性疾病的病程有关,即多发性硬化症、类风湿性关节炎和系统性红斑狼疮;它与多发性硬化症的活动性和严重程度呈正相关。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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