Phenotypic profile of peripheral blood lymphocytes in patients with inflammatory bowel diseases

M. Zafranskaya, H. Y. Adamovich, A. U. Varabei, A. M. Starastin, D. Nizheharodava
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Abstract

Mechanisms of recognition and effector responses of immune system upon initiation and maintenance of immune-mediated inflammation and tissue damage in inflammatory bowel diseases, including Crohn’s disease and ulcerative colitis (UC), have been actively studied over recent time. Existing evidence suggests these diseases to be caused by abnormal immune response against intestinal flora microorganisms in genetically susceptible individuals. Despite available data on the features of immune disorders in ulcerative colitis and Crohn’s disease, there are still many questions about the involved minor lymphocyte subpopulations and contribution of various functionally active molecules, which play a key role in recognition and initiation of the immune response and can be considered biomarkers of a pathological process in inflammatory bowel diseases. The populations of T lymphocytes with γδT cell receptor, B1 cells and NK T lymphocytes are of greatest interest, as well as functionally active TLRs (Toll-like receptors), CD89, CD314, etc. Due to substantial progress in studying the nature of recognition and activation of the immune cells, the paper presents phenotypic and functional characteristics of major and minor subpopulations of peripheral blood lymphocytes observed in 25 patients treated at the Surgery Department of the State Institution “Minsk Regional Clinical Hospital” (Republic of Belarus) from 2018 to 2020. The detected changes in peripheral blood lymphocyte phenotype of inflammatory bowel diseases patients suggest distinct immunological profiles prevailing in the damage mechanisms in Crohn’s disease and ulcerative colitis. I.e., in Crohn’s disease patients, B1 lymphocytes with CD19+CD5+ and NK cells in combination with increased CD56bright population, as well as NK T cells with anti-inflammatory and regulatory activity are involved into genesis of the disease. In ulcerative colitis, T, B, NK lymphocytes with pro-inflammatory phenotype and T lymphocytes with γδ T cell receptor may play a pathogenetic role in maintenance of chronic inflammation. With respect to functional significance of activating receptors, the number of TLR4- и CD89-positive cells may be used for developing immunological criteria/ biomarkers of therapeutic efficacy of new drugs. Studying interactions between innate and adaptive immunity will open new perspectives in understanding immunological disorders associated with chronic gastrointestinal inflammation.
炎症性肠病患者外周血淋巴细胞的表型特征
在炎症性肠病(包括克罗恩病和溃疡性结肠炎)中,免疫系统对免疫介导的炎症和组织损伤的启动和维持的识别和效应反应机制近年来得到了积极的研究。现有证据表明,这些疾病是由遗传易感个体对肠道菌群微生物的异常免疫反应引起的。尽管有关于溃疡性结肠炎和克罗恩病免疫紊乱特征的现有数据,但关于所涉及的次要淋巴细胞亚群和各种功能活性分子的贡献仍然存在许多问题,这些分子在免疫应答的识别和启动中起着关键作用,可以被认为是炎症性肠病病理过程的生物标志物。具有γδT细胞受体的T淋巴细胞,B1细胞和NK T淋巴细胞,以及功能活跃的tlr (toll样受体),CD89, CD314等群体是最感兴趣的。由于在研究免疫细胞识别和激活的性质方面取得了实质性进展,本文介绍了2018年至2020年在白俄罗斯共和国明斯克地区临床医院国家机构外科治疗的25例患者中观察到的外周血淋巴细胞主要和次要亚群的表型和功能特征。检测到炎症性肠病患者外周血淋巴细胞表型的变化提示在克罗恩病和溃疡性结肠炎的损伤机制中普遍存在不同的免疫学特征。即在克罗恩病患者中,具有CD19+CD5+和NK细胞的B1淋巴细胞结合CD56bright群体增加,以及具有抗炎和调节活性的NK T细胞参与了疾病的发生。在溃疡性结肠炎中,具有促炎表型的T、B、NK淋巴细胞和具有γδ T细胞受体的T淋巴细胞可能在慢性炎症的维持中起病理作用。就激活受体的功能意义而言,TLR4- cd89阳性细胞的数量可能用于开发新药治疗效果的免疫学标准/生物标志物。研究先天免疫和适应性免疫之间的相互作用将为理解慢性胃肠道炎症相关的免疫紊乱开辟新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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