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单核细胞 CD86 的表达影响无症状慢性恰加斯病患者的免疫调节谱。

CD86 Expression by Monocytes Influences an Immunomodulatory Profile in Asymptomatic Patients with Chronic Chagas Disease.

机构信息

Laboratório de Biologia das Interações Celulares, Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Instituto René Rachou, Fundação Oswaldo Cruz - FIOCRUZ, Belo Horizonte, Brazil.

出版信息

Front Immunol. 2018 Mar 12;9:454. doi: 10.3389/fimmu.2018.00454. eCollection 2018.

Abstract

In the chronic phase of Chagas disease, 60% of the patients develop the asymptomatic form known as indeterminate (IND). The remaining 30% of the patients develop a life-threatening form in which digestive and/or cardiac (CARD) alterations take place. The mechanisms underlying the development of severe forms of Chagas disease remain poorly understood. It is well known that interactions between immune cells such as monocytes and lymphocytes drive immune responses. Further, the co-stimulatory molecules CD80 and CD86 expressed by monocytes and subsets induce lymphocyte activation, thereby triggering cellular immune response. Here, we revealed, for the first time, the functional-phenotypic profile of monocytes subsets in Chagas disease. Using flow cytometry, we evaluated the effect of stimulation with antigens on the expression of the co-stimulatory molecules CD80 and CD86 in different monocyte subsets of patients with IND and CARD clinical forms of Chagas disease. We also assessed the expression of toll-like receptor (TLR)-2, TLR-4, TLR-9, HLA-DR, IL-10, and IL-12 in the monocyte subsets and of CTLA-4 and CD28, ligands of CD80 and CD86, in T lymphocytes. CD86 expression in all monocyte subsets was higher in IND patients when compared with non-infected (NI) individuals. After stimulation with , these patients also showed a higher frequency of CD4CTLA-4 T lymphocytes than NI individuals. We found an association between CD80 and CD28, and between CD86 and CTLA-4 expression, with a high frequency of regulatory T (Treg) cells in IND patients. We proposed that CD86 may be involved in immunoregulation by its association with CTLA-4 in asymptomatic patients. CD86 and CTLA-4 interaction may influence Treg activation, and this could represent a new strategy to control inflammation and tissue damage.

摘要

在恰加斯病的慢性期,60%的患者会发展为无症状的不定型(IND)。剩下的 30%的患者会发展为危及生命的形式,其中会发生消化和/或心脏(CARD)改变。导致恰加斯病严重形式发展的机制仍知之甚少。众所周知,免疫细胞(如单核细胞和淋巴细胞)之间的相互作用会驱动免疫反应。此外,单核细胞和亚群表达的共刺激分子 CD80 和 CD86 诱导淋巴细胞激活,从而触发细胞免疫反应。在这里,我们首次揭示了恰加斯病患者单核细胞亚群的功能表型特征。我们使用流式细胞术评估了抗原刺激对 IND 和 CARD 临床形式的恰加斯病患者不同单核细胞亚群中共刺激分子 CD80 和 CD86 表达的影响。我们还评估了单核细胞亚群中 toll 样受体(TLR)-2、TLR-4、TLR-9、HLA-DR、IL-10 和 IL-12 的表达以及 CTLA-4 和 CD28 的表达,CD80 和 CD86 的配体在 T 淋巴细胞中。与未感染(NI)个体相比,IND 患者的所有单核细胞亚群的 CD86 表达均升高。在用刺激后,这些患者还显示出比 NI 个体更高频率的 CD4CTLA-4 T 淋巴细胞。我们发现 CD80 和 CD28 之间以及 CD86 和 CTLA-4 表达之间存在关联,与 IND 患者中调节性 T(Treg)细胞的高频率有关。我们提出 CD86 可能通过与无症状患者中的 CTLA-4 结合参与免疫调节。CD86 和 CTLA-4 相互作用可能影响 Treg 激活,这可能代表一种控制炎症和组织损伤的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/465d/5857740/b68e3538855f/fimmu-09-00454-g001.jpg

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