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HIV 感染者胸腺中 CD4+ T 细胞耗竭、免疫激活和调节性 T 细胞产生增加。

CD4+ T cell depletion, immune activation and increased production of regulatory T cells in the thymus of HIV-infected individuals.

机构信息

Division of Infectious Diseases, Department of Internal Medicine, San Gerardo Hospital, University of Milan-Bicocca, Monza, Italy.

出版信息

PLoS One. 2010 May 24;5(5):e10788. doi: 10.1371/journal.pone.0010788.

Abstract

Mechanisms by which HIV affects the thymus are multiple and only partially known, and the role of thymic dysfunction in HIV/AIDS immunopathogenesis remains poorly understood. To evaluate the effects of HIV infection on intra-thymic precursors of T cells in HIV-infected adults, we conducted a detailed immunophenotypic study of thymic tissue isolated from 7 HIV-infected and 10 HIV-negative adults who were to undergo heart surgery. We found that thymuses of HIV-infected individuals were characterized by a relative depletion of CD4+ single positive T cells and a corresponding enrichment of CD8+ single positive T cells. In addition, thymocytes derived from HIV-infected subjects showed increased levels of activated and proliferating cells. Our analysis also revealed a decreased expression of interleukin-7 receptor in early thymocytes from HIV-infected individuals, along with an increase in this same expression in mature double- and single-positive cells. Frequency of regulatory T cells (CD25+FoxP3+) was significantly increased in HIV-infected thymuses, particularly in priorly-committed CD4 single positive cells. Our data suggest that HIV infection is associated with a complex set of changes in the immunophenotype of thymocytes, including a reduction of intrathymic CD4+ T cell precursors, increased expression of activation markers, changes in the expression pattern of IL-7R and enrichment of T regulatory cells generation.

摘要

HIV 影响胸腺的机制是多样的,目前仅部分被了解,而胸腺功能障碍在 HIV/AIDS 免疫发病机制中的作用仍知之甚少。为了评估 HIV 感染对 HIV 感染者体内 T 细胞前体的影响,我们对 7 名 HIV 感染者和 10 名 HIV 阴性成年人的胸腺组织进行了详细的免疫表型研究,这些人将接受心脏手术。我们发现,HIV 感染者的胸腺表现为 CD4+单阳性 T 细胞相对耗竭,CD8+单阳性 T 细胞相应富集。此外,来自 HIV 感染者的胸腺细胞显示出激活和增殖细胞水平升高。我们的分析还揭示了 HIV 感染者早期胸腺细胞中白细胞介素 7 受体表达减少,同时成熟的双阳性和单阳性细胞中该受体表达增加。HIV 感染者的调节性 T 细胞(CD25+FoxP3+)频率显著增加,尤其是在前承诺的 CD4 单阳性细胞中。我们的数据表明,HIV 感染与胸腺细胞免疫表型的一系列复杂变化相关,包括 intrathymic CD4+T 细胞前体减少、激活标志物表达增加、IL-7R 表达模式变化以及 T 调节细胞生成增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a60f/2875388/4558ffe33d0b/pone.0010788.g001.jpg

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