HIV感染中的淋巴结退化、t细胞适应和t细胞死亡。

HIV therapy Pub Date : 2010-12-14 DOI:10.2217/HIV.10.56
I. Picerno, G. Visalli, R. Lentile, G. Piedimonte
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引用次数: 2

摘要

纤维化组织退化发生在多种慢性疾病中。作为滤泡萎缩和耗竭的最后阶段,弥漫性纤维化是HIV感染特征的淋巴结退化的慢性过程的更严重的后果。本文综述了hiv诱导的淋巴结纤维化与其他慢性纤维增生性疾病的比较,包括参与这一过程的细胞类型和共同导致胶原沉积和重塑正常组织结构的信号中间体。鉴于这种类型纤维化的组织学定量不容易作为临床病理学的常规方法引入,我们将讨论利用一些功能修饰的可能性,这些功能修饰表达T细胞对纤维化/缺氧环境的适应性,作为淋巴结损伤演变的生化标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lymph node involution, T-cell adaptation and T-cell death in HIV infection.
Fibrotic tissue involution occurs in a large variety of chronic diseases. As the final phase of follicular atrophy and depletion, a diffuse fibrosis is the more severe consequence of the chronic process of lymph node involution that characterizes HIV infection. This review focuses on the comparison between HIV-induced lymph node fibrosis and other chronic fibroproliferative diseases, in terms of cell types participating in the process and signaling intermediates that together cause the deposition of collagen and remodel normal tissue architecture. Given that the histological quantification of this type of fibrosis cannot be easily introduced as a routine method in clinical pathology, we will discuss the possibility of exploiting some functional modifications, which express the adaptation of T cells to the fibrotic/hypoxic environment, as biochemical markers of the evolution of lymph node damage.
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