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与感染猴免疫缺陷病毒(SIV)的猕猴淋巴器官中CD4/CD8比值下降相关的免疫和病毒学变化。

Immunological and virological changes associated with decline in CD4/CD8 ratios in lymphoid organs of SIV-infected macaques.

作者信息

Rosenberg Y J, Zack P M, Leon E C, White B D, Papermaster S F, Hall E, Greenhouse J J, Eddy G A, Lewis M G

机构信息

Henry M. Jackson Foundation, Rockville, Maryland 20850.

出版信息

AIDS Res Hum Retroviruses. 1994 Jul;10(7):863-72. doi: 10.1089/aid.1994.10.863.

Abstract

The decline in CD4/CD8 ratios in lymph nodes (LNs) of SIV macaques and HIV-infected individuals occurs later than that in blood. In a previous study, long-term SIV-infected macaques were delineated into two groups: (1) those whose LNs had normal CD4/CD8 ratios and (2) those whose LNs had low CD4/CD8 ratios. In the present investigation, LNs, spleens, and blood from these groups have been further analyzed to ascertain the cellular and virological events, particularly those involving CD8+ cells, that occur concomitantly with LN CD4% decline. An increase in the percent of CD69-, IL-2R(p75)-, CD45RA1o CD8+ cells was the most constant event observed in lymphoid tissue from mid- to late-stage SIV-infected monkeys. Such cells were sometimes observed in LNs prior to any other immunological or morphological changes. However, decline in LN CD4/CD8 ratios and the associated degeneration of follicular dendritic cells (FDCs) in the germinal centers (GCs) of these nodes were observed only when both CD8+ cell infiltration of GCs and accumulation of viral antigens within the FDC network could be demonstrated. These dramatic changes were also associated with significantly reduced responsiveness to mitogens throughout the lymphoid compartment. In terms of viral burden, immunological and structural collapse of LNs was not always associated with increased viral DNA levels. Despite the CD4+ cell decline in blood during HIV and SIV infections, the immunological and architectural collapse of the lymphoid compartment, which comprises the bulk of the lymphocytes in the body, appears to be a critical event leading to the onset of AIDS. The present findings suggest that increased CD8+ cell activity as well as decrease in CD4+ cell function both contribute to this process.

摘要

在感染猴免疫缺陷病毒(SIV)的猕猴和感染人类免疫缺陷病毒(HIV)的个体中,淋巴结(LN)内CD4/CD8比值的下降比血液中出现得更晚。在先前的一项研究中,长期感染SIV的猕猴被分为两组:(1)淋巴结CD4/CD8比值正常的猕猴;(2)淋巴结CD4/CD8比值低的猕猴。在本研究中,对这些组的淋巴结、脾脏和血液进行了进一步分析,以确定与淋巴结CD4%下降同时发生的细胞和病毒学事件,特别是那些涉及CD8+细胞的事件。在感染SIV的中晚期猴子的淋巴组织中,观察到最常见的事件是CD69-、白细胞介素-2受体(p75)-、CD45RA1o CD8+细胞百分比增加。在出现任何其他免疫或形态学变化之前,有时在淋巴结中就能观察到这类细胞。然而,只有当生发中心(GC)的CD8+细胞浸润和滤泡树突状细胞(FDC)网络内病毒抗原的积累都能被证实时,才会观察到这些淋巴结中CD4/CD8比值下降以及生发中心滤泡树突状细胞的相关退变。这些显著变化还与整个淋巴区对丝裂原的反应性显著降低有关。就病毒载量而言,淋巴结的免疫和结构崩溃并不总是与病毒DNA水平升高相关。尽管在HIV和SIV感染期间血液中的CD4+细胞数量下降,但构成体内大部分淋巴细胞的淋巴区的免疫和结构崩溃似乎是导致艾滋病发病的关键事件。目前的研究结果表明,CD8+细胞活性增加以及CD4+细胞功能下降都促成了这一过程。

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