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体内人类淋巴组织中CD8 +细胞与HIV - 1产生细胞之间的微观解剖关系。

Microanatomic relationships between CD8+ cells and HIV-1-producing cells in human lymphoid tissue in vivo.

作者信息

Folkvord Joy M, Anderson Deborah M, Arya Jyoti, MaWhinney Samantha, Connick Elizabeth

机构信息

Division of Infectious Disease, University of Colorado Health Sciences Center, 4200 East Ninth Avenue, Denver, CO 80262, USA.

出版信息

J Acquir Immune Defic Syndr. 2003 Apr 15;32(5):469-76. doi: 10.1097/00126334-200304150-00001.

Abstract

OBJECTIVE

Host immune responses are unable to fully suppress HIV-1 replication in lymphoid tissues. Microanatomic relationships between HIV-1-producing cells and CD8+ cells in lymphoid tissues were analyzed to determine whether there was evidence for an immune privileged site or impaired recognition of virus-producing cells.

METHODS

CD8+ cell phenotypes were determined on disaggregated inguinal lymph node cells by flow cytometry for seven untreated HIV-1-infected subjects. Microanatomic relationships between HIV-1-producing cells and CD8+ cells were analyzed in lymph node sections from 15 HIV-1-infected individuals using in situ hybridization and immunohistochemical staining.

RESULTS

Most (median, 96%) lymph node CD8+ cells coexpressed CD3. Frequencies of virus-producing cells detected by in situ hybridization correlated with plasma HIV-1 RNA concentration (Spearman rho = 0.70; p =.02; n = 11). The percentage of lymph node cells adjacent to virus-producing cells that were CD8+ (median, 29%) was not statistically different from the percentage of CD8+ cells in lymphoid tissue overall (median, 34%; p =.09).

CONCLUSIONS

Multiple explanations could account for the observation that CD8+ cells do not preferentially accumulate around virus-producing cells including the possibility that HIV-1-specific CD8+ cells cannot recognize virus-producing cells. Further studies are necessary to determine whether HIV-1-specific CD8+ T cells aggregate around virus-producing cells in lymphoid tissue.

摘要

目的

宿主免疫反应无法完全抑制HIV-1在淋巴组织中的复制。分析了淋巴组织中产生HIV-1的细胞与CD8+细胞之间的微观解剖关系,以确定是否有证据表明存在免疫特权部位或对产生病毒的细胞的识别受损。

方法

通过流式细胞术对7名未经治疗的HIV-1感染受试者腹股沟淋巴结细胞进行分离,以确定CD8+细胞表型。使用原位杂交和免疫组织化学染色,对15名HIV-1感染个体的淋巴结切片中产生HIV-1的细胞与CD8+细胞之间的微观解剖关系进行分析。

结果

大多数(中位数为96%)淋巴结CD8+细胞共表达CD3。原位杂交检测到的产生病毒的细胞频率与血浆HIV-1 RNA浓度相关(Spearman相关系数=0.70;p=0.02;n=11)。与产生病毒的细胞相邻的淋巴结细胞中CD8+细胞的百分比(中位数为29%)与淋巴组织中CD8+细胞的总体百分比(中位数为34%)无统计学差异(p=0.09)。

结论

对于CD8+细胞未优先在产生病毒的细胞周围聚集这一现象,可能有多种解释,包括HIV-1特异性CD8+细胞无法识别产生病毒的细胞。需要进一步研究以确定HIV-1特异性CD8+T细胞是否在淋巴组织中产生病毒的细胞周围聚集。

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