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Evidence of early B-cell dysregulation in simian immunodeficiency virus infection: rapid depletion of naïve and memory B-cell subsets with delayed reconstitution of the naïve B-cell population.在猿猴免疫缺陷病毒感染中存在早期 B 细胞失调的证据:幼稚和记忆 B 细胞亚群迅速耗竭,而幼稚 B 细胞群体的重建延迟。
J Virol. 2010 Mar;84(5):2466-76. doi: 10.1128/JVI.01966-09. Epub 2009 Dec 23.
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Tissue-specific B-cell dysfunction and generalized memory B-cell loss during acute SIV infection.急性猴免疫缺陷病毒感染期间的组织特异性B细胞功能障碍和全身性记忆B细胞损失。
PLoS One. 2009 Jun 19;4(6):e5966. doi: 10.1371/journal.pone.0005966.
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Immunol Rev. 2009 May;229(1):216-31. doi: 10.1111/j.1600-065X.2009.00774.x.
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Primary B cell immunodeficiencies: comparisons and contrasts.原发性B细胞免疫缺陷:比较与对比
Annu Rev Immunol. 2009;27:199-227. doi: 10.1146/annurev.immunol.021908.132649.
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Resting human memory B cells are intrinsically programmed for enhanced survival and responsiveness to diverse stimuli compared to naive B cells.与初始B细胞相比,静息的人类记忆B细胞具有内在的程序设定,以增强其存活能力及对多种刺激的反应性。
J Immunol. 2009 Jan 15;182(2):890-901. doi: 10.4049/jimmunol.182.2.890.
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HIV infection and the gastrointestinal immune system.HIV感染与胃肠道免疫系统。
Mucosal Immunol. 2008 Jan;1(1):23-30. doi: 10.1038/mi.2007.1.
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A new memory CD27-IgG+ B cell population in peripheral blood expressing VH genes with low frequency of somatic mutation.外周血中一种新的记忆性CD27-IgG⁺ B细胞群体,其表达的VH基因体细胞突变频率较低。
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Germinal center function in the spleen during simian HIV infection in rhesus monkeys.恒河猴感染猿类HIV期间脾脏生发中心的功能
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Delineation of multiple subpopulations of natural killer cells in rhesus macaques.恒河猴体内自然杀伤细胞多个亚群的描绘。
Immunology. 2005 Jun;115(2):206-14. doi: 10.1111/j.1365-2567.2005.02147.x.
10
Peak SIV replication in resting memory CD4+ T cells depletes gut lamina propria CD4+ T cells.静息记忆性CD4+ T细胞中的SIV复制高峰会消耗肠道固有层CD4+ T细胞。
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恒河猴幼稚 B 细胞和记忆 B 细胞可通过表面表达 CD27 区分,并且对 CD40 配体的反应存在差异。

Naïve and memory B cells in the rhesus macaque can be differentiated by surface expression of CD27 and have differential responses to CD40 ligation.

机构信息

Department of Immunology, University of Pittsburgh, Pittsburgh PA 15261, USA.

出版信息

J Immunol Methods. 2011 Jan 5;363(2):166-76. doi: 10.1016/j.jim.2010.09.017. Epub 2010 Sep 24.

DOI:10.1016/j.jim.2010.09.017
PMID:20875419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3357916/
Abstract

The rhesus macaque (RM) model has the potential to be an invaluable tool for studying B cell populations during pathogenic infections, however, to date, there has been no definitive delineation of naïve and memory B cell populations in the RM. This has precluded a rigorous analysis of the generation, persistence and resolution of a pathogen-specific memory B cell response. The present study utilized multiple analyses to demonstrate that CD27 expression on B cells is consistent with a memory phenotype. Compared to CD20+CD27- B cells, CD20+CD27+ B cells were larger in size, and preferentially accumulated at effector sites. Direct sequence analysis revealed that CD20+CD27+ B cells had an increased frequency of point mutations that were consistent with somatic hypermutation and at a functional level, CD40 ligation improved CD20+CD27- but not CD20+CD27+ B cell survival in vitro. These data provide definitive evidence that the naïve and memory B cell populations of the RM can be differentiated using surface expression of CD27.

摘要

恒河猴(RM)模型有可能成为研究致病感染期间 B 细胞群体的宝贵工具,然而,迄今为止,RM 中尚未明确界定幼稚和记忆 B 细胞群体。这使得对病原体特异性记忆 B 细胞反应的产生、持续存在和解决进行严格分析变得不可能。本研究利用多种分析方法证明 B 细胞上的 CD27 表达与其记忆表型一致。与 CD20+CD27-B 细胞相比,CD20+CD27+B 细胞体积更大,并且优先聚集在效应部位。直接序列分析表明,CD20+CD27+B 细胞的点突变频率增加,与体细胞高频突变一致,在功能水平上,CD40 配体可提高 CD20+CD27-B 细胞的存活,但不能提高 CD20+CD27+B 细胞的存活。这些数据提供了明确的证据,表明可以使用 CD27 的表面表达来区分 RM 的幼稚和记忆 B 细胞群体。