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Chronic HIV-1 infection impairs superantigen-induced activation of peripheral CD4+CXCR5+PD-1+ cells with relative preservation of recall antigen-specific responses

机译:慢性HIV-1感染削弱了超抗原诱导的外周CD4 + CXCR5 + PD-1 +细胞的激活同时保留了召回抗原特异性应答

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摘要

Peripheral CD4+CXCR5+PD-1+ T cells are a putative circulating counterpart to germinal center T follicular helper (TFH) cells. They show both phenotypic and functional similarities to TFH cells, which provide necessary help for the differentiation of B cells to antibody-secreting plasmablasts. In this study we evaluated the frequency, phenotypes, and responses of peripheral TFH-like (pTFH) cells to superantigen and recall antigen stimulation in 10 healthy and 34 chronically infected treatment-naïve HIV-1+ individuals. There was no difference in the frequency of pTFH cells between HIV+ and HIV− individuals. Surface expression of ICOS, but not CD40L, was higher on pTFH cells at baseline in HIV+ individuals. Compared to HIV− individuals, pTFH cells from HIV+ individuals had decreased maximal expression of ICOS and CD40L in response to in vitro superantigen stimulation. This decreased response did not correlate with viral control, CD4+ T cell count, duration of infection, or the degree of neutralizing antibody breadth. Despite a decreased maximal response, however, pTFH responses to HIV gag and tetanus toxoid recall antigens were preserved.
机译:外周CD4 + CXCR5 + PD-1 + T细胞是生发中心T滤泡辅助细胞(TFH)的假定循环对应物。它们显示了与TFH细胞的表型和功能相似性,这为B细胞分化为分泌抗体的成浆细胞提供了必要的帮助。在这项研究中,我们评估了10名健康和34名长期未接受过治疗的HIV-1 +个体的外周TFH样(pTFH)细胞对超抗原的频率,表型和反应,并回忆了抗原刺激。 HIV +和HIV-个体之间pTFH细胞的频率没有差异。 HIV +个体在基线时在pTFH细胞上ICOS的表面表达较高,而CD40L没有。与HIV-个体相比,来自HIV +个体的pTFH细胞响应体外超抗原刺激而降低了ICOS和CD40L的最大表达。这种降低的反应与病毒控制,CD4 + T细胞计数,感染持续时间或中和抗体的广度无关。尽管最大反应降低,但是,pTFH对HIV gag和破伤风类毒素召回抗原的反应得以保留。

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