首页> 外文OA文献 >Induction of Anti-Human Immunodeficiency Virus Type 1 (HIV-1) CD8+ and CD4+ T-Cell Reactivity by Dendritic Cells Loaded with HIV-1 X4-Infected Apoptotic Cells
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Induction of Anti-Human Immunodeficiency Virus Type 1 (HIV-1) CD8+ and CD4+ T-Cell Reactivity by Dendritic Cells Loaded with HIV-1 X4-Infected Apoptotic Cells

机译:载有HIV-1 X4感染的树突状细胞的树突状细胞诱导抗人类免疫缺陷病毒1型(HIV-1)CD8 +和CD4 + T细胞反应性。

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摘要

T-cell responses to X4 strains of human immunodeficiency virus type 1 (HIV-1) are considered important in controlling progression of HIV-1 infection. We investigated the ability of dendritic cells (DC) and various forms of HIV-1 X4 antigen to induce anti-HIV-1 T-cell responses in autologous peripheral blood mononuclear cells from HIV-1-infected persons. Immature DC loaded with HIV-1 IIIB-infected, autologous, apoptotic CD8− cells and matured with CD40 ligand induced gamma interferon production in autologous CD8+ and CD4+ T cells. In contrast, mature DC loaded with HIV-1 IIIB-infected, necrotic cells or directly infected with cell-free HIV-1 IIIB were poorly immunogenic. Thus, HIV-1-infected cells undergoing apoptosis serve as a rich source of X4 antigen for CD8+ and CD4+ T cells by DC. This may be an important mechanism of HIV-1 immunogenicity and provides a strategy for immunotherapy of HIV-1-infected patients on combination antiretroviral therapy.
机译:对1型人类免疫缺陷病毒(HIV-1)的X4株的T细胞应答被认为对控制HIV-1感染的进展很重要。我们调查了树突状细胞(DC)和各种形式的HIV-1 X4抗原在来自HIV-1感染者的自体外周血单核细胞中诱导抗HIV-1 T细胞反应的能力。未成熟的DC装有HIV-1 IIIB感染的自体凋亡CD8-细胞,并与CD40配体成熟,可诱导自体CD8 +和CD4 + T细胞中的γ干扰素产生。相反,成熟的DC装有HIV-1 IIIB感染的坏死细胞或直接感染无细胞的HIV-1 IIIB,其免疫原性较差。因此,经历凋亡的HIV-1感染的细胞通过DC充当了CD8 +和CD4 + T细胞的X4抗原的丰富来源。这可能是HIV-1免疫原性的重要机制,并为联合抗逆转录病毒疗法对HIV-1感染患者的免疫治疗提供了策略。

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