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具有效应细胞表型且能控制病毒复制的HIV-1特异性CD8+ T细胞。

HIV-1 specific CD8+ T cells with an effector phenotype and control of viral replication.

作者信息

Hess Christoph, Altfeld Marcus, Thomas Seddon Y, Addo Marylyn M, Rosenberg Eric S, Allen Todd M, Draenert Rika, Eldrige Robert L, van Lunzen Jan, Stellbrink Hans-J, Walker Bruce D, Luster Andrew D

机构信息

Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Harvard Medical School, Massachusetts, USA.

出版信息

Lancet. 2004 Mar 13;363(9412):863-6. doi: 10.1016/S0140-6736(04)15735-8.

Abstract

Most people infected with HIV-1 cannot control viral replication despite the presence of virus-specific CD8+ T cells. It has been postulated that this inability is related to the failure of these cells to mature into fully differentiated effector cells. We tested this hypothesis by comparing the maturation phenotype of virus-specific CD8+ T cells in people who could control viral replication off anti-retroviral therapy with those who could not. In five patients with treated acute HIV-1-infection, structured treatment interruption (STI) induced control of viral replication was associated with expansion of virus-specific CD8+ T cells with a fully differentiated effector phenotype. These effector cells were also expanded in treatment-naive chronically infected individuals who spontaneously controlled viral replication, and augmented expression of perforin was noted in both settings. Our data show that full maturation of virus-specific CD8+ T cells is possible in the context of HIV-1-infection, and suggest that such maturation might be important in viral control.

摘要

大多数感染HIV-1的人尽管存在病毒特异性CD8+T细胞,但仍无法控制病毒复制。据推测,这种无能与这些细胞未能成熟为完全分化的效应细胞有关。我们通过比较接受抗逆转录病毒治疗后能够控制病毒复制的人与无法控制病毒复制的人之间病毒特异性CD8+T细胞的成熟表型,来检验这一假设。在5例接受治疗的急性HIV-1感染患者中,结构化治疗中断(STI)诱导的病毒复制控制与具有完全分化效应表型的病毒特异性CD8+T细胞的扩增有关。这些效应细胞在未经治疗的慢性感染个体中也有扩增,这些个体可自发控制病毒复制,并且在两种情况下均观察到穿孔素表达增加。我们的数据表明,在HIV-1感染的情况下,病毒特异性CD8+T细胞完全成熟是可能的,并且表明这种成熟可能在病毒控制中起重要作用。

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