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CD4(+)和CD8(+) T细胞在控制HIV感染中的作用。

The Role of CD4(+) and CD8(+) T Cells in Controlling HIV Infection.

作者信息

Migueles Stephen A., Connors Mark

机构信息

LIR, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Building 10, Room 11B-09, 10 Center Drive MSC 1876, Bethesda, MD 20892-1876, USA.

出版信息

Curr Infect Dis Rep. 2002 Oct;4(5):461-467. doi: 10.1007/s11908-002-0014-2.

Abstract

Presently, it is thought that virus-specific T cells play a major role in restricting lentiviral replication and determining the rate of disease progression in humans. However, it remains unclear why this restriction fails in the majority of infected individuals. The major exception is a rare subgroup of HIV-infected long-term nonprogressors (LTNPs) who have been infected for approximately 20 years yet maintain normal CD4(+) T-cell counts and less than 50 copies of viral RNA/mL of plasma. Although virus-specific cellular (CD4(+) and CD8(+) T lymphocytes) immune responses have been shown to exert some degree of in vivo control of HIV replication, the precise correlates of protective immunity differentiating LTNPs from patients with progressive disease remain unknown. A greater understanding of the components and magnitude of an effective immune response to HIV is an important step toward the development of effective vaccines and immunotherapies.

摘要

目前,人们认为病毒特异性T细胞在限制慢病毒复制和决定人类疾病进展速度方面发挥着主要作用。然而,尚不清楚为何这种限制在大多数受感染个体中会失效。主要的例外是一小部分罕见的长期不进展者(LTNP),他们感染HIV约20年,但仍保持正常的CD4(+) T细胞计数,且血浆中病毒RNA水平低于50拷贝/毫升。尽管病毒特异性细胞免疫反应(CD4(+)和CD8(+) T淋巴细胞)已被证明在体内对HIV复制有一定程度的控制作用,但区分LTNP和疾病进展患者的保护性免疫的确切相关因素仍不清楚。更深入了解针对HIV的有效免疫反应的组成部分和强度是开发有效疫苗和免疫疗法的重要一步。

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