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在小鼠和人类中鉴定出的人类免疫缺陷病毒逆转录酶T辅助表位:与细胞毒性T细胞表位的相关性

Human immunodeficiency virus reverse transcriptase T helper epitopes identified in mice and humans: correlation with a cytotoxic T cell epitope.

作者信息

De Groot A S, Clerici M, Hosmalin A, Hughes S H, Barnd D, Hendrix C W, Houghten R, Shearer G M, Berzofsky J A

机构信息

Molecular Immunogenetics and Vaccine Research Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Infect Dis. 1991 Dec;164(6):1058-65. doi: 10.1093/infdis/164.6.1058.

Abstract

T cell immunity may be critical to development of a vaccine for human immunodeficiency virus (HIV-1). T helper epitopes were identified in three predominantly conserved regions in the HIV-1 reverse transcriptase by using reverse transcriptase-immunized mice of five major histocompatibility complex haplotypes. One peptide (residues 38-52) that stimulated H-2k T cells also contained an epitope recognized by cytotoxic T cells from the same mice and from HIV-infected patients. Such concordance between helper and cytotoxic T lymphocyte epitopes, observed in four cases, may be important in vaccine development. Peptide 36-52 was recognized by interleukin-2-producing peripheral blood T cells from 9 of 17 HIV-seropositive humans studied, of multiple human leukocyte antigen-DR and -DQ types. The broad recognition of this peptide by both helper and cytotoxic T cells substantiates its potential importance in a vaccine.

摘要

T细胞免疫对于人类免疫缺陷病毒(HIV-1)疫苗的研发可能至关重要。通过使用具有五种主要组织相容性复合体单倍型的逆转录酶免疫小鼠,在HIV-1逆转录酶的三个主要保守区域中鉴定出了T辅助表位。一种刺激H-2k T细胞的肽(第38-52位氨基酸残基)也包含一个表位,该表位可被来自相同小鼠和HIV感染患者的细胞毒性T细胞识别。在四个案例中观察到的辅助性T淋巴细胞表位和细胞毒性T淋巴细胞表位之间的这种一致性,在疫苗研发中可能很重要。在研究的17名HIV血清阳性的人类中,有9名的产生白细胞介素-2的外周血T细胞识别肽36-52,这些人具有多种人类白细胞抗原-DR和-DQ类型。辅助性T细胞和细胞毒性T细胞对该肽的广泛识别证实了其在疫苗中的潜在重要性。

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