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与HLA - B8结合的具有免疫原性的HIV变异肽可能无法刺激细胞毒性T淋巴细胞反应。

Immunogenic HIV variant peptides that bind to HLA-B8 can fail to stimulate cytotoxic T lymphocyte responses.

作者信息

McAdam S, Klenerman P, Tussey L, Rowland-Jones S, Lalloo D, Phillips R, Edwards A, Giangrande P, Brown A L, Gotch F

机构信息

Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.

出版信息

J Immunol. 1995 Sep 1;155(5):2729-36.

PMID:7544382
Abstract

Cytotoxic T lymphocyte responses in HIV infection can be impaired through variation in the epitope regions of viral proteins such as a gag. We report here an analysis of variant epitope peptides in three gag epitopes presented by HLA B8. Fifteen variant peptides were examined for their binding to HLA-B8; all but one bound at concentrations comparable to known epitopes. All except two of those that bound could be recognized by CTL from an HLA-B8 positive HIV-1-infected patient and were therefore immunogenic. However, in a hemophiliac patient studied in detail, there was a failure to respond to two immunogenic peptide epitopes representing virus present as provirus in the patient's peripheral blood. In one case, the patient's CTL had previously responded to the peptide; in the other case, there was a good response to a peptide of closely related sequence. Thus there was a selective failure of the CTL response to some proviral epitopes. This impaired reaction to new variants could contribute to the loss of immune control of the infection.

摘要

在HIV感染中,细胞毒性T淋巴细胞反应可能会因病毒蛋白(如gag)表位区域的变异而受损。我们在此报告对HLA B8所呈递的三个gag表位中的变异表位肽进行的分析。检测了15种变异肽与HLA - B8的结合情况;除一种外,所有变异肽在与已知表位相当的浓度下均可结合。在那些能够结合的变异肽中,除两种外,其余均可被一名HLA - B8阳性的HIV - 1感染患者的CTL识别,因此具有免疫原性。然而,在一名经过详细研究的血友病患者中,其对代表存在于该患者外周血中作为前病毒的病毒的两种免疫原性肽表位未能产生反应。在一个病例中,该患者的CTL此前曾对该肽产生反应;在另一个病例中,对一个序列密切相关的肽有良好反应。因此,CTL对某些前病毒表位的反应存在选择性缺失。这种对新变异体的反应受损可能会导致感染的免疫控制丧失。

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