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HIV感染的黑猩猩对人类免疫缺陷病毒(HIV)及其重组抗原的T细胞反应。

T-cell responses to human immunodeficiency virus (HIV) and its recombinant antigens in HIV-infected chimpanzees.

作者信息

Eichberg J W, Zarling J M, Alter H J, Levy J A, Berman P W, Gregory T, Lasky L A, McClure J, Cobb K E, Moran P A

机构信息

Southwest Foundation for Biomedical Research, San Antonio, Texas 78284.

出版信息

J Virol. 1987 Dec;61(12):3804-8. doi: 10.1128/JVI.61.12.3804-3808.1987.

Abstract

Peripheral blood lymphocytes from chimpanzees infected for 3 months to more than 3 years with human immunodeficiency virus (HIV) had normal T-cell proliferative responses after stimulation with a variety of recall antigens and mitogens, indicating that HIV infection does not cause detectable immunological impairment in chimpanzees. This finding contrasts with that obtained in HIV-infected humans, who often have impaired T-cell reactivity. Peripheral blood lymphocytes from most HIV-infected chimpanzees that were studied also had strong proliferative responses to purified HIV as well as to HIV envelope glycoproteins isolated from the virus, to recombinant HIV envelope glycoproteins gp120 and gp41, and to HIV gag protein p24. The HIV-specific T-cell responses in HIV-infected chimpanzees may contribute to prevention of the development of acquired immunodeficiency syndrome in this species.

摘要

感染人类免疫缺陷病毒(HIV)3个月至3年以上的黑猩猩的外周血淋巴细胞,在用多种回忆抗原和有丝分裂原刺激后,具有正常的T细胞增殖反应,这表明HIV感染在黑猩猩中不会引起可检测到的免疫损伤。这一发现与在HIV感染的人类中获得的结果形成对比,HIV感染的人类通常T细胞反应受损。大多数接受研究的感染HIV的黑猩猩的外周血淋巴细胞,对纯化的HIV以及从病毒中分离出的HIV包膜糖蛋白、重组HIV包膜糖蛋白gp120和gp41以及HIV gag蛋白p24也有强烈的增殖反应。感染HIV的黑猩猩中针对HIV的T细胞反应可能有助于预防该物种获得性免疫缺陷综合征的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0057/255996/b0565eaa8622/jvirol00103-0168-a.jpg

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