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恒河猴感染猕猴猿猴免疫缺陷病毒急性感染中的免疫致病事件。

Immunopathogenic events in acute infection of rhesus monkeys with simian immunodeficiency virus of macaques.

作者信息

Reimann K A, Tenner-Racz K, Racz P, Montefiori D C, Yasutomi Y, Lin W, Ransil B J, Letvin N L

机构信息

New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772.

出版信息

J Virol. 1994 Apr;68(4):2362-70. doi: 10.1128/JVI.68.4.2362-2370.1994.

Abstract

Infection of the rhesus monkey with simian immunodeficiency virus of macaques (SIVmax) was employed to explore the early immune events associated with the initial containment of an acute AIDS virus infection. In nine rhesus monkeys infected intravenously with uncloned SIVmac strain 251, high-level p27 plasma antigenemia was usually detected transiently from approximately day 7 through day 21 following virus inoculation. SIVmac replication in lymph nodes measured by in situ RNA hybridization closely paralleled the time course and magnitude of viremia. The containment of SIVmac spread by 3 to 4 weeks following infection suggests an efficient, early immune control of this virus infection. Anti-SIVmac antibodies were first detected in the blood at approximately day 14. At the time antigenemia was decreased or cleared, SIVmac neutralizing antibodies were present. A rise in circulating and lymph node CD8+ T cells also occurred coincident with the clearance of antigenemia and persisted thereafter. These CD8+ lymphocytes in lymph nodes had increased expression of both major histocompatibility complex class II and the adhesion molecule LFA-1; they also demonstrated decreased expression of the naive T-cell-associated CD45RA molecule. SIVmac-specific cytotoxic T-lymphocyte precursors were detected in both blood and lymph node by 7 days post-virus inoculation. These studies indicate that both virus-specific humoral and cellular immune mechanisms in blood and lymph node are associated with the clearance of viremia that occurs within the first month of infection of rhesus monkeys with SIVmac.

摘要

利用猕猴感染猕猴猿猴免疫缺陷病毒(SIVmax)来探索与急性艾滋病病毒感染的初始控制相关的早期免疫事件。在9只静脉注射未克隆的SIVmac毒株251的猕猴中,通常在病毒接种后约第7天至第21天短暂检测到高水平的p27血浆抗原血症。通过原位RNA杂交测量的淋巴结中SIVmac复制与病毒血症的时间进程和程度密切平行。感染后3至4周SIVmac传播得到控制,表明对这种病毒感染有高效的早期免疫控制。抗SIVmac抗体最早在大约第14天在血液中被检测到。在抗原血症降低或清除时,存在SIVmac中和抗体。循环和淋巴结CD8 + T细胞的增加也与抗原血症的清除同时发生,并在其后持续存在。淋巴结中的这些CD8 +淋巴细胞主要组织相容性复合体II类和黏附分子LFA-1的表达增加;它们还表现出与幼稚T细胞相关的CD45RA分子的表达降低。在病毒接种后7天在血液和淋巴结中均检测到SIVmac特异性细胞毒性T淋巴细胞前体。这些研究表明,血液和淋巴结中的病毒特异性体液免疫和细胞免疫机制均与猕猴感染SIVmac后第一个月内发生的病毒血症清除有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/268d/236713/6f35b744a366/jvirol00013-0341-a.jpg

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