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急性感染的人外周血淋巴细胞-重症联合免疫缺陷(Hu-PBL-SCID)小鼠人源异种移植中1型人类免疫缺陷病毒复制的定量评估

Quantitative assessment of human immunodeficiency virus type 1 replication in human xenografts of acutely infected Hu-PBL-SCID mice.

作者信息

Koup R A, Hesselton R M, Safrit J T, Somasundaran M, Sullivan J L

机构信息

Aaron Diamond AIDS Research Center, New York University School of Medicine, New York 10016.

出版信息

AIDS Res Hum Retroviruses. 1994 Mar;10(3):279-84. doi: 10.1089/aid.1994.10.279.

Abstract

Replication of the IIIB strain of human immunodeficiency virus type 1 (HIV-1IIIB) in CB.17 scid/scid mice reconstituted with human peripheral blood lymphocytes (Hu-PBL-SCID) was investigated. Hu-PBL-SCID mice could be infected, in a dose-dependent manner, when HIV-1IIIB was injected intraperitoneally. Replication-competent HIV-1 could be recovered from spleen, peripheral blood, bone marrow, thymus, lymph node, and peritoneal cavity, indicating the ability of the infection to spread to human tissue throughout the chimeric animals. HIV-1 infection was quantitated using p24 determination, end-point dilution culture, and polymerase chain reaction amplification. The level of HIV-1 replication in Hu-PBL-SCID mice was found to approximate the level reported in human infection. No HIV-1-specific immune response was generated to this infection, but nonspecific immune activation did occur, as also reported in human infection. Similarities therefore exist between HIV-1 infection of humans and Hu-PBL-SCID mice, which makes the latter an in vivo model in which to study HIV-1 replication.

摘要

研究了1型人类免疫缺陷病毒IIIB株(HIV-1IIIB)在用人外周血淋巴细胞重建的CB.17 scid/scid小鼠(Hu-PBL-SCID)中的复制情况。当腹腔注射HIV-1IIIB时,Hu-PBL-SCID小鼠能够以剂量依赖的方式被感染。从脾脏、外周血、骨髓、胸腺、淋巴结和腹腔中可回收具有复制能力的HIV-1,这表明感染能够在整个嵌合动物体内扩散到人体组织。使用p24测定、终点稀释培养和聚合酶链反应扩增对HIV-1感染进行定量。发现Hu-PBL-SCID小鼠中HIV-1的复制水平接近人类感染中报道的水平。对这种感染未产生HIV-1特异性免疫反应,但确实发生了非特异性免疫激活,这在人类感染中也有报道。因此,人类HIV-1感染与Hu-PBL-SCID小鼠之间存在相似性,这使得后者成为研究HIV-1复制的体内模型。

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