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人类免疫缺陷病毒对人外周血淋巴细胞-重症联合免疫缺陷小鼠的感染。

Human immunodeficiency virus infection of human-PBL-SCID mice.

作者信息

Mosier D E, Gulizia R J, Baird S M, Wilson D B, Spector D H, Spector S A

机构信息

Division of Immunology, Medical Biology Institute, La Jolla, CA 92037.

出版信息

Science. 1991 Feb 15;251(4995):791-4. doi: 10.1126/science.1990441.

Abstract

Severe combined immunodeficient (SCID) mice reconstituted with human peripheral blood leukocytes (hu-PBL-SCID mice) have inducible human immune function and may be useful as a small animal model for acquired immunodeficiency syndrome (AIDS) research. Hu-PBL-SCID mice infected with human immunodeficiency virus-1 (HIV-1) contained virus that was recoverable by culture from the peritoneal cavity, spleen, peripheral blood, and lymph nodes for up to 16 weeks after infection; viral sequences were also detected by in situ hybridization and by amplification with the polymerase chain reaction (PCR). Mice could be infected with multiple strains of HIV-1, including LAV-1/Bru, IIIB, MN, SF2, and SF13. HIV-1 infection affected the concentration of human immunoglobulin and the number of CD4+ T cells in the mice. These results support the use of the hu-PBL-SCID mouse for studies of the pathogenesis and treatment of AIDS.

摘要

用人外周血白细胞重建的严重联合免疫缺陷(SCID)小鼠(人外周血白细胞-SCID小鼠)具有可诱导的人类免疫功能,可用作获得性免疫缺陷综合征(艾滋病)研究的小动物模型。感染了人类免疫缺陷病毒1型(HIV-1)的人外周血白细胞-SCID小鼠体内含有可通过培养从腹腔、脾脏、外周血和淋巴结中回收的病毒,感染后长达16周均可回收;病毒序列也可通过原位杂交和聚合酶链反应(PCR)扩增检测到。小鼠可感染多种HIV-1毒株,包括LAV-1/Bru、IIIB、MN、SF2和SF13。HIV-1感染影响小鼠体内人类免疫球蛋白的浓度和CD4+T细胞的数量。这些结果支持将人外周血白细胞-SCID小鼠用于艾滋病发病机制和治疗的研究。

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