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1型人类免疫缺陷病毒分离株对人外周血树突状细胞的不依赖CD4感染。

CD4-independent infection of human peripheral blood dendritic cells with isolates of human immunodeficiency virus type 1.

作者信息

Chehimi J, Prakash K, Shanmugam V, Collman R, Jackson S J, Bandyopadhyay S, Starr S E

机构信息

Division of Allergy, Immunology and Infectious Diseases, Joseph Stokes Jr Research Institute, Children's Hospital of Philadelphia, Pennsylvania 19104.

出版信息

J Gen Virol. 1993 Jul;74 ( Pt 7):1277-85. doi: 10.1099/0022-1317-74-7-1277.

Abstract

Dendritic cells (DC) are members of a distinct family of bone marrow-derived leukocytes. DC are potent accessory cells for a number of T cell-mediated immune responses, including autologous and allogeneic mixed leukocyte reactions, and mitogen- and antigen-stimulated lymphocyte proliferation. In the present study, DC purified from human peripheral blood were inoculated with various strains (IIIB, SF2, WMJ1, SF162, 89.6 and clone HXB2) of human immunodeficiency virus type 1 (HIV-1) displaying different patterns of cellular tropism. Viral replication was demonstrated by detection of p24 antigen (Ag) intracellularly and in culture supernatants, and by Southern and Northern blot analyses for the presence of HIV DNA and RNA, respectively, within infected cells. Cell-free and cell-associated p24 Ag levels rose substantially when DC were inoculated with strains SF162, 89.6 and clone HXB2. In contrast, p24 Ag levels rose only marginally after inoculation of DC with strains IIIB, SF2 and WMJ1. Purified DC did not express detectable membrane CD4, although CD4 mRNA was detected by reverse transcriptase PCR. The presence of anti-CD4 monoclonal antibodies failed to block infection of DC by any of the HIV strains tested, suggesting the existence of a CD4-independent alternative pathway of viral entry. The possibility that DC serve as a reservoir for HIV-1 must be considered.

摘要

树突状细胞(DC)是源自骨髓的一类独特白细胞家族的成员。DC是多种T细胞介导的免疫反应的有效辅助细胞,包括自体和异体混合淋巴细胞反应,以及丝裂原和抗原刺激的淋巴细胞增殖。在本研究中,从人外周血中纯化的DC接种了1型人类免疫缺陷病毒(HIV-1)的各种毒株(IIIB、SF2、WMJ1、SF162、89.6和克隆HXB2),这些毒株表现出不同的细胞嗜性模式。通过检测细胞内和培养上清液中的p24抗原(Ag),以及分别通过Southern和Northern印迹分析检测感染细胞内HIV DNA和RNA的存在,证实了病毒复制。当DC接种毒株SF162、89.6和克隆HXB2时,无细胞和细胞相关的p24 Ag水平大幅上升。相比之下,DC接种毒株IIIB、SF2和WMJ1后,p24 Ag水平仅略有上升。纯化的DC不表达可检测到的膜CD4,尽管通过逆转录酶PCR检测到了CD4 mRNA。抗CD4单克隆抗体的存在未能阻断所测试的任何HIV毒株对DC的感染,这表明存在一种不依赖CD4的病毒进入替代途径。必须考虑DC作为HIV-1储存库的可能性。

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