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HIV-1在重建阴道黏膜中对朗格汉斯细胞的感染。

HIV-1 infection of Langerhans cells in a reconstructed vaginal mucosa.

作者信息

Sivard Peggy, Berlier Willy, Picard Bertrand, Sabido Odile, Genin Christian, Misery Laurent

机构信息

Groupe Immunite des Muqueuses et Agents Pathogenes, Jean Monnet University, Saint-Etienne, France.

出版信息

J Infect Dis. 2004 Jul 15;190(2):227-35. doi: 10.1086/421704. Epub 2004 Jun 14.

Abstract

We have developed an in vitro reconstructed vaginal mucosa integrating Langerhans cells (LCs), obtained by differentiation of umbilical cord blood CD34(+) hematopoietic progenitor cells, and, in this model, we have investigated the infection of LCs by human immunodeficiency virus type 1 (HIV-1). Proviral DNA of X4 (LAI and NL4-3) and R5 (Ba-L) HIV-1 strains were detected in LCs integrated in the reconstituted mucosa. Infection of LCs could be specifically inhibited by the chemokines stromal cell-derived factor 1 (SDF-1) and RANTES (regulated on activation, normally T cell-expressed and -secreted), confirming the presence of functional coreceptors on LCs generated in vitro. A complete inhibition of LCs, by use of azidothymidine, a reverse-transcriptase inhibitor, was also observed. Moreover, HIV-1-infected LCs of the reconstructed mucosa were able to transmit R5 or X4 HIV-1 strains to activated peripheral blood mononuclear cells. Such a model could be a useful tool to study the mechanisms involved in transmission of HIV in the female genital tract.

摘要

我们构建了一种体外重建的阴道黏膜,其中整合了通过脐带血CD34(+)造血祖细胞分化获得的朗格汉斯细胞(LCs),并在此模型中研究了1型人类免疫缺陷病毒(HIV-1)对LCs的感染情况。在重建黏膜中整合的LCs中检测到了X4(LAI和NL4-3)和R5(Ba-L)HIV-1毒株的前病毒DNA。趋化因子基质细胞衍生因子1(SDF-1)和调节激活正常T细胞表达和分泌因子(RANTES)可特异性抑制LCs的感染,这证实了体外生成的LCs上存在功能性共受体。使用逆转录酶抑制剂叠氮胸苷也观察到对LCs的完全抑制作用。此外,重建黏膜中被HIV-1感染的LCs能够将R5或X4 HIV-1毒株传播给活化的外周血单个核细胞。这样的模型可能是研究HIV在女性生殖道传播所涉及机制的有用工具。

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