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通过竞争性聚合酶链反应对HIV感染患者表皮朗格汉斯细胞中HIV-1前病毒DNA进行定量分析。

Quantitation by competitive PCR of HIV-1 proviral DNA in epidermal Langerhans cells of HIV-infected patients.

作者信息

Cimarelli A, Zambruno G, Marconi A, Girolomoni G, Bertazzoni U, Giannetti A

机构信息

Istituto di Genetica Biochimica ed Evoluzionistica, CNR, Pavia, Italy.

出版信息

J Acquir Immune Defic Syndr (1988). 1994 Mar;7(3):230-5.

PMID:8106964
Abstract

Langerhans cells (LC) belong to the dendritic cell family and represent the principal antigen presenting cells populating squamous epithelia. We have reported the presence of human immunodeficiency virus Type 1 (HIV-1) proviral DNA and RNA in purified LC from the epidermis of seropositive patients. The aim of this study was to quantify HIV-1 proviral DNA in LC of infected patients using a competitive polymerase chain reaction (PCR) assay. Bulk epidermal cell (EC) suspensions were obtained from the skin of nine AIDS patients and six seronegative subjects. Purified LC and LC-depleted EC were prepared by immunomagnetic separation using an anti-CD1a monoclonal antibody. LC preparations did not contain T cells, as assessed by reverse transcription PCR analysis of the T cell receptor beta-chain gene (C region). In addition, no CD14+ cells could be detected in LC fractions by immunostaining of cytospin preparations. To quantify HIV-1 DNA, a new competitive PCR system was devised using SK145/150 as primers (gag) and a competitor plasmid DNA with a modified sequence (209 instead of 142 bp). The number of HIV-1 DNA copies found in the LC of AIDS patients ranged from 107 to 3,645/10(5) LC. In contrast, LC-depleted EC from the same subjects were all negative. The results indicate that in AIDS patients the frequency of infected LC is comparable to that reported for peripheral blood CD4+ T cells.

摘要

朗格汉斯细胞(LC)属于树突状细胞家族,是鳞状上皮中主要的抗原呈递细胞。我们曾报道在血清反应阳性患者表皮纯化的LC中存在1型人类免疫缺陷病毒(HIV-1)前病毒DNA和RNA。本研究的目的是使用竞争性聚合酶链反应(PCR)测定法对感染患者LC中的HIV-1前病毒DNA进行定量。从9名艾滋病患者和6名血清反应阴性受试者的皮肤中获取大量表皮细胞(EC)悬液。使用抗CD1a单克隆抗体通过免疫磁珠分离制备纯化的LC和去除LC的EC。通过对T细胞受体β链基因(C区)的逆转录PCR分析评估,LC制剂不含T细胞。此外,通过细胞涂片制剂的免疫染色在LC组分中未检测到CD14+细胞。为了定量HIV-1 DNA,设计了一种新的竞争性PCR系统,使用SK145/150作为引物(gag)和具有修饰序列(209而非142 bp)的竞争性质粒DNA。在艾滋病患者的LC中发现的HIV-1 DNA拷贝数范围为107至3645/10(5) LC。相比之下,来自相同受试者的去除LC的EC均为阴性。结果表明,在艾滋病患者中,被感染LC的频率与外周血CD4+ T细胞的报道频率相当。

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