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培养的人胸腺上皮单层细胞在体外可诱导艾滋病患者单核细胞表达CD4。

Cultured human thymus epithelial monolayer cells induce CD4 expression on mononuclear cells of AIDS patients in vitro.

作者信息

Schuurman H J, Hendriks R W, Lange J M, van der Linden J A, Gmelig Meyling F H, Danner S A, Kater L

出版信息

Clin Exp Immunol. 1986 May;64(2):348-55.

Abstract

We investigated the in vitro effect of cultured human thymic epithelial monolayer cells on mononuclear cells (MNC) from patients with Acquired Immune Deficiency Syndrome (AIDS) and AIDS-related complex (ARC). Patients having undergone bone-marrow transplantation (BMT), who showed a similar deficiency of T-lymphocytes expressing CD4 (Leu-3, T4), and healthy blood donors served as controls. Most epithelial monolayer cells were of thymic medulla origin, as documented using a panel of monoclonal antibodies to thymic epithelial cells. In AIDS/ARC patients the CD4-positive cells (ranging between 4 and 30% of MNC) increased by a factor of 1.56 (s.e.m. 0.15, n = 12) during a 2 h incubation on the monolayer. Human fetal lung fibroblasts were inactive in this respect. There was no consistent change in cells expressing CD3 (Leu-4, T3), CD5 (Leu-1) or CD8 (Leu-2, T8). In BMT patients and healthy controls, neither thymus epithelium nor fibroblasts had any effect on T cell marker expression. Incorporation of tritiated thymidine by stimulated or unstimulated lymphocytes was increased after incubation for 3 days on either epithelium or fibroblasts. We conclude that CD4 expression is induced on MNC from AIDS/ARC patients during a 2 h incubation on epithelial monolayers.

摘要

我们研究了培养的人胸腺上皮单层细胞对获得性免疫缺陷综合征(AIDS)和艾滋病相关综合征(ARC)患者单核细胞(MNC)的体外作用。接受过骨髓移植(BMT)且表现出类似表达CD4(Leu-3,T4)的T淋巴细胞缺乏的患者,以及健康献血者作为对照。如使用一组针对胸腺上皮细胞的单克隆抗体所证明的,大多数上皮单层细胞起源于胸腺髓质。在AIDS/ARC患者中,CD4阳性细胞(占MNC的4%至30%)在单层上孵育2小时期间增加了1.56倍(标准误0.15,n = 12)。人胎儿肺成纤维细胞在这方面没有活性。表达CD3(Leu-4,T3)、CD5(Leu-1)或CD8(Leu-2,T8)的细胞没有一致的变化。在BMT患者和健康对照中,胸腺上皮和成纤维细胞对T细胞标志物表达均无影响。在与上皮或成纤维细胞孵育3天后,受刺激或未受刺激的淋巴细胞掺入氚标记胸腺嘧啶核苷的量增加。我们得出结论,AIDS/ARC患者的MNC在与上皮单层孵育2小时期间诱导了CD4表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/1542350/9bf17409baa1/clinexpimmunol00122-0129-a.jpg

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