Sadat-Sowti B, Debré P, Idziorek T, Guillon J M, Hadida F, Okzenhendler E, Katlama C, Mayaud C, Autran B
Laboratoire d'Immunologie Cellulaire et Tissulaire, CNRS UA 0186, CHU Pitié-Salpétrière, Paris.
Eur J Immunol. 1991 Mar;21(3):737-41. doi: 10.1002/eji.1830210329.
CD8+CD57+ T cells, expanded in peripheral blood lymphocytes of AIDS patients, inhibit the effector phase of HLA-specific cytotoxic T lymphocytes, natural killer and lymphocyte-activated killer cells in a 4-h chromium-release assay. This inhibitory activity present in supernatants of purified sorted CD8+CD57+ cells is mediated by a non-antigen-specific inhibitory factor which is distinct from prostaglandin E2, T cell growth factor (TGF)-beta, latent-TGF-beta, tumor necrosis factor (TNF)-alpha and TNF-beta. Partial biochemical characterization demonstrates that the CD8+CD57+ inhibitory activity (a) is heat, trypsin and acid resistant, (b) binds to concanavalin A columns, indicating its glycosylation state and (c) is mediated by a 20-30-kDa soluble molecule.
在艾滋病患者外周血淋巴细胞中扩增的CD8 + CD57 + T细胞,在4小时铬释放试验中可抑制HLA特异性细胞毒性T淋巴细胞、自然杀伤细胞和淋巴细胞激活杀伤细胞的效应阶段。纯化分选的CD8 + CD57 +细胞上清液中存在的这种抑制活性由一种非抗原特异性抑制因子介导,该因子不同于前列腺素E2、T细胞生长因子(TGF)-β、潜伏性TGF-β、肿瘤坏死因子(TNF)-α和TNF-β。部分生化特性表明,CD8 + CD57 +抑制活性(a)耐热、耐胰蛋白酶和耐酸,(b)与伴刀豆球蛋白A柱结合,表明其糖基化状态,(c)由一种20 - 30 kDa的可溶性分子介导。