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首页> 外文期刊>The Journal of Experomental Medicine >Antigen-specific T-cell-mediated suppression. I. Induction of L-glutamic acid(60)-L-alanine(30)-L-tyrosine(10) specific suppressor T cells in vitro requires both antigen-specific T-cell-suppressor factor and antigen
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Antigen-specific T-cell-mediated suppression. I. Induction of L-glutamic acid(60)-L-alanine(30)-L-tyrosine(10) specific suppressor T cells in vitro requires both antigen-specific T-cell-suppressor factor and antigen

机译:抗原特异性T细胞介导的抑制作用。 I.体外诱导L-谷氨酸(60)-L-丙氨酸(30)-L-酪氨酸(10)特异性抑制性T细胞既需要抗原特异性T细胞抑制因子又需要抗原

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摘要

A combination of in vitro and in vivo techniques were used to explore the mode of action of both crude and purified suppressive extracts specific for the random copolymer L-giutamic acid(60)-L-alanine(30)-L-tyrosine(10) (GAT- T(s)F) obtained from nonresponder DBA/1 (H-2(q)) mice. Normal DBA/1 spleen cells were incubated under modified Mishell-Dutton culture conditions for 2 days together with crude or purified GAT-T(s)F, and in the presence or absence of free GAT. These cells were then washed extensively and 3 × 10(6) viable cells transferred to syngeneic recipients, which were challenged at the same time with the immunogenic form of GAT complexed to methylated bovine serum albumin (GAT-MBSA). GAT-specific IgG plaque-forming cells (PFC) in the spleen were assayed 7 days later. In agreement with earlier in vitro studies on the action of GAT-T(s)F, it was demonstrated that under these conditions, low concentrations of GAT-T(s)F stimulated the development of cells which, aider transfer, are able to suppress the GAT PFC response to GAT-MBSA. The cells responsible for this suppression were shown to be T lymphocytes by using nylon wool-purified T cells for suppressor cell induction and by eliminating suppressive activity in cells cultured with crude GAT-T(s)F by treatment with anti-Thy 1.2 plus C before transfer. The suppressor T cells act in a specific manner failing to suppress significantly either anti-sheep erythrocyte or trinitrophenyl-ovalbumin primary PFC responses. For the induction of GAT-specific suppressor T cells in culture, a moiety bearing H- 2(K(q) or I(q)) determinants and also GAT, either bound to the crude GAT- T(s)F or added in nanogram amounts to antigen (GAT)-free purified GAT-T(s)F, were both required.
机译:结合了体内和体外技术,研究了对无规共聚物L-谷氨酸(60)-L-丙氨酸(30)-L-酪氨酸(10)特异的粗制和纯化抑制性提取物的作用方式从无反应者DBA / 1(H-2(q))小鼠获得的(GAT-T(s)F)。在改良的Mishell-Dutton培养条件下,将正常的DBA / 1脾细胞与粗制或纯化的GAT-T(F)F在存在或不存在游离GAT的条件下孵育2天。然后将这些细胞充分洗涤,并将3×10(6)活细胞转移至同系受体,同时用复合至甲基化牛血清白蛋白(GAT-MBSA)的免疫原性GAT攻击。 7天后测定脾脏中的GAT特异性IgG斑块形成细胞(PFC)。与早期有关GAT-T(F)F作用的体外研究一致,研究表明在这些条件下,低浓度的GAT-T(F)F刺激了细胞的发育,并有助于转移。抑制GAT PFC对GAT-MBSA的响应。通过使用尼龙羊毛纯化的T细胞抑制细胞诱导,并通过用抗Thy 1.2加C处理消除了用粗GAT-T(F)F培养的细胞中的抑制活性,证明了负责这种抑制的细胞是T淋巴细胞。转移之前。抑制性T细胞以特定的方式起作用,不能显着抑制抗绵羊红细胞或三硝基苯基-卵清蛋白的初级PFC应答。为了诱导培养中的GAT特异性抑制性T细胞,可将带有H-2(K(q)或I(q))决定簇以及GAT的部分结合至粗GAT-T(s)F或添加至都需要10毫微克量的无抗原(GAT)的纯化GAT-T(s)F。

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