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混合淋巴细胞培养的无细胞培养基增强小鼠T淋巴细胞体外对同种异体成纤维细胞的致敏作用。

Cell-free media of mixed lymphocyte cultures augmenting sensitization in vitro of mouse T lymphocytes against allogeneic fibroblasts.

作者信息

Altman A, Cohen I R

出版信息

Eur J Immunol. 1976 Jul;5(7):437-44. doi: 10.1002/eji.1830050702.

Abstract

Using an in vitro mouse lymphocyte anti-fibroblast reaction (AFR), we recently reported that the addition of allogeneic stimulator lymphocytes to the sensitization phase of the AFR enhanced sensitization to fibroblast antigens as evidenced by a marked increase in the cytolytic activity of the sensitized lymphocyte population. In the present report we studied the mechanism of this helper effect by testing the capacity of cell-free media derived from 48-h mixed spleen cultures to enhance anti-fibroblast sensitization. We found that such cell-free media could produce a marked helper effect when applied to the sensitization phase of the AFR, but not when added to the cytolytic effector phase. The stimulator cells in the mixed lymphocyte culture (MLC) did not have to be syngeneic with the sensitizing fibroblasts in the AFR in order for the helper effect to be demonstrated. Lymphocytes sensitized to fibroblast antigens in the presence of MLC medium retained their specificity of the effector phase. Our data suggest that the MLC medium acts by enhancing differentiation processes of antigen-triggered lymphocytes. Generation of helper activity by the MLC was abolished by 1000 r irradiation of the responder cells. By using nu/nu and normal spleens, both from two different strains, as cell sources for the MLC, we found that the generation of helper activity depended on T cells capable of proliferation. Furthermore, stimulator lymphocytes differing from responder lymphocytes by non-H-2 alloantigens as well as by point mutation with the H-2 complex were capable of eliciting helper factor(s). Thus, soluble factor(s) produced in a MLC, which are dependent on T lymphocyte proliferation, have the capacity to enhance the sensitization of mouse lymphocytes against antigens present on allogeneic fibroblasts.

摘要

利用体外小鼠淋巴细胞抗成纤维细胞反应(AFR),我们最近报道,在AFR的致敏阶段添加同种异体刺激淋巴细胞可增强对成纤维细胞抗原的致敏作用,致敏淋巴细胞群体的细胞溶解活性显著增加即证明了这一点。在本报告中,我们通过测试来自48小时混合脾细胞培养物的无细胞培养基增强抗成纤维细胞致敏作用的能力,研究了这种辅助效应的机制。我们发现,这种无细胞培养基应用于AFR的致敏阶段时可产生显著的辅助效应,但添加到细胞溶解效应阶段时则不然。混合淋巴细胞培养(MLC)中的刺激细胞不必与AFR中致敏的成纤维细胞同基因,即可证明辅助效应。在MLC培养基存在下对成纤维细胞抗原致敏的淋巴细胞保留了其效应阶段的特异性。我们的数据表明,MLC培养基通过增强抗原触发淋巴细胞的分化过程发挥作用。对反应细胞进行1000伦琴照射可消除MLC产生的辅助活性。通过使用来自两种不同品系的裸鼠和正常脾脏作为MLC的细胞来源,我们发现辅助活性的产生依赖于能够增殖的T细胞。此外,与反应淋巴细胞在非H-2同种异体抗原以及H-2复合体的点突变方面不同的刺激淋巴细胞能够引发辅助因子。因此,MLC中产生的可溶性因子依赖于T淋巴细胞增殖,具有增强小鼠淋巴细胞对同种异体成纤维细胞上存在的抗原的致敏作用的能力。

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