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针对2,4,6-三硝基苯基(TNP)修饰细胞的细胞毒性淋巴细胞的克隆分析。

The clonal analysis of cytotoxic lymphocytes against 2,4,6-trinitrophenyl (TNP)-modified cells.

作者信息

Ching L M, Marbrook J

出版信息

Eur J Immunol. 1979 Jan;9(1):22-7. doi: 10.1002/eji.1830090106.

Abstract

The frequency and specificity of clones of cytotoxic lymphocytes (CL) produced when (CBA X C57BL)F1 spleen cell populations were cultured with 2,4,6-trinitrophenyl (TNP)-modified syngeneic F1 cells, was examined. The frequency of clones which lysed F1-TNP targets was 1/3.3 X 10(4) spleen cells, and the frequency of clones which lysed the modified parental cells, CBA-TNP and C57BL-TNP was 1/6.7 X 10(4) and 1/2.9 X 10(5) spleen cells, respectively. Using a clonal analysis of the specificity of the CL, it was shown that the majority of the clones of CL which lysed the two modified parental tarets, were specific for one or the other of the targets. Activity against modified allogeneic DBA/2-TNP targets was also detected. The activity against DBA/2-TNP targets was due mainly to clones of CL which were specific for DBA/2-TNP targets. Only a minor part of the activity was due to clones which were cross-reactive for both F1-TNP and DBA/2-TNP target cells.

摘要

研究了用2,4,6-三硝基苯(TNP)修饰的同基因F1细胞培养(CBA×C57BL)F1脾细胞群体时产生的细胞毒性淋巴细胞(CL)克隆的频率和特异性。裂解F1-TNP靶标的克隆频率为1/3.3×10⁴个脾细胞,裂解修饰的亲代细胞CBA-TNP和C57BL-TNP的克隆频率分别为1/6.7×10⁴和1/2.9×10⁵个脾细胞。通过对CL特异性的克隆分析表明,裂解两个修饰亲代靶标的CL克隆大多数对其中一个靶标具有特异性。还检测到针对修饰的异基因DBA/2-TNP靶标的活性。针对DBA/2-TNP靶标的活性主要归因于对DBA/2-TNP靶标具有特异性的CL克隆。只有一小部分活性归因于对F1-TNP和DBA/2-TNP靶细胞都具有交叉反应性的克隆。

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