首页> 美国卫生研究院文献>Immunology >Regulatory role of suppressor T cells in the expression of delayed-type hypersensitivity in mice. II. Soluble factor from thymic suppressor cells stimulated with antigen in vitro and its possible interaction with macrophages.
【2h】

Regulatory role of suppressor T cells in the expression of delayed-type hypersensitivity in mice. II. Soluble factor from thymic suppressor cells stimulated with antigen in vitro and its possible interaction with macrophages.

机译:抑制性T细胞在小鼠迟发型超敏反应表达中的调节作用。二。胸腺抑制细胞中的可溶性因子在体外被抗原刺激并可能与巨噬细胞发生相互作用。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Thymus cells from mice primed s.c. with a high dose (10 mg) of lysozyme (Lys) specifically suppressed delayed footpad reaction (FPR) in mice previously immuned with lipid-conjugated lysozyme (D.Lys), and also suppressed the transfer of FPR by D.Lys-immune spleen cells into normal mice. Furthermore, they inhibited antigen-stimulated DNA synthesis of D.Lys-immune spleen cells in vitro. If the suppressor thymus cells were cultured with Lys in vitro, they produced soluble factor which depressed the ability of D.Lys-immune spleen cells to transfer FPR. Both supernatant of culture without Lys and extract of suppressor thymus cells were inactive in supression of FPR. The suppressor factor was antigen-specific because its suppressive activity was absorbed with Lys but not with an unrelated antigen lactalbumin. The factor failed to depress the ability of D.Lys-immune spleen cells to transfer FPR when the spleen cells were depleted of glass-adherent cells. In addition, incubation of peritoneal exudate cells from normal mice with the factor rendered the cells suppressive for passive transfer of FPR. These results suggest that the suppressor factor depresses the effector function of T cells responsible for FPR possibly via macrophage.
机译:来自小鼠的胸腺细胞可引发s.c.用高剂量(10 mg)溶菌酶(Lys)特异性抑制先前用脂质结合溶菌酶(D.Lys)免疫的小鼠的延迟足垫反应(FPR),还抑制D.Lys免疫脾脏转移FPR细胞进入正常小鼠。此外,它们在体外抑制D.Lys-免疫脾细胞的抗原刺激的DNA合成。如果抑制性胸腺细胞与Lys一起在体外培养,它们会产生可溶因子,从而降低D.Lys免疫脾细胞转移FPR的能力。不含Lys的培养上清液和抑制性胸腺细胞提取物在FPR抑制中均无活性。抑制因子是抗原特异性的,因为其抑制活性被Lys吸收,但不被无关的抗原乳白蛋白吸收。当脾细胞中缺乏玻璃粘附细胞时,该因子不能降低免疫D.Lys的脾细胞转移FPR的能力。此外,正常小鼠腹膜渗出细胞与该因子的孵育使细胞抑制了FPR的被动转移。这些结果表明抑制因子可能通过巨噬细胞降低了负责FPR的T细胞的效应子功能。

著录项

  • 期刊名称 Immunology
  • 作者

    A Kojima; S I Tamura; Y Egashira;

  • 作者单位
  • 年(卷),期 1979(37),3
  • 年度 1979
  • 页码 577–585
  • 总页数 9
  • 原文格式 PDF
  • 正文语种
  • 中图分类 免疫学;
  • 关键词

  • 入库时间 2022-08-17 12:05:45

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号