Suppr超能文献

小鼠移植物抗宿主反应激活的两种非特异性抑制细胞的证据。

Evidence for two types of non-specific suppressor cells activated by the graft-versus-host reaction in mice.

作者信息

Parthenais E, Lapp W S

出版信息

Scand J Immunol. 1978 Mar;7(3):215-20. doi: 10.1111/j.1365-3083.1978.tb00446.x.

Abstract

In vitro experiments were carried out to investigate the immunosuppressive efect of different populations of spleen cells obtained from animal experiencing a graft-versus-host reaction (GVHR). To induce the GVHR, parental lymphoid cells were injected into adult F1 hybrid mice. GVHR-activated spleen cells (GVH-sc) taken at different times post-GVHR induction were separated into adherent and non-adherent fractions and treated with anti-theta serum plus complement. The different types of GVH-SC were added to either parental (donor-type) of F1 (host-type) normal spleen cells and cultured with sheep erythrocytes in a modified Marbrook chamber. It was found that both adherent and non-adherent 10-day GVH-SC significantly inhibited the plaque-forming cell response of F1 normal spleen cells but not that of parental normal spleen cells. Significant suppression of the parental response was observed following the addition of 15-day GVH-SC or anti-theta treated adherent and non-adherent 7-day GVH-SC. The results suggest that the non-specific immunosuppressive effect of GVH-SC is mediated by GVHR-activated macrophages and B lymphocytes found in the anti-theta treated adherent and non-adherent fractions of the GVH-SC suspensions respectively.

摘要

进行了体外实验,以研究从经历移植物抗宿主反应(GVHR)的动物获得的不同群体脾细胞的免疫抑制作用。为诱导GVHR,将亲代淋巴细胞注射到成年F1杂种小鼠体内。在GVHR诱导后不同时间采集的GVHR激活的脾细胞(GVH-sc)被分离为贴壁和非贴壁部分,并用抗θ血清加补体处理。将不同类型的GVH-SC添加到亲代(供体型)或F1(宿主型)正常脾细胞中,并在改良的Marbrook小室中与绵羊红细胞一起培养。发现贴壁和非贴壁的10天GVH-SC均显著抑制F1正常脾细胞的空斑形成细胞反应,但不抑制亲代正常脾细胞的反应。在添加15天GVH-SC或抗θ处理的贴壁和非贴壁7天GVH-SC后,观察到亲代反应受到显著抑制。结果表明,GVH-SC的非特异性免疫抑制作用分别由GVHR激活的巨噬细胞和B淋巴细胞介导,它们分别存在于GVH-SC悬浮液的抗θ处理的贴壁和非贴壁部分中。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验