Suppr超能文献

移植前使用非清除性抗CD4单克隆抗体和供体特异性输血诱导移植耐受的动力学。免疫无反应性的发展需要一段关键的时间。

Kinetics of induction of transplantation tolerance with a nondepleting anti-Cd4 monoclonal antibody and donor-specific transfusion before transplantation. A critical period of time is required for development of immunological unresponsiveness.

作者信息

Saitovitch D, Bushell A, Mabbs D W, Morris P J, Wood K J

机构信息

Nuffield Department of Surgery, University of Oxford, John Radcliffe Hospital, Headington, Oxford, England.

出版信息

Transplantation. 1996 Jun 15;61(11):1642-7. doi: 10.1097/00007890-199606150-00016.

Abstract

The combination of a depleting anti-Cd43 monoclonal antibody (mAb) and a single donor-specific transfusion before transplantation has been shown to induce operational transplantation tolerance in the majority of cardiac allograft recipients in a mouse model. To examine a protocol which might be more clinically relevant, we have modified this tolerance-inducing protocol by substituting the depleting with a nondepleting anti-Cd4 mAb. We show that this form of pretreatment can also induce immunologic unresponsiveness in most recipients (C3H/He, H2(k)), provided a critical period of time, in this case 28 days, is allowed between pretreatment and transplantation of a fully mismatched heart graft (H2(b)). When only 1 or 2 weeks were allowed between pretreatment and transplantation, only slight graft prolongation was obtained when compared with recipients receiving anti-Cd4 mAb alone, at these time points. Maintenance of tolerance in this model was due, at least in part, to active mechanisms as immunologic unresponsiveness to donor antigens could be transferred to naive syngeneic mice by splenocytes from recipients bearing long-term functioning grafts. These findings suggest that a population of regulatory cells develop after pretreatment with nondepleting anti-Cd4 mAb and donor-specific transfusion, and that it takes at least 1 month for these cells to expand and effectively drive the recipient's immune system toward immunologic unresponsiveness.

摘要

在小鼠模型中,已证明移植前使用耗竭性抗Cd43单克隆抗体(mAb)与单次供体特异性输血相结合,可使大多数心脏同种异体移植受者产生操作性移植耐受。为了研究一种可能更具临床相关性的方案,我们通过用非耗竭性抗Cd4 mAb替代耗竭性抗体,对这种诱导耐受的方案进行了修改。我们发现,这种预处理形式在大多数受者(C3H/He,H2(k))中也能诱导免疫无反应性,前提是在预处理和完全不匹配的心脏移植物(H2(b))移植之间留出一个关键时间段,在这种情况下为28天。当预处理和移植之间只允许1或2周时,与仅接受抗Cd4 mAb的受者相比,在这些时间点仅获得轻微的移植物延长。在该模型中,耐受的维持至少部分归因于主动机制,因为对供体抗原的免疫无反应性可通过来自长期具有功能移植物的受者的脾细胞转移至同基因的未致敏小鼠。这些发现表明,在用非耗竭性抗Cd4 mAb和供体特异性输血进行预处理后,会产生一群调节性细胞,并且这些细胞至少需要1个月才能扩增并有效地促使受者的免疫系统产生免疫无反应性。

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