Song H K, Noorchashm H, Lieu Y K, Rostami S, Greeley S A, Barker C F, Naji A
Harrison Department of Surgical Research, University of Pennsylvania Medical Center, Philadelphia 19104, USA.
Transplantation. 1999 Jul 27;68(2):297-9. doi: 10.1097/00007890-199907270-00024.
The study of alloimmune responses has been limited by a lack of assays that can track the behavior of alloreactive lymphocytes in vivo. Here we utilize an experimental system that allows the identification and study of alloreactive CD4+ lymphocytes responding to major histocompatibility antigens in vivo.
Responder mouse lymphocytes were labeled with a fluorescein-based dye, adoptively transferred into irradiated allogeneic stimulator mice, and recovered at serial time points for analysis by flow cytometry.
Discrete generations of CD4+ responder lymphocytes proliferating specifically in response to allogeneic MHC class II were distinguished by fluorescein intensity. Successive division of alloreactive CD4+ lymphocytes was traced up to six generations after 60 hr.
This experimental system provides information on the division kinetics of alloreactive CD4+ cells. Other applications include immunophenotyping of alloreactive lymphocyte subsets. Further study of systems such as this will allow the detailed characterization of how alloimmune responses are initiated and proceed in vivo.
同种免疫反应的研究因缺乏能够在体内追踪同种反应性淋巴细胞行为的检测方法而受到限制。在此,我们利用一种实验系统,该系统能够在体内识别和研究对主要组织相容性抗原产生反应的同种反应性CD4 +淋巴细胞。
将应答小鼠淋巴细胞用基于荧光素的染料标记,过继转移到经辐照的同种异体刺激小鼠体内,并在连续的时间点回收,用于流式细胞术分析。
通过荧光素强度区分了对同种异体MHC II类特异性增殖的不同代CD4 +应答淋巴细胞。在60小时后,追踪到同种反应性CD4 +淋巴细胞连续分裂多达六代。
该实验系统提供了关于同种反应性CD4 +细胞分裂动力学的信息。其他应用包括同种反应性淋巴细胞亚群的免疫表型分析。对这样的系统进行进一步研究将能够详细表征同种免疫反应在体内是如何启动和进行的。