细胞毒性T细胞
CTL公司*
免疫学
抗原
过继性细胞移植
免疫疗法
病毒学
MHC I级
主要组织相容性复合体
生物
T细胞
免疫系统
CD8型
体外
生物化学
作者
Uluhan Sili,M. Helen Huls,Alan R. Davis,Stephen Gottschalk,Malcolm K. Brenner,Helen E. Heslop,Cliona M. Rooney
标识
DOI:10.1097/00002371-200305000-00008
摘要
Dendritic cells (DCs) have been shown to activate cytotoxic T-lymphocytes (CTLs) for many tumor and virus-associated antigens in vitro. In this study, the authors tested the feasibility of using DCs to expand polyclonal, cytomegalovirus (CMV)-specific CTL lines for adoptive immunotherapy. Two stimulations with DCs expressing pp65, the immunodominant antigen of CMV, effectively activated and expanded MHC-class I restricted, CMV-specific CTLs from peripheral blood mononuclear cells. However, limiting monocyte-derived DC numbers precluded the authors from expanding the CTLs to the numbers required for adoptive transfer protocols. Nonspecific stimulation methods failed to expand CTL lines specifically. However, the authors found that lymphoblastoid cell lines (LCLs) expressing pp65 expanded pp65-specific CTL lines without competition from EBV-specific CTLs. An unlimited source of antigen presenting cells that could present antigen in the appropriate MHC context emerged as a critical point for expansion of polyclonal, antigen-specific CTL lines.
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