细胞毒性T细胞
免疫学
抗原
免疫疗法
生物
主要组织相容性复合体
过继性细胞移植
CD8型
CTL公司*
人类白细胞抗原
癌症研究
免疫系统
T细胞
体外
生物化学
作者
Mathias Oelke,Marcela V. Maus,Dominic Didiano,Carl H. June,Andréas Mackensen,Jonathan P. Schneck
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2003-04-21
卷期号:9 (5): 619-625
被引量:300
摘要
Adoptive immunotherapy holds promise as a treatment for cancer and infectious diseases, but its development has been impeded by the lack of reproducible methods for generating therapeutic numbers of antigen-specific CD8(+) cytotoxic T lymphocytes (CTLs). As a result, there are only limited reports of expansion of antigen-specific CTLs to the levels required for clinical therapy. To address this issue, artificial antigen-presenting cells (aAPCs) were made by coupling a soluble human leukocyte antigen-immunoglobulin fusion protein (HLA-Ig) and CD28-specific antibody to beads. HLA-Ig-based aAPCs were used to induce and expand CTLs specific for cytomegalovirus (CMV) or melanoma. aAPC-induced cultures showed robust antigen-specific CTL expansion over successive rounds of stimulation, resulting in the generation of clinically relevant antigen-specific CTLs that recognized endogenous antigen-major histocompatibility complex complexes presented on melanoma cells. These studies show the value of HLA-Ig-based aAPCs for reproducible expansion of disease-specific CTLs for clinical approaches to adoptive immunotherapy.
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