OLIGOCLONAL EXPANSION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I RESTRICTED CYTOLYTIC T-LYMPHOCYTES DURING A PRIMARY IMMUNE-RESPONSE INVIVO - DIRECT MONITORING BY FLOW-CYTOMETRY AND POLYMERASE CHAIN-REACTION

被引:79
作者
MACDONALD, HR
CASANOVA, JL
MARYANSKI, JL
CEROTTINI, JC
机构
[1] Ludwig Institute for Cancer Research, Lausanne Branch, Epalinges
关键词
D O I
10.1084/jem.177.5.1487
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous T cell receptor (TCR) sequence analysis of a panel of 23 H-2K(d) restricted cytotoxic T lymphocyte (CTL) clones recognizing the decapeptide HLA-CW3 170-179 revealed a striking conservation of TCR structure, in that all clones examined used Vbeta10 and Jalpha pHDS58 segments. We show here that the primary response in vivo after intraperitoneal injection of DBA/2 mice with HLA-CW3 expressing transfectants of syngeneic P815 (H-2d) tumor cells is characterized by a dramatic expansion of CD8+ Vbeta10+ CTL in the peritoneal cavity and draining (mesenteric) lymph node, as well as in peripheral blood. Additional analysis of TCR on HLA-CW3 immune populations by flow cytometry and polymerase chain reaction further indicates that the vast majority of responding CD8+ cells express restricted Valpha domains, a dominant Jalpha segment (pHDS58), and a conserved CDR3 length for both alpha and beta chains. This novel system provides a unique opportunity to directly monitor an oligoclonal primary antigen specific immune response in vivo at the single cell level independently of functional assays.
引用
收藏
页码:1487 / 1492
页数:6
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