Induction of antigen-specific T cell anergy: An early event in the course of tumor progression

Kevin F. Staveley-O’Carroll(Johns Hopkins University), Eduardo M. Sotomayor(Johns Hopkins University), Jami Montgomery(Johns Hopkins University), Ivan Borrello(Johns Hopkins University), Leon Hwang(Johns Hopkins University), Steve Fein(Johns Hopkins University), Drew M. Pardoll(Johns Hopkins University), Hyam I. Levitsky(Johns Hopkins University)
Proceedings of the National Academy of Sciences
February 3, 1998
Cited by 696Open Access

Abstract

The priming of tumor-antigen-specific T cells is critical for the initiation of successful anti-tumor immune responses, yet the fate of such cells during tumor progression is unknown. Naive CD4(+) T cells specific for an antigen expressed by tumor cells were transferred into tumor-bearing mice. Transient clonal expansion occurred early after transfer, accompanied by phenotypic changes associated with antigen recognition. Nevertheless, these cells had a diminished response to peptide antigen in vitro and were unable to be primed in vivo. The development of antigen-specific T cell anergy is an early event in the tumor-bearing host, and it suggests that tolerance to tumor antigens may impose a significant barrier to therapeutic vaccination.


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