Tumor Cell Programmed Death Ligand 1-Mediated T Cell Suppression Is Overcome by Coexpression of CD80
Author(s) -
Samuel Haile,
Jacobus J. Bosch,
Nnenna Agu,
Annette M. Zeender,
Preethi Somasundaram,
Minu K. Srivastava,
Sabine Britting,
Julie Wolf,
Bruce R. Ksander,
Suzanne OstrandRosenberg
Publication year - 2011
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1003682
Subject(s) - cd80 , biology , cancer research , melanoma , cell , immune system , microbiology and biotechnology , t cell , cancer cell , programmed cell death , cancer , immunology , apoptosis , cytotoxic t cell , cd40 , in vitro , genetics
Programmed death ligand 1 (PDL1, or B7-H1) is expressed constitutively or is induced by IFN-γ on the cell surface of most human cancer cells and acts as a "molecular shield" by protecting tumor cells from T cell-mediated destruction. Using seven cell lines representing four histologically distinct solid tumors (lung adenocarcinoma, mammary carcinoma, cutaneous melanoma, and uveal melanoma), we demonstrate that transfection of human tumor cells with the gene encoding the costimulatory molecule CD80 prevents PDL1-mediated immune suppression by tumor cells and restores T cell activation. Mechanistically, CD80 mediates its effects through its extracellular domain, which blocks the cell surface expression of PDL1 but does not prevent intracellular expression of PDL1 protein. These studies demonstrate a new role for CD80 in facilitating antitumor immunity and suggest new therapeutic avenues for preventing tumor cell PDL1-induced immune suppression.
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