4.6 Article

Tumor Cell Programmed Death Ligand 1-Mediated T Cell Suppression Is Overcome by Coexpression of CD80

Journal

JOURNAL OF IMMUNOLOGY
Volume 186, Issue 12, Pages 6822-6829

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1003682

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Funding

  1. National Institutes of Health [R01CA115880, R01CA84232, R01EY016486, T32 GM066706, R25-GM55036]
  2. Graduate Assistance in Areas of National Need predoctoral fellowship
  3. Rotterdamse Vereniging Blindenbelangen
  4. Stichting Blindenhulp
  5. Stichting Blinden-Penning
  6. Stichting Dondersfonds
  7. Stichting Nelly Reef Fund
  8. Gratama Stichting
  9. Stichting Admiraal van Kinsbergen Fonds
  10. Foundation De Drie Lichten fellowships
  11. Deutsche Forschungsgemeinschaft [DFG-SFB643 (C8)]

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Programmed death ligand 1 (PDL1, or B7-H1) is expressed constitutively or is induced by IFN-gamma 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. The Journal of Immunology, 2011, 186: 6822-6829.

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