A Critical Role for Granzymes in Antigen Cross-Presentation through Regulating Phagocytosis of Killed Tumor Cells
Author(s) -
Sabine Hoves,
Vivien R. Sutton,
Nicole M. Haynes,
Edwin D. Hawkins,
Daniel FernandezRuiz,
Nikola Baschuk,
Karin Sedelies,
Maximilian Schnurr,
John Stagg,
Daniel M. Andrews,
José A. Villadangos,
Joseph A. Trapani
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.1001670
Subject(s) - granzyme , perforin , cytotoxic t cell , priming (agriculture) , cd8 , biology , microbiology and biotechnology , antigen , immune system , immunogenicity , phagocytosis , t cell , immunology , in vitro , biochemistry , botany , germination
Granzymes A and B (GrAB) are known principally for their role in mediating perforin-dependent death of virus-infected or malignant cells targeted by CTL. In this study, we show that granzymes also play a critical role as inducers of Ag cross-presentation by dendritic cells (DC). This was demonstrated by the markedly reduced priming of naive CD8(+) T cells specific for the model Ag OVA both in vitro and in vivo in response to tumor cells killed in the absence of granzymes. Reduced cross-priming was due to impairment of phagocytosis of tumor cell corpses by CD8α(+) DC but not CD8α(-) DC, demonstrating the importance of granzymes in inducing the exposure of prophagocytic "eat-me" signals on the dying target cell. Our data reveal a critical and previously unsuspected role for granzymes A and B in dictating immunogenicity by influencing the mode of tumor cell death and indicate that granzymes contribute to the efficient generation of immune effector pathways in addition to their well-known role in apoptosis induction.
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