Tumor growth enhances cross-presentation leading to limited T cell activation without tolerance

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info:eu-repo/semantics/altIdentifier/doi/10.1084/jem.20010032

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info:eu-repo/semantics/altIdentifier/pmid/11854356

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info:eu-repo/semantics/altIdentifier/pissn/0022-1007

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_061A829BB9D33

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L. T. Nguyen et al., « Tumor growth enhances cross-presentation leading to limited T cell activation without tolerance », Serveur académique Lausannois, ID : 10.1084/jem.20010032


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Using a tumor model of spontaneously arising insulinomas expressing a defined tumor-associated antigen, we investigated whether tumor growth promotes cross-presentation and tolerance of tumor-specific T cells. We found that an advanced tumor burden enhanced cross-presentation of tumor-associated antigens to high avidity tumor-specific T cells, inducing T cell proliferation and limited effector function in vivo. However, contrary to other models, tumor-specific T cells were not tolerized despite a high tumor burden. In fact, in tumor-bearing mice, persistence and responsiveness of adoptively transferred tumor-specific T cells were enhanced. Accordingly, a potent T cell-mediated antitumor response could be elicited by intravenous administration of tumor-derived peptide and agonistic anti-CD40 antibody or viral immunization and reimmunization. Thus, in this model, tumor growth promotes activation of high avidity tumor-specific T cells instead of tolerance. Therefore, the host remains responsive to T cell immunotherapy.

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