Original paper
Combination CTLA-4 Blockade and 4-1BB Activation Enhances Tumor Rejection by Increasing T-Cell Infiltration, Proliferation, and Cytokine Production
Abstract
Background The co-inhibitory receptor Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) attenuates immune responses and prevent autoimmunity, however, tumors exploit this pathway to evade the host T-cell response. The T-cell co-stimulatory receptor 4-1BB is transiently upregulated on T-cells following activation and increases their proliferation and inflammatory cytokine production when engaged. Antibodies which block CTLA-4 or which activate 4-1BB can...
Figures & Tables

Figure 1. Anti-CTLA-4 and a4-1BB synergize in the context of FVAX. Kaplan-Meier ...

Figure 2. Combination aCTLA-4/a4-1BB therapy promotes high effector to regulator...

Figure 3. 4-1BB activation cooperates with CTLA-4 blockade to induce peripheral ...

Figure 4. Combination aCTLA-4/a4-1BB therapy enhances intra-tumoral T-cell cytok...

Figure 5. Combination aCTLA-4/a4-1BB therapy induces KLRG1 and PD-1 expression b...

Figure 6. High KLRG1 expression by tumor-infiltrating effector T-cells at Day-25...

Figure 7. Combination aCTLA-4/a4-1BB therapy induces higher tumor infiltration b...

Figure 8. Combination aCTLA-4/a4-1BB treatment generates more pro-inflammatory r...
Paper Details
Title
Combination CTLA-4 Blockade and 4-1BB Activation Enhances Tumor Rejection by Increasing T-Cell Infiltration, Proliferation, and Cytokine Production
Published Date
Apr 29, 2011
Journal
Volume
6
Issue
4
Pages
e19499 - e19499
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