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Fundamental Mechanisms of Immune Checkpoint Blockade Therapy
Spencer C Wei1, Colm R Duffy2, James P Allison1,3
1Department of Immunology, The University of Texas MD Anderson Cancer Center, Houston, Texas. scwei@mdanderson.org jallison@mdanderson.org.
Abstract:
Immune checkpoint blockade is able to induce durable responses across multiple types of cancer, which has enabled the oncology community to begin to envision potentially curative therapeutic approaches. However, the remarkable responses to immunotherapies are currently limited to a minority of patients and indications, highlighting the need for more effective and novel approaches. Indeed, an extraordinary amount of preclinical and clinical investigation is exploring the therapeutic potential of negative and positive costimulatory molecules. Insights into the underlying biological mechanisms and functions of these molecules have, however, lagged significantly behind. Such understanding will be essential for the rational design of next-generation immunotherapies. Here, we review the current state of our understanding of T-cell costimulatory mechanisms and checkpoint blockade, primarily of CTLA4 and PD-1, and highlight conceptual gaps in knowledge.Significance: This review provides an overview of immune checkpoint blockade therapy from a basic biology and immunologic perspective for the cancer research community. Cancer Discov; 8(9); 1069-86. ©2018 AACR.
Insights
Immune checkpoint blockade offers durable cancer responses but benefits few. Further research into T-cell costimulatory molecules is crucial for developing next-generation immunotherapies.
Area of Science:
- Immunology
- Oncology
Background:
- Immune checkpoint blockade (ICB) has shown promise for durable cancer responses.
- However, current ICBs benefit only a subset of patients, necessitating novel therapeutic strategies.
Purpose of the Study:
- To review the current understanding of T-cell costimulatory mechanisms and ICB.
- To identify knowledge gaps essential for designing next-generation immunotherapies.
Main Methods:
- Review of preclinical and clinical investigations.
- Focus on T-cell costimulatory molecules, CTLA-4, and PD-1.
Main Results:
- Significant research is exploring costimulatory molecules for cancer therapy.
- Understanding of these molecules' biological mechanisms lags behind therapeutic exploration.
Conclusions:
- Enhanced knowledge of T-cell costimulation is vital for advancing cancer immunotherapy.
- Addressing conceptual gaps in ICB and costimulatory molecule function is critical for future treatments.
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