The double-edged sword: Harnessing PD-1 blockade in tumor and autoimmunity

Author:

Kuchroo Juhi R.12ORCID,Hafler David A.34ORCID,Sharpe Arlene H.1245ORCID,Lucca Liliana E.3ORCID

Affiliation:

1. Department of Immunology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.

2. Evergrande Center for Immunological Diseases, Harvard Medical School and Brigham and Women’s Hospital, Boston, MA, USA.

3. Departments of Neurology and Immunobiology, Yale School of Medicine, New Haven, CT, USA.

4. Broad Institute of MIT and Harvard University, Cambridge, MA, USA.

5. Department of Pathology, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA.

Abstract

PD-1 restrains both effector T cells and T regs ; therefore, PD-1 may be uniquely modulated to enhance tumor rejection while maintaining immune tolerance.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine,Immunology

Reference194 articles.

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2. Safety, Activity, and Immune Correlates of Anti–PD-1 Antibody in Cancer

3. Toxicities of the anti-PD-1 and anti-PD-L1 immune checkpoint antibodies

4. Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases;Sakaguchi S.;J. Immunol.,1995

5. CD4+CD25high Regulatory Cells in Human Peripheral Blood

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