2023 - Research.com Immunology in United States Leader Award
2019 - Benjamin Franklin Medal, Franklin Institute
2019 - Distinguished Fellows of the American Association of Immunologists (AAI)
2018 - Nobel Prize for their discovery of cancer therapy by inhibition of negative immune regulation
2018 - King Faisal Prize
2018 - Albany Medical Center Prize in Medicine and Biomedical Research
2018 - Jessie Stevenson Kovalenko Medal, US National Academy of Sciences For important medical discoveries related to the body’s immune response to tumors.
2018 - Dr. Paul Janssen Award for Biomedical Research, Johnson & Johnson for pioneering a novel and effective strategy to harness the immune system for treating solid tumor cancers.
2017 - Fellow of the American Academy of Arts and Sciences
2017 - BBVA Foundation Frontiers of Knowledge Award
2015 - Paul Ehrlich and Ludwig Darmstaedter Prize
2014 - Canada Gairdner International Award
2014 - Breakthrough Prize in Life Sciences for the discovery of T cell checkpoint blockade as effective cancer therapy.
2014 - Szent-Györgyi Prize for Progress in Cancer Research, National Foundation for Cancer Research (NFCR)
2014 - Louisa Gross Horwitz Prize, Columbia University
2011 - American Association of Immunologists Lifetime Achievement Award
2011 - AAI Lifetime Achievement Award, American Association of Immunologists
2008 - AAI-Steinman Award for Human Immunology Research, American Association of Immunologists
2007 - Member of the National Academy of Medicine (NAM)
2006 - Fellow of the American Association for the Advancement of Science (AAAS)
1997 - Member of the National Academy of Sciences
1930 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary scientific interests are in Immunology, T cell, Cytotoxic T cell, Antigen and Immune system. His biological study spans a wide range of topics, including Blockade and Melanoma. The study incorporates disciplines such as Molecular biology, Tremelimumab and Cell biology in addition to T cell.
In his research on the topic of Cytotoxic T cell, FOXP3 is strongly related with CD8. His study focuses on the intersection of Antigen and fields such as Antibody with connections in the field of Nivolumab. His Immune system research incorporates themes from Mutation, Cancer and Cancer research.
His primary areas of study are Immunology, T cell, Immune system, Antigen and Cytotoxic T cell. His Immunology research includes elements of Cancer, Cancer research and Blockade. His T cell research includes themes of Receptor, CD8 and Cell biology.
His studies in Immune checkpoint and Immunity are all subfields of Immune system research. His Antigen study integrates concerns from other disciplines, such as Molecular biology, Antibody and Cellular differentiation. His Cytotoxic T cell study often links to related topics such as FOXP3.
James P. Allison mainly focuses on Internal medicine, Cancer research, Oncology, Immune checkpoint and Immune system. His research integrates issues of T cell, CD8 and Immunotherapy in his study of Cancer research. His work deals with themes such as Cytotoxic T cell and Antigen, which intersect with T cell.
As a member of one scientific family, James P. Allison mostly works in the field of Oncology, focusing on Ipilimumab and, on occasion, Prostate cancer. Blockade, Cancer and Immunology are the main areas of his Immune checkpoint studies. His work carried out in the field of Immune system brings together such families of science as Receptor, Antibody and Cytokine.
His scientific interests lie mostly in Immune checkpoint, Cancer research, Immunotherapy, Melanoma and Cancer. His studies deal with areas such as Ipilimumab and Oncology as well as Immune checkpoint. The concepts of his Cancer research study are interwoven with issues in T cell, CD8, Immune system and Cytotoxic T cell.
His T cell research integrates issues from Precision medicine, Targeted therapy and Antigen. His study in the field of CTLA-4 and T cell differentiation also crosses realms of Context. His Immunology study combines topics from a wide range of disciplines, such as Microbiome and Feces.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Restoring function in exhausted CD8 T cells during chronic viral infection.
Daniel L. Barber;E. John Wherry;David Masopust;Baogong Zhu.
Nature (2006)
Enhancement of antitumor immunity by CTLA-4 blockade.
Dana R. Leach;Matthew F. Krummel;James P. Allison.
Science (1996)
The future of immune checkpoint therapy
Padmanee Sharma;James P. Allison.
Science (2015)
Gut microbiome modulates response to anti–PD-1 immunotherapy in melanoma patients
V. Gopalakrishnan;V. Gopalakrishnan;C. N. Spencer;C. N. Spencer;L. Nezi;A. Reuben.
Science (2018)
CD28 and CTLA-4 have opposing effects on the response of T cells to stimulation.
Matthew F. Krummel;James P. Allison.
Journal of Experimental Medicine (1995)
CD28-mediated signalling co-stimulates murine T cells and prevents induction of anergy in T-cell clones.
Fiona A. Harding;James G. McArthur;Jane A. Gross;David H. Raulet.
Nature (1992)
Immunologic Correlates of the Abscopal Effect in a Patient with Melanoma
Michael A. Postow;Margaret K. Callahan;Margaret K. Callahan;Christopher A. Barker;Christopher A. Barker;Yoshiya Yamada;Yoshiya Yamada.
The New England Journal of Medicine (2012)
Depletion of Carcinoma-Associated Fibroblasts and Fibrosis Induces Immunosuppression and Accelerates Pancreas Cancer with Reduced Survival.
Berna C. Özdemir;Berna C. Özdemir;Tsvetelina Pentcheva-Hoang;Julienne L. Carstens;Xiaofeng Zheng.
Cancer Cell (2014)
Immune Checkpoint Targeting in Cancer Therapy: Toward Combination Strategies with Curative Potential
Padmanee Sharma;James P. Allison.
Cell (2015)
Cancer regression and autoimmunity induced by cytotoxic T lymphocyte-associated antigen 4 blockade in patients with metastatic melanoma
Giao Q. Phan;James C. Yang;Richard M. Sherry;Patrick Hwu.
Proceedings of the National Academy of Sciences of the United States of America (2003)
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