James Patrick Allison

Affiliations: 
1985-1997 Molecular and Cell Biology University of California, Berkeley, Berkeley, CA, United States 
 1997-2004 Rheumatology University of California, San Francisco, San Francisco, CA 
 2004-2012 Weill Cornell Medical College, New York, NY, United States 
 2006-2012 Memorial Sloan-Kettering Cancer Center, Rockville Centre, NY, United States 
 2012- Immunology M. D. Anderson Cancer Center, Houston, TX, United States 
Area:
Immunotherapy
Website:
https://faculty.mdanderson.org/profiles/james_allison.html
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"James Patrick Allison"
Bio:

The Nobel Prize in Physiology or Medicine 2018 was awarded jointly to James P. Allison and Tasuku Honjo "for their discovery of cancer therapy by inhibition of negative immune regulation"
http://www.nasonline.org/member-directory/members/3003904.html
http://www.whatisbiotechnology.org/index.php/people/summary/Allison
https://kingfaisalprize.org/professor-james-p-allison/
http://digitalassets.lib.berkeley.edu/rohoia/ucb/text/oralhisttransretro00maririch.pdf

Cross-listing: Chemistry Tree

Parents

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G Barrie Kitto grad student 1973 UT Austin (Chemistry Tree)
 (I. Isolation and characterization of a tumor inhibitory asparaginase from Alcaligenes eutrophus. II. Insolubilization of L-Asparaginase by covalent attachment to nylon tubing.)
Ralph Alfred Reisfeld post-doc 1974-1977 Scripps Institute (Chemistry Tree)

Children

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Jackson G. Egen grad student 2002 UC Berkeley (Chemistry Tree)
Dilnawaz Kapadia grad student 2003 UC Berkeley (Chemistry Tree)
Virginia A. Pedicord grad student 2010 Weill Cornell Medical College (Chemistry Tree)
Rachel A. Gottschalk grad student 2012 Weill Cornell Medical College (Chemistry Tree)
Xiaozhou Fan grad student 2013 Weill Cornell Medical College (Chemistry Tree)
Tyler R. Simpson grad student 2013 Weill Cornell Medical College (Chemistry Tree)
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Publications

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Sultan H, Takeuchi Y, Ward JP, et al. (2024) Neoantigen-specific cytotoxic Tr1 CD4 T cells suppress cancer immunotherapy. Nature
Mok S, Ağaç Çobanoğlu D, Liu H, et al. (2024) Post-immunotherapy CTLA-4 Ig treatment improves antitumor efficacy. Proceedings of the National Academy of Sciences of the United States of America. 121: e2404661121
Siddiqui BA, Palaskas NL, Basu S, et al. (2024) Molecular pathways and cellular subsets associated with adverse clinical outcomes in overlapping immune-related myocarditis and myositis. Cancer Immunology Research
Sharma N, Fan X, Atolagbe OT, et al. (2024) ICOS costimulation in combination with CTLA-4 blockade remodels tumor-associated macrophages toward an antitumor phenotype. The Journal of Experimental Medicine. 221
Axelrod ML, Meijers WC, Screever EM, et al. (2022) T cells specific for α-myosin drive immunotherapy-related myocarditis. Nature
Hailemichael Y, Johnson DH, Abdel-Wahab N, et al. (2022) Interleukin-6 blockade abrogates immunotherapy toxicity and promotes tumor immunity. Cancer Cell. 40: 509-523.e6
Abbas HA, Hao D, Tomczak K, et al. (2021) Single cell T cell landscape and T cell receptor repertoire profiling of AML in context of PD-1 blockade therapy. Nature Communications. 12: 6071
Sharma N, Atolagbe OT, Ge Z, et al. (2021) LILRB4 suppresses immunity in solid tumors and is a potential target for immunotherapy. The Journal of Experimental Medicine. 218
Goswami S, Chen Y, Anandhan S, et al. (2020) mutation plus CXCL13 expression act as combinatorial biomarkers to predict responses to immune checkpoint therapy in mUCC. Science Translational Medicine. 12
Mitra A, Andrews MC, Roh W, et al. (2020) Spatially resolved analyses link genomic and immune diversity and reveal unfavorable neutrophil activation in melanoma. Nature Communications. 11: 1839
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