2020 - AAI Excellence in Mentoring Award, American Association of Immunologists
2019 - Distinguished Fellows of the American Association of Immunologists (AAI)
2013 - Member of the National Academy of Medicine (NAM)
2006 - Fellow of the American Academy of Arts and Sciences
1997 - Fellow of John Simon Guggenheim Memorial Foundation
Jeffrey A. Bluestone mainly investigates Immunology, T cell, IL-2 receptor, Antigen and CD28. His Immunology study is mostly concerned with Autoimmunity, FOXP3, Autoimmune disease, NOD mice and Immune tolerance. His research in T cell intersects with topics in Interleukin 2, In vivo and Cell biology.
His study on IL-2 receptor also encompasses disciplines like
Jeffrey A. Bluestone focuses on Immunology, T cell, Cell biology, Immune system and Antigen. His study involves Autoimmunity, T-cell receptor, IL-2 receptor, Immune tolerance and Immunotherapy, a branch of Immunology. His work in IL-2 receptor addresses subjects such as FOXP3, which are connected to disciplines such as Regulatory T cell and Transcription factor.
His T cell study incorporates themes from Molecular biology, Cytotoxic T cell, T lymphocyte and CD8. His Molecular biology research focuses on Monoclonal antibody and how it connects with In vivo. His study ties his expertise on Antibody together with the subject of Antigen.
Jeffrey A. Bluestone spends much of his time researching Immunology, Immune system, Autoimmunity, Immunotherapy and Cell biology. His Immunology study which covers Disease that intersects with Phenotype. Jeffrey A. Bluestone combines subjects such as Cancer, Cytokine and Antigen with his study of Immune system.
His biological study spans a wide range of topics, including Adoptive cell transfer, Nod, Type 1 diabetes and Transplantation. His study in Immunotherapy is interdisciplinary in nature, drawing from both Cancer research, Clinical trial, Bioinformatics and Cell therapy. Jeffrey A. Bluestone has included themes like CD28, CD8 and Gene targeting in his Cell biology study.
His scientific interests lie mostly in Immunology, Immune system, Autoimmunity, Immunotherapy and FOXP3. In his study, Phenotype is strongly linked to Disease, which falls under the umbrella field of Immunology. His work on T-cell receptor and CD28 as part of general Immune system research is often related to Mechanism, thus linking different fields of science.
His Autoimmunity research is multidisciplinary, incorporating elements of Cancer, Immunity, Transplant rejection, Transplantation and Effector. His Immunotherapy research is multidisciplinary, relying on both Encephalomyelitis, T cell, Adoptive cell transfer and Heel. His work deals with themes such as Peripheral tolerance and Regulatory T cell, IL-2 receptor, which intersect with FOXP3.
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.
CD28/B7 SYSTEM OF T CELL COSTIMULATION
Deborah J. Lenschow;Theresa L. Walunas;Jeffrey A. Bluestone.
Annual Review of Immunology (1996)
Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4
Elizabeth A. Tivol;Frank Borriello;A.Nicola Schweitzer;William P. Lynch.
Immunity (1995)
CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells
Weihong Liu;Amy L Putnam;Zhou Xu-yu;Gregory L. Szot.
Journal of Experimental Medicine (2006)
B7/CD28 costimulation is essential for the homeostasis of the CD4+CD25+ immunoregulatory T cells that control autoimmune diabetes.
Benoît Salomon;Deborah J Lenschow;Lesley Rhee;Neda Ashourian.
Immunity (2000)
CTLA-4 can function as a negative regulator of T cell activation
Theresa L. Walunas;Deborah J. Lenschow;Christina Y. Bakker;Peter S. Linsley.
Immunity (1994)
International Trial of the Edmonton Protocol for Islet Transplantation
A. M James Shapiro;Camillo Ricordi;Bernhard J. Hering;Hugh Auchincloss.
The New England Journal of Medicine (2006)
Identification of a monoclonal antibody specific for a murine T3 polypeptide
Oberdan Leo;Michele Foo;David H. Sachs;Lawrence E. Samelson.
Proceedings of the National Academy of Sciences of the United States of America (1987)
Innate immunity and intestinal microbiota in the development of Type 1 diabetes
Li Wen;Ruth E. Ley;Ruth E. Ley;Pavel Yu. Volchkov;Peter B. Stranges.
Nature (2008)
Anti-CD3 Monoclonal Antibody in New-Onset Type 1 Diabetes Mellitus
Kevan C. Herold;William Hagopian;Julie A. Auger;Ena Poumian-Ruiz.
The New England Journal of Medicine (2002)
The B7 and CD28 receptor families
Carl H. June;Jeffrey A. Bluestone;Lee M. Nadler;Craig B. Thompson.
Immunology Today (1994)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of California, San Francisco
Yale University
Icahn School of Medicine at Mount Sinai
Memorial Sloan Kettering Cancer Center
University of Chicago
Necker-Enfants Malades Hospital
Northwestern University
University of California, San Francisco
Alexion Pharma (Switzerland)
Harvard University
University of Manchester
Google (United States)
Ronin Institute
MSD (United States)
Georgia Institute of Technology
Pfizer (United States)
The University of Texas Health Science Center at San Antonio
University of Pennsylvania
Washington University in St. Louis
University of Georgia
University of Glasgow
University of Manchester
Alfred Wegener Institute for Polar and Marine Research
University of Groningen
Flinders University
University of California, Berkeley