- Source: Pramod Kumar Srivastava
Pramod Kumar Srivastava (born 15 August 1955) is an American immunologist and physician serving as the Eversource Energy chairman in experimental oncology at the University of Connecticut School of Medicine. He is known for his work on cancer vaccines.
He is the scientific founder of Antigenics (AGEN), the New York-based biotech company.
Early life and education
Srivastava completed his Ph.D. at the Centre for Cellular and Molecular Biology, Hyderabad, India, and his MD from the University of Connecticut School of Medicine.
Career
Srivastava was appointed Assistant Professor in the Department of Pharmacology, Mount Sinai School of Medicine, in 1989. He moved to Fordham University as an associate professor of biology in 1993 and became a full Professor in 1995. During this time, Srivastava co-founded a biotechnology company, Antigenics, in 1994.
In 1997, he was appointed physician health services professor of medicine at the University of Connecticut School of Medicine. He became the founding director of the Center for Immunotherapy of Cancer and Infectious Diseases.He was also the founding chairman of the Department of Immunology. Since 2011, he has been the director of the Carole and Neag Comprehensive Cancer Center at the University of Connecticut School of Medicine.
= Scientific and clinical work
=Srivastava made contributions to neuroimmunology. His laboratory first identified the temperature receptors (TRPV receptors) on dendritic cells and reported the consequences of the engagement of these receptors on immune tolerance in the gut. In addition, Srivastava investigated neuroimmunology interactions and showed how the sympathetic nervous system is critical for the normal development of neutrophils and that dysregulation of this pathway leads to the generation of the immune suppressive myeloid-derived suppressor cells, which promotes the proliferation of regulatory T cells.
Publications
Srivastava has more than 200 peer-reviewed publications and more than 200 awarded patents in the field of cancer immunology including:
Reversion analysis reveals the in vivo immunogenicity of a poorly MHC I-binding cancer neoepitope. Doi: https://doi.org/10.1038/s41467-021-26646-5
An unbiased approach to defining bona fide cancer neoepitopes that elicit immune-mediated cancer rejection. Doi: https://doi.org/10.1172/jci142823
Sympathetic nervous tone limits the development of myeloid-derived suppressor cells Doi: https://doi.org/10.1126/sciimmunol.aay9368
Cross-dressing of CD8α+ Dendritic Cells with Antigens from Live Mouse Tumor Cells Is a Major Mechanism of Cross-priming Doi: https://doi.org/10.1158/2326-6066.cir-20-0248
New epitopes in ovalbumin provide insights into cancer neoepitopes Doi: https://doi.org/10.1172/jci.insight.127882
Mass spectrometry driven exploration reveals nuances of neoepitope-driven tumor rejection Doi: https://doi.org/10.1172/jci.insight.129152
Endocannabinoid system acts as a regulator of immune homeostasis in the gut Doi: https://doi.org/10.1073/pnas.1612177114
Tumor Control Index as a new tool to assess tumor growth in experimental animals Doi: https://doi.org/10.1016/j.jim.2017.03.013
Oral ingestion of Capsaicin, the pungent component of chili pepper, enhances a discreet population of macrophages and confers protection from autoimmune diabetes.Doi: https://doi.org/10.1038/mi.2011.50
Duan F, Duitama J, Al Seesi S, Ayres CM, Corcelli SA, Pawashe AP, Blanchard T, McMahon D, Sidney J, Sette A, Mandoiu II, Srivastava PK. Genomic and bioinformatic profiling of mutational neoepitopes reveals new rules to predict anticancer immunogenicity. J Exp Med. (2014) 211:2231-48. PMID: 25245761
Binder RJ, Srivastava PK. Peptides chaperoned by heat shock proteins are a necessary and sufficient source of antigen in cross-priming CD8+ T cells. Nature Immunology (2005) 6(6):593-9. PMID: 15864309 Doi: https://doi.org/10.1038/ni1201
Basu S, Binder RJ, Srivastava PK. CD91 is a common receptor for heat shock proteins gp96, hsp90, hsp70, and calreticulin, Immunity (2001) 14, 303-313, PMID: 11290339 Doi : https://doi.org/10.1016/s1074-7613(01)00111-x
Basu S, Binder RJ, Suto R, Anderson KM, Srivastava PK. Necrotic but not apoptotic cell death releases heat shock proteins, which deliver maturation signal to dendritic cells and activate the NFB pathway. International Immunology (2000) 12 (11), 1539-1546. PMID: 11058573 Doi: https://doi.org/10.1093/intimm/12.11.1539
Binder RJ, Han DK, Srivastava PK. CD91 is a receptor for heat shock protein gp96. Nature Immunology (2000) 1 (2), 151-155. PMID: 11248808 Doi: https://doi.org/10.1038/77835
Tamura Y, Peng P, Liu K, Daou M, Srivastava PK. Immunotherapy of metastatic lung cancer by heat shock protein preparations. Science (1997) 278(5335):117-120,1997. PMID: 9311915 Doi: https://doi.org/10.1126/science.278.5335.117
Suto R, Srivastava PK. A mechanism for the specific immunogenicity of heat shock protein - chaperoned peptides. Science (1995) 269, 1585-1588. PMID: 7545313 Doi: https://doi.org/10.1126/science.7545313
Further reading
Srivastava and Das 1984 International Journal of Cancer
Srivastava and Maki 1991 Current Topics in Microbiology and Immunology
Udono and Srivastava 1993 Journal of Experimental Medicine
Srivastava 2002 Annual review of Immunology
Binder et al. 2000 Nature Immunology
Basu et al. 2001 Immunity
Srivastava 1993 Advances in Cancer Research
Ebrahimi-Nik et al. 2021 Nature Communications
Brennick et al. 2021 Journal of Clinical Investigation
Duan et al. 2014 Journal of Experimental Medicine.
Basu and Srivastava 2005 PNAS
Acharya et al. 2017 PNAS
Nevin et al. 2020 Science Immunology
References
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