Steven A. Rosenberg
史蒂文·罗森伯格
MD, PhD
Chief, Surgery Branch, NCI Center for Cancer Research; NIH Distinguished InvestigatorNCI癌症研究中心外科部主任;NIH杰出研究员
👥Biography 个人简介
Steven A. Rosenberg, MD, PhD is Chief of the Surgery Branch at the NCI Center for Cancer Research and an NIH Distinguished Investigator. He is universally recognized as the founder of cancer immunotherapy as a clinical discipline and the pioneer of adoptive T cell transfer (ACT) using tumor-infiltrating lymphocytes (TILs). Beginning in the late 1980s, Dr. Rosenberg's Surgery Branch at NCI conducted the first successful clinical trials demonstrating that TILs — T cells isolated from excised tumors, expanded ex vivo to massive numbers, and reinfused after lymphodepleting chemotherapy — could induce complete durable remissions in patients with metastatic melanoma, including in patients who had failed all prior therapy. His development of the lymphodepletion-plus-IL-2 conditioning regimen was essential to achieving durable T cell engraftment and antitumor responses. His 2002 Science paper reporting 6 of 13 metastatic melanoma patients achieving objective responses including two complete remissions with ACT is considered a landmark. Dr. Rosenberg's laboratory has also pioneered TCR-engineered T cell therapy — genetically modifying peripheral blood T cells to express high-affinity TCRs against tumor antigens — and has extended ACT to common epithelial cancers including colorectal cancer and breast cancer by identifying and expanding neoantigen-reactive TILs. He has published more than 1,000 peer-reviewed papers and has received virtually every major award in oncology and immunology.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
TIL Therapy — First Clinical Proof-of-Concept for ACT in Metastatic Cancer
Conducted the first successful clinical trials of adoptive transfer of ex vivo expanded tumor-infiltrating lymphocytes in metastatic melanoma at NCI from 1988 onward; demonstrated that TILs combined with IL-2 administration could induce objective tumor responses including complete remissions in patients with refractory disease — establishing the first clinical proof-of-concept that ACT with autologous T cells is a viable treatment for metastatic solid tumors.
Lymphodepletion Conditioning — Essential Innovation for TIL Persistence
Developed the lymphodepleting non-myeloablative chemotherapy conditioning regimen preceding TIL infusion, demonstrating that eliminating endogenous lymphocytes creates "immunologic space" for transferred T cells to expand, survive, and mediate durable antitumor responses — a fundamental principle now applied in all ACT protocols including CAR-T cell therapy.
TCR-Engineered T Cell Therapy for Common Epithelial Cancers
Pioneered clinical translation of TCR gene-modified T cells expressing high-affinity TCRs against MART-1, gp100, CEA, NY-ESO-1, and MAGE-A3 tumor antigens, demonstrating that peripheral blood T cells can be genetically redirected to recognize tumor-associated peptide-MHC complexes and mediate antitumor responses — extending T cell therapy beyond melanoma to lung, colon, synovial cell sarcoma, and other cancers.
Neoantigen-Reactive TIL Therapy in Common Epithelial Cancers
Led development of approaches to identify, select, and expand neoantigen-reactive TIL subpopulations from common epithelial cancers (colorectal, lung, breast, bile duct), demonstrating that neoantigen-reactive T cells can mediate objective tumor regressions in these cancers — extending ACT beyond melanoma and establishing neoantigen-targeted TIL therapy as a universal personalized cancer immunotherapy approach.
Representative Works 代表性著作
Use of tumor-infiltrating lymphocytes and interleukin-2 in the immunotherapy of patients with metastatic melanoma
New England Journal of Medicine (1988)
First clinical paper reporting objective responses in metastatic melanoma patients treated with TIL plus high-dose IL-2, founding the ACT field.
Durable complete responses in heavily pretreated patients with metastatic melanoma using T-cell transfer immunotherapy
Clinical Cancer Research (2011)
Reported updated long-term results of TIL therapy in metastatic melanoma demonstrating durable complete responses exceeding 3 years in a subset of patients.
Cancer regression and autoimmunity induced by cytotoxic T lymphocyte-associated antigen 4 blockade in patients with metastatic melanoma
Proceedings of the National Academy of Sciences (2003)
Demonstrated that CTLA-4 blockade combined with peptide vaccination induced tumor regression in metastatic melanoma patients, one of the first clinical demonstrations of anti-CTLA-4 antitumor activity.
Neoantigen-based cell therapies
Nature (2019)
Landmark study demonstrating that neoantigen-reactive TILs can be isolated and expanded from common epithelial cancers and mediate objective tumor regressions, extending personalized TIL therapy to colorectal, lung, and breast cancers.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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