Peter P. Lee
Academic Appointments
- Associate Professor, Medicine - Hematology
- Member, Cancer Center
Contact Information
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Clinical Offices
Hematology Clinic 875 Blake Wilbur Dr Clinic C Stanford, CA 94305-5820 Tel Work (650) 498-6000 Fax (650) 498-5030
- Academic Offices
Personal Information EmailNot for medical emergencies or patient use
Professional Snapshot
Clinical Focus
- Cancer > Hematology
- Cancer > Hematology > Leukemia - Acute and Chronic
- Hematology
- Leukemia - Hematology
Professional Education
| Fellowship: | SUMC - Graduate Medical Education, CA (1999) |
| Residency: | Scripps Clinic & Research Foun, CA (1992) |
| Internship: | Scripps Clinic & Research Foun, CA (1990) |
| Medical Education: | UC San Diego, CA USA (1989) |
Postdoctoral Advisees
Damiano Cereghetti , Andrea Miyahira , Alvernia Setiadi , Ning Yan , Hongxiang Yu
Graduate & Fellowship Program Affiliations
Web Site Links
Industry Relationships
Stanford is committed to ethical and transparent interactions with our industry partners. It is our policy to disclose payments of $5,000 or more, equity valued at $5,000 or more in a publicly traded company, or any equity in a privately held company, to physicians and scientists employed by Stanford University from companies or other commercial entities with which they interact as part of their professional activities. View Full Information
| Service on Board of Directors: | Osel Inc. |
Scientific Focus
Research Interests
My research focuses on understanding the biology of the immune response to cancer. It is becoming clear that the immune system plays an important role in controlling cancer development and modulating cancer growth. Even patients with metastatic cancer can be shown to have an on-going immune response to their cancer. Why the immune response fails to be protective in the cancer patient remains unclear. A better understanding of this fundamental question may lead to improved strategies to manipulate the immune response as novel cancer therapy.
Key questions being pursued:
1. How does the immune system tell a cancer cell from a normal cell?
2. What are the molecular mechanisms by which cancer cells modulate the immune response?
3. How do different treatments - chemotherapy, radiation, transplantation, biotherapies (e.g. IL-2, Interferon, etc.) - impact on the balance between tumor cell proliferation and the immune response?
To address these questions, we are utilizing state-of-the-art technologies such as dendritic cell and T cell cloning, multi-color (up to 11 color) FACS analysis and sorting, peptide/MHC tetramers, and cDNA microarrays. We are also utilizing mathematical models and simulation with supercomputers to gain insights into the dynamics (systems biology) of these responses.
Clinical Trials
- Immunobiology of Breast Cancer Recruiting
- Immunobiology of Cancer Recruiting
Publications
- Modeling imatinib-treated chronic myelogenous leukemia: reducing the complexity of agent-based models. Bull Math Biol. 2008; (3): 728-44
- Development and dynamics of robust T-cell responses to CML under imatinib treatment. Blood. 2008; (11): 5342-9
- Engineering of a human vaginal Lactobacillus strain for surface expression of two-domain CD4 molecules. Appl Environ Microbiol. 2008; (15): 4626-35
- Down-regulation of the interferon signaling pathway in T lymphocytes from patients with metastatic melanoma. PLoS Med. 2007; (5): e176
- Gene expression network analysis and applications to immunology. Bioinformatics. 2007; (7): 850-8

