The job of the immune system is to respond to signals released by tissues that are being destroyed by foreign invaders, such as viruses and bacteria, and to destroy the invaders. These signals have been termed “danger” signals (1). Destruction of tissues by uncontrolled cell growth characteristic of cancer is expected to also generate danger signals, albeit possibly qualitatively different due to the absence of infectious agents. Evidence that the immune system not only detects the presence of cancer but also destroys it and remembers it through the recognition of tumor-specific antigens was provided in the late 1950's (2) and has been confirmed many times in increasingly more sophisticated animal models and in cancer patients. What has not been fully accepted, however, in part because supporting data are only now emerging, is that the immune system can recognize precursors of cancer...
Skip Nav Destination
Article navigation
Commentary|
November 24 2003
Premalignant Lesions as Targets for Cancer Vaccines
Olivera J. Finn
Olivera J. Finn
University of Pittsburgh School of Medicine, Department of Immunology, Pittsburgh, PA 15261
Search for other works by this author on:
Olivera J. Finn
University of Pittsburgh School of Medicine, Department of Immunology, Pittsburgh, PA 15261
Address correspondence to Olivera J. Finn, University of Pittsburgh School of Medicine, Dept. of Immunology, Biomedical Science Tower, Terrace and DeSoto Streets, Pittsburgh, PA 15261. Phone: (412) 648-9816; Fax: (412) 383-7042; email: [email protected]
Received:
October 13 2003
Accepted:
October 13 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2003
J Exp Med (2003) 198 (11): 1623–1626.
Article history
Received:
October 13 2003
Accepted:
October 13 2003
Citation
Olivera J. Finn; Premalignant Lesions as Targets for Cancer Vaccines . J Exp Med 1 December 2003; 198 (11): 1623–1626. doi: https://doi.org/10.1084/jem.20031787
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement