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Infiltration of cervical cancer tissue with human papillomavirus-specific cytotoxic T-lymphocytes.

Abstract
CTLs specific for high-risk human papillomaviruses (HPVs) have recently been found in the peripheral blood of cervical cancer patients. Although cell-mediated immunity is thought to be important in the control of HPV infection, the functional relevance and site of activation of HPV-specific CTLs are unclear. We identified HLA-A*0201-restricted HPV-16 E7 peptide-specific CTLs in the peripheral blood (four of five patients), draining lymph nodes (three of four patients) and tumors (one of three patients) of cervical cancer patients. In four of four cancer patients, the frequency of CTLs specific for a recombinant vaccinia virus expressing HPV-16 and -18 E6/E7 gene products was found to be higher in tumors and lymph nodes compared with that of peripheral blood. HPV-specific CTLs were not identified in any of seven healthy controls, but primary responses could be generated by peptide-pulsed dendritic cells (four of four controls). In a non-HLA-A*0201 subject with invasive carcinoma, other HLA alleles also presented HPV antigens. This is the first demonstration that virus-specific CTLs infiltrate the virus-associated tumor, where they may play an important role in restricting disease progression.
AuthorsE M Evans, S Man, A S Evans, L K Borysiewicz
JournalCancer research (Cancer Res) Vol. 57 Issue 14 Pg. 2943-50 (Jul 15 1997) ISSN: 0008-5472 [Print] United States
PMID9230206 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • E6 protein, Human papillomavirus type 16
  • Oncogene Proteins, Viral
  • Papillomavirus E7 Proteins
  • Repressor Proteins
  • oncogene protein E7, Human papillomavirus type 16
Topics
  • Adult
  • Aged
  • Female
  • Genes, MHC Class I
  • Humans
  • Middle Aged
  • Oncogene Proteins, Viral (immunology)
  • Papillomaviridae (immunology)
  • Papillomavirus E7 Proteins
  • Repressor Proteins
  • T-Lymphocytes, Cytotoxic (immunology)
  • Uterine Cervical Neoplasms (immunology, virology)

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