| Literature DB >> 22290207 |
Astrid M Bedoya1,2, Roberto Jaramillo3, Armando Baena1,2, Jorge Castaño4, Natalia Olaya4, Arnold H Zea5, Rolando Herrero6, Gloria I Sanchez7.
Abstract
Only a small proportion of women infected with Human Papillomavirus (HPV) develop cervical cancer. Host immune response seems to play a role eliminating the viral infection and preventing progression to cancer. Characterization of tumor infiltrating lymphocytes (TILs) in cervical pre-neoplastic lesions and cervical cancer may be helpful to understand the mechanisms that mediate this protection. The aim of this study was to determine if there are differences in the localization and density (cells/mm(2)) of CD8+ T-cells, CD4+ T-cells and Tregs (CD25 + Foxp3+) in cervical pre-neoplastic lesions and cervical cancer. Immunohistochemical analysis of sections of 96 (26 CIN1, 21 CIN2, 25 CIN3, and 24 SCC) samples revealed that regardless of CIN grades, CD8+ T-cells are more abundant than CD4+, CD25+ and Foxp3+ cells in both the stroma and epithelium. There was a higher density of CD8+ cells in the stroma of cervical cancer compared to CIN3 (OR = 4.20, 95% CI 1.2-15), CIN2 (OR = 7.86, 95% CI 1.7-36.4) and CIN1 (OR = 4.25, 95% CI 1.1-17). Studies evaluating whether these cells are recruited before or after cancer progression will be helpful to understand the role of these cells in the natural history of HPV-induced lesions.Entities:
Keywords: Cervical cancer; HPV infection; Immunohistochemistry; Tumor infiltrating cells
Year: 2012 PMID: 22290207 PMCID: PMC3601215 DOI: 10.1007/s12307-012-0097-8
Source DB: PubMed Journal: Cancer Microenviron ISSN: 1875-2284