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Cancer-testis antigens and immunosurveillance in human cutaneous squamous cell and basal cell carcinomas.

Authors :
Walter A
Barysch MJ
Behnke S
Dziunycz P
Schmid B
Ritter E
Gnjatic S
Kristiansen G
Moch H
Knuth A
Dummer R
van den Broek M
Source :
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2010 Jul 15; Vol. 16 (14), pp. 3562-70. Date of Electronic Publication: 2010 Jun 02.
Publication Year :
2010

Abstract

Purpose: Nonmelanoma skin cancer is the most common cancer and comprises basal cell carcinoma (BCC) and squamous cell carcinoma (SCC). The incidence of SCC increases drastically in immunosuppressed individuals, suggesting a critical role of the immune system in controlling SCC. To find an explanation for the selective immunosurveillance of SCC, we investigated the expression of cancer-testis (CT) antigens and MHC class I (MHC-I) and the infiltration by immune cells in BCC and SCC.<br />Experimental Design: We determined the expression of 23 different CT-antigens in 63 BCC and 40 SCC biopsies of immunocompetent and in 20 biopsies of immunosuppressed SCC patients by reverse transcription-PCR and immunohistochemistry. IgG responses to 36 tumor antigens were measured by Western blotting and ELISA. MHC-I expression and CD8(+) T-cell infiltration were analyzed by immunohistochemistry in BCC and SCC of immunocompetent and immunosuppressed patients and in imiquimod-treated BCC patients.<br />Results: We found expression of at least one CT-antigen in 81% of BCC and in 40% of SCC. We did not detect CT-antigen-specific serum IgG. Most SCC, but not BCC, expressed MHC-I and were infiltrated with CD8(+) cells. Imiquimod-treated BCC expressed MHC-I and were infiltrated by CD8(+) T cells.<br />Conclusions: We propose that immunosurveillance controls SCC, but not BCC, because the latter lacks MHC-I. This fits with the increased incidence of SCC in immunosuppressed individuals and may explain the relatively low prevalence of CT-antigen expression in SCC as a result of CD8(+) T-cell-driven immunoediting.<br /> (Copyright 2010 AACR.)

Details

Language :
English
ISSN :
1557-3265
Volume :
16
Issue :
14
Database :
MEDLINE
Journal :
Clinical cancer research : an official journal of the American Association for Cancer Research
Publication Type :
Academic Journal
Accession number :
20519358
Full Text :
https://doi.org/10.1158/1078-0432.CCR-09-3136