Back to Search Start Over

Intense Foxp3+CD25+ regulatory T-cell infiltration is associated with high-grade cutaneous squamous cell carcinoma and counterbalanced by CD8+/Foxp3+CD25+ ratio.

Authors :
Azzimonti, B.
Zavattaro, E.
Provasi, M.
Vidali, M.
Conca, A.
Catalano, E.
Rimondini, L.
Colombo, E.
Valente, G.
Source :
British Journal of Dermatology; Jan2015, Vol. 172 Issue 1, p64-73, 10p
Publication Year :
2015

Abstract

Background Recent reports have revealed the therapeutic potential of cell-mediated immunity in neoplasms such as cutaneous squamous cell carcinoma ( SCC). Objectives To define the antigenic coexpression of regulatory T cells (Tregs) and plasmacytoid dendritic cells ( pDCs) and assess the CD8<superscript>+</superscript>/Foxp3<superscript>+</superscript>CD25<superscript>+</superscript> cell ratio at peritumoral and intratumoral levels in order to investigate a correlation with the aggressiveness of SCC tumours. Methods We evaluated the content and distribution of Foxp3<superscript>+</superscript>CD25<superscript>+</superscript> Treg and CD123<superscript>+</superscript> pDC infiltration and assessed CD8<superscript>+</superscript>/Foxp3<superscript>+</superscript>CD25<superscript>+</superscript> cell ratio at peritumoral and intratumoral levels in 40 SCCs (20 well-differentiated, G1; and 20 moderately to poorly differentiated, G2-G3) to investigate a correlation with their aggressiveness. We determined the profiles of Tregs and CD123<superscript>+</superscript> cells; immunostained for CD4, CD8, CD123, interleukin (IL)-1 and transforming growth factor (TGF)-β1; and unequivocally double stained for Foxp3CD25. Results Peritumorally, CD4, CD8 and Foxp3 expression showed no difference between the two groups. CD123<superscript>+</superscript> cells were fewer in G2-G3 ( P = 0·0005), while Foxp3<superscript>+</superscript> CD25<superscript>+</superscript> cells were more numerous ( P = 0·0005). The Foxp3<superscript>+</superscript> CD25<superscript>+</superscript>/Foxp3<superscript>+</superscript> ratio was higher in G2-G3 cases ( P = 0·0005), confirming the trend in this group of activated T lymphocytes towards total Treg Foxp3<superscript>+</superscript> cells, while the CD8<superscript>+</superscript>/Foxp3<superscript>+</superscript> CD25<superscript>+</superscript> ratio was higher in G1 ( P = 0·0005). Intratumorally, CD4<superscript>+</superscript> and CD8<superscript>+</superscript> cells infiltrated G2-G3 ( P = 0·048) more than G1 ( P = 0·004), whereas almost all cells were CD123 negative. Regarding Foxp3 CD25, TGF-β1 and IL-10, they were less expressed in G1, whereas they were positive in G2-G3 ( P < 0·05). The CD8<superscript>+</superscript>/Foxp3<superscript>+</superscript> CD25<superscript>+</superscript> ratio was similar to that observed in peritumoral infiltration. Conclusions Our data suggest that intratumoral recruitment of Tregs, high expression of TGF-β1 and IL-10, almost negative CD123+, and a low CD8<superscript>+</superscript>/Foxp3<superscript>+</superscript> CD25<superscript>+</superscript> T-cell ratio may contribute to the aggressiveness of cutaneous SCC, as already evidenced for other solid tumours. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070963
Volume :
172
Issue :
1
Database :
Complementary Index
Journal :
British Journal of Dermatology
Publication Type :
Academic Journal
Accession number :
100352071
Full Text :
https://doi.org/10.1111/bjd.13172