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

被引:33
作者
Azzimonti, B. [1 ]
Zavattaro, E. [2 ]
Provasi, M. [2 ]
Vidali, M. [3 ]
Conca, A. [4 ]
Catalano, E. [1 ,5 ]
Rimondini, L. [1 ]
Colombo, E. [2 ]
Valente, G. [4 ,5 ]
机构
[1] Univ Piemonte Orientale, Hlth Sci, I-28100 Novara, Italy
[2] Univ Piemonte Orientale, Azienda Ospedaliero Univ Maggiore della Carita, Dept Dermatol, I-28100 Novara, Italy
[3] Univ Piemonte Orientale, Azienda Ospedaliero Univ Maggiore della Carita, Dept Clin Chem, I-28100 Novara, Italy
[4] Univ Piemonte Orientale, Azienda Ospedaliero Univ Maggiore della Carita, Pathol Units, I-28100 Novara, Italy
[5] Univ Piemonte Orientale, Sch Med, Dept Translat Med, I-28100 Novara, Italy
关键词
COMPREHENSIVE CLINICOPATHOLOGICAL CLASSIFICATION; PLASMACYTOID DENDRITIC CELLS; NONMELANOMA SKIN-CANCER; TRANSPLANT RECIPIENTS; IMMUNE-RESPONSES; NECK-CANCER; EXPRESSION; HEAD; PROGNOSIS; GROWTH;
D O I
10.1111/bjd.13172
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BackgroundRecent reports have revealed the therapeutic potential of cell-mediated immunity in neoplasms such as cutaneous squamous cell carcinoma (SCC). ObjectivesTo define the antigenic coexpression of regulatory T cells (Tregs) and plasmacytoid dendritic cells (pDCs) and assess the CD8(+)/Foxp3(+)CD25(+) cell ratio at peritumoral and intratumoral levels in order to investigate a correlation with the aggressiveness of SCC tumours. MethodsWe evaluated the content and distribution of Foxp3(+)CD25(+) Treg and CD123(+) pDC infiltration and assessed CD8(+)/Foxp3(+)CD25(+) 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(+) cells; immunostained for CD4, CD8, CD123, interleukin (IL)-1 and transforming growth factor (TGF)-1; and unequivocally double stained for Foxp3CD25. ResultsPeritumorally, CD4, CD8 and Foxp3 expression showed no difference between the two groups. CD123(+) cells were fewer in G2-G3 (P=00005), while Foxp3(+)CD25(+) cells were more numerous (P=00005). The Foxp3(+)CD25(+)/Foxp3(+) ratio was higher in G2-G3 cases (P=00005), confirming the trend in this group of activated T lymphocytes towards total Treg Foxp3(+) cells, while the CD8(+)/Foxp3(+)CD25(+) ratio was higher in G1 (P=00005). Intratumorally, CD4(+) and CD8(+) cells infiltrated G2-G3 (P=0048) more than G1 (P=0004), whereas almost all cells were CD123 negative. Regarding Foxp3CD25, TGF-1 and IL-10, they were less expressed in G1, whereas they were positive in G2-G3 (P<005). The CD8(+)/Foxp3(+)CD25(+) ratio was similar to that observed in peritumoral infiltration. ConclusionsOur data suggest that intratumoral recruitment of Tregs, high expression of TGF-1 and IL-10, almost negative CD123+, and a low CD8(+)/Foxp3(+)CD25(+) T-cell ratio may contribute to the aggressiveness of cutaneous SCC, as already evidenced for other solid tumours.
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收藏
页码:64 / 73
页数:10
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