Langerhans, plasmacytoid dendritic and myeloid-derived suppressor cell levels in mycosis fungoides vary according to the stage of the disease

被引:17
|
作者
Pileri, Alessandro [1 ,2 ]
Agostinelli, Claudio [3 ]
Sessa, Maurizio [4 ]
Quaglino, Pietro [5 ]
Santucci, Marco [6 ]
Tomasini, Carlo [7 ]
Grandi, Vieri [2 ]
Fava, Paolo [5 ]
Astrua, Chiara [5 ]
Righi, Simona [3 ]
Patrizi, Annalisa [1 ]
Pileri, Stefano A. [8 ,9 ]
Pimpinelli, Nicola [2 ]
机构
[1] Univ Bologna, Dept Expt Diagnost & Specialty Med, Dermatol Unit, Via Massarenti 1, I-40138 Bologna, Italy
[2] Univ Florence, Sch Med, Dermatol Unit, Dept Surg & Translat Med, Florence, Italy
[3] Univ Bologna, Dept Expt Diagnost & Specialty Med, Haematopathol Unit, Bologna, Italy
[4] Univ Naples 2, Sect Pharmacol L Donatelli, Dept Expt Med, Naples, Italy
[5] Univ Turin, Dept Med Sci, Dermatol Unit, Turin, Italy
[6] Univ Florence, Div Anat Pathol, Dept Surg & Translat Med, Sch Med, Florence, Italy
[7] Univ Turin, Dermatopathol Sect, Azienda Osped Citta Salute & Sci, Turin, Italy
[8] European Inst Oncol, Unit Diagnost Haematopathol, Milan, Italy
[9] Univ Bologna, Dept Expt Diagnost & Specialty Med, Bologna, Italy
关键词
Mycosis fungoides; Dendritic cell; Myeloid-derived suppressor cell; Immunohistochemistry; ENDOTHELIAL GROWTH-FACTOR; T-REGULATORY CELLS; SEZARY-SYNDROME; TUMOR MICROENVIRONMENT; NONPARAMETRIC ANALYSIS; CANCER-IMMUNOTHERAPY; LYMPHOMA; SKIN; IMMUNOSURVEILLANCE; MODEL;
D O I
10.1007/s00428-017-2107-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Mycosis fungoides (MF) is characterized by a switch from indolent behaviour in the early stages to a worse clinical outcome in the advanced ones. Recently, various studies have investigated the role the microenvironment might play in such a switch. We have analysed the distribution of Langerhans cells, plasmacytoid dendritic cells and myeloid-derived suppressor cells in 46 MF cases in various stages, aiming to assess whether changes occur from early to advanced stage. We have investigated the number of langerin, CD303 and arginase-1 positive cells and their distribution at high power. Data were analysed using t test for continuous variables, chi (2) tests or Fisher's exact test for categorical variables, as well as analysis of covariance. In comparing stages IA/B to IIB, we observed a significant decrease in Langerhans cells (p value 0.03) and a significant increase in CD303 and arginase-1 positive cells (p value < 0.01 for both markers). Furthermore, a significant increase in Langerhans cells only was observed in stage IIB in comparison to stage III (p = 0.02), while in stage IV, a significant decrease in Langerhans cells was noted in comparison to stage III (p = 0.02). Our data suggest that changes in the microenvironment might influence disease progression, especially from stages IA/B to IIB, opening new scenarios in MF therapy.
引用
收藏
页码:575 / 582
页数:8
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