PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells

Author:

Caraban Bogdan Marian1,Matei Elena2ORCID,Cozaru Georgeta Camelia23,Aşchie Mariana23,Deacu Mariana13,Enciu Manuela13ORCID,Bălţătescu Gabriela Izabela23ORCID,Chisoi Anca23,Dobrin Nicolae3,Petcu Lucian4,Gheorghe Emma1,Hangan Laurențiu-Tony1,Roșu Mihai Cătălin2,Orasanu Cristian Ionuț23ORCID,Nicolau Antonela-Anca23ORCID

Affiliation:

1. Faculty of Medicine, “Ovidius” University of Constanta, 900470 Constanta, Romania

2. Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, “Ovidius” University of Constanta, 900591 Constanta, Romania

3. Clinical Service of Pathology, “Sf. Apostol Andrei” Emergency County Hospital, 900591 Constanta, Romania

4. Dental Medicine Faculty, “Ovidius” University of Constanta, 900470 Constanta, Romania

Abstract

(1) Background: Because melanoma is an aggressive tumor with an unfavorable prognosis, we aimed to characterize the PD-L1 expression in melanomas in association with T cell infiltrates because PD-1/PD-L1 blockade represents the target in treating melanoma strategy. (2) Methods: The immunohistochemical manual quantitative methods of PD-L1, CD4, and CD8 TILs were performed in melanoma tumor microenvironment cells. (3) Results: Most of the PD-L1 positive, expressing tumors, have a moderate score of CD4+ TILs and CD8+TILs (5−50% of tumor area) in tumoral melanoma environment cells. The PD-L1 expression in TILs was correlated with different degrees of lymphocytic infiltration described by the Clark system (X2 = 8.383, p = 0.020). PD-L1 expression was observed often in melanoma cases, with more than 2−4 mm of Breslow tumor thickness being the associated parameters (X2 = 9.933, p = 0.014). (4) Conclusions: PD-L1 expression represents a predictive biomarker with very good accuracy for discriminating the presence or absence of malign tumoral melanoma cells. PD-L1 expression was an independent predictor of good prognosis in patients with melanomas.

Funder

the result indicators assumed within a SEPMEL grant

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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