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PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells
(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 immunohistochemic...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965691/ https://www.ncbi.nlm.nih.gov/pubmed/36836455 http://dx.doi.org/10.3390/jpm13020221 |
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author | Caraban, Bogdan Marian Matei, Elena Cozaru, Georgeta Camelia Aşchie, Mariana Deacu, Mariana Enciu, Manuela Bălţătescu, Gabriela Izabela Chisoi, Anca Dobrin, Nicolae Petcu, Lucian Gheorghe, Emma Hangan, Laurențiu-Tony Roșu, Mihai Cătălin Orasanu, Cristian Ionuț Nicolau, Antonela-Anca |
author_facet | Caraban, Bogdan Marian Matei, Elena Cozaru, Georgeta Camelia Aşchie, Mariana Deacu, Mariana Enciu, Manuela Bălţătescu, Gabriela Izabela Chisoi, Anca Dobrin, Nicolae Petcu, Lucian Gheorghe, Emma Hangan, Laurențiu-Tony Roșu, Mihai Cătălin Orasanu, Cristian Ionuț Nicolau, Antonela-Anca |
author_sort | Caraban, Bogdan Marian |
collection | PubMed |
description | (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 (X(2) = 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 (X(2) = 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. |
format | Online Article Text |
id | pubmed-9965691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99656912023-02-26 PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells Caraban, Bogdan Marian Matei, Elena Cozaru, Georgeta Camelia Aşchie, Mariana Deacu, Mariana Enciu, Manuela Bălţătescu, Gabriela Izabela Chisoi, Anca Dobrin, Nicolae Petcu, Lucian Gheorghe, Emma Hangan, Laurențiu-Tony Roșu, Mihai Cătălin Orasanu, Cristian Ionuț Nicolau, Antonela-Anca J Pers Med Article (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 (X(2) = 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 (X(2) = 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. MDPI 2023-01-27 /pmc/articles/PMC9965691/ /pubmed/36836455 http://dx.doi.org/10.3390/jpm13020221 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Caraban, Bogdan Marian Matei, Elena Cozaru, Georgeta Camelia Aşchie, Mariana Deacu, Mariana Enciu, Manuela Bălţătescu, Gabriela Izabela Chisoi, Anca Dobrin, Nicolae Petcu, Lucian Gheorghe, Emma Hangan, Laurențiu-Tony Roșu, Mihai Cătălin Orasanu, Cristian Ionuț Nicolau, Antonela-Anca PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells |
title | PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells |
title_full | PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells |
title_fullStr | PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells |
title_full_unstemmed | PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells |
title_short | PD-L1, CD4+, and CD8+ Tumor-Infiltrating Lymphocytes (TILs) Expression Profiles in Melanoma Tumor Microenvironment Cells |
title_sort | pd-l1, cd4+, and cd8+ tumor-infiltrating lymphocytes (tils) expression profiles in melanoma tumor microenvironment cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965691/ https://www.ncbi.nlm.nih.gov/pubmed/36836455 http://dx.doi.org/10.3390/jpm13020221 |
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