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Distribution of tumor-infiltrating immune cells in glioblastoma
AIM: Evaluation of features related to infiltrating immune cell level in glioblastoma. METHODS: Tumor-infiltrating lymphocytes (TILs) through H&E staining, and TILs (CD3, CD4, CD8 and CD20) and macrophage (CD68 and CD163) levels through immunohistochemistry were evaluated through digital analysi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Medicine Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331699/ https://www.ncbi.nlm.nih.gov/pubmed/30299157 http://dx.doi.org/10.2217/cns-2017-0037 |
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author | Orrego, Enrique Castaneda, Carlos A Castillo, Miluska Bernabe, Luis A Casavilca, Sandro Chakravarti, Arnab Meng, Wei Garcia-Corrochano, Pamela Villa-Robles, Maria R Zevallos, Rocio Mejia, Omar Deza, Pedro Belmar-Lopez, Carolina Ojeda, Luis |
author_facet | Orrego, Enrique Castaneda, Carlos A Castillo, Miluska Bernabe, Luis A Casavilca, Sandro Chakravarti, Arnab Meng, Wei Garcia-Corrochano, Pamela Villa-Robles, Maria R Zevallos, Rocio Mejia, Omar Deza, Pedro Belmar-Lopez, Carolina Ojeda, Luis |
author_sort | Orrego, Enrique |
collection | PubMed |
description | AIM: Evaluation of features related to infiltrating immune cell level in glioblastoma. METHODS: Tumor-infiltrating lymphocytes (TILs) through H&E staining, and TILs (CD3, CD4, CD8 and CD20) and macrophage (CD68 and CD163) levels through immunohistochemistry were evaluated through digital analysis. RESULTS: CD68 (9.1%), CD163 (2.2%), CD3 (1.6%) and CD8 (1.6%) had the highest density. Higher CD4(+) was associated with unmethylated MGMT (p = 0.016). Higher CD8(+) was associated with larger tumoral size (p = 0.027). Higher CD163(+) was associated with higher age (p = 0.044) and recursive partitioning analysis = 4. Women (p < 0.05), total resection (p < 0.05), MGMT-methylation (p < 0.001), radiotherapy (p < 0.001), chemotherapy (p < 0.001) and lower CD4(+) (p < 0.05) were associated with longer overall survival. CONCLUSION: Macrophages are more frequent than TILs. Some subsets are associated with clinical features. |
format | Online Article Text |
id | pubmed-6331699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Future Medicine Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63316992019-01-16 Distribution of tumor-infiltrating immune cells in glioblastoma Orrego, Enrique Castaneda, Carlos A Castillo, Miluska Bernabe, Luis A Casavilca, Sandro Chakravarti, Arnab Meng, Wei Garcia-Corrochano, Pamela Villa-Robles, Maria R Zevallos, Rocio Mejia, Omar Deza, Pedro Belmar-Lopez, Carolina Ojeda, Luis CNS Oncol Research Article AIM: Evaluation of features related to infiltrating immune cell level in glioblastoma. METHODS: Tumor-infiltrating lymphocytes (TILs) through H&E staining, and TILs (CD3, CD4, CD8 and CD20) and macrophage (CD68 and CD163) levels through immunohistochemistry were evaluated through digital analysis. RESULTS: CD68 (9.1%), CD163 (2.2%), CD3 (1.6%) and CD8 (1.6%) had the highest density. Higher CD4(+) was associated with unmethylated MGMT (p = 0.016). Higher CD8(+) was associated with larger tumoral size (p = 0.027). Higher CD163(+) was associated with higher age (p = 0.044) and recursive partitioning analysis = 4. Women (p < 0.05), total resection (p < 0.05), MGMT-methylation (p < 0.001), radiotherapy (p < 0.001), chemotherapy (p < 0.001) and lower CD4(+) (p < 0.05) were associated with longer overall survival. CONCLUSION: Macrophages are more frequent than TILs. Some subsets are associated with clinical features. Future Medicine Ltd 2018-10-09 /pmc/articles/PMC6331699/ /pubmed/30299157 http://dx.doi.org/10.2217/cns-2017-0037 Text en © 2018 Orrego, Castaneda, Castillo et al. This work is licensed under a Creative Commons Attribution-NonCommercial NonDerivative 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Research Article Orrego, Enrique Castaneda, Carlos A Castillo, Miluska Bernabe, Luis A Casavilca, Sandro Chakravarti, Arnab Meng, Wei Garcia-Corrochano, Pamela Villa-Robles, Maria R Zevallos, Rocio Mejia, Omar Deza, Pedro Belmar-Lopez, Carolina Ojeda, Luis Distribution of tumor-infiltrating immune cells in glioblastoma |
title | Distribution of tumor-infiltrating immune cells in glioblastoma |
title_full | Distribution of tumor-infiltrating immune cells in glioblastoma |
title_fullStr | Distribution of tumor-infiltrating immune cells in glioblastoma |
title_full_unstemmed | Distribution of tumor-infiltrating immune cells in glioblastoma |
title_short | Distribution of tumor-infiltrating immune cells in glioblastoma |
title_sort | distribution of tumor-infiltrating immune cells in glioblastoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331699/ https://www.ncbi.nlm.nih.gov/pubmed/30299157 http://dx.doi.org/10.2217/cns-2017-0037 |
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