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CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia

Currently, no prognostic factors exist for determining the host immune status of chronic lymphocytic leukemia (CLL) patients. Therefore, the present report analyzed cluster of differentiation 14 (CD14)(+) human leukocyte antigen (HLA)-DR(low/−) myeloid-derived suppressor cells (MDSC) from 49 CLL pat...

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Detalles Bibliográficos
Autores principales: LIU, JINLIN, ZHOU, YONGLIE, HUANG, QIANG, QIU, LIANNV
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314977/
https://www.ncbi.nlm.nih.gov/pubmed/25663875
http://dx.doi.org/10.3892/ol.2014.2808
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author LIU, JINLIN
ZHOU, YONGLIE
HUANG, QIANG
QIU, LIANNV
author_facet LIU, JINLIN
ZHOU, YONGLIE
HUANG, QIANG
QIU, LIANNV
author_sort LIU, JINLIN
collection PubMed
description Currently, no prognostic factors exist for determining the host immune status of chronic lymphocytic leukemia (CLL) patients. Therefore, the present report analyzed cluster of differentiation 14 (CD14)(+) human leukocyte antigen (HLA)-DR(low/−) myeloid-derived suppressor cells (MDSC) from 49 CLL patients and demonstrated that these cells were significantly expanded in all CLL patients when compared with monoclonal B cell lymphocytosis patients and healthy volunteers. Furthermore, upregulation of CD14(+)HLA-DR(low/−) MDSCs was correlated with CLL tumor progression and a poor prognosis for CLL patients, and CD14(+)HLA-DR(low/−) MDSCs were significantly correlated with the presence of CD4(+) T and CD5(+)CD19(+) cells in CLL patients, which could significantly inhibit the CD4(+) T-cell immune response, contributing to CLL cell progression in CLL patients.
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spelling pubmed-43149772015-02-06 CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia LIU, JINLIN ZHOU, YONGLIE HUANG, QIANG QIU, LIANNV Oncol Lett Articles Currently, no prognostic factors exist for determining the host immune status of chronic lymphocytic leukemia (CLL) patients. Therefore, the present report analyzed cluster of differentiation 14 (CD14)(+) human leukocyte antigen (HLA)-DR(low/−) myeloid-derived suppressor cells (MDSC) from 49 CLL patients and demonstrated that these cells were significantly expanded in all CLL patients when compared with monoclonal B cell lymphocytosis patients and healthy volunteers. Furthermore, upregulation of CD14(+)HLA-DR(low/−) MDSCs was correlated with CLL tumor progression and a poor prognosis for CLL patients, and CD14(+)HLA-DR(low/−) MDSCs were significantly correlated with the presence of CD4(+) T and CD5(+)CD19(+) cells in CLL patients, which could significantly inhibit the CD4(+) T-cell immune response, contributing to CLL cell progression in CLL patients. D.A. Spandidos 2015-03 2014-12-17 /pmc/articles/PMC4314977/ /pubmed/25663875 http://dx.doi.org/10.3892/ol.2014.2808 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
LIU, JINLIN
ZHOU, YONGLIE
HUANG, QIANG
QIU, LIANNV
CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia
title CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia
title_full CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia
title_fullStr CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia
title_full_unstemmed CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia
title_short CD14(+)HLA-DR(low/−) expression: A novel prognostic factor in chronic lymphocytic leukemia
title_sort cd14(+)hla-dr(low/−) expression: a novel prognostic factor in chronic lymphocytic leukemia
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314977/
https://www.ncbi.nlm.nih.gov/pubmed/25663875
http://dx.doi.org/10.3892/ol.2014.2808
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