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Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study

BACKGROUND: Regulation of tumor microenvironment is closely involved in the prognosis of Hodgkin lymphoma (HL). Indoleamine 2,3-dioxygenase (IDO) is an enzyme acting as immune modulator through suppression of T-cell immunity. This study aims to investigate role of IDO in the microenvironment of HL....

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Autores principales: Choe, Ji-Young, Yun, Ji Yun, Jeon, Yoon Kyoung, Kim, Se Hoon, Park, Gyeongsin, Huh, Joo Ryoung, Oh, Sohee, Kim, Ji Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026588/
https://www.ncbi.nlm.nih.gov/pubmed/24886161
http://dx.doi.org/10.1186/1471-2407-14-335
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author Choe, Ji-Young
Yun, Ji Yun
Jeon, Yoon Kyoung
Kim, Se Hoon
Park, Gyeongsin
Huh, Joo Ryoung
Oh, Sohee
Kim, Ji Eun
author_facet Choe, Ji-Young
Yun, Ji Yun
Jeon, Yoon Kyoung
Kim, Se Hoon
Park, Gyeongsin
Huh, Joo Ryoung
Oh, Sohee
Kim, Ji Eun
author_sort Choe, Ji-Young
collection PubMed
description BACKGROUND: Regulation of tumor microenvironment is closely involved in the prognosis of Hodgkin lymphoma (HL). Indoleamine 2,3-dioxygenase (IDO) is an enzyme acting as immune modulator through suppression of T-cell immunity. This study aims to investigate role of IDO in the microenvironment of HL. METHODS: A total of 121 cases of HL were enrolled to do immunohistochemistry for IDO, CD163, CD68, CD4, CD8, and FoxP3. Positivity was evaluated from area fractions or numbers of positive cells using automated image analyzer. Correlations between IDO expression and various cellular infiltrates and clinicopathologic parameters were examined and survival analyses were performed. RESULTS: IDO was expressed in histiocytes, dendritic cells and some endothelial cells with variable degrees, but not in tumor cells. IDO positive cells were more frequently found in mixed cellularity type than other histologic types, and in cases with EBV+, high Ann Arbor stages, B symptoms, and high IPS (all p < 0.05). High IDO expression was associated with inferior survival (p < 0.001) and reflects an independent prognostic factor in nodular sclerosis HL. CONCLUSIONS: This is the first study suggesting that IDO is the principle immunomodulator and is involved to adverse clinical outcomes of HL.
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spelling pubmed-40265882014-05-21 Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study Choe, Ji-Young Yun, Ji Yun Jeon, Yoon Kyoung Kim, Se Hoon Park, Gyeongsin Huh, Joo Ryoung Oh, Sohee Kim, Ji Eun BMC Cancer Research Article BACKGROUND: Regulation of tumor microenvironment is closely involved in the prognosis of Hodgkin lymphoma (HL). Indoleamine 2,3-dioxygenase (IDO) is an enzyme acting as immune modulator through suppression of T-cell immunity. This study aims to investigate role of IDO in the microenvironment of HL. METHODS: A total of 121 cases of HL were enrolled to do immunohistochemistry for IDO, CD163, CD68, CD4, CD8, and FoxP3. Positivity was evaluated from area fractions or numbers of positive cells using automated image analyzer. Correlations between IDO expression and various cellular infiltrates and clinicopathologic parameters were examined and survival analyses were performed. RESULTS: IDO was expressed in histiocytes, dendritic cells and some endothelial cells with variable degrees, but not in tumor cells. IDO positive cells were more frequently found in mixed cellularity type than other histologic types, and in cases with EBV+, high Ann Arbor stages, B symptoms, and high IPS (all p < 0.05). High IDO expression was associated with inferior survival (p < 0.001) and reflects an independent prognostic factor in nodular sclerosis HL. CONCLUSIONS: This is the first study suggesting that IDO is the principle immunomodulator and is involved to adverse clinical outcomes of HL. BioMed Central 2014-05-15 /pmc/articles/PMC4026588/ /pubmed/24886161 http://dx.doi.org/10.1186/1471-2407-14-335 Text en Copyright © 2014 Choe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Choe, Ji-Young
Yun, Ji Yun
Jeon, Yoon Kyoung
Kim, Se Hoon
Park, Gyeongsin
Huh, Joo Ryoung
Oh, Sohee
Kim, Ji Eun
Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
title Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
title_full Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
title_fullStr Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
title_full_unstemmed Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
title_short Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
title_sort indoleamine 2,3-dioxygenase (ido) is frequently expressed in stromal cells of hodgkin lymphoma and is associated with adverse clinical features: a retrospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026588/
https://www.ncbi.nlm.nih.gov/pubmed/24886161
http://dx.doi.org/10.1186/1471-2407-14-335
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