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Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct

Regulatory T cells, Tregs, are a subset of lymphocytes that have immunosuppressive attributes. They are elevated in blood of glioblastoma patients and within this tumor's tissue itself. Indoleamine 2,3-dioxygenase, IDO, converts tryptophan to kynurenine. IDO activity enhances Treg formation by...

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Autores principales: Söderlund, Johan, Erhardt, Sophie, Kast, Richard E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925358/
https://www.ncbi.nlm.nih.gov/pubmed/20691089
http://dx.doi.org/10.1186/1742-2094-7-44
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author Söderlund, Johan
Erhardt, Sophie
Kast, Richard E
author_facet Söderlund, Johan
Erhardt, Sophie
Kast, Richard E
author_sort Söderlund, Johan
collection PubMed
description Regulatory T cells, Tregs, are a subset of lymphocytes that have immunosuppressive attributes. They are elevated in blood of glioblastoma patients and within this tumor's tissue itself. Indoleamine 2,3-dioxygenase, IDO, converts tryptophan to kynurenine. IDO activity enhances Treg formation by pathways that are unknown. Experimentally, inhibition of IDO decreases Treg function and number in rodents. The common anti-viral agent acyclovir inhibits IDO. Acyclovir may thereby decrease Treg function in glioblastoma. If it can be confirmed that Treg counts are elevated in glioblastoma patients' tumor tissue, and if we can document acyclovir's lowering of tissue Treg counts by a small trial of acyclovir in pre-operative glioblastoma patients, a trial of acyclovir effect on survival should be done given the current poor prognosis of glioblastoma and the well-established safety and low side effect burden of acyclovir.
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spelling pubmed-29253582010-08-24 Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct Söderlund, Johan Erhardt, Sophie Kast, Richard E J Neuroinflammation Hypothesis Regulatory T cells, Tregs, are a subset of lymphocytes that have immunosuppressive attributes. They are elevated in blood of glioblastoma patients and within this tumor's tissue itself. Indoleamine 2,3-dioxygenase, IDO, converts tryptophan to kynurenine. IDO activity enhances Treg formation by pathways that are unknown. Experimentally, inhibition of IDO decreases Treg function and number in rodents. The common anti-viral agent acyclovir inhibits IDO. Acyclovir may thereby decrease Treg function in glioblastoma. If it can be confirmed that Treg counts are elevated in glioblastoma patients' tumor tissue, and if we can document acyclovir's lowering of tissue Treg counts by a small trial of acyclovir in pre-operative glioblastoma patients, a trial of acyclovir effect on survival should be done given the current poor prognosis of glioblastoma and the well-established safety and low side effect burden of acyclovir. BioMed Central 2010-08-06 /pmc/articles/PMC2925358/ /pubmed/20691089 http://dx.doi.org/10.1186/1742-2094-7-44 Text en Copyright ©2010 Söderlund 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 cited.
spellingShingle Hypothesis
Söderlund, Johan
Erhardt, Sophie
Kast, Richard E
Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct
title Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct
title_full Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct
title_fullStr Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct
title_full_unstemmed Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct
title_short Acyclovir inhibition of IDO to decrease Tregs as a glioblastoma treatment adjunct
title_sort acyclovir inhibition of ido to decrease tregs as a glioblastoma treatment adjunct
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925358/
https://www.ncbi.nlm.nih.gov/pubmed/20691089
http://dx.doi.org/10.1186/1742-2094-7-44
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