Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.

Th17 cells, a recently discovered subset of T helper cells that secrete IL-17A, can affect the inflammation process autoimmune and cancer diseases development. The purpose of this study was to evaluate the role of Th17 cells and IL17A in biology of CLL. The study group included 294 untreated CLL pat...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Iwona Hus, Agnieszka Bojarska-Junak, Sylwia Chocholska, Waldemar Tomczak, Justyna Woś, Anna Dmoszyńska, Jacek Roliński
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/0125662e64694743bde82038d5ca9420
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:0125662e64694743bde82038d5ca9420
record_format dspace
spelling oai:doaj.org-article:0125662e64694743bde82038d5ca94202021-11-18T08:48:46ZTh17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.1932-620310.1371/journal.pone.0078091https://doaj.org/article/0125662e64694743bde82038d5ca94202013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24223764/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Th17 cells, a recently discovered subset of T helper cells that secrete IL-17A, can affect the inflammation process autoimmune and cancer diseases development. The purpose of this study was to evaluate the role of Th17 cells and IL17A in biology of CLL. The study group included 294 untreated CLL patients in different clinical stages. Here, we show that higher Th17 and IL-17A values were associated with less advanced clinical stage of CLL. Th17 cells' percentages in PB were lower in patients who died due to CLL during follow-up due to CLL (as compared to surviving patients) and in patients responding to first-line therapy with fludarabine-based regimens (as compared to non-responders). IL-17A inversely correlated with the time from CLL diagnosis to the start of therapy and was lower in patients who required treatment during follow-up. Th-17 and IL-17A values were lower in patients with adverse prognostic factors (17p and 11q deletion, CD38 and ZAP-70 expression). CLL patients with detectable IL-17A mRNA in T cells were in Rai Stage 0 and negative for both ZAP-70 and CD38 expression. Th17 percentages positively correlated with iNKT and adversely with Treg cells. The results of this study suggest that Th17 may play a beneficial role in CLL immunity.Iwona HusAgnieszka Bojarska-JunakSylwia ChocholskaWaldemar TomczakJustyna WośAnna DmoszyńskaJacek RolińskiJacek RolińskiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 11, p e78091 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Iwona Hus
Agnieszka Bojarska-Junak
Sylwia Chocholska
Waldemar Tomczak
Justyna Woś
Anna Dmoszyńska
Jacek Roliński
Jacek Roliński
Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.
description Th17 cells, a recently discovered subset of T helper cells that secrete IL-17A, can affect the inflammation process autoimmune and cancer diseases development. The purpose of this study was to evaluate the role of Th17 cells and IL17A in biology of CLL. The study group included 294 untreated CLL patients in different clinical stages. Here, we show that higher Th17 and IL-17A values were associated with less advanced clinical stage of CLL. Th17 cells' percentages in PB were lower in patients who died due to CLL during follow-up due to CLL (as compared to surviving patients) and in patients responding to first-line therapy with fludarabine-based regimens (as compared to non-responders). IL-17A inversely correlated with the time from CLL diagnosis to the start of therapy and was lower in patients who required treatment during follow-up. Th-17 and IL-17A values were lower in patients with adverse prognostic factors (17p and 11q deletion, CD38 and ZAP-70 expression). CLL patients with detectable IL-17A mRNA in T cells were in Rai Stage 0 and negative for both ZAP-70 and CD38 expression. Th17 percentages positively correlated with iNKT and adversely with Treg cells. The results of this study suggest that Th17 may play a beneficial role in CLL immunity.
format article
author Iwona Hus
Agnieszka Bojarska-Junak
Sylwia Chocholska
Waldemar Tomczak
Justyna Woś
Anna Dmoszyńska
Jacek Roliński
Jacek Roliński
author_facet Iwona Hus
Agnieszka Bojarska-Junak
Sylwia Chocholska
Waldemar Tomczak
Justyna Woś
Anna Dmoszyńska
Jacek Roliński
Jacek Roliński
author_sort Iwona Hus
title Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.
title_short Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.
title_full Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.
title_fullStr Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.
title_full_unstemmed Th17/IL-17A might play a protective role in chronic lymphocytic leukemia immunity.
title_sort th17/il-17a might play a protective role in chronic lymphocytic leukemia immunity.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/0125662e64694743bde82038d5ca9420
work_keys_str_mv AT iwonahus th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT agnieszkabojarskajunak th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT sylwiachocholska th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT waldemartomczak th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT justynawos th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT annadmoszynska th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT jacekrolinski th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
AT jacekrolinski th17il17amightplayaprotectiveroleinchroniclymphocyticleukemiaimmunity
_version_ 1718421242907721728