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Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum
High IL-10 levels are pivotal to parasite survival in visceral leishmaniasis (VL). Antigenic stimuli induce IL-10 expression and release of adenosine by CD39/CD73. Due their intrinsic ability to express IL-10 and produce adenosine from extracellular ATP, we evaluated the IL-10, CD39, and CD73 expres...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864225/ https://www.ncbi.nlm.nih.gov/pubmed/36668925 http://dx.doi.org/10.3390/tropicalmed8010018 |
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author | Peixoto, Rephany F. Gois, Bruna M. Martins, Marineuma Palmeira, Pedro Henrique S. Rocha, Juliana C. Gomes, Juliana A. S. Azevedo, Fátima L. A. A. Veras, Robson C. de Medeiros, Isac A. Grisi, Teresa C. S. L. de Araújo, Demétrius A. M. Amaral, Ian P. G. Keesen, Tatjana S. L. |
author_facet | Peixoto, Rephany F. Gois, Bruna M. Martins, Marineuma Palmeira, Pedro Henrique S. Rocha, Juliana C. Gomes, Juliana A. S. Azevedo, Fátima L. A. A. Veras, Robson C. de Medeiros, Isac A. Grisi, Teresa C. S. L. de Araújo, Demétrius A. M. Amaral, Ian P. G. Keesen, Tatjana S. L. |
author_sort | Peixoto, Rephany F. |
collection | PubMed |
description | High IL-10 levels are pivotal to parasite survival in visceral leishmaniasis (VL). Antigenic stimuli induce IL-10 expression and release of adenosine by CD39/CD73. Due their intrinsic ability to express IL-10 and produce adenosine from extracellular ATP, we evaluated the IL-10, CD39, and CD73 expression by Regulatory T cells (Treg) correlated with VL pathology. Using flow cytometry, Treg cells was analyzed in peripheral blood samples from VL patients (in the presence and absence of Leishmania infantum soluble antigen (SLA)) and healthy individuals (negative endemic control—NEC group), without any treatment. Additionally, IL-10 levels in leukocytes culture supernatant were measured in all groups by ELISA assay. VL patients presented more Treg frequency than NEC group, independently of stimulation. ELISA results demonstrated that SLA induced higher IL-10 expression in the VL group. However, the NEC group had a higher Treg IL-10(+) compared to the VL group without stimulation and SLA restored the IL-10 in Treg. Additionally, an increase in Treg CD73(+) in the VL group independently of stimuli compared to that in the NEC group was observed. We suggest that Treg are not the main source of IL-10, while the CD73 pathway may be an attempt to modulate the exacerbation of immune response in VL disease. |
format | Online Article Text |
id | pubmed-9864225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98642252023-01-22 Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum Peixoto, Rephany F. Gois, Bruna M. Martins, Marineuma Palmeira, Pedro Henrique S. Rocha, Juliana C. Gomes, Juliana A. S. Azevedo, Fátima L. A. A. Veras, Robson C. de Medeiros, Isac A. Grisi, Teresa C. S. L. de Araújo, Demétrius A. M. Amaral, Ian P. G. Keesen, Tatjana S. L. Trop Med Infect Dis Article High IL-10 levels are pivotal to parasite survival in visceral leishmaniasis (VL). Antigenic stimuli induce IL-10 expression and release of adenosine by CD39/CD73. Due their intrinsic ability to express IL-10 and produce adenosine from extracellular ATP, we evaluated the IL-10, CD39, and CD73 expression by Regulatory T cells (Treg) correlated with VL pathology. Using flow cytometry, Treg cells was analyzed in peripheral blood samples from VL patients (in the presence and absence of Leishmania infantum soluble antigen (SLA)) and healthy individuals (negative endemic control—NEC group), without any treatment. Additionally, IL-10 levels in leukocytes culture supernatant were measured in all groups by ELISA assay. VL patients presented more Treg frequency than NEC group, independently of stimulation. ELISA results demonstrated that SLA induced higher IL-10 expression in the VL group. However, the NEC group had a higher Treg IL-10(+) compared to the VL group without stimulation and SLA restored the IL-10 in Treg. Additionally, an increase in Treg CD73(+) in the VL group independently of stimuli compared to that in the NEC group was observed. We suggest that Treg are not the main source of IL-10, while the CD73 pathway may be an attempt to modulate the exacerbation of immune response in VL disease. MDPI 2022-12-27 /pmc/articles/PMC9864225/ /pubmed/36668925 http://dx.doi.org/10.3390/tropicalmed8010018 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Peixoto, Rephany F. Gois, Bruna M. Martins, Marineuma Palmeira, Pedro Henrique S. Rocha, Juliana C. Gomes, Juliana A. S. Azevedo, Fátima L. A. A. Veras, Robson C. de Medeiros, Isac A. Grisi, Teresa C. S. L. de Araújo, Demétrius A. M. Amaral, Ian P. G. Keesen, Tatjana S. L. Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum |
title | Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum |
title_full | Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum |
title_fullStr | Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum |
title_full_unstemmed | Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum |
title_short | Characterization of Regulatory T Cells in Patients Infected by Leishmania Infantum |
title_sort | characterization of regulatory t cells in patients infected by leishmania infantum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864225/ https://www.ncbi.nlm.nih.gov/pubmed/36668925 http://dx.doi.org/10.3390/tropicalmed8010018 |
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