Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis

Detalhes bibliográficos
Autor(a) principal: Correa, Frederico J.S.
Data de Publicação: 2022
Outros Autores: Andres, Marina Paula, Rocha, Tainá Pezzin, Carvalho, Ana Eduarda Z., Aloia, Thiago P.A., Corpa, Marcus V.N., Kallas, Esper G., Mangueira, Cristóvão L.P., Baracat, Edmund C., Carvalho, Karina I., Abrão, Mauricio S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/213316
Resumo: Objective: To evaluate the frequencies of iNKT cells and their subsets in patients with deep endometriosis. Methods: A case-control study was conducted between 2013 and 2015, with 73 patients distributed into two groups: 47 women with a histological diagnosis of endometriosis and 26 controls. Peripheral blood, endometriosis lesions, and healthy peritoneal samples were collected on the day of surgery to determine the frequencies of iNKT cells and subtypes via flow cytometry analysis. Results: The authors observed a lower number of iNKT (p = 0.01) and Double-Negative (DN) iNKT cells (p = 0.02) in the blood of patients with endometriosis than in the control group. The number of DN iNKT IL-17+ cells in the secretory phase was lower in the endometriosis group (p = 0.049). There was an increase in the secretion of IL-17 by CD4+ iNKT cells in the blood of patients with endometriosis and severe dysmenorrhea (p = 0.038), and severe acyclic pelvic pain (p = 0.048). Patients with severe dysmenorrhea also had a decreased number of CD4+ CCR7+ cells (p = 0.022). Conclusion: The decreased number of total iNKT and DN iNKT cells in patients with endometriosis suggests that iNKT cells play a role in the pathogenesis of endometriosis and can be used to develop new diagnostic and therapeutic agents.
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spelling Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosisDeep endometriosisInvariant natural Killer T-cellsCytokinesFlow cytometryObjective: To evaluate the frequencies of iNKT cells and their subsets in patients with deep endometriosis. Methods: A case-control study was conducted between 2013 and 2015, with 73 patients distributed into two groups: 47 women with a histological diagnosis of endometriosis and 26 controls. Peripheral blood, endometriosis lesions, and healthy peritoneal samples were collected on the day of surgery to determine the frequencies of iNKT cells and subtypes via flow cytometry analysis. Results: The authors observed a lower number of iNKT (p = 0.01) and Double-Negative (DN) iNKT cells (p = 0.02) in the blood of patients with endometriosis than in the control group. The number of DN iNKT IL-17+ cells in the secretory phase was lower in the endometriosis group (p = 0.049). There was an increase in the secretion of IL-17 by CD4+ iNKT cells in the blood of patients with endometriosis and severe dysmenorrhea (p = 0.038), and severe acyclic pelvic pain (p = 0.048). Patients with severe dysmenorrhea also had a decreased number of CD4+ CCR7+ cells (p = 0.022). Conclusion: The decreased number of total iNKT and DN iNKT cells in patients with endometriosis suggests that iNKT cells play a role in the pathogenesis of endometriosis and can be used to develop new diagnostic and therapeutic agents.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2022-05-13info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/21331610.1016/j.clinsp.2022.100032Clinics; Vol. 77 (2022); 100032Clinics; v. 77 (2022); 100032Clinics; Vol. 77 (2022); 1000321980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/213316/195265Copyright (c) 2023 Clinicsinfo:eu-repo/semantics/openAccessCorrea, Frederico J.S.Andres, Marina PaulaRocha, Tainá PezzinCarvalho, Ana Eduarda Z.Aloia, Thiago P.A.Corpa, Marcus V.N.Kallas, Esper G.Mangueira, Cristóvão L.P.Baracat, Edmund C.Carvalho, Karina I.Abrão, Mauricio S.2023-07-06T13:04:56Zoai:revistas.usp.br:article/213316Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2023-07-06T13:04:56Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
title Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
spellingShingle Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
Correa, Frederico J.S.
Deep endometriosis
Invariant natural Killer T-cells
Cytokines
Flow cytometry
title_short Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
title_full Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
title_fullStr Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
title_full_unstemmed Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
title_sort Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis
author Correa, Frederico J.S.
author_facet Correa, Frederico J.S.
Andres, Marina Paula
Rocha, Tainá Pezzin
Carvalho, Ana Eduarda Z.
Aloia, Thiago P.A.
Corpa, Marcus V.N.
Kallas, Esper G.
Mangueira, Cristóvão L.P.
Baracat, Edmund C.
Carvalho, Karina I.
Abrão, Mauricio S.
author_role author
author2 Andres, Marina Paula
Rocha, Tainá Pezzin
Carvalho, Ana Eduarda Z.
Aloia, Thiago P.A.
Corpa, Marcus V.N.
Kallas, Esper G.
Mangueira, Cristóvão L.P.
Baracat, Edmund C.
Carvalho, Karina I.
Abrão, Mauricio S.
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Correa, Frederico J.S.
Andres, Marina Paula
Rocha, Tainá Pezzin
Carvalho, Ana Eduarda Z.
Aloia, Thiago P.A.
Corpa, Marcus V.N.
Kallas, Esper G.
Mangueira, Cristóvão L.P.
Baracat, Edmund C.
Carvalho, Karina I.
Abrão, Mauricio S.
dc.subject.por.fl_str_mv Deep endometriosis
Invariant natural Killer T-cells
Cytokines
Flow cytometry
topic Deep endometriosis
Invariant natural Killer T-cells
Cytokines
Flow cytometry
description Objective: To evaluate the frequencies of iNKT cells and their subsets in patients with deep endometriosis. Methods: A case-control study was conducted between 2013 and 2015, with 73 patients distributed into two groups: 47 women with a histological diagnosis of endometriosis and 26 controls. Peripheral blood, endometriosis lesions, and healthy peritoneal samples were collected on the day of surgery to determine the frequencies of iNKT cells and subtypes via flow cytometry analysis. Results: The authors observed a lower number of iNKT (p = 0.01) and Double-Negative (DN) iNKT cells (p = 0.02) in the blood of patients with endometriosis than in the control group. The number of DN iNKT IL-17+ cells in the secretory phase was lower in the endometriosis group (p = 0.049). There was an increase in the secretion of IL-17 by CD4+ iNKT cells in the blood of patients with endometriosis and severe dysmenorrhea (p = 0.038), and severe acyclic pelvic pain (p = 0.048). Patients with severe dysmenorrhea also had a decreased number of CD4+ CCR7+ cells (p = 0.022). Conclusion: The decreased number of total iNKT and DN iNKT cells in patients with endometriosis suggests that iNKT cells play a role in the pathogenesis of endometriosis and can be used to develop new diagnostic and therapeutic agents.
publishDate 2022
dc.date.none.fl_str_mv 2022-05-13
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/213316
10.1016/j.clinsp.2022.100032
url https://www.revistas.usp.br/clinics/article/view/213316
identifier_str_mv 10.1016/j.clinsp.2022.100032
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/213316/195265
dc.rights.driver.fl_str_mv Copyright (c) 2023 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 77 (2022); 100032
Clinics; v. 77 (2022); 100032
Clinics; Vol. 77 (2022); 100032
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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