Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome,
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Anais brasileiros de dermatologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962021000500544 |
Resumo: | Abstract Background: The treatment of cutaneous leishmaniasis is a challenge. A better understanding of the in situ mechanisms involved in the evolution and cure of the disease is essential for the development of new therapies. Objective: Correlate histopathological and immunological characteristics of cutaneous leishmaniasis lesions with clinical outcome after different treatment regimens. Methods: The authors analyzed cellular infiltration and immunohistochemistry staining for CD4, CD8 and IL-17 in biopsy samples from 33 patients with cutaneous leishmaniasis before treatment. All patients were recruited in a randomized clinical trial at Corte de Pedra (Bahia-Brazil) and assigned to receive Glucantime®, Glucantime® + Oral Tamoxifen or Glucantime® + Topical Tamoxifen. Patients were followed for 2 to 6 months to define disease outcome. Results: A similar expression of CD4, CD8 and IL-17 was observed in lesion samples regardless of clinical outcome. In general, a higher amount of CD8 cells were observed compared with CD4 cells. An important observation was that all patients whose cellular infiltrate did not contain plasma cells were cured after treatment. Study limitations: Isolated quantification of TCD8 and IL-17 using immunohistochemistry is insufficient to analyze the role of these molecules in the immunopathogenesis of cutaneous leishmaniasis. In addition, the expansion of the immunohistochemistry panel would allow a more complete analysis of the immune response in situ. Conclusions: The absence of plasma cells in cutaneous leishmaniasis lesions was related to a favorable therapeutic outcome. |
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Anais brasileiros de dermatologia (Online) |
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Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome,CD4 antigensCD8 antigensImmunohistochemistryInterleukin-17LeishmaniasiscutaneousPlasma cellsAbstract Background: The treatment of cutaneous leishmaniasis is a challenge. A better understanding of the in situ mechanisms involved in the evolution and cure of the disease is essential for the development of new therapies. Objective: Correlate histopathological and immunological characteristics of cutaneous leishmaniasis lesions with clinical outcome after different treatment regimens. Methods: The authors analyzed cellular infiltration and immunohistochemistry staining for CD4, CD8 and IL-17 in biopsy samples from 33 patients with cutaneous leishmaniasis before treatment. All patients were recruited in a randomized clinical trial at Corte de Pedra (Bahia-Brazil) and assigned to receive Glucantime®, Glucantime® + Oral Tamoxifen or Glucantime® + Topical Tamoxifen. Patients were followed for 2 to 6 months to define disease outcome. Results: A similar expression of CD4, CD8 and IL-17 was observed in lesion samples regardless of clinical outcome. In general, a higher amount of CD8 cells were observed compared with CD4 cells. An important observation was that all patients whose cellular infiltrate did not contain plasma cells were cured after treatment. Study limitations: Isolated quantification of TCD8 and IL-17 using immunohistochemistry is insufficient to analyze the role of these molecules in the immunopathogenesis of cutaneous leishmaniasis. In addition, the expansion of the immunohistochemistry panel would allow a more complete analysis of the immune response in situ. Conclusions: The absence of plasma cells in cutaneous leishmaniasis lesions was related to a favorable therapeutic outcome.Sociedade Brasileira de Dermatologia2021-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962021000500544Anais Brasileiros de Dermatologia v.96 n.5 2021reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1016/j.abd.2021.02.006info:eu-repo/semantics/openAccessRibeiro,Camila SampaioFrança,Riam RochaSilva,Juliana AlmeidaSilva,Silvana Conceição daUliana,Sílvia R.B.Boaventura,Viviane SampaioMachado,Paulo R.L.eng2021-10-14T00:00:00Zoai:scielo:S0365-05962021000500544Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2021-10-14T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
title |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
spellingShingle |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, Ribeiro,Camila Sampaio CD4 antigens CD8 antigens Immunohistochemistry Interleukin-17 Leishmaniasis cutaneous Plasma cells |
title_short |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
title_full |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
title_fullStr |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
title_full_unstemmed |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
title_sort |
Cellular infiltrate in cutaneous leishmaniasis lesions and therapeutic outcome, |
author |
Ribeiro,Camila Sampaio |
author_facet |
Ribeiro,Camila Sampaio França,Riam Rocha Silva,Juliana Almeida Silva,Silvana Conceição da Uliana,Sílvia R.B. Boaventura,Viviane Sampaio Machado,Paulo R.L. |
author_role |
author |
author2 |
França,Riam Rocha Silva,Juliana Almeida Silva,Silvana Conceição da Uliana,Sílvia R.B. Boaventura,Viviane Sampaio Machado,Paulo R.L. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Ribeiro,Camila Sampaio França,Riam Rocha Silva,Juliana Almeida Silva,Silvana Conceição da Uliana,Sílvia R.B. Boaventura,Viviane Sampaio Machado,Paulo R.L. |
dc.subject.por.fl_str_mv |
CD4 antigens CD8 antigens Immunohistochemistry Interleukin-17 Leishmaniasis cutaneous Plasma cells |
topic |
CD4 antigens CD8 antigens Immunohistochemistry Interleukin-17 Leishmaniasis cutaneous Plasma cells |
description |
Abstract Background: The treatment of cutaneous leishmaniasis is a challenge. A better understanding of the in situ mechanisms involved in the evolution and cure of the disease is essential for the development of new therapies. Objective: Correlate histopathological and immunological characteristics of cutaneous leishmaniasis lesions with clinical outcome after different treatment regimens. Methods: The authors analyzed cellular infiltration and immunohistochemistry staining for CD4, CD8 and IL-17 in biopsy samples from 33 patients with cutaneous leishmaniasis before treatment. All patients were recruited in a randomized clinical trial at Corte de Pedra (Bahia-Brazil) and assigned to receive Glucantime®, Glucantime® + Oral Tamoxifen or Glucantime® + Topical Tamoxifen. Patients were followed for 2 to 6 months to define disease outcome. Results: A similar expression of CD4, CD8 and IL-17 was observed in lesion samples regardless of clinical outcome. In general, a higher amount of CD8 cells were observed compared with CD4 cells. An important observation was that all patients whose cellular infiltrate did not contain plasma cells were cured after treatment. Study limitations: Isolated quantification of TCD8 and IL-17 using immunohistochemistry is insufficient to analyze the role of these molecules in the immunopathogenesis of cutaneous leishmaniasis. In addition, the expansion of the immunohistochemistry panel would allow a more complete analysis of the immune response in situ. Conclusions: The absence of plasma cells in cutaneous leishmaniasis lesions was related to a favorable therapeutic outcome. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962021000500544 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962021000500544 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.abd.2021.02.006 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
dc.source.none.fl_str_mv |
Anais Brasileiros de Dermatologia v.96 n.5 2021 reponame:Anais brasileiros de dermatologia (Online) instname:Sociedade Brasileira de Dermatologia (SBD) instacron:SBD |
instname_str |
Sociedade Brasileira de Dermatologia (SBD) |
instacron_str |
SBD |
institution |
SBD |
reponame_str |
Anais brasileiros de dermatologia (Online) |
collection |
Anais brasileiros de dermatologia (Online) |
repository.name.fl_str_mv |
Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD) |
repository.mail.fl_str_mv |
abd@sbd.org.br||revista@sbd.org.br |
_version_ |
1752126424578260992 |