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In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection

BACKGROUND: Skin lesions of patients affected by non-ulcerated cutaneous leishmaniasis (NUCL) caused by L. (L.) infantum chagasi are characterized by lymphohistiocytic inflammatory infiltrate associated with epithelioid granuloma and scarce parasitism. However, the in situ cellular immune response o...

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Autores principales: Sandoval, Carmen, Araujo, Gabriela, Sosa, Wilfredo, Avalos, Sara, Silveira, Fernando, Corbett, Carlos, Zúniga, Concepción, Laurenti, Marcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centro de Estudos de Venenos e Animais Peçonhentos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909480/
https://www.ncbi.nlm.nih.gov/pubmed/33708246
http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0149
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author Sandoval, Carmen
Araujo, Gabriela
Sosa, Wilfredo
Avalos, Sara
Silveira, Fernando
Corbett, Carlos
Zúniga, Concepción
Laurenti, Marcia
author_facet Sandoval, Carmen
Araujo, Gabriela
Sosa, Wilfredo
Avalos, Sara
Silveira, Fernando
Corbett, Carlos
Zúniga, Concepción
Laurenti, Marcia
author_sort Sandoval, Carmen
collection PubMed
description BACKGROUND: Skin lesions of patients affected by non-ulcerated cutaneous leishmaniasis (NUCL) caused by L. (L.) infantum chagasi are characterized by lymphohistiocytic inflammatory infiltrate associated with epithelioid granuloma and scarce parasitism. However, the in situ cellular immune response of these patients is unclear. Therefore, the aim of the present study was to characterize the cellular immune response in the skin lesions of patients affected by NUCL. METHODS: Twenty biopsies were processed by immunohistochemistry using primary antibodies to T lymphocytes (CD4, CD8), NK cells, B lymphocytes, macrophages, nitric oxide synthase and interferon-gamma. RESULTS: Immunohistochemistry revealed higher expression of all cellular types and molecules (IFN-γ, iNOS) in the dermis of diseased skin compared to the skin of healthy individuals (p < 0.05). Morphometric analysis performed in the skin lesions sections showed the predominance of CD8(+) T lymphocytes in the mononuclear infiltrate, followed by macrophages, mostly iNOS(+), a response that could be mediated by IFN-γ. CONCLUSION: Our study improves knowledge of the cellular immune response in non-ulcerated or atypical cutaneous leishmaniasis caused by L. (L.) infantum chagasi in Central America and pointed to the pivotal participation of CD8(+) T lymphocytes in the host defense mechanisms against the parasite in patients with NUCL.
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spelling pubmed-79094802021-03-10 In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection Sandoval, Carmen Araujo, Gabriela Sosa, Wilfredo Avalos, Sara Silveira, Fernando Corbett, Carlos Zúniga, Concepción Laurenti, Marcia J Venom Anim Toxins Incl Trop Dis Short Report BACKGROUND: Skin lesions of patients affected by non-ulcerated cutaneous leishmaniasis (NUCL) caused by L. (L.) infantum chagasi are characterized by lymphohistiocytic inflammatory infiltrate associated with epithelioid granuloma and scarce parasitism. However, the in situ cellular immune response of these patients is unclear. Therefore, the aim of the present study was to characterize the cellular immune response in the skin lesions of patients affected by NUCL. METHODS: Twenty biopsies were processed by immunohistochemistry using primary antibodies to T lymphocytes (CD4, CD8), NK cells, B lymphocytes, macrophages, nitric oxide synthase and interferon-gamma. RESULTS: Immunohistochemistry revealed higher expression of all cellular types and molecules (IFN-γ, iNOS) in the dermis of diseased skin compared to the skin of healthy individuals (p < 0.05). Morphometric analysis performed in the skin lesions sections showed the predominance of CD8(+) T lymphocytes in the mononuclear infiltrate, followed by macrophages, mostly iNOS(+), a response that could be mediated by IFN-γ. CONCLUSION: Our study improves knowledge of the cellular immune response in non-ulcerated or atypical cutaneous leishmaniasis caused by L. (L.) infantum chagasi in Central America and pointed to the pivotal participation of CD8(+) T lymphocytes in the host defense mechanisms against the parasite in patients with NUCL. Centro de Estudos de Venenos e Animais Peçonhentos 2021-02-26 /pmc/articles/PMC7909480/ /pubmed/33708246 http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0149 Text en This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Sandoval, Carmen
Araujo, Gabriela
Sosa, Wilfredo
Avalos, Sara
Silveira, Fernando
Corbett, Carlos
Zúniga, Concepción
Laurenti, Marcia
In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection
title In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection
title_full In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection
title_fullStr In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection
title_full_unstemmed In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection
title_short In situ cellular immune response in non-ulcerated skin lesions due to Leishmania (L.) infantum chagasi infection
title_sort in situ cellular immune response in non-ulcerated skin lesions due to leishmania (l.) infantum chagasi infection
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909480/
https://www.ncbi.nlm.nih.gov/pubmed/33708246
http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0149
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