Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp

Detalhes bibliográficos
Autor(a) principal: Pacheco, Carmen M. Sandoval
Data de Publicação: 2021
Outros Autores: Flores, Gabriela Venicia Araújo, Gonzalez, Kadir, Gomes, Claudia Maria de Castro, Passero, Luiz F. D, Tomokane, Thaise Yumie, Sosa-Ochoa, Wilfredo, Valeriano, Concepción Zúniga, Calzada, Jose, Saldaña, Azael, Corbett, Carlos Eduardo Pereira, Silveira, Fernando Tobias, Laurenti, Márcia Dalastra
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Digital do Instituto Evandro Chagas (Patuá)
Texto Completo: https://patua.iec.gov.br/handle/iec/4308
Resumo: Macrophages play important roles in the innate and acquired immune responses against Leishmania parasites. Depending on the subset and activation status, macrophages may eliminate intracellular parasites; however, these host cells also can offer a safe environment for Leishmania replication. In this sense, the fate of the parasite may be influenced by the phenotype of the infected macrophage, linked to the subtype of classically activated (M1) or alternatively activated (M2) macrophages. In the present study, M1 and M2 macrophage subsets were analyzed by double-staining immunohistochemistry in skin biopsies from patients with American cutaneous leishmaniasis (ACL) caused by L. (L.) amazonensis, L. (V.) braziliensis, L. (V.) panamensis ,and L. (L.) infantum chagasi. High number of M1 macrophages was detected in nonulcerated cutaneous leishmaniasis (NUCL) caused by L. (L.) infantum chagasi (M1 = 112 ± 12, M2 = 43 ± 12 cells/mm2). On the other side, high density of M2 macrophages was observed in the skin lesions of patients with anergic diffuse cutaneous leishmaniasis (ADCL) (M1 = 195 ± 25, M2 = 616 ± 114), followed by cases of localized cutaneous leishmaniasis (LCL) caused by L. (L.) amazonensis (M1 = 97 ± 24, M2 = 219 ± 29), L. (V.) panamensis (M1 = 71 ± 14, M2 = 164 ± 14), and L. (V.) braziliensis (M1 = 50 ± 13, M2 = 53 ± 10); however, low density of M2 macrophages was observed in NUCL. The data presented herein show the polarization of macrophages in skin lesions caused by different Leishmania species that may be related with the outcome of the disease.
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spelling Pacheco, Carmen M. SandovalFlores, Gabriela Venicia AraújoGonzalez, KadirGomes, Claudia Maria de CastroPassero, Luiz F. DTomokane, Thaise YumieSosa-Ochoa, WilfredoValeriano, Concepción ZúnigaCalzada, JoseSaldaña, AzaelCorbett, Carlos Eduardo PereiraSilveira, Fernando TobiasLaurenti, Márcia Dalastra2021-05-13T16:06:23Z2021-05-13T16:06:23Z2021PACHECO, Carmen M. Sandoval et al. Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp. Journal of Immunology Research, v. 2021, n. ID 5596876, p. 1-8, 2021.2314-7156https://patua.iec.gov.br/handle/iec/430810.1155/2021/5596876Macrophages play important roles in the innate and acquired immune responses against Leishmania parasites. Depending on the subset and activation status, macrophages may eliminate intracellular parasites; however, these host cells also can offer a safe environment for Leishmania replication. In this sense, the fate of the parasite may be influenced by the phenotype of the infected macrophage, linked to the subtype of classically activated (M1) or alternatively activated (M2) macrophages. In the present study, M1 and M2 macrophage subsets were analyzed by double-staining immunohistochemistry in skin biopsies from patients with American cutaneous leishmaniasis (ACL) caused by L. (L.) amazonensis, L. (V.) braziliensis, L. (V.) panamensis ,and L. (L.) infantum chagasi. High number of M1 macrophages was detected in nonulcerated cutaneous leishmaniasis (NUCL) caused by L. (L.) infantum chagasi (M1 = 112 ± 12, M2 = 43 ± 12 cells/mm2). On the other side, high density of M2 macrophages was observed in the skin lesions of patients with anergic diffuse cutaneous leishmaniasis (ADCL) (M1 = 195 ± 25, M2 = 616 ± 114), followed by cases of localized cutaneous leishmaniasis (LCL) caused by L. (L.) amazonensis (M1 = 97 ± 24, M2 = 219 ± 29), L. (V.) panamensis (M1 = 71 ± 14, M2 = 164 ± 14), and L. (V.) braziliensis (M1 = 50 ± 13, M2 = 53 ± 10); however, low density of M2 macrophages was observed in NUCL. The data presented herein show the polarization of macrophages in skin lesions caused by different Leishmania species that may be related with the outcome of the disease.This study was supported by the Sao Paulo Research Foundation (FAPESP) grants #2014/50315-0, #2015/01154-7, #2017/24834-9, #2018/04698-6 and GVAF and CMSP Scholarship from CAPES (Social Demand) and Laboratório de Patologia de Moléstias Infecciosas (LIM50 HC-FMUSP). MDL is a research fellow from the National Research Council-CNPq, Brazil, grant #302174/2017-6.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. São Paulo, SP, Brazil.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. São Paulo, SP, Brazil.Instituto Conmemorativo Gorgas de Estudios de la Salud. Departamento de Parasitología Molecular. Calidonia, Panama.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. São Paulo, SP, Brazil.São Paulo State University. Institute of Biosciences. Institute for Advanced Studies of Ocean. São Vicente, SP, Brazil.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. São Paulo, SP, Brazil.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. São Paulo, SP, Brazil / Universidad Nacional Autónoma de Honduras. Instituto de Investigación en Microbiología. Tegucigalpa, Honduras.Hospital Escuela. Departamento de Vigilancia de la Salud. Tegucigalpa, Honduras.Instituto Conmemorativo Gorgas de Estudios de la Salud. Departamento de Parasitología Molecular. Calidonia, Panama / Universidad de Panamá - Campus Harmodio Arias Madrid. Facultad de Medicina Veterinaria. Albrook, Panama.Instituto Conmemorativo Gorgas de Estudios de la Salud. Departamento de Parasitología Molecular. Calidonia, Panama / Universidad de Panamá. Facultad de Medicina. Centro de Investigación y Diagnóstico de Enfermedades Parasitarias. Panama.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. São Paulo, SP, Brazil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Laboratório de Microbiologia Ambiental. Ananindeua, PA, Brasil / Universidade Federal de Pará. Núcleo de Medicina Tropical. Belém, PA, Brazil.Universidade de São Paulo. Faculdade de Medicina. Departamento de Patologia. Laboratório de Patologia de Moléstias Infecciosas. 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dc.title.pt_BR.fl_str_mv Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
title Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
spellingShingle Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
Pacheco, Carmen M. Sandoval
Leishmania / parasitologia
Macrófagos / imunologia
Desenluvamentos Cutâneos / parasitologia
Pele / lesões
Coloração e Rotulagem
title_short Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
title_full Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
title_fullStr Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
title_full_unstemmed Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
title_sort Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp
author Pacheco, Carmen M. Sandoval
author_facet Pacheco, Carmen M. Sandoval
Flores, Gabriela Venicia Araújo
Gonzalez, Kadir
Gomes, Claudia Maria de Castro
Passero, Luiz F. D
Tomokane, Thaise Yumie
Sosa-Ochoa, Wilfredo
Valeriano, Concepción Zúniga
Calzada, Jose
Saldaña, Azael
Corbett, Carlos Eduardo Pereira
Silveira, Fernando Tobias
Laurenti, Márcia Dalastra
author_role author
author2 Flores, Gabriela Venicia Araújo
Gonzalez, Kadir
Gomes, Claudia Maria de Castro
Passero, Luiz F. D
Tomokane, Thaise Yumie
Sosa-Ochoa, Wilfredo
Valeriano, Concepción Zúniga
Calzada, Jose
Saldaña, Azael
Corbett, Carlos Eduardo Pereira
Silveira, Fernando Tobias
Laurenti, Márcia Dalastra
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pacheco, Carmen M. Sandoval
Flores, Gabriela Venicia Araújo
Gonzalez, Kadir
Gomes, Claudia Maria de Castro
Passero, Luiz F. D
Tomokane, Thaise Yumie
Sosa-Ochoa, Wilfredo
Valeriano, Concepción Zúniga
Calzada, Jose
Saldaña, Azael
Corbett, Carlos Eduardo Pereira
Silveira, Fernando Tobias
Laurenti, Márcia Dalastra
dc.subject.decsPrimary.pt_BR.fl_str_mv Leishmania / parasitologia
Macrófagos / imunologia
Desenluvamentos Cutâneos / parasitologia
Pele / lesões
Coloração e Rotulagem
topic Leishmania / parasitologia
Macrófagos / imunologia
Desenluvamentos Cutâneos / parasitologia
Pele / lesões
Coloração e Rotulagem
description Macrophages play important roles in the innate and acquired immune responses against Leishmania parasites. Depending on the subset and activation status, macrophages may eliminate intracellular parasites; however, these host cells also can offer a safe environment for Leishmania replication. In this sense, the fate of the parasite may be influenced by the phenotype of the infected macrophage, linked to the subtype of classically activated (M1) or alternatively activated (M2) macrophages. In the present study, M1 and M2 macrophage subsets were analyzed by double-staining immunohistochemistry in skin biopsies from patients with American cutaneous leishmaniasis (ACL) caused by L. (L.) amazonensis, L. (V.) braziliensis, L. (V.) panamensis ,and L. (L.) infantum chagasi. High number of M1 macrophages was detected in nonulcerated cutaneous leishmaniasis (NUCL) caused by L. (L.) infantum chagasi (M1 = 112 ± 12, M2 = 43 ± 12 cells/mm2). On the other side, high density of M2 macrophages was observed in the skin lesions of patients with anergic diffuse cutaneous leishmaniasis (ADCL) (M1 = 195 ± 25, M2 = 616 ± 114), followed by cases of localized cutaneous leishmaniasis (LCL) caused by L. (L.) amazonensis (M1 = 97 ± 24, M2 = 219 ± 29), L. (V.) panamensis (M1 = 71 ± 14, M2 = 164 ± 14), and L. (V.) braziliensis (M1 = 50 ± 13, M2 = 53 ± 10); however, low density of M2 macrophages was observed in NUCL. The data presented herein show the polarization of macrophages in skin lesions caused by different Leishmania species that may be related with the outcome of the disease.
publishDate 2021
dc.date.accessioned.fl_str_mv 2021-05-13T16:06:23Z
dc.date.available.fl_str_mv 2021-05-13T16:06:23Z
dc.date.issued.fl_str_mv 2021
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv PACHECO, Carmen M. Sandoval et al. Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp. Journal of Immunology Research, v. 2021, n. ID 5596876, p. 1-8, 2021.
dc.identifier.uri.fl_str_mv https://patua.iec.gov.br/handle/iec/4308
dc.identifier.issn.-.fl_str_mv 2314-7156
dc.identifier.doi.-.fl_str_mv 10.1155/2021/5596876
identifier_str_mv PACHECO, Carmen M. Sandoval et al. Macrophage polarization in the skin lesion caused by neotropical species of Leishmania sp. Journal of Immunology Research, v. 2021, n. ID 5596876, p. 1-8, 2021.
2314-7156
10.1155/2021/5596876
url https://patua.iec.gov.br/handle/iec/4308
dc.language.iso.fl_str_mv eng
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