Cargando…

Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions

INTRODUCTION: Zoonotic cutaneous leishmaniasis (ZCL), due to infection by Leishmania (L). major, is characterized by polymorphic clinical manifestations which could be attributed to the host's immune response. In this study we investigated the involvement of cytotoxic cells on the outcome of th...

Descripción completa

Detalles Bibliográficos
Autores principales: Boussoffara, Thouraya, Boubaker, Mohamed Samir, Ben Ahmed, Melika, Mokni, Mourad, Feriani, Salma, Ben Salah, Afif, Louzir, Hechmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688079/
https://www.ncbi.nlm.nih.gov/pubmed/30997749
http://dx.doi.org/10.1002/iid3.240
_version_ 1783442817957232640
author Boussoffara, Thouraya
Boubaker, Mohamed Samir
Ben Ahmed, Melika
Mokni, Mourad
Feriani, Salma
Ben Salah, Afif
Louzir, Hechmi
author_facet Boussoffara, Thouraya
Boubaker, Mohamed Samir
Ben Ahmed, Melika
Mokni, Mourad
Feriani, Salma
Ben Salah, Afif
Louzir, Hechmi
author_sort Boussoffara, Thouraya
collection PubMed
description INTRODUCTION: Zoonotic cutaneous leishmaniasis (ZCL), due to infection by Leishmania (L). major, is characterized by polymorphic clinical manifestations which could be attributed to the host's immune response. In this study we investigated the involvement of cytotoxic cells on the outcome of the disease. METHODS: Expression of granzyme B (GrB), granulysine (Grly), and interferon (IFN)‐γ was evaluated within ZCL lesion specimens using the technique of real‐time quantitative polymerase chain reaction (RT‐qPCR). Immunohistochemical staining was performed using anti‐CD3, CD4, CD8, CD56, GrB, and IFN‐γ antibodies to identify the phenotype of GrB and IFN‐γ‐producing cells. RESULTS: GrB and Grly mRNA was detected within 75% and 80% of ZCL lesions, respectively. Statistical analysis demonstrated a significant correlation between levels of GrB and Grly. Interestingly, expression of these molecules correlates negatively with the lesion's age. The highest levels were measured in early lesions (E‐ZCL) (lesion age ≤1 month) comparing to late lesions (L‐ZCL) (lesion age >1 month). Otherwise, IFN‐γ mRNA was detected only within 56% and a positive correlation was found between levels of this cytokine and those of GrB. Immunohistochemical analysis showed that GrB is produced essentially by CD8(+)T cells whereas IFN‐γ is produced by both CD4(+) and CD8(+)T cells. CONCLUSION: Together our results demonstrate the presence of cytotoxic cells producing GrB and Grly within leishmaniasis cutaneous lesions.
format Online
Article
Text
id pubmed-6688079
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-66880792019-08-14 Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions Boussoffara, Thouraya Boubaker, Mohamed Samir Ben Ahmed, Melika Mokni, Mourad Feriani, Salma Ben Salah, Afif Louzir, Hechmi Immun Inflamm Dis Original Research INTRODUCTION: Zoonotic cutaneous leishmaniasis (ZCL), due to infection by Leishmania (L). major, is characterized by polymorphic clinical manifestations which could be attributed to the host's immune response. In this study we investigated the involvement of cytotoxic cells on the outcome of the disease. METHODS: Expression of granzyme B (GrB), granulysine (Grly), and interferon (IFN)‐γ was evaluated within ZCL lesion specimens using the technique of real‐time quantitative polymerase chain reaction (RT‐qPCR). Immunohistochemical staining was performed using anti‐CD3, CD4, CD8, CD56, GrB, and IFN‐γ antibodies to identify the phenotype of GrB and IFN‐γ‐producing cells. RESULTS: GrB and Grly mRNA was detected within 75% and 80% of ZCL lesions, respectively. Statistical analysis demonstrated a significant correlation between levels of GrB and Grly. Interestingly, expression of these molecules correlates negatively with the lesion's age. The highest levels were measured in early lesions (E‐ZCL) (lesion age ≤1 month) comparing to late lesions (L‐ZCL) (lesion age >1 month). Otherwise, IFN‐γ mRNA was detected only within 56% and a positive correlation was found between levels of this cytokine and those of GrB. Immunohistochemical analysis showed that GrB is produced essentially by CD8(+)T cells whereas IFN‐γ is produced by both CD4(+) and CD8(+)T cells. CONCLUSION: Together our results demonstrate the presence of cytotoxic cells producing GrB and Grly within leishmaniasis cutaneous lesions. John Wiley and Sons Inc. 2019-04-17 /pmc/articles/PMC6688079/ /pubmed/30997749 http://dx.doi.org/10.1002/iid3.240 Text en © 2019 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Boussoffara, Thouraya
Boubaker, Mohamed Samir
Ben Ahmed, Melika
Mokni, Mourad
Feriani, Salma
Ben Salah, Afif
Louzir, Hechmi
Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions
title Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions
title_full Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions
title_fullStr Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions
title_full_unstemmed Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions
title_short Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions
title_sort activated cytotoxic t cells within zoonotic cutaneous leishmaniasis lesions
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688079/
https://www.ncbi.nlm.nih.gov/pubmed/30997749
http://dx.doi.org/10.1002/iid3.240
work_keys_str_mv AT boussoffarathouraya activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions
AT boubakermohamedsamir activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions
AT benahmedmelika activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions
AT moknimourad activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions
AT ferianisalma activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions
AT bensalahafif activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions
AT louzirhechmi activatedcytotoxictcellswithinzoonoticcutaneousleishmaniasislesions