Is There Any Difference in the In Situ Immune Response in Active Localized Cutaneous Leishmaniasis That Respond Well or Poorly to Meglumine Antimoniate Treatment or Spontaneously Heal?
Authors:
- Jéssica Leite-SilvaJéssica Leite-Silva
- Carla Oliveira-RibeiroCarla Oliveira-Ribeiro
- Fernanda Nazaré MorgadoFernanda Nazaré Morgado
- Maria Inês Fernandes PimentelMaria Inês Fernandes Pimentel
- Marcelo Rosandiski LyraMarcelo Rosandiski Lyra
- Aline FagundesAline Fagundes
- Luciana Freitas Campos MirandaLuciana Freitas Campos Miranda
- Claudia Maria Valete-RosalinoClaudia Maria Valete-Rosalino
- Armando Oliveira SchubachArmando Oliveira Schubach
- Fátima Conceição-SilvaFátima Conceição-Silva
Open Access
- 22 June 2023
- journal article
- research article
- Published by MDPI AG in Microorganisms
- Vol. 11 (7) , 1631
Abstract
Localized cutaneous leishmaniasis caused by Leishmania braziliensis can either respond well or poorly to the treatment or heal spontaneously; It seems to be dependent on the parasite and/or host factors, but the mechanisms are not fully understood. We evaluated the in situ immune response in eighty-two active lesions from fifty-eight patients prior to treatment classified as early spontaneous regression (SRL-n = 14); treatment responders (GRL-n = 20); and non-responders (before first treatment/relapse, PRL1/PRL2-n = 24 each). Immunohistochemistry was used to identify cell/functional markers which were correlated with the clinical characteristics. PRL showed significant differences in lesion number/size, clinical evolution, and positive parasitological examinations when compared with the other groups. SRL presented a more efficient immune response than GRL and PRL, with higher IFN-γ/NOS2 and a lower percentage of macrophages, neutrophils, NK, B cells, and Ki-67+ cells. Compared to SRL, PRL had fewer CD4+ Tcells and more CD163+ macrophages. PRL1 had more CD68+ macrophages and Ki-67+ cells but less IFN-γ than GRL. PRL present a less efficient immune profile, which could explain the poor treatment response, while SRL had a more balanced immune response profile for lesion healing. Altogether, these evaluations suggest a differentiated profile of the organization of the inflammatory process for lesions of different tegumentary leishmaniasis evolution.Keywords
Funding Information
- PAEF-IOC (008-F10–22-2-49, e-26/211-707/2021)
- APQ1 (008-F10–22-2-49, e-26/211-707/2021)
This publication has 85 references indexed in Scilit:
- The IL-33/ST2 Axis Is Associated with Human Visceral Leishmaniasis and Suppresses Th1 Responses in the Livers of BALB/c Mice Infected with Leishmania donovanimBio, 2013
- Regulatory T Cells in the Pathogenesis and Healing of Chronic Human Dermal Leishmaniasis Caused by Leishmania (Viannia) SpeciesPLOS Neglected Tropical Diseases, 2012
- Neutrophils cast extracellular traps in response to protozoan parasitesFrontiers in Immunology, 2012
- Foxp3 and IL-10 Expression Correlates with Parasite Burden in Lesional Tissues of Post Kala Azar Dermal Leishmaniasis (PKDL) PatientsPLOS Neglected Tropical Diseases, 2011
- Role of IL-33 in inflammation and diseaseJournal of Inflammation, 2011
- Therapeutic failure in American cutaneous leishmaniasis is associated with gelatinase activity and cytokine expressionClinical and Experimental Immunology, 2010
- Recruitment of CD8+ T cells expressing granzyme A is associated with lesion progression in human cutaneous leishmaniasisParasite Immunology, 2009
- Interleukin 17 Production among Patients with American Cutaneous LeishmaniasisThe Journal of Infectious Diseases, 2009
- Leishmania amazonensispromastigotes induce and are killed by neutrophil extracellular trapsProceedings of the National Academy of Sciences, 2009
- CD4+CD25−Foxp3− Th1 cells are the source of IL-10–mediated immune suppression in chronic cutaneous leishmaniasisJournal of Experimental Medicine, 2007