Platelet-Derived Microvesicles Contribute to the Pathophysiogenesis of Human Cutaneous Leishmaniasis: A Nano-Flow Cytometric Approach in Plasma Samples from Patients before and under Antimonial Treatment

Author:

Costa Vanessa Fernandes de Abreu12,Chometon Thaize Quiroga12,de Castro Katherine Kelda Gomes2,Ponte Melissa Silva Gonçalves12,Pimentel Maria Inês Fernandes3ORCID,Lyra Marcelo Rosandiski3,Bertho Alvaro Luiz12

Affiliation:

1. Laboratory of Immunoparasitology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil

2. Flow Cytometry Core Facility, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil

3. Laboratory of Clinical Research and Surveillance in Leishmaniasis, Evandro Chagas National Institute of Infectious Diseases, FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil

Abstract

Cutaneous leishmaniasis is a neglected tropical disease caused, in Brazil, mainly by Leishmania braziliensis, which is a protozoan transmitted during the blood feeding of infected female sandflies. To control leishmaniasis, the participation of CD4+ Th1 cells together with macrophages, neutrophils, and other peripheral blood cells, including platelets, is necessary. These anuclear fragments, when activated, produce microvesicles (MVs) that can reach locations outside the blood, carrying molecules responsible for activating pro-inflammatory responses and antigen presentation. Using flow cytometry, this current study evaluated the frequency and concentration of platelet-derived MVs (pMVs) in plasma samples obtained from patients in the acute phase and undergoing treatment, as well as from healthy volunteers. Our results revealed a higher frequency and concentration of pMVs in the plasma of patients with acute CL when compared to all other groups studied. These results highlight the impact of pMVs in modulating the immune response of CL patients, correlating their higher concentrations and frequencies in CL-patient plasmas, with the acute inflammatory status of the disease and their reduction with beneficial results of systemic treatment with antimony. This knowledge is essential to define potential treatment protocols, as well as highlight pMVs as biomarkers for the different clinical stages of CL.

Funder

Oswaldo Cruz Institute, FIOCRUZ

FAPERJ

TCT-FAPERJ

CAPES

Publisher

MDPI AG

Reference45 articles.

1. BRASIL, Ministério da Saúde (2023, December 15). Manual de Vigilância da Leishmaniose Tegumentar, Available online: https://bvsms.saude.gov.br/bvs/publicacoes/manual_vigilancia_leishmaniose_tegumentar.pdf.

2. (2023, December 23). OPAS, OMS Américas. Available online: https://www.paho.org/pt/topicos/leishmaniose.

3. BRASIL, Ministério da Saúde (2023, December 20). DATASUS, Available online: http://tabnet.datasus.gov.br/cgi/tabcgi.exe?sinannet/cnv/ltarj.def.

4. BRASIL, Ministério da Saúde (2023, December 20). Distribuição da Leishmaniose Tegumentar, Available online: https://www.gov.br/saude/pt-br/assuntos/saude-de-a-a-z/l/lt/situacao-epidemiologica.

5. Cutaneous Leishmaniasis: The Complexity of Host’s Effective Immune Response against a Polymorphic Parasitic Disease;Gabriel;J. Immunol. Res.,2019

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