Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/164497
Título: High seroprevalence of Leishmania infantum is linked to immune activation in people with HIV
Autor: de Moraes, Laise
Santos, Luciane Amorim
Arruda, Liã Bárbara
Silva, Maria da Purificação Pereira da
Silva, Márcio de Oliveira
Silva, José Adriano Góes
Ramos, André
Santos, Marcos Bastos dos
Torres, Felipe Guimarães
Orge, Cibele
Teixeira, Antonio Marcos dos Santos
Vieira, Thiago Santos
Ramírez, Laura
Soto, Manuel
Grassi, Maria Fernanda Rios
Siqueira, Isadora Cristina de
Costa, Dorcas Lamounier
Costa, Carlos Henrique Nery
Andrade, Bruno de Bezerril
Akrami, Kevan
de Oliveira, Camila Indiani
Boaventura, Viviane Sampaio
Barral-Netto, Manoel
Barral, Aldina
Vandamme, Anne Mieke
Van Weyenbergh, Johan
Khouri, Ricardo
Palavras-chave: HIV-1
hostpathogen interaction
immune activation
Leishmania infantum
visceral leishmaniasis
QR180 Immunology
RA0421 Public health. Hygiene. Preventive Medicine
Microbiology
Microbiology (medical)
Parasitology
Virology
Immunology
Applied Microbiology and Biotechnology
SDG 3 - Good Health and Well-being
SDG 9 - Industry, Innovation, and Infrastructure
SDG 10 - Reduced Inequalities
Data: 2023
Resumo: Visceral leishmaniasis is an opportunistic disease in HIV-1 infected individuals, unrecognized as a determining factor for AIDS diagnosis. The growing geographical overlap of HIV-1 and Leishmania infections is an emerging challenge worldwide, as co-infection increases morbidity and mortality for both infections. Here, we determined the prevalence of people living with HIV (PWH) with a previous or ongoing infection by Leishmania infantum and investigated the virological and immunological factors associated with co-infection. We adopted a two-stage cross-sectional cohort (CSC) design (CSC-I, n = 5,346 and CSC-II, n = 317) of treatment-naïve HIV-1-infected individuals in Bahia, Brazil. In CSC-I, samples collected between 1998 and 2013 were used for serological screening for leishmaniasis by an in-house Enzyme-Linked Immunosorbent Assay (ELISA) with SLA (Soluble Leishmania infantum Antigen), resulting in a prevalence of previous or ongoing infection of 16.27%. Next, 317 PWH were prospectively recruited from July 2014 to December 2015 with the collection of sociodemographic and clinical data. Serological validation by two different immunoassays confirmed a prevalence of 15.46 and 8.20% by anti-SLA, and anti-HSP70 serology, respectively, whereas 4.73% were double-positive (DP). Stratification of these 317 individuals in DP and double-negative (DN) revealed a significant reduction of CD4+ counts and CD4+/CD8+ ratios and a tendency of increased viral load in the DP group, as compared to DN. No statistical differences in HIV-1 subtype distribution were observed between the two groups. However, we found a significant increase of CXCL10 (p = 0.0076) and a tendency of increased CXCL9 (p = 0.061) in individuals with DP serology, demonstrating intensified immune activation in this group. These findings were corroborated at the transcriptome level in independent Leishmania- and HIV-1-infected cohorts (Swiss HIV Cohort and Piaui Northeast Brazil Cohort), indicating that CXCL10 transcripts are shared by the IFN-dominated immune activation gene signatures of both pathogens and positively correlated to viral load in untreated PWH. This study demonstrated a high prevalence of PWH with L. infantum seropositivity in Bahia, Brazil, linked to IFN-mediated immune activation and a significant decrease in CD4+ levels. Our results highlight the urgent need to increase awareness and define public health strategies for the management and prevention of HIV-1 and L. infantum co-infection.
Descrição: Funding Information: This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001, RK; Fundação de Amparo à Pesquisa do Estado da Bahia (FAPESB, grant APP0032/2016, RK); Brazilian National Council for Scientific and Technological Development (CNPq, grant 65083/2015-8, LS); FAPESB/CNPq (008/2014 PRONEX grant 8111/2014, AB); Fonds voor Wetenschappelijk Onderzoek Vlaanderen (grant G0D6817N, A-MV and JW). None of the funding organizations had any role in the study design, data collection, data interpretation or writing of this report. Publisher Copyright: Copyright © 2023 de Moraes, Santos, Arruda, Silva, Silva, Silva, Ramos, Santos, Torres, Orge, Teixeira, Vieira, Ramírez, Soto, Grassi, Siqueira, Costa, Costa, Andrade, Akrami, de Oliveira, Boaventura, Barral-Netto, Barral, Vandamme, Van Weyenbergh and Khouri.
Peer review: yes
URI: http://hdl.handle.net/10362/164497
DOI: https://doi.org/10.3389/fmicb.2023.1221682
ISSN: 1664-302X
Aparece nas colecções:Home collection (IHMT)

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