Evidence map›Paper›PMID 40096173›Full record

ArticlePLoS neglected tropical diseases2025

T-cell activation and senescence in asymptomatic HIV/Leishmania infantum co-infection.

Carolina de Oliveira Mendes-Aguiar, Manoella do Monte Alves, Amanda de Albuquerque Lopes Machado, Glória Regina de Góis Monteiro, Iara Marques Medeiros, Jose Wilton Queiroz, Iraci Duarte Lima, Eliardo G Costa, Richard D Pearson, Mary E Wilson and 3 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Assessment of asymptomaticFrontiers in medicine · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Carolina de Oliveira Mendes-AguiarInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Manoella do Monte AlvesDepartment of Infectious Disease, Health Science Center, Federal University of Rio Grande do Norte, Natal, Brazil.
Amanda de Albuquerque Lopes MachadoInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Glória Regina de Góis MonteiroInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Iara Marques MedeirosInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Jose Wilton QueirozInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Iraci Duarte LimaInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Eliardo G CostaDepartment of Statistics, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Richard D PearsonDivision of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia, United States of America.
Mary E WilsonDepartments of Internal Medicine and Microbiology & Immunology, University of Iowa and the Veterans' Affairs Medical Center, Iowa City, Iowa, United States of America.
Marshall J GlesbyDivision of Infectious Disease, Weill Cornell Medical College, New York, New York, United States of America.
Eliana Lúcia Tomaz do NascimentoInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.
Selma Maria Bezerra JerônimoInstitute of Tropical Medicine of Rio Grande do Norte, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID 0000-0002-4784-9904

Funding

CNPqNational Institute of Science and Technology of Tropical Diseases INCT-DT, 465229/2014-0
6 · The paper itself

Abstract

backgroundLeishmania infantum can be an opportunistic pathogen, with an immunocompromised status increasing the risk of converting asymptomatic infection to symptomatic visceral leishmaniasis (VL). VL has approximately 5% fatality rate; and HIV coinfection (AIDS/VL) increases this risk. We hypothesized that, relative to those with HIV alone, people with co-infection would have altered T cell activation which could impact on the risk of VL.

methodsA cross-sectional study was performed between 2014 and 2016 to determine the prevalence of L. infantum infection in people living with HIV (PLHIV) residing in Brazil (n = 1,372). Subsequent incident cases of VL were ascertained from a public health database through 2018 and from a cohort of families with VL. Immune status of 69 participants was evaluated and comparisons made between those with and without HIV, with latent or with active Leishmania infection and those without HIV but with active or resolved Leishmania or T cell hypersensitivity to Leishmania antigen and healthy control subjects.

resultsA total of 24.2% of PLHIV had positive anti-IgG L. infantum antibodies. The relative risk of developing AIDS/VL was 2.27 (95% CI: 0.920 to 5.59; p = 0.07) to HIV/Leish coinfected subjects with positive leishmania serology compared to HIV subjects without leishmania serology. Poor adherence to antiretroviral therapy (p = 0.0008) or prior opportunistic infections (p = 0.0007) was associated with development of AIDS/VL in asymptomatic HIV/Leish. CD4+ and CD8+ T cells counts or viral load were similar between asymptomatic HIV/Leish and HIV subjects. However, activated CD8+CD38+HLA-DR+ T cells were higher in asymptomatic HIV/Leish than HIV. Likewise, senescent (CD57+) and PD1+ CD8+ T cells were higher in asymptomatic HIV/Leish than in AIDS/VL or HIV groups.

conclusionAlthough asymptomatic HIV/Leish subjects had CD4+ and CD8+ T cells similar to HIV alone, their CD8+T cells had increased activation and senescence which could contribute to risk of developing VL.

Indexed as

CoinfectionHIV InfectionsLeishmania infantumLeishmaniasis, VisceralLymphocyte ActivationT-LymphocytesAdultAsymptomatic InfectionsBrazilCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCellular SenescenceCross-Sectional StudiesFemaleHumansMale

Identifiers

PMID40096173
PMCPMC11964262

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.