Evidence map›Paper›PMID 38064516›Full record

ArticlePLoS neglected tropical diseases2023

A Prospective cohort study of zoonotic cutaneous leishmaniasis in tunisia: Clinical and Immunological features and immune correlates of protection.

Ikbel Naouar, Wafa Kammoun Rebai, Afif Ben Salah, Hind Bouguerra, Amine Toumi, Nabil Belhadj Hamida, Hechmi Louzir, Amel Meddeb-Garnaoui

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 28% of its field
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 4 countries.

Ikbel NaouarLaboratory of Transmission Control and Immunobiology of Infection, Pasteur Institute of Tunis, Tunis, Tunisia.
Wafa Kammoun RebaiFaculty of Sciences, University of Tunis El Manar, Tunis, Tunisia.ORCID 0000-0002-2872-7282
Afif Ben SalahLaboratory of Transmission Control and Immunobiology of Infection, Pasteur Institute of Tunis, Tunis, Tunisia.
Hind BouguerraNational Observatory of New and Emerging Diseases, Tunis, Tunisia.
Amine ToumiHealth Information and Intelligence Section, Ministry of Public Health, Doha, Qatar.
Nabil Belhadj HamidaLaboratory of Transmission Control and Immunobiology of Infection, Pasteur Institute of Tunis, Tunis, Tunisia.
Hechmi LouzirLaboratory of Transmission Control and Immunobiology of Infection, Pasteur Institute of Tunis, Tunis, Tunisia.
Amel Meddeb-GarnaouiLaboratory of Medical Parasitology, Biotechnology and Biomolecular, Pasteur Institute of Tunis, Tunis, Tunisia.
Institut Pasteur de Tunis · TNMinistry of Public Health · QATunis University · TNUniversity of Toronto · CA

Funding

L. major infection: Natural history and determinants of resistanceP50AI074178 · NIAID · INSTITUT PASTEUR DE TUNIS · PI BEN SALAH, AFIF · 2007 to 2011
$2.4M
NIAID NIH HHS P50 AI074178
6 · The paper itself

Abstract

backgroundThis study aimed to define immunological markers of exposure to L. major parasites and identify correlates of protection against infection.

methodsWe analyzed a cohort of 790 individuals at risk of developing ZCL living in endemic areas with varying L. major infection prevalence. One area had a high infection prevalence indicated by high proportions of leishmanin skin test (LST) positive subjects, while the other areas were recent foci with lower infection prevalence. Blood samples were collected before the transmission season to measure Interferon gamma (IFN-γ), Interleukin 10 (IL-10), and Granzyme B (GrB) levels in response to parasite stimulation in peripheral blood mononuclear cells. A one-year follow-up period involved active detection of new ZCL cases to estimate disease incidence after a transmission season and identify immune correlates of protection.

resultsThe study population showed heterogeneity in parasite contact, evident from specific scars and/or positive LST results, significantly higher in the old focus compared to recent foci. IFN-γ and GrB were markers of parasite exposure and reliable indicators of immunity to L. major. Positive correlations were observed between IFN-γ/IL-10 and GrB/IL-10 ratios and LST results. Unexpectedly, only 29 new ZCL cases (4%) appeared after a transmission season, with 27 cases reported in recent foci and 2 in the oldest focus. Our findings indicate that individuals in L. major endemic areas are likely to develop ZCL regardless of their LST status. We showed that high pre-transmission season levels of IFN-γ and GrB produced by PBMC, along with a high IFN-γ/IL-10 ratio, were associated with protection.

conclusionThis study on a large cohort at risk of ZCL confirmed IFN-γ and GrB as protective factors against the disease. A high IFN-γ/IL-10 ratio, but not GrB/IL-10 ratio was associated with resistance. These results are valuable for developing and evaluating of a vaccine against human leishmaniasis.

Indexed as

Interleukin-10Leishmaniasis, CutaneousHumansInterferon-gammaLeukocytes, MononuclearProspective StudiesTunisiaInterferon-gammaInterleukin-10

Identifiers

PMID38064516
PMCPMC10732404
OpenAlexW4389475061

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Registered trials

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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.