Evidence map›Paper›PMID 30997749›Full record

ArticleImmunity, inflammation and disease2019

Activated cytotoxic T cells within zoonotic cutaneous leishmaniasis lesions.

Thouraya Boussoffara, Mohamed Samir Boubaker, Melika Ben Ahmed, Mourad Mokni, Salma Feriani, Afif Ben Salah, Hechmi Louzir

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2019. 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
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. LmjF.22.0810 fromBiomedicines · 2020
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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

7 authors at 2 institutions in 2 countries.

Thouraya BoussoffaraLaboratory of Transmission, Control and Immunobiology of Infections, Pasteur Institute of Tunis, Tunis, Tunisia.ORCID 0000-0001-9827-6440
Mohamed Samir BoubakerUniversité de Tunis El Manar, Tunis, Tunisia.
Melika Ben AhmedLaboratory of Transmission, Control and Immunobiology of Infections, Pasteur Institute of Tunis, Tunis, Tunisia.
Mourad MokniFaculté de Médecine de Tunis, Tunis, Tunisia.
Salma FerianiLaboratory of Human and Experimental Pathology, Pasteur Institute of Tunis, Tunis, Tunisia.
Afif Ben SalahLaboratory of Transmission, Control and Immunobiology of Infections, Pasteur Institute of Tunis, Tunis, Tunisia.
Hechmi LouzirLaboratory of Transmission, Control and Immunobiology of Infections, Pasteur Institute of Tunis, Tunis, Tunisia.
Tunis University · TNInstitut Pasteur de Tunis · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionZoonotic cutaneous leishmaniasis (ZCL), due to infection by Leishmania (L). major, is characterized by polymorphic clinical manifestations which could be attributed to the host's immune response. In this study we investigated the involvement of cytotoxic cells on the outcome of the disease.

methodsExpression of granzyme B (GrB), granulysine (Grly), and interferon (IFN)-γ was evaluated within ZCL lesion specimens using the technique of real-time quantitative polymerase chain reaction (RT-qPCR). Immunohistochemical staining was performed using anti-CD3, CD4, CD8, CD56, GrB, and IFN-γ antibodies to identify the phenotype of GrB and IFN-γ-producing cells.

resultsGrB and Grly mRNA was detected within 75% and 80% of ZCL lesions, respectively. Statistical analysis demonstrated a significant correlation between levels of GrB and Grly. Interestingly, expression of these molecules correlates negatively with the lesion's age. The highest levels were measured in early lesions (E-ZCL) (lesion age ≤1 month) comparing to late lesions (L-ZCL) (lesion age >1 month). Otherwise, IFN-γ mRNA was detected only within 56% and a positive correlation was found between levels of this cytokine and those of GrB. Immunohistochemical analysis showed that GrB is produced essentially by CD8

conclusionTogether our results demonstrate the presence of cytotoxic cells producing GrB and Grly within leishmaniasis cutaneous lesions.

Indexed as

AdultAnimalsAntigens, Differentiation, T-LymphocyteChildChild, PreschoolCytokinesFemaleGene ExpressionGranzymesHumansInfantInfant, NewbornInterferon-gammaLeishmania majorLeishmaniasis, CutaneousLymphocyte ActivationAntigens, Differentiation, T-LymphocyteCytokinesGNLY protein, humanGranzymesInterferon-gammacytotoxic cellsgranulysingranzyme BIFN-γLeishmania majorLeishmaniasis lesion

Identifiers

PMID30997749
PMCPMC6688079
OpenAlexW2939759343

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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.