Evidence map›Paper›PMID 39308868›Full record

SynthesisFrontiers in immunology2024

An update on leprosy immunopathogenesis: systematic review.

Marcos Jessé Abrahão Silva, Caroliny Soares Silva, Thiago Pinto Brasil, Ana Karoliny Alves, Everaldina Cordeiro Dos Santos, Cristiane Cunha Frota, Karla Valéria Batista Lima, Luana Nepomuceno Gondim Costa Lima

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Decoding leprosy: immune response, clinical manifestations and emerging diagnostic approaches.Transactions of the Royal Society of Tropical Medicine and Hygiene · 2025
    Review
  7. Article
  8. Article
  9. IFN-γ-Driven macrophage responses in the immunity toFrontiers in cellular and infection microbiology · 2025
    Review
  10. Review
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.

Marcos Jessé Abrahão Silva *Postgraduate Program in Parasitic Biology in the Amazon (PPGBPA), University of Pará State (UEPA), Belém, Brazil.
Caroliny Soares Silva *Postgraduate Program in Parasitic Biology in the Amazon (PPGBPA), University of Pará State (UEPA), Belém, Brazil.
Thiago Pinto BrasilDepartment of Biomedicine, Federal University of Ceará (UFC), Fortaleza, Brazil.
Ana Karoliny AlvesDepartment of Biomedicine, Federal University of Ceará (UFC), Fortaleza, Brazil.
Everaldina Cordeiro Dos SantosBacteriology and Mycology Section (SABMI), Evandro Chagas Institute (IEC), Ananindeua, Brazil.
Cristiane Cunha FrotaDepartment of Pathology and Legal Medicine, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza, Brazil.
Karla Valéria Batista LimaBacteriology and Mycology Section (SABMI), Evandro Chagas Institute (IEC), Ananindeua, Brazil.
Luana Nepomuceno Gondim Costa LimaBacteriology and Mycology Section (SABMI), Evandro Chagas Institute (IEC), Ananindeua, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Leprosy is a chronic infectious condition and the main cause of neuropathy that occurs brought on by Methods: A systematic review following the PRISMA 2020 recommendations was conducted in the PUBMED, LILACS, SciELO and Science Direct databases using articles in English, Portuguese or Spanish between January 2011 and May 2022 with the descriptors "Leprosy/Immunology", "Cytokines" and " Results: A total of 49 articles were included. There is a relationship of greater severity of infection associated with lower release of MHC molecules in response to PGL-1 that inhibit the promotion of resolving T lymphocytes arising from dendritic cells (DCs) stimulation. In addition, the differentiation of macrophage phenotypes dependent on the activation of PRRs can define activation and the distinct type of T helper (Th) cells involved according to severity. Activated CD8+ T cells also have distinct types at the appropriate poles of the disease, and B cells show at the most severe pole of the LL, specific induction of IgA and more Treg-type CD8+ T cells that further contribute to T cell anergy. Conclusion: Therefore, the adaptive immune system aggravates nerve damage and defines the type of leprosy, while the innate immune system is considerably more significant in the onset of nerve damage, symptomatic of the initial presentation of illness and in several critical immune responses, including inflammation and elimination of dead

Indexed as

LeprosyMycobacterium lepraeAnimalsCytokinesHumansCytokinesimmunityleprosymolecularmycobacterium lepraenerve damagepathology

Identifiers

PMID39308868
PMCPMC11412872

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.