Evidence map›Paper›PMID 27190181›Full record

ArticleThe Journal of infectious diseases2016

Immunologic Markers of Protection in Leishmania (Viannia) braziliensis Infection: A 5-Year Cohort Study.

Aline C Muniz, Olívia Bacellar, Ednaldo Lima Lago, Augusto M Carvalho, Pedro Paulo Carneiro, Luiz Henrique Guimarães, Paulo N Rocha, Lucas P Carvalho, Marshall Glesby, Edgar M Carvalho

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  7. Immune Response to LinB13, a Lutzomyia Intermedia Salivary Protein Correlates With Disease Severity in Tegumentary Leishmaniasis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Article
  8. Protection and Pathology inPathogens (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Review
  11. A Genome-wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis in Brazil.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  12. Anti-Leishmania IgG is a marker of disseminated leishmaniasis caused by Leishmania braziliensis.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article
  13. Article
  14. The Influence of Infection by DifferentFrontiers in cellular and infection microbiology · 2021
    Article
  15. Article
  16. Article
  17. Frontiers in cellular and infection microbiology · 2019
    Article
  18. Mucosal leishmaniasis: A Retrospective Study of 327 Cases from an Endemic Area ofThe American journal of tropical medicine and hygiene · 2017
    Article
  19. Article
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

10 authors at 5 institutions in 2 countries.

Aline C MunizServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine.
Olívia BacellarServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine Instituto Nacional de Ciência e Tecnologia em Doenças Tropicais.
Ednaldo Lima LagoServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia.
Augusto M CarvalhoPostgraduate Program in Health Sciences, Federal University of Bahia School of Medicine Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ), Salvador.
Pedro Paulo CarneiroServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine.
Luiz Henrique GuimarãesServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia.
Paulo N RochaPostgraduate Program in Health Sciences, Federal University of Bahia School of Medicine Department of Medicine and Diagnostic Support, Federal University of Bahia School of Medicine, Brazil.
Lucas P CarvalhoServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine Instituto Nacional de Ciência e Tecnologia em Doenças Tropicais Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ), Salvador.
Marshall GlesbyWeill Cornell Medical College, New York, New York.
Edgar M CarvalhoServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal University of Bahia Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine Instituto Nacional de Ciência e Tecnologia em Doenças Tropicais Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ), Salvador.
Universidade Federal da Bahia · BRComplexo Hospitalar Universitário Professor Edgard Santos · BRInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais · BRCornell University · USFundação Oswaldo Cruz · BR

Funding

The role of Leishmania braziliensis strain polymorphism on disease outcome and ..P50AI030639 · NIAID · FEDERAL UNIVERSITY OF BAHIA · PI CARVALHO, EDGAR M · 1991 to 2023
$9.1M
NIAID NIH HHS P50 AI030639
6 · The paper itself

Abstract

backgroundThe control of Leishmania braziliensis by individuals with subclinical infection (SC) are unknown.

methodsA cohort of 308 household contacts (HCs) of patients with cutaneous leishmaniasis (CL) was established in 2010 in an endemic area and followed up for 5 years. Whole-blood cultures stimulated with soluble Leishmania antigen and a Leishmania skin test (LST) were performed in years 0, 2, and 4. The identification of the lymphocyte subsets secreting interferon (IFN) γ and the ability of monocytes to control Leishmania were determined.

resultsDuring follow-up, 118 subjects (38.3%) had evidence of L. braziliensis infection. Of the HCs, CL was documented in 45 (14.6%), 101 (32.8%) had SC infection, and 162 (52.6%) did not have evidence of exposure to L. braziliensis The ratio of infection to disease was 3.2:1. IFN-γ production, mainly by natural killer cells, was associated with protection, and a positive LST result did not prevent development of disease. Moreover, monocytes from subjects with SC infection were less permissive to parasite penetration and had a greater ability to control L. braziliensis than cells from patients with CL.

conclusionsProtection against CL was associated with IFN-γ production, negative LST results, impaired ability of Leishmania to penetrate monocytes, and increased ability to control Leishmania growth.

Indexed as

BiomarkersAdolescentAdultBloodChildFemaleFollow-Up StudiesHumansInterferon-gammaLeishmania braziliensisLeishmaniasis, CutaneousLeukocytes, MononuclearMaleSkin TestsYoung AdultBiomarkersInterferon-gammacutaneous leishmaniasishousehold contactsIFN-γLeishmania braziliensisLeishmania skin testsubclinical leishmaniasis

Identifiers

PMID27190181
PMCPMC4957441
OpenAlexW2460356985

What OpenQuestion holds

Textmetadata
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.