Evidence map›Paper›PMID 22685406›Full record

ArticlePLoS pathogens2012

Circulating microbial products and acute phase proteins as markers of pathogenesis in lymphatic filarial disease.

R Anuradha, P Jovvian George, N Pavan Kumar, Michael P Fay, V Kumaraswami, Thomas B Nutman, Subash Babu

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Heightened Microbial Translocation Is a Prognostic Biomarker of Recurrent Tuberculosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Anti-The Indian journal of medical research · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Observational
  13. Article
  14. Immunology of lymphatic filariasis.Parasite immunology · 2014
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Immunopathogenesis of lymphatic filarial disease.Seminars in immunopathology · 2012
    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

7 authors at 3 institutions in 2 countries.

R AnuradhaNational Institutes of Health, International Center for Excellence in Research, Chennai, India.
P Jovvian George
N Pavan Kumar
Michael P Fay
V Kumaraswami
Thomas B Nutman
Subash Babu
International Centers for Excellence in Research · INNational Institutes of Health · USNational Institute of Research in Tuberculosis · IN

Funding

Immunoregulation /Immune Recognition In Filarial/Nonfilarial Parasitic InfectionZIAAI000197 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI NUTMAN, THOMAS · 2009 to 2025
$23.4M
India International Center for Excellence in ResearchZIAAI001065 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI NUTMAN, THOMAS · 2009 to 2025
$19.0M
Intramural NIH HHS
6 · The paper itself

Abstract

Lymphatic filariasis can be associated with development of serious pathology in the form of lymphedema, hydrocele, and elephantiasis in a subset of infected patients. Dysregulated host inflammatory responses leading to systemic immune activation are thought to play a central role in filarial disease pathogenesis. We measured the plasma levels of microbial translocation markers, acute phase proteins, and inflammatory cytokines in individuals with chronic filarial pathology with (CP Ag+) or without (CP Ag-) active infection; with clinically asymptomatic infections (INF); and in those without infection (endemic normal [EN]). Comparisons between the two actively infected groups (CP Ag+ compared to INF) and those without active infection (CP Ag- compared to EN) were used preliminarily to identify markers of pathogenesis. Thereafter, we tested for group effects among all the four groups using linear models on the log transformed responses of the markers. Our data suggest that circulating levels of microbial translocation products (lipopolysaccharide and LPS-binding protein), acute phase proteins (haptoglobin and serum amyloid protein-A), and inflammatory cytokines (IL-1β, IL-12, and TNF-α) are associated with pathogenesis of disease in lymphatic filarial infection and implicate an important role for circulating microbial products and acute phase proteins.

Indexed as

Acute-Phase ProteinsAdultBiomarkersCarrier ProteinsCytokinesElephantiasis, FilarialFemaleHumansLipopolysaccharide-Binding ProteinLipopolysaccharidesMaleMembrane GlycoproteinsMiddle AgedYoung AdultAcute-Phase ProteinsBiomarkersCarrier ProteinsCytokinesLipopolysaccharide-Binding ProteinLipopolysaccharidesMembrane Glycoproteins

Identifiers

PMID22685406
PMCPMC3369944
OpenAlexW2082172279

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.