Evidence map›Paper›PMID 10225839›Full record

ArticleClinical and diagnostic laboratory immunology1999

Helicobacter pylori heat shock protein A: serologic responses and genetic diversity.

E K Ng, S A Thompson, G I Pérez-Pérez, I Kansau, A van der Ende, A Labigne, J J Sung, S C Chung, M J Blaser

Open access · diamondAbstract read
In one paragraph

Article in Clinical and diagnostic laboratory immunology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular mimicry inWorld journal of gastroenterology · 2017
    Review
  4. Review
  5. Article
  6. Seroepidemiological study of Pneumocystis jirovecii infection in healthy infants in Chile using recombinant fragments of the P. jirovecii major surface glycoprotein.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2010
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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

9 authors at 5 institutions in 5 countries.

E K NgDivision of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA. endersng@netvigator.com
S A Thompson
G I Pérez-Pérez
I Kansau
A van der Ende
A Labigne
J J Sung
S C Chung
M J Blaser
Vanderbilt University · USChinese University of Hong Kong · HKInstitut Pasteur · FRAmsterdam UMC Location University of Amsterdam · NLIo Therapeutics (United States) · US

Funding

NIDDK NIH HHS R01 DK 58834
6 · The paper itself

Abstract

Helicobacter pylori synthesizes an unusual GroES homolog, heat shock protein A (HspA). The present study was aimed at an assessment of the serological response to HspA in a group of Chinese patients with defined gastroduodenal pathologies and determination of whether diversity is present in the nucleotide sequences encoding HspA in isolates from these patients. Serum samples collected from 154 patients who had an upper gastrointestinal pathology and the presence of H. pylori defined by biopsy were tested for an immunoglobulin G (IgG) serologic response to H. pylori HspA by an enzyme linked immunosorbant assay. HspA-encoding nucleotide sequences in H. pylori isolates from 14 patients (7 seropositive and 7 seronegative for HspA) were analyzed by PCR and direct sequencing of the PCR products. The sequencing results were compared to those of 48 isolates from other parts of the world. Of the 154 known H. pylori-positive patients, 54 (35.1%) were seropositive for HspA. The A domain (GroES homology) of HspA was highly conserved in the 14 isolates tested. Although the B domain (metal-binding site unique to H. pylori) resembled that in the known major variant, particular amino acid substitutions allowed definition of an HspA variant associated with isolates from East Asia. There were no associations between patient characteristics and HspA seropositivity or amino acid sequences. We confirmed in this study that the clinical outcomes of H. pylori infection are not related to HspA antigenicity or to sequence variation. However, B-domain sequence variation may be a marker for the study of the genetic diversity of H. pylori strains of different geographic origins.

Indexed as

Bacterial ProteinsGenetic VariationAdultAmino Acid SequenceAntibodies, BacterialAntigens, BacterialAsian PeopleDNA, BacterialEnzyme-Linked Immunosorbent AssayFemaleGastrointestinal DiseasesHeat-Shock ProteinsHelicobacter InfectionsHelicobacter pyloriHong KongHumansAntibodies, BacterialAntigens, BacterialBacterial ProteinsDNA, BacterialHeat-Shock ProteinsHspA protein, bacteriaImmunoglobulin G

Identifiers

PMID10225839
PMCPMC103726
OpenAlexW2162880221

What OpenQuestion holds

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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.