Evidence map›Paper›PMID 19211772›Full record

ArticleClinical and vaccine immunology : CVI2009

Lateral flow immunoassay for diagnosis of Trypanosoma cruzi infection with high correlation to the radioimmunoprecipitation assay.

Raymond L Houghton, Yvonne Y Stevens, Kathryn Hjerrild, Jeff Guderian, Masahiko Okamoto, Mazbahul Kabir, Steven G Reed, David A Leiby, W John W Morrow, Myriam Lorca and 1 more

Open access · diamondAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Review
  5. Review
  6. Article
  7. AssessingPathogens (Basel, Switzerland) · 2021
    Article
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  11. The American journal of tropical medicine and hygiene · 2017
    Article
  12. Review
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  16. Observational
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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

11 authors at 4 institutions in 2 countries.

Raymond L HoughtonInBios International, Inc., Seattle, WA 98104, USA. raymond@inbios.com
Yvonne Y Stevens
Kathryn Hjerrild
Jeff Guderian
Masahiko Okamoto
Mazbahul Kabir
Steven G Reed
David A Leiby
W John W Morrow
Myriam Lorca
Syamal Raychaudhuri
Infectious Disease Research Institute · USInBios International (United States) · USAmerican Red Cross · USUniversity of Chile · CL

Funding

Geographically robust rapid assay for T. cruzi infectionR44AI052683 · NIAID · INBIOS INTERNATIONAL, INC. · PI RAYCHAUDHURI, SYAMAL X · 2004 to 2010
$1.8M
NIAID NIH HHS R44 AI0522683-02NIAID NIH HHS R44 AI052683
6 · The paper itself

Abstract

The incidence of blood donors seropositive for Trypanosoma cruzi in North America has increased with population migration and more rigorous surveillance. The United States, considered nonendemic for T. cruzi, could therefore be at risk to exposure to parasite transmission through blood or organ donations. Current tests show variable reactivity, especially with Central American sera. Here we describe the development of a lateral flow immunoassay for the rapid detection of T. cruzi infection that has a strong correlation to the radioimmunoprecipitation assay (RIPA) "gold standard" in the United States. Such a test could have utility in small blood banks for prescreening donors, as well as in cardiac transplantation evaluation. T. cruzi consensus and/or RIPA-positive sera from Central and South America were evaluated in enzyme immunoassays (EIAs). These included commercial panels from Boston Biomedica, Inc. (BBI) (n = 14), and HemaBio (n = 21). Other sources included RIPA-positive sera from the American Red Cross (ARC) (n = 42), as well as from Chile. Sera were tested with the multiepitope recombinant TcF. All but one of the BBI samples were positive and 7 of 21 HemaBio samples and 6 of 42 ARC samples were low positive or negative. This observation indicated the need for additional antigens. To complement TcF reactivity, we tested the sera with peptides 30, 36, SAPA, and 1.1, 1.2, and 1.3 His fragments of 85-kDa trans-sialidase. We identified a promising combination of the tested antigens and constructed a single recombinant protein, ITC6, that enhanced the relative sensitivity in U.S. blood donor sera compared to that of TcF. The data on its evaluation using RIPA-confirmed positive sera in EIA and lateral flow immunoassay studies are presented, along with an additional recombinant protein, ITC8.2, with two additional sequences for peptide 1 and Kmp-11. The latter, when evaluated in a dipstick assay with consensus positive sera, had a sensitivity of 99.2% and a specificity of 99.1%.

Indexed as

Amino Acid SequenceAnimalsAntibodies, ProtozoanAntigens, ProtozoanChagas DiseaseHumansImmunoassayMolecular Sequence DataRadioimmunoprecipitation AssayRecombinant Fusion ProteinsSensitivity and SpecificityTrypanosoma cruziAntibodies, ProtozoanAntigens, ProtozoanRecombinant Fusion Proteins

Identifiers

PMID19211772
PMCPMC2668284
OpenAlexW2098021042

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.