Evidence map›Paper›PMID 33788861›Full record

ArticlePLoS neglected tropical diseases2021

Boosting understanding of Lassa Fever virus epidemiology: Field testing a novel assay to identify past Lassa Fever virus infection in blood and oral fluids of survivors and unexposed controls in Sierra Leone.

Onome Akpogheneta, Steve Dicks, Donald Grant, Zainab Kanneh, Brima Jusu, Joseph Edem-Hotah, Lansana Kanneh, Foday Alhasan, Michael Gbakie, John Schieffelin and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 6 institutions in 3 countries.

Onome AkpoghenetaDepartment of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Steve DicksBlood Borne Virus Unit, Public Health England, Colindale, United Kingdom.ORCID 0000-0002-4709-9664
Donald GrantKenema Government Hospital Lassa Fever Unit, Kenema, Sierra Leone.
Zainab KannehKenema Government Hospital Lassa Fever Unit, Kenema, Sierra Leone.
Brima JusuKenema Government Hospital Lassa Fever Unit, Kenema, Sierra Leone.
Joseph Edem-HotahFaculty of Nursing, University of Sierra Leone, Freetown, Sierra Leone.ORCID 0000-0002-6086-181X
Lansana KannehKenema Government Hospital Lassa Fever Unit, Kenema, Sierra Leone.
Foday AlhasanKenema Government Hospital Lassa Fever Unit, Kenema, Sierra Leone.
Michael GbakieKenema Government Hospital Lassa Fever Unit, Kenema, Sierra Leone.
John SchieffelinSections of Infectious Disease, Tulane University School of Medicine, New Orleans, Louisiana, United States of America.ORCID 0000-0001-6642-5739
Samreen IjazBlood Borne Virus Unit, Public Health England, Colindale, United Kingdom.ORCID 0000-0001-6658-3542
Richard TedderDepartment of Infectious Disease, Imperial College, London, United Kingdom.ORCID 0000-0002-9672-5721
Hilary BowerUK Public Health Rapid Support Team, London School of Hygiene & Tropical Medicine/Public Health England, London, United Kingdom.ORCID 0000-0002-1541-6637
Public Health England · GBImperial College London · GBLondon School of Hygiene & Tropical Medicine · GBNHS Blood and Transplant · GBTulane University · USUniversity of Sierra Leone · SL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite identification 50 years ago, the true burden of Lassa Fever (LF) across Africa remains undefined for reasons including research focus on hospitalised patients, lack of validated field-feasible tools which reliably identify past infection, and the fact that all assays require blood samples making large-scale surveys difficult. Designated a priority pathogen of epidemic potential requiring urgent research by the World Health Organisation, a better understanding of LF sero-epidemiology is essential to developing and evaluating new interventions including vaccines. We describe the first field testing of a novel species-neutral Double Antigen Binding Assay (DABA) designed to detect antibodies to LF in plasma and oral fluid. METHODOLOGY/PRINCIPAL

findingsPaired plasma and oral fluid were collected in Sierra Leone from survivors discharged from Kenema Government Hospital Lassa Fever Unit between 1980 and 2018, and from controls recruited in Freetown in 2019. Epidemiological sensitivity and specificity of the DABA measured against historical diagnosis in survivors and self-declared non-exposed controls was 81.7% (95% CI 70.7%- 89.9%) and 83.3% (72.7%- 91.1%) respectively in plasma, and 71.8% (60.0%- 81.9%) and 83.3% (72.7%- 91.1%) respectively in oral fluid. Antibodies were identified in people infected up to 15 years and, in one case, 40 years previously. Participants found oral fluid collection easy and painless with 80% happy to give an oral fluid sample regularly. CONCLUSIONS/SIGNIFICANCE: Given the difficulties of assay validation in a resource-limited setting, including unexpected exposures and diagnostics of varying accuracy, the new assay performed well in both plasma and oral fluid. Sensitivity and specificity are expected to be higher when case/control ascertainment is more definitive and further work is planned to investigate this. Even at the performance levels achieved, the species-neutral DABA has the potential to facilitate the large-scale seroprevalence surveys needed to underpin essential developments in LF control, as well as support zoonotic investigations.

Indexed as

AdultAntibodies, ViralFemaleHumansLassa FeverLassa virusMaleMiddle AgedSalivaSierra LeoneSurvivorsViremiaAntibodies, Viral

Identifiers

PMID33788861
PMCPMC8041174
OpenAlexW3143660864

What OpenQuestion holds

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LicenceCC BY
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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.