Evidence map›Paper›PMID 39883706›Full record

ArticlePLoS neglected tropical diseases2025

Sensitivity of anti-filarial antibodies for lymphatic filariasis surveillance: Insights from a serological survey in Samoa in 2018.

Harriet L S Lawford, Benn Sartorius, Helen J Mayfield, Filipina Amosa-Lei Sam, Satupaitea Viali, Tito Kamu, Robert Thomsen, Colleen L Lau

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

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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

8 authors.

Harriet L S LawfordUQ Centre for Clinical Research, Faculty of Health, Medicine, and Behavioural Sciences, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-9699-8201
Benn SartoriusUQ Centre for Clinical Research, Faculty of Health, Medicine, and Behavioural Sciences, The University of Queensland, Brisbane, Queensland, Australia.
Helen J MayfieldUQ Centre for Clinical Research, Faculty of Health, Medicine, and Behavioural Sciences, The University of Queensland, Brisbane, Queensland, Australia.
Filipina Amosa-Lei SamNational University of Samoa, Apia, Samoa.
Satupaitea VialiNational University of Samoa, Apia, Samoa.
Tito KamuTupua Tamasese Meaole Hospital, Apia, Samoa.
Robert ThomsenMinistry of Health, Apia, Samoa.
Colleen L LauUQ Centre for Clinical Research, Faculty of Health, Medicine, and Behavioural Sciences, The University of Queensland, Brisbane, Queensland, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSensitive diagnostic tools that signal lymphatic filariasis (LF) transmission are needed to monitor the progress of LF elimination programs. Anti-filarial antibody (Ab) markers could be more sensitive than antigen (Ag) point-of-care tests for monitoring LF transmission in some settings. This study aimed to investigate the sensitivity of anti-filarial Abs for detecting signals of LF transmission in Samoa by i) investigating the sensitivity and specificity of Ab to identify Ag-positives; ii) estimating the average number needed to test (NNTestav) to identify LF-seropositives (seropositive for Ag and/or any Ab), and iii) compare the efficiency of the different serological indicators by target age group and sampling design.

methodsA community-based serological survey of participants aged ≥5 years was conducted 1.5-3.5 months following the first round of triple-drug mass drug administration in Samoa in 2018, covering 35 primary sampling units (PSUs) (30 randomly selected and five purposively selected 'suspected hotspots'). Ag-positivity was detected using Alere Filariasis Test Strips, and Ab-seropositivity (Bm14, Wb123, Bm33 Abs) were measured using multiplex bead assays. Seroprevalence was adjusted for study design and standardised for age and gender. NNTestav was calculated using the formula 1/p, where p was the adjusted seroprevalence for each subgroup.

resultsOf 3795 participants (mean age: 20.7; 51.2% female), 1892 (49.9%) were LF-seropositive. If Ag alone was used to identify LF-seropositives, only 5% (117/1892) would be identified. Of the three Ab seromarkers, Bm14 Ab had the highest area under the Receiver-Operating Characteristic Curve ([ROC]=0.88) to classify participants as Ag-positive, followed by Wb123 Ab (ROC=0.83) and Bm33 Ab (ROC=0.76). Participants aged ≥10 years had lower NNTestav compared to participants aged 5-9 years for all seromarkers. NNTestav was lower in purposively versus randomly selected PSUs.

conclusionsAll Ab seromarkers had high ROC values to classify patients as Ag-positive and may be useful tools for LF surveillance in some settings. However, further research is required to fully understand how best Ab serosurveillance can be incorporated into LF elimination programmes.

Indexed as

Antibodies, HelminthElephantiasis, FilarialAdolescentAdultAgedAnimalsAntigens, HelminthChildChild, PreschoolEpidemiological MonitoringFemaleHumansMaleMiddle AgedSamoaSensitivity and SpecificityAntibodies, HelminthAntigens, Helminth

Identifiers

PMID39883706
PMCPMC11922241

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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.