Evidence map›Paper›PMID 41728319›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Clinical Performance of a Mp1p Antibody Detection Immunoassay For Talaromycosis.

Shanti Narayanasamy, Nguyen T M Thu, Matthew T Burke, Lottie Brown, Helen Xu, Sruthi Venugopalan, Joseph R Egger, Vo Trieu Ly, Ngo Thi Hoa, Thuy Le

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Shanti NarayanasamyDuke Global Health Institute, Duke University, Durham, NC, USA.ORCID 0000-0002-6667-2868
Nguyen T M ThuDivision of Infectious Diseases and International Health, Duke University School of Medicine, Durham, North Carolina, USA.
Matthew T BurkeDivision of Infectious Diseases and International Health, Duke University School of Medicine, Durham, North Carolina, USA.
Lottie BrownInstitute of Infection and Immunity, City St George's University, School of Health & Medical Sciences, London, UK.
Helen XuDivision of Infectious Diseases and International Health, Duke University School of Medicine, Durham, North Carolina, USA.
Sruthi VenugopalanDepartment of Internal Medicine, University of Nevada Reno School of Medicine, Nevada, USA.
Joseph R EggerDuke Global Health Institute, Duke University, Durham, NC, USA.
Vo Trieu LyUniversity of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Ngo Thi HoaOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.ORCID 0000-0001-9320-4050
Thuy LeDivision of Infectious Diseases and International Health, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0002-3393-6580

Funding

Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
Liposomal Amphotericin B and Flucytosine Antifungal Strategies for Talaromycosis (LAmB-FAST)R01AI181764 · NIAID · DUKE UNIVERSITY · PI Thuy Le · 2024 to 2026
$3.9M
Development, Clinical Validation, and Readiness for Implementation of a Novel Mp1p D4 Poin Diagnosis of Talaromycosist of Care Test for RapidR01AI177098 · NIAID · DUKE UNIVERSITY · PI Ashutosh Chilkoti, Thuy Le · 2023 to 2026
$2.8M
Making an early diagnosis of talaromycosis - an approach to reduce morbidity and mortality in advanced HIV disease in Southeast AsiaR01AI143409 · NIAID · DUKE UNIVERSITY · PI LE, THUY · 2019 to 2024
$2.8M
Tropical Medicine Research Center for Talaromycosis in VietnamU01AI169358 · NIAID · DUKE UNIVERSITY · PI Thuy Le · 2022 to 2026
$2.5M
NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI143409NIAID NIH HHS R01 AI177098NIAID NIH HHS R01 AI181764NIAID NIH HHS U01 AI169358
6 · The paper itself

Abstract

Background: Talaromycosis, caused by the fungus Methods: This diagnostic study included 423 adults with advanced HIV disease and culture-confirmed talaromycosis as cases, and 206 non-talaromycosis individuals with and without HIV who have never traveled to Asia as controls. Anti-Mp1p IgM and IgG antibodies were measured using conventional double-sandwich EIA. Diagnostic performance was assessed using the healthy control group and the HIV control group separately. Assay cut-offs were based on both the Youden index generated from the receiver operating characteristic curves, and separately using a pre-defined specificity of 95%. Results: At the pre-defined 95% specificity, IgM had low to moderate accuracy of 62.3% and 87.9%, and a low sensitivity of 8.3% and 21.3%, when evaluated with healthy and HIV controls, respectively. IgG had similarly low accuracy of 52.2% and 78.4%, and a low sensitivity of 21.5% and 30.5%, when evaluated using healthy and HIV controls, respectively. Both IgM and IgG assays performed better in HIV controls than healthy controls. Conclusions: The anti-Mp1p IgM and IgG EIAs show low utility for the diagnosis of acute talaromycosis. However, at the high specificity cut-off of 95%, the assays have utility in the detection of

Indexed as

antibodyMp1ppenicilliosisPenicillium marneffeiserologyTalaromyces marneffeitalaromycosis

Identifiers

PMID41728319
PMCPMC12919142

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.