Title
Lipoarabinomannan antigenic epitope differences in tuberculosis disease subtypes
Date Issued
01 December 2020
Access level
open access
Resource Type
journal article
Author(s)
Magni R.
Rruga F.
Alsaab F.
Sharif S.
Howard M.
Espina V.
Kim B.
Lepene B.
Lee G.
Alayouni M.A.
Steinberg H.
Araujo R.
Kashanchi F.
Riccardi F.
Morreira S.
Araujo A.
Poli F.
Jaganath D.
Semitala F.C.
Worodria W.
Andama A.
Choudhary A.
Honnen W.J.
Petricoin E.F.
Cattamanchi A.
Colombatti R.
de Waard J.H.
Oberhelman R.
Pinter A.
Liotta L.A.
Luchini A.
Publisher(s)
Nature Research
Abstract
An accurate urine test for diverse populations with active tuberculosis could be transformative for preventing TB deaths. Urinary liporabinomannan (LAM) testing has been previously restricted to HIV co-infected TB patients. In this study we evaluate urinary LAM in HIV negative, pediatric and adult, pulmonary and extrapulmonary tuberculosis patients. We measured 430 microbiologically confirmed pretreatment tuberculosis patients and controls from Peru, Guinea Bissau, Venezuela, Uganda and the United States using three monoclonal antibodies, MoAb1, CS35, and A194, which recognize distinct LAM epitopes, a one-sided immunoassay, and blinded cohorts. We evaluated sources of assay variability and comorbidities (HIV and diabetes). All antibodies successfully discriminated TB positive from TB negative patients. ROAUC from the average of three antibodies’ responses was 0.90; 95% CI 0.87–0.93, 90% sensitivity, 73.5% specificity (80 pg/mL). MoAb1, recognizing the 5-methylthio-d-xylofuranose(MTX)-mannose(Man) cap epitope, performed the best, was less influenced by glycosuria and identified culture positive pediatric (N = 19) and extrapulmonary (N = 24) patients with high accuracy (ROAUC 0.87, 95% CI 0.77–0.98, 0.90 sensitivity 0.80 specificity at 80 pg/mL; ROAUC = 0.96, 95% CI 0.92–0.99, 96% sensitivity, 80% specificity at 82 pg/mL, respectively). The MoAb1 antibody, recognizing the MTX-Man cap epitope, is a novel analyte for active TB detection in pediatric and extrapulmonary disease.
Volume
10
Issue
1
Language
English
OCDE Knowledge area
Sistema respiratorio Enfermedades infecciosas
Scopus EID
2-s2.0-85089542282
PubMed ID
Source
Scientific Reports
ISSN of the container
20452322
Sponsor(s)
This research was made possible through support from the Bill and Melinda Gates Foundation Global Health Program OPP1198385 to LAL, the Eunice Kennedy Shriver National Institute of Child Health and Human Development Grant R21HD097472 to LAL, and the National Institute of Allergy and Infectious Diseases Grants R21AI138135 to AL and R01AI136722 to RHG. The funders of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the manuscript. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.
Sources of information: Directorio de Producción Científica Scopus