4.7 Article

Diagnostic Performance of Tuberculosis-Specific IgG Antibody Profiles in Patients with Presumptive Tuberculosis from Two Continents

期刊

CLINICAL INFECTIOUS DISEASES
卷 64, 期 7, 页码 947-955

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/cix023

关键词

serologic tests; tuberculosis; biomarkers; antibodies; diagnosis

资金

  1. FIND
  2. Bill & Melinda Gates Foundation [OPP1018924]
  3. Ministry of Foreign Affairs, Government of the Netherlands [22211]
  4. Medical Research Council [MR/K023446/1] Funding Source: researchfish
  5. Bill and Melinda Gates Foundation [OPP1018924] Funding Source: Bill and Melinda Gates Foundation
  6. MRC [MR/K023446/1] Funding Source: UKRI

向作者/读者索取更多资源

Background. Development of rapid diagnostic tests for tuberculosis is a global priority. A whole proteome screen identified Mycobacterium tuberculosis antigens associated with serological responses in tuberculosis patients. We used World Health Organization (WHO) target product profile (TPP) criteria for a detection test and triage test to evaluate these antigens. Methods. Consecutive patients presenting to microscopy centers and district hospitals in Peru and to outpatient clinics at a tuberculosis reference center in Vietnam were recruited. We tested blood samples from 755 HIV-uninfected adults with presumptive pulmonary tuberculosis to measure IgG antibody responses to 57 M. tuberculosis antigens using a field-based multiplexed serological assay and a 132-antigen bead-based reference assay. We evaluated single antigen performance and models of all possible 3-antigen combinations and multiantigen combinations. Results. Three-antigen and multiantigen models performed similarly and were superior to single antigens. With specificity set at 90% for a detection test, the best sensitivity of a 3-antigen model was 35% (95% confidence interval [CI], 31-40). With sensitivity set at 85% for a triage test, the specificity of the best 3-antigen model was 34% (95% CI, 29-40). The reference assay also did not meet study targets. Antigen performance differed significantly between the study sites for 7/22 of the best-performing antigens. Conclusions. Although M. tuberculosis antigens were recognized by the IgG response during tuberculosis, no single antigen or multiantigen set performance approached WHO TPP criteria for clinical utility among HIV-uninfected adults with presumed tuberculosis in high-volume, urban settings in tuberculosis-endemic countries.

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