4.8 Article

Evaluation of Host Serum Protein Biomarkers of Tuberculosis in sub-Saharan Africa

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.639174

Keywords

serum; protein; biomarker; tuberculosis; diagnosis; HIV; Africa

Categories

Funding

  1. James Maxwell Grant Prophit Fellowship (Royal College of Physicians, London)
  2. Wellcome [104803, 203135, FC0010218]
  3. UKRI-MRC [FC0010218]
  4. CRUK [FC0010218]
  5. National Institutes of Health [AI115940]
  6. Foundation for National Institutes of Health [WILK116PTB]
  7. EDCTP2 [SRIA2015-1065]
  8. ILULU-TB project which was EU Action for Diseases of Poverty program grant [Sante/2006/105-061]

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A study evaluated serum protein biomarkers discovered in primary care cohorts from Africa reapplied to patients from secondary care, discovering a nine-protein signature to distinguish tuberculosis from other diseases. This signature showed high sensitivity and specificity, indicating the potential for serum proteins as point-of-care screening tests for TB in African hospitals. Additionally, complement factor H was identified as a new biomarker for such signatures.
Accurate and affordable point-of-care diagnostics for tuberculosis (TB) are needed. Host serum protein signatures have been derived for use in primary care settings, however validation of these in secondary care settings is lacking. We evaluated serum protein biomarkers discovered in primary care cohorts from Africa reapplied to patients from secondary care. In this nested case-control study, concentrations of 22 proteins were quantified in sera from 292 patients from Malawi and South Africa who presented predominantly to secondary care. Recruitment was based upon intention of local clinicians to test for TB. The case definition for TB was culture positivity for Mycobacterium tuberculosis; and for other diseases (OD) a confirmed alternative diagnosis. Equal numbers of TB and OD patients were selected. Within each group, there were equal numbers with and without HIV and from each site. Patients were split into training and test sets for biosignature discovery. A nine-protein signature to distinguish TB from OD was discovered comprising fibrinogen, alpha-2-macroglobulin, CRP, MMP-9, transthyretin, complement factor H, IFN-gamma, IP-10, and TNF-alpha. This signature had an area under the receiver operating characteristic curve in the training set of 90% (95% CI 86-95%), and, after adjusting the cut-off for increased sensitivity, a sensitivity and specificity in the test set of 92% (95% CI 80-98%) and 71% (95% CI 56-84%), respectively. The best single biomarker was complement factor H [area under the receiver operating characteristic curve 70% (95% CI 64-76%)]. Biosignatures consisting of host serum proteins may function as point-of-care screening tests for TB in African hospitals. Complement factor H is identified as a new biomarker for such signatures.

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