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EBioMedicine. 2017 Nov;25:112-121. doi: 10.1016/j.ebiom.2017.10.018. Epub 2017 Oct 24.

Biomarkers of Tuberculosis Severity and Treatment Effect: A Directed Screen of 70 Host Markers in a Randomized Clinical Trial.

Author information

1
Meso Scale Diagnostics, LLC, Rockville, MD, USA. Electronic address: gsigal@meso-scale.com.
2
University of California, San Francisco, CA, USA.
3
Meso Scale Diagnostics, LLC, Rockville, MD, USA.
4
Yale School of Public Health and Yale School of Medicine, New Haven, CT, USA.
5
San Antonio VA Medical Center, San Antonio, TX, USA.
6
Centers for Disease Control and Prevention, Atlanta, GA, USA.
7
Pacific Northwest National Laboratory, Richland, WA, USA.
8
University of Notre Dame, Notre Dame, IN, USA.
9
Oregon Health and Science University, Portland, OR, USA.
10
University of California, San Francisco, CA, USA. Electronic address: pnahid@ucsf.edu.

Abstract

More efficacious treatment regimens are needed for tuberculosis, however, drug development is impeded by a lack of reliable biomarkers of disease severity and of treatment effect. We conducted a directed screen of host biomarkers in participants enrolled in a tuberculosis clinical trial to address this need. Serum samples from 319 protocol-correct, culture-confirmed pulmonary tuberculosis patients treated under direct observation as part of an international, phase 2 trial were screened for 70 markers of infection, inflammation, and metabolism. Biomarker assays were specifically developed for this study and quantified using a novel, multiplexed electrochemiluminescence assay. We evaluated the association of biomarkers with baseline characteristics, as well as with detailed microbiologic data, using Bonferroni-adjusted, linear regression models. Across numerous analyses, seven proteins, SAA1, PCT, IL-1β, IL-6, CRP, PTX-3 and MMP-8, showed recurring strong associations with markers of baseline disease severity, smear grade and cavitation; were strongly modulated by tuberculosis treatment; and had responses that were greater for patients who culture-converted at 8weeks. With treatment, all proteins decreased, except for osteocalcin, MCP-1 and MCP-4, which significantly increased. Several previously reported putative tuberculosis-associated biomarkers (HOMX1, neopterin, and cathelicidin) were not significantly associated with treatment response. In conclusion, across a geographically diverse and large population of tuberculosis patients enrolled in a clinical trial, several previously reported putative biomarkers were not significantly associated with treatment response, however, seven proteins had recurring strong associations with baseline radiographic and microbiologic measures of disease severity, as well as with early treatment response, deserving additional study.

KEYWORDS:

Biomarkers; Clinical trials; Host immune response; Tuberculosis

PMID:
29100778
PMCID:
PMC5704068
DOI:
10.1016/j.ebiom.2017.10.018
[Indexed for MEDLINE]
Free PMC Article

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