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Tuberculosis (Edinb). 2012 May;92(3):243-7. doi: 10.1016/j.tube.2012.02.004. Epub 2012 Mar 10.

Anti-phospholipid antibody levels as biomarker for monitoring tuberculosis treatment response.

Author information

1
Division of Infectious Diseases and Vaccinology, School of Public Health, 201 Hildebrand Hall, University of California, Berkeley, CA 94720, USA. agoodridge@cal.berkeley.edu

Abstract

Standard methods to monitor tuberculosis (TB) treatment response rely on sputum microscopy and culture conversion. Alternatives to these methods are needed for those patients whose sputum tests are smear or culture negative. Here, we examine anti-phospholipid IgM antibody level changes as a biomarker for treatment response in smear positive TB patients. Serum samples were obtained from 40 pulmonary TB patients at the start and end of the intensive phase treatment (IPT) from the CDC-TB Trials Consortium randomized clinical trial in Kampala, Uganda. Samples were screened by ELISA for IgM levels against five phospholipids found in Mycobacterium tuberculosis and host cells. Lipid antigens included cardiolipin (CL), phosphatidyl inositol (PI), phosphatidyl ethanolamine (PE), phosphatidyl choline (PTC), and sphingolipid (SL). Levels of IgM against all phospholipids significantly decreased (p = 0.034, 0.001, 0.008 0.008, 0.040, respectively) following anti-TB drug treatment in patients without lung cavitary disease at baseline. The mean sensitivity of this test in these patients was 83% when the IgM response to a single lipid antigen was used; it was >90% when responses to 2 or more lipids were assessed. In contrast, cavitary TB patients showed an overall IgM increase, with a significant rise against PE (p = 0.025). There was no significant difference in the change in antibody levels between patients who remained culture-positive and those who culture-converted after 40 doses of drug therapy. The measurement of IgM anti-phospholipid antibodies may be a useful biomarker to monitor treatment response in non-cavitary TB patients.

PMID:
22406155
PMCID:
PMC4408545
DOI:
10.1016/j.tube.2012.02.004
[Indexed for MEDLINE]
Free PMC Article

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