Persistently elevated abnormal B‐cell subpopulations and anti‐core antibodies in patients co‐infected with HIV/HCV who relapse. Issue 4 (21st January 2015)

• Record Type: Journal Article
• Authors: Kohli, Anita; Funk, Emily; Burbelo, Peter; Barrett, Lisa; Meissner, Eric G.; Santich, Brian; Shaffer, Ashton; Johl, Jessica; Sidharthan, Sreetha; Moir, Susan; Kottilil, Shyam; Fauci, Anthony S.
• Is Part Of: Journal of medical virology. Volume 87:Issue 4(2015:Apr.)
• Page Start: 544
• Page End: 552
• Publication Date: 2015-01-21
• Subjects: Virology -- Periodicals; 616
• DOI: 10.1002/jmv.24089
• Languages: English
• ISSNs: 0146-6615

Abstract

<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jmv24089-sec-0001" sec-type="section"> <p>Hepatitis C (HCV) treatment for patients coinfected with human immunodeficiency virus (HIV) and HCV is associated with modest rates of sustained virologic response (SVR) and an increased rate of relapse when compared to HCV monoinfected patients. As patients who attain SVR and patients who relapse are clinically indistinguishable during treatment, where both groups have fully suppressed HCV viral load, it has not been possible to identify in advance those who will relapse. Biomarkers that may distinguish patients with differential treatment response may be clinically useful and provide insight into mechanisms of relapse. In this retrospective study, serum and PBMCs were obtained from 41 HIV/HCV co‐infected patients and 17 healthy volunteers. Changes in antibody titers to various regions of the HCV proteome during treatment for HCV were determined using a novel luciferase immunoprecipitation assay. Changes in B‐cell subtypes in patients with differential treatment response as well as healthy volunteers were compared. This study demonstrates that elevated anti‐HCV core antibody titers persisted during HCV treatment in patients who relapsed when compared to those who attained SVR. Furthermore, characterization of B cells in patients who relapsed demonstrated an abnormal B‐cell phenotype distribution characterized by elevated frequencies of exhausted B cells among relapsers at baseline, which persisted despite suppression of HCV viremia at 24 weeks, along with increased frequencies of plasmablasts. These data suggest that anti‐HCV specific B cells may be responding to ongoing subclinical HCV replication in patients who will relapse. <bold><italic>J. Med. Virol. 87:544–552, 2015</italic>.</bold> © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract>