Nonsuppressive anti-HBV therapy may select for drug-resistant mutants that could escape vaccine-induced protection from infection.
Hepatitis B virus (HBV) polymerase and envelope genes overlap, such that polymerase mutations associated with drug resistance may alter antigenic sites in hepatitis B surface antigen (HBsAg). A triple mutational pattern that confers lamivudine (3TC) resistance (rtV173L + rtL180M + rtM204V) reduces binding of antibody to HBsAg; if transmitted, this mutant virus could escape vaccine-induced protection. How frequently does selection of vaccine-escape mutants occur in patients on anti-HBV therapy?
To address this question, investigators performed HBV sequencing in 19 monoinfected and 52 HIV-coinfected patients who were treated for at least 12 months with anti-HBV nucleosides (3TC or emtricitabine), nucleotides (tenofovir or adefovir), or both. T…
Reviewing Author
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)