In Taiwan, HIV-infected patients are provided free access to HIV care that includes monitoring of CD4 count and plasma HIV RNA load, and combination antiretroviral therapy (cART) that was introduced

in Taiwan in 1997. CART was defined as the use of at least three agents from at least two classes of antiretroviral agents according to the local treatment guidelines for adults with HIV infection. The study was approved by the Research Ethics Committee of the hospital and subjects gave written informed consent (NCT registration no. 01102296). HIV-infected subjects were MG-132 price sequentially enrolled to receive two doses and three doses of HAV vaccine (1440 ELISA units) (HAVRIX 1440; GlaxoSmithKline, Biologicals, Rixensart, Osimertinib solubility dmso Belgium). Enrollment of HIV-infected subjects to receive three doses of HAV vaccine began after completion of enrollment of HIV-infected subjects to receive two doses of vaccine. In the two-dose vaccination schedule in HIV-infected and HIV-uninfected subjects, HAV vaccine was administered at week 0 and week 24, while in the three-dose schedule, HAV vaccine was administered at week 0, week 4, and week 24. The subjects were contacted by cell phone to inquire reactions following vaccination.

Anti-HAV antibody was determined at week 24 (before the last dose was administered) and week 48. The primary endpoint was seroconversion at week 48. The secondary endpoints were seroconversion at week 24 and the geometric mean concentration (GMC) of anti-HAV antibody at weeks 48 and 72. Patients who had no serum available for determination of anti-HAV antibody at week 24 were considered as nonresponders. At week 48, those patients who had no serum samples available, but had achieved seroconversion at week 24, were considered as responders; those without seroconversion at week 48, or having no serologic data available before the last dose of vaccination at week 24 were considered as nonresponders (intention-to-treat [ITT] analysis using last-observation-carried-forward

principle). Sensitivity analyses were performed in patients who had available results of anti-HAV antibody at different time points (per-protocol [PP] analysis). Because the baseline characteristics were statistically significantly different in age and immunologic and virologic characteristics filipin between the two-dose HIV-infected and three-dose HIV-infected group (Table 1), pairs from the two groups were selected that were matched for CD4 count (±20 cells/μL) and age (±2 years) to better assess the serologic responses to HAV vaccination between the two groups receiving different doses of HAV vaccine. Serum samples were collected before vaccination (week 0) and at weeks 24, 48, and 72. The determinations of anti-HAV antibody of serum samples were performed at the central laboratory of the hospital via chemiluminescence immunoassay according to the manufacturer’s protocol (ARCHITECT HAVAb-IgG, Abbott Diagnostics, Wiesbaden, Germany).