the drugs, suboptimal pharmacokinetic states, and suboptimal virology patency (4). Currently, treatment success may be summarized as the suppression of the VL and achieving of undetectable levels, immunological success, and the prevention of HIV-related events. (3). We aimed to assess the 24-week virological and immunological success of treatment-naive and treatment-experienced patients included in the Action against HIV in Istanbul (ACTHIV-IST) database. MATERIALS AND METHODS Data collection: The ACTHIV-IST database was used in our study. ACTHIV-IST consists of 5 centers following up treatment-naive and treatment-experienced patients in Istanbul, which is the most populated city in Turkey. ACTHIV-IST was established in 2012, and new cases are being enrolled in the database retrospectively. Study design and study participants: The ACTHIV-IST database was screened retrospectively from January 2012 to January 2014. One thousand two hundred eighty-nine patients older than 18-years were included in this study. The ART initiation decision was based on the up-to-date international guidelines at the time of the study. Three hundred thirty-nine treatment-naive and treatment-experienced patients were recorded in the database during the time span of the study. Of those, 256 patients had initiated ART, and 32 were excluded because of the absence of CD4+ cell count and VL follow up results in the 24th week. Two hundred twenty-SUMMARY: We aimed to assess the 24-week virological and immunological success of the treatment of treatment-naive and treatment-experienced patients included in the Action against HIV in Istanbul (ACTHIV-IST) database. The ACTHIV-IST database was screened retrospectively from January 2012 to January 2014. The data for these patients such as age, sex, treatment-naive or treatment-experienced status, date of diagnosis, date of commencing antiretroviral therapy, antiretroviral therapy regimen, CD4+ cell count, and viral load before and after therapy were analyzed. In the 24th week of antiretroviral therapy, there were 40 (17.9) and 29 (14.1) virological and immunological failures, respectively. Virological failure (VF) was associated with a baseline viral load > 100,000 copies (p = 0.004). A CD4+ cell count lower than 200 cells µl was not found to be associated with VF (p = 0.843). Immunological failure was substantially rare in patients with a baseline CD4+ cell count > 200 cells µl (p = 0.005). Although an HIV-RNA 100,000 copies ml was protective against VF in the 24th week, in individuals with an HIV-RNA > 100,000 copies ml, VF was 3.2 times more likely to occur. Baseline VF was the most predictive parameter to estimate 24th week virological success and VF. VF is an important prognostic parameter resulting in CD4+ cell depletion, AIDS-related events, and increased mortality.