Long-Term Hepatitis B Virus (HBV) Response to Lamivudine-Containing Highly Active Antiretroviral Therapy in HIV-HBV Co-Infected Patients in Thailand

被引:8
|
作者
Khamduang, Woottichai [1 ,2 ,3 ]
Gaudy-Graffin, Catherine [2 ]
Ngo-Giang-Huong, Nicole [1 ,3 ,4 ]
Jourdain, Gonzague [1 ,3 ,4 ]
Moreau, Alain [2 ]
Luekamlung, Nuananong [5 ]
Halue, Guttiga [6 ]
Buranawanitchakorn, Yuwadee [7 ]
Kunkongkapan, Sura [8 ]
Buranabanjasatean, Sudanee [9 ]
Lallemant, Marc [1 ,3 ,4 ]
Sirirungsi, Wasna [1 ]
Goudeau, Alain [2 ]
机构
[1] Chiang Mai Univ, Fac Associated Med Sci, Chiang Mai 50000, Thailand
[2] Univ Tours, Fac Med, INSERM, U966,CHRU Tours, Tours, France
[3] IRD, UMI Programs HIV Prevent & Treatment PHPT 174, Chiang Mai, Thailand
[4] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[5] Lamphun Hosp, Lamphun, Thailand
[6] Phayao Hosp, Phayao, Thailand
[7] Chiang Kham Hosp, Phayao, Thailand
[8] Mae Sai Hosp, Chiangrai, Thailand
[9] Mae Chan Hosp, Chiangrai, Thailand
来源
PLOS ONE | 2012年 / 7卷 / 07期
关键词
PATIENTS RECEIVING LAMIVUDINE; HIV-1-INFECTED ADULTS; INDIVIDUALS; RESISTANT; EFFICACY; ADOLESCENTS; GUIDELINES; MORTALITY; IMPACT; COHORT;
D O I
10.1371/journal.pone.0042184
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Approximately 4 million of people are co-infected with HIV and Hepatitis B virus (HBV). In resource-limited settings, the majority of HIV-infected patients initiate first-line highly active antiretroviral therapy containing lamivudine (3TC-containing-HAART) and long-term virological response of HBV to lamivudine-containing HAART in co-infected patients is not well known. Methodology/Principal Finding: HIV-HBV co-infected patients enrolled in the PHPT cohort (ClinicalTrials. gov NCT00433030) and initiating a 3TC-containing-HAART regimen were included. HBV-DNA, HIV-RNA, CD4+ T-cell counts and alanine transaminase were measured at baseline, 3 months, 12 months and then every 6 months up to 5 years. Kaplan-Meier analysis was used to estimate the cumulative rates of patients who achieved and maintained HBV-DNA suppression. Of 30 co-infected patients, 19 were positive for HBe antigen (HBeAg). At initiation of 3TC-containing-HAART, median HBV DNA and HIV RNA levels were 7.35 log10 IU/mL and 4.47 log10 copies/mL, respectively. At 12 months, 67% of patients achieved HBV DNA suppression: 100% of HBeAg-negative patients and 47% of HBeAg-positive. Seventy-three percent of patients had HIV RNA below 50 copies/mL. The cumulative rates of maintained HBV-DNA suppression among the 23 patients who achieved HBV-DNA suppression were 91%, 87%, and 80% at 1, 2, and 4 years respectively. Of 17 patients who maintained HBV-DNA suppression while still on 3TC, 4 (24%) lost HBsAg and 7 of 8 (88%) HBeAg-positive patients lost HBeAg at their last visit (median duration, 59 months). HBV breakthrough was observed only in HBeAg-positive patients and 6 of 7 patients presenting HBV breakthrough had the rtM204I/V mutations associated with 3TC resistance along with rtL180M and/or rtV173L. Conclusions: All HBeAg-negative patients and 63% of HBeAg-positive HIV-HBV co-infected patients achieved long-term HBV DNA suppression while on 3TC-containing-HAART. This study provides information useful for the management of co-infected patients in resource-limited countries where the vast majority of co-infected patients are currently receiving 3TC.
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