Prasitsuebsai Wasana, Teeraananchai Sirinya, Singtoroj Thida, Truong Khanh Huu, Ananworanich Jintanat, Do Viet Chau, Nguyen Lam Van, Kosalaraksa Pope, Kurniati Nia, Sudjaritruk Tavitiya, Chokephaibulkit Kulkanya, Kerr Stephen J, Sohn Annette H
*HIV-NAT, Thai Red Cross AIDS Research Centre, Bangkok, Thailand;†TREAT Asia/amfAR-The Foundation for AIDS Research, Bangkok, Thailand;‡Infectious Disease Department, Children's Hospital 1, Ho Chi Minh City, Vietnam;§US Military HIV Research Program, Walter Reed Army Institute of Research/Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD;‖Infectious Disease Department, Children's Hospital 2, Ho Chi Minh City, Vietnam;¶Infectious Disease Department, National Hospital of Pediatrics, Hanoi, Vietnam;#Division of Infectious Diseases, Department of Pediatrics, Khon Kaen University, Khon Kaen, Thailand;**Cipto Mangunkusumo General Hospital, Jakarta, Indonesia;††Faculty of Medicine and Research Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand;‡‡Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand;§§The Kirby Institute, University of New South Wales, Sydney, Australia; and‖‖Department of Global Health, Academic Medical Center, University of Amsterdam, Amsterdam Institute for Global Health and Development, Amsterdam, the Netherlands.
J Acquir Immune Defic Syndr. 2016 Aug 1;72(4):380-6. doi: 10.1097/QAI.0000000000000971.
Data on pediatric treatment outcomes and drug resistance while on second-line antiretroviral therapy (ART) are needed to guide HIV care in resource-limited countries.
HIV-infected children <18 years who were switched or switching to second-line ART after first-line failure were enrolled from 8 sites in Indonesia, Thailand, and Vietnam. Genotyping was performed at virologic failure (VF; HIV-RNA >1000 copies/mL). Cox proportional hazards regression was used to evaluate factors predicting VF.
Of 277 children, 41% were female. At second-line switch, age was 7.5 (5.3-10.3) years, CD4 count was 300 (146-562) cells per cubic millimeter, and percentage was 13 (7-20%); HIV-RNA was 5.0 (4.4-5.5) log10 copies per milliliter. Second-line regimens contained lamivudine (90%), tenofovir (43%), zidovudine or abacavir (30%), lopinavir (LPV/r; 91%), and atazanavir (ATV; 7%). After 3.3 (1.8-5.3) years on second-line ART, CD4 was 763 (556-1060) cells per cubic millimeter and 26% (20-31%). VF occurred in 73 (27%), with an incidence of 7.25 per 100 person-years (95% confidence interval [CI]: 5.77 to 9.12). Resistance mutations in 50 of 73 children with available genotyping at first VF included M184V (56%), ≥1 thymidine analogue mutation (TAM; 40%), ≥4 TAMs (10%), Q151M (4%), any major LPV mutation (8%), ≥6 LPV mutations (2%), and any major ATV mutation (4%). Associations with VF included age >11 years (hazard ratio [HR] 4.06; 95% CI: 2.15 to 7.66) and HIV-RNA >5.0 log10 copies per milliliter (HR 2.42; 95% CI: 1.27 to 4.59) at switch and were seen more commonly in children from Vietnam (HR 2.79; 95% CI: 1.55 to 5.02).
One-fourth of children developed VF while on second-line ART. However, few developed major mutations to protease inhibitors.
在资源有限的国家,需要有关儿科二线抗逆转录病毒疗法(ART)治疗结果和耐药性的数据来指导艾滋病护理。
从印度尼西亚、泰国和越南的8个地点招募了18岁以下在一线治疗失败后改用或正在改用二线ART的艾滋病毒感染儿童。在病毒学失败(VF;HIV-RNA>1000拷贝/毫升)时进行基因分型。使用Cox比例风险回归来评估预测VF的因素。
277名儿童中,41%为女性。在改用二线治疗时,年龄为7.5(5.3-10.3)岁,CD4细胞计数为每立方毫米300(146-562)个,百分比为13(7-20)%;HIV-RNA为每毫升5.0(4.4-5.5)log10拷贝。二线治疗方案包括拉米夫定(90%)、替诺福韦(43%)、齐多夫定或阿巴卡韦(30%)、洛匹那韦(LPV/r;91%)和阿扎那韦(ATV;7%)。在接受二线ART治疗3.3(1.8-5.3)年后,CD4细胞计数为每立方毫米763(556-1060)个,百分比为26(20-31)%。73名(27%)出现VF,发病率为每100人年7.25例(95%置信区间[CI]:5.77至9.12)。73名在首次VF时进行基因分型的儿童中有50名出现耐药突变,包括M184V(56%)、≥1个胸苷类似物突变(TAM;40%)、≥4个TAM(10%)、Q151M(4%)、任何主要LPV突变(8%)、≥6个LPV突变(2%)和任何主要ATV突变(4%)。与VF相关的因素包括改用二线治疗时年龄>11岁(风险比[HR]4.06;95%CI:2.15至7.66)和HIV-RNA>每毫升5.0 log10拷贝(HR 2.42;95%CI:1.27至4.59),在越南儿童中更常见(HR 2.79;95%CI:1.55至5.02)。
四分之一的儿童在接受二线ART治疗时出现VF。然而,很少有儿童出现针对蛋白酶抑制剂的主要突变。