摘要
目的探讨某AIDS治疗示范区3种高效抗反转录病毒疗法(HAART)的疗效,为进一步合理使用抗病毒治疗方案奠定基础。方法回顾性分析AIDS治疗示范区抗病毒治疗6个月以上的3种治疗方案:叠氮胸苷(AZT)+双脱氧肌苷(DDI)+奈韦拉平(NVP),拉米夫定(3TC)+司他夫定(D4T)+NVP.D4T+DDI+NVP。分别检测HIV RNA、CD4^+细胞、耐药位点,统计学分析采用t检验或四格表法检验。结果3种治疗方案中,抗病毒治疗前后HIV RNA的转阴率比较.AZT+ DDI+NVP组与3TC+D4T+NVP组差异无统计学意义(P>0.05),D4T+DDI+NVP组与AZT +DDI+NVP组差异有统计学意义(P<0.05);3组CD4^+T淋巴细胞计数在治疗前后差异有统计学意义(P<0.05);其中AZT+DDI+NVP组CD4^+T淋巴细胞计数为(100~350)×10~6/L,HIV RNA转阴率较其他各组差异有统计学意义(P<0.05);AZT+DDI+NVP组核苷类反转录酶抑制剂(NRTIs.AZT+DDI)发生的耐药位点是M41L、E44A、K70KR、D67N、L210W、T215Y、K219W等.属于高度耐药;非核苷类反转录酶抑制剂(NNRTIs,NVP)是A98G、V179H、Y181C、K103N、G190A等,属于高度耐药;3TC+D4T+NVP组NNRTIs(NVP)发生的耐药位点是Y181C,未见3TC突变位点。DDI+D4T+NVP组NNRTIs发生的耐药位点是Y181C;但以上各组均未发现对蛋白酶抑制剂(PIs)耐药位点。结论AZT+DDI+NVP与3TC+D4T+NVP组疗效优于DDI+D4T+ NVP组,可获得较好疗效。
Objective To compare the effects of three kinds of high active anti-retroviral therapy(HAART) in acquired immune deficiency syndrome(AIDS) area and provide the basis for applying HAART better in the future. Methods The effects of three kinds of HAART [Zidovudine(AZT)+ Dideoxyinosine(DDI) + Nevirapine ( NVP), Lamivudine (3TC) + Stavudine (D4T) + NVP and D4T + DDI+NVP)] in AIDS area over 6 months were analyzed retrospectively. HIV RNA, CD4^+ T cells, the sites of drug resistance were detected. The data were analyzed using t test or 2 × 2 table test. Results Of the three kinds of HAART, there were no difference of HIV RNA negative rate between AZT+ DDI+ NVP group and 3TC+ D4T+ NVP group(P 〉 0.05 ); however there were significant difference between D4T+DDI+NVP group and AZT+DDI+NVP group(P 〈 0.05 ) ; furthermore, the CD4^+ cell counts were different in these three groups before and after treatment (P 〈 0.05 ) and the HIV RNA negative rate in AZT+ DDI+NVP group was much higher than the other groups(P 〈 0.05 )when the CD4^ + cell counts were ( 100- 350) )× 10^6 / L. The detection of sites of drug resistance: the major mutant sites to AZT+DDI were M41L, E44A, K70KR, D67N, L210W, T215Y or K219W which were highly resistant and to NVP were A98G, V179H, Y181C, K103N or G190A which were highly resistant in AZT+DDI+NVP group. Meanwhile, the site to NVP was Y181C and no sites to 3TC in 3TC+D4T+ NVP and DDI+D4T+NVP group. There were no mutant sites of drug resistance to protease inhibitors (PIs) in all the HAART groups. Conclusion It will be better choice of AZT+DDI+NVP or 3TC+D4T +NVP group than DDI+D4T+NVP group for treatment in Chinese AIDS patients.
出处
《中华传染病杂志》
CAS
CSCD
北大核心
2007年第12期726-730,共5页
Chinese Journal of Infectious Diseases
关键词
获得性免疫缺陷综合征
抗反转录病毒治疗
高效
回顾性研究
抗药性
病毒
Acquired immunodeficiency syndrome
Antiretroviral therapy, highly active
Retrospective studies
Drug resistance, viral