Violin M, Forbici F, Cozzi-Lepri A, Velleca R, Bertoli A, Riva C, Giannella S, Manconi P E, Lazzarin A, Pasquinucci S, Tacconi L, Carnevale G, Mazzotta F, Bonazzi L, Montroni M, Chirianni A, Capobianchi M, Ippolito G, Moroni M, Perno C F, D'Arminio-Monforte A
Institute of Infectious and Tropical Diseases, University of Milan, L Sacco Hospital, Italy.
J Biol Regul Homeost Agents. 2002 Jan-Mar;16(1):37-43.
The risk of acquiring HIV-1 drug resistance at time of infection has become a public health problem following the widespread use of antiretroviral drugs in developed countries. Although a number of studies have reported data regarding the prevalence of HIV-1 primary resistance in developed countries over the past years, limited knowledge is available regarding the proportion of mutations related to drug resistance in antiretroviral naive subjects with chronic HIV-1 disease. In this study, we evaluated the prevalence of mutations in the reverse-transcriptase (RT) and protease region both in a representative group of recently HIV-1 infected subjects (n=68) and a cohort of chronically-infected HIV-positive patients (n=347) enrolled in the Italian Cohort of Antiretroviral Naive patients (I.CO.NA.). In recently infected individuals, the overall prevalence of mutations for nucleoside RTI (NRTIs) was 10/68 (14.7%). The distribution of mutations by calendar year were 0, 1 in 1996, 9, 3 in 1997 and 1, 0 in 1998 for NRTIs and protease inhibitors (PIs) respectively. Thymidine associated mutations were identified in six subjects (8.8%), five of whom had one mutation [41L, 70K (n=2), 215Y] and one had two mutations (67N+219Q). Four subjects (5.9%) showed the changes associated with resistance to lamivudine (184V or 118I). No non nucleoside-RTI (NNRTI) mutations were present in the study period. Primary PIs mutations (two 46L and two 82I) were present in four subjects (5.9%). Of note, mutations related to resistance to more than one class of antiretrovirals were present in one (1.5%). Among patients with chronic infection a large proportion (88.5%) carried no mutations in RT region, 11.5% individuals carried one or more mutations associated with resistance to NRTI (7.8%), or NNRTI (4.9%), with 4 patients carrying mutations to both classes. Among mutations associated with high-level resistance to RTI, T215Y was found in only 2 patients, M184V in 2 cases, T69D in another case, and K103N in only 1 patient, for a total of 6 patients (one carrying both T215Y and M184V) (1.7%). Primary mutations associated with substantial resistance to PIs were found in only 5/347 patients (1.4%); all the other patients carried only secondary mutations. Prevalence of mutations associated with high-level resistance to antiretroviral drugs is stable in recently infected individuals and low in patients with established HIV infection. The potential impact of transmitted mutations on the response to first regimen in individuals carrying transmitted mutations needs to be assessed by prospective studies.
在发达国家广泛使用抗逆转录病毒药物之后,感染时获得HIV-1耐药性的风险已成为一个公共卫生问题。尽管过去几年有多项研究报告了发达国家HIV-1原发性耐药的流行数据,但对于慢性HIV-1疾病的初治抗逆转录病毒治疗患者中与耐药相关的突变比例,了解有限。在本研究中,我们评估了意大利初治抗逆转录病毒治疗患者队列(I.CO.NA.)中一组具有代表性的近期HIV-1感染患者(n = 68)以及一组慢性感染的HIV阳性患者(n = 347)中逆转录酶(RT)和蛋白酶区域的突变流行情况。在近期感染的个体中,核苷类逆转录酶抑制剂(NRTIs)的突变总体流行率为10/68(14.7%)。按日历年划分的NRTIs和蛋白酶抑制剂(PIs)突变分布情况分别为:1996年为0、1,1997年为9、3,1998年为1、0。在6名受试者(8.8%)中鉴定出与胸苷相关的突变,其中5名有一个突变[41L、70K(n = 2)、215Y],1名有两个突变(67N + 219Q)。4名受试者(5.9%)出现了与拉米夫定耐药相关的变化(184V或118I)。在研究期间未发现非核苷类逆转录酶抑制剂(NNRTIs)突变。4名受试者(5.9%)存在原发性PIs突变(两个46L和两个82I)。值得注意的是,1名(1.5%)患者存在与对不止一类抗逆转录病毒药物耐药相关的突变。在慢性感染患者中,很大一部分(88.5%)RT区域无突变,11.5%的个体携带一个或多个与对NRTI(7.8%)或NNRTI(4.9%)耐药相关的突变,有4名患者对两类药物均有突变。在与对RTI高水平耐药相关的突变中,仅在2名患者中发现T215Y,2例发现M184V,另1例发现T69D,仅1名患者发现K103N,共6名患者(1名同时携带T215Y和M184V)(1.7%)。仅在5/347名患者(1.4%)中发现与对PIs显著耐药相关的原发性突变;所有其他患者仅携带继发性突变。在近期感染个体中,与对抗逆转录病毒药物高水平耐药相关的突变流行率稳定,在已确诊HIV感染的患者中较低。携带传播性突变的个体中传播性突变对首个治疗方案反应的潜在影响需要通过前瞻性研究进行评估。