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首页> 外文期刊>BMC Infectious Diseases >HLA-B*57:01 allele prevalence in HIV-infected North American subjects and the impact of allele testing on the incidence of abacavir-associated hypersensitivity reaction in HLA-B*57:01-negative subjects
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HLA-B*57:01 allele prevalence in HIV-infected North American subjects and the impact of allele testing on the incidence of abacavir-associated hypersensitivity reaction in HLA-B*57:01-negative subjects

机译:HLA-B * 57:01阴性受试者中HLA-B * 57:01等位基因患病率在HIV感染的北美受试者中以及等位基因检测对阿巴卡韦相关的超敏反应发生率的影响

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Background The presence of the HLA-B*57:01 allele in HIV-infected subjects is associated with a higher risk of abacavir-associated hypersensitivity reaction (ABC HSR). HLA-B*57:01 allele prevalence varies in different populations, but HLA-B*57:01 testing with immunological confirmation has had a negative predictive value for ABC HSR between 97 and 100%. Methods In the ASSURE study (EPZ113734), the HLA-B*57:01 prevalence in virologically suppressed, antiretroviral treatment–experienced, HIV-infected subjects from the United States, including Puerto Rico, was assessed. Results Three hundred eighty-five subjects were screened; 13 were HLA-B*57:01 positive and 372 were negative. Only HLA-B*57:01-negative, abacavir-naive subjects were eligible to enroll into the ASSURE trial. Eleven of the 13 subjects who possessed the HLA-B*57:01 allele were white, the other 2 were African-American. There was no geographic clustering of HLA-B*57:01-positive subjects, and the incidence correlated roughly with those states with the greatest numbers of subjects screened. Similarly, there was no statistically significant correlation between subjects who possessed or lacked the allele and age, gender, ethnicity or CD4+ T-cell numbers. The incidence of ABC HSR following abacavir initiation was also evaluated. Only 1 of 199 HLA-B*57:01-negative subjects (an African-American male) randomized to receive abacavir-containing treatment developed symptoms consistent with suspected ABC HSR; ABC HSR was not immunologically confirmed. Conclusions These findings confirm the utility of HLA-B*57:01 allele testing to reduce the frequency of ABC HSR. The prevalence of HLA-B*57:01 positivity was higher in white than in African-American subjects. In HLA-B*57:01-negative subjects, suspected ABC HSR is very rare, but should lead to discontinuation of abacavir when ABC HSR cannot be definitively excluded from the differential diagnosis. Trial registration The ASSURE (EPZ113734) study was registered on ClinicalTrials.gov registration on April 8th 2010 and the registration number is NCT01102972.
机译:背景HIV感染受试者中HLA-B * 57:01等位基因的存在与阿巴卡韦相关的超敏反应(ABC HSR)的较高风险相关。 HLA-B * 57:01等位基因患病率在不同人群中有所不同,但是具有免疫学证实的HLA-B * 57:01检测对ABC HSR的阴性预测值为97%至100%。方法在ASSURE研究(EPZ113734)中,评估了来自美国(包括波多黎各)的受病毒抑制,抗逆转录病毒治疗,有HIV感染的受试者中HLA-B * 57:01的患病率。结果筛选出385名受试者。 HLA-B * 57:01阳性13例,阴性372例。只有HLA-B * 57:01阴性,无abacavir的受试者才有资格参加ASSURE试验。拥有HLA-B * 57:01等位基因的13位受试者中有11位是白人,另外2位是非裔美国人。没有HLA-B * 57:01阳性受试者的地理聚类,并且发病率与那些受试者数量最多的州大致相关。同样,在拥有或缺乏等位基因的受试者与年龄,性别,种族或CD4 + T细胞数量之间也没有统计学上的显着相关性。还评估了阿巴卡韦启动后ABC HSR的发生率。 199名HLA-B * 57:01阴性受试者(非洲裔美国男性)中只有1名被随机接受含阿巴卡韦的治疗,其症状与可疑ABC HSR相符。未通过免疫学证实ABC HSR。结论这些发现证实了HLA-B * 57:01等位基因测试可降低ABC HSR的频率。白人中HLA-B * 57:01阳性的患病率高于非裔美国人受试者。在HLA-B * 57:01阴性患者中,疑似ABC HSR非常罕见,但是当不能明确将ABC HSR排除在鉴别诊断之外时,应该导致阿巴卡韦停药。试验注册ASSURE(EPZ113734)研究于2010年4月8日在ClinicalTrials.gov注册上进行了注册,注册号为NCT01102972。

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