Busch M P, Kleinman S H, Williams A E, Smith J W, Ownby H E, Laycock M E, Lee L L, Pau C P, Schreiber G B
Irwin Memorial Blood Centers, San Francisco, California, USA.
Transfusion. 1996 Jan;36(1):37-44. doi: 10.1046/j.1537-2995.1996.36196190513.x.
Follow-up studies from the mid-1980s showed that 1 to 5 percent of blood donors testing reactive in anti-human immunodeficiency virus type 1 (HIV-1) enzyme immunoassay (EIA) and testing indeterminate in Western blot were infected with HIV-1 and were in the process of seroconverting. The present study was conducted to establish the rate of HIV infection among contemporary anti-HIV-1/HIV type 2 (HIV-2) EIA-reactive, Western blot-indeterminate donors.
Donations (n = 607) with indeterminate HIV supplemental test results were identified by screening 3,021,342 donations given from November 1990 through August 1993 at five participating blood centers. Consenting donors were enrolled and samples taken 4 to 8 weeks after donation. Follow-up sera were tested by EIA and Western blot for anti-HIV-1 seroconversion and by type-specific peptide assays for antibodies to HIV-2 and HIV-1 subtype O. Peripheral blood mononuclear cells and/or plasma from the follow-up samples were tested for HIV-1 DNA and/or RNA by polymerase chain reaction. The rate of HIV-1 infection among Western blot-indeterminate donors was also estimated by multiplying the incidence rate of HIV-1 seroconversion in this donor population by the estimated duration of the EIA-reactive and Western blot-indeterminate window during seroconversion (8.5 days).
Supplemental test-indeterminate donors (n = 355) enrolled a median of 38 days after donation; 265 (75%) of these donors were identified as indeterminate after an anti-HIV-1/2 EIA-reactive donation. Enrolled and non-enrolled donors had similar distributions of demographic characteristics and band patterns. Follow-up samples from all 355 donors tested negative for HIV-1 in polymerase chain reaction. Follow-up sera tested Western blot-negative in 54 cases (15%) and Western blot-indeterminate in 299 (84%). Two follow-up sera (0.6%) were interpreted, according to manufacturer's package insert criteria, as Western blot positive with p24 and gp41 bands and/or gp120/160 bands; however, paired testing of index and follow-up sera from these two cases showed identical Western blot and EIA reactivity, and polymerase chain reaction was negative for HIV RNA and DNA, which ruled out HIV infection. The absence of HIV infection in 355 Western blot-indeterminate donors was consistent with our incidence-based model analysis, which yielded an estimate of one HIV-1 infection for every 215 Western blot-indeterminate donations (95% CI, 1/39-1/8333).
Contemporary blood donors classified as indeterminate in supplemental HIV testing are infrequently infected with HIV. Donors whose follow-up samples test negative in anti-HIV-1/2 EIAs and negative or persistently indeterminate in Western blots should be considered eligible for reinstatement.
20世纪80年代中期的随访研究表明,在抗人类免疫缺陷病毒1型(HIV-1)酶免疫测定(EIA)中检测呈反应性且在免疫印迹法中检测结果不确定的献血者中,有1%至5%感染了HIV-1,且正处于血清转化过程中。本研究旨在确定当代抗HIV-1/2型免疫缺陷病毒(HIV-2)EIA反应性、免疫印迹法结果不确定的献血者中的HIV感染率。
通过筛查1990年11月至1993年8月期间在五个参与研究的血液中心进行的3,021,342次献血,确定了607份HIV补充检测结果不确定的献血样本。获得同意的献血者被纳入研究,并在献血后4至8周采集样本。随访血清通过EIA和免疫印迹法检测抗HIV-1血清转化情况,并通过型特异性肽分析检测针对HIV-2和HIV-1 O亚型的抗体。通过聚合酶链反应检测随访样本中的外周血单个核细胞和/或血浆中的HIV-1 DNA和/或RNA。还通过将该献血者群体中HIV-1血清转化的发病率乘以血清转化期间EIA反应性和免疫印迹法结果不确定窗口的估计持续时间(8.5天),来估计免疫印迹法结果不确定的献血者中HIV-1的感染率。
补充检测结果不确定的献血者(n = 355)在献血后中位时间38天被纳入研究;其中265名(75%)献血者在抗HIV-1/2 EIA反应性献血后被确定为结果不确定。纳入和未纳入的献血者在人口统计学特征和条带模式分布上相似。所有355名献血者的随访样本在聚合酶链反应中检测HIV-1均为阴性。随访血清在54例(15%)中免疫印迹法检测为阴性,在299例(84%)中免疫印迹法结果不确定。根据制造商包装说明书标准,两份随访血清(0.6%)被解释为免疫印迹法p24和gp41条带和/或gp120/160条带阳性;然而,这两例的索引血清和随访血清的配对检测显示免疫印迹法和EIA反应性相同,聚合酶链反应检测HIV RNA和DNA均为阴性,排除了HIV感染。355名免疫印迹法结果不确定的献血者未感染HIV,这与我们基于发病率的模型分析一致,该分析得出每215份免疫印迹法结果不确定的献血中有1例HIV-1感染(95%可信区间,1/39 - 1/8333)。
当代在HIV补充检测中被分类为结果不确定的献血者很少感染HIV,可以考虑恢复那些随访样本抗HIV-1/2 EIA检测为阴性且免疫印迹法检测为阴性或持续结果不确定的献血者的资格。