Palumbo P, Skurnick J, Lewis D, Eisenberg M
Department of Pediatrics, University of Medicine and Dentistry, New Jersey Medical School, Newark 07103, USA.
J Acquir Immune Defic Syndr Hum Retrovirol. 1995 Dec 1;10(4):436-40. doi: 10.1097/00042560-199512000-00006.
A cohort of human immunodeficiency virus (HIV)-discordant couples was established to evaluate risk factors associated with heterosexual viral transmission. Polymerase chain reaction (PCR) was utilized to document the HIV-uninfected status among members of discordant heterosexual couples and to rule out immunosilent infection. HIV DNA PCR specific for a gag gene region was performed on peripheral blood mononuclear cell samples from 203 HIV antibody-negative adults who have long-term heterosexual relationships with HIV-infected partners. The results were negative for 200 but consistently positive in three individuals. More extensive evaluation of these three individuals with an additional primer pair specific for the envelope gene, quantitative DNA PCR, multiple additional time points, and variable nucleotide tandem repeat analyses revealed specimen processing problems in two cases but an apparent true positive PCR assay in the third case. This subject remains antibody and PCR negative for a 32-month follow-up period. These results confirm previous studies that document a negligible incidence of occult HIV infection as delineated by PCR in antibody negative heterosexual partners of HIV-infected individuals. Specimen processing errors occur at a low rate (1% in this study) and require careful evaluation. The possibility of transient, aborted infection versus successful infection with a long immunosilent period was observed in a single individual. Definitive resolution of infection status will require long-term evaluation.
建立了一组艾滋病毒(HIV)不一致的异性伴侣队列,以评估与异性间病毒传播相关的危险因素。采用聚合酶链反应(PCR)记录不一致异性伴侣中未感染HIV的成员的状态,并排除免疫沉默感染。对203名与HIV感染伴侣有长期异性关系的HIV抗体阴性成年人的外周血单个核细胞样本进行了针对gag基因区域的HIV DNA PCR检测。结果显示,200人的检测结果为阴性,但有三人持续呈阳性。对这三人进行了更广泛的评估,使用了另一对针对包膜基因的引物、定量DNA PCR、多个额外的时间点以及可变核苷酸串联重复分析,结果显示其中两例存在样本处理问题,但第三例的PCR检测结果明显为真阳性。该受试者在32个月的随访期内抗体和PCR检测均为阴性。这些结果证实了之前的研究,即通过PCR检测,在HIV感染个体的抗体阴性异性伴侣中,隐匿性HIV感染的发生率可忽略不计。样本处理错误的发生率较低(本研究中为1%),需要仔细评估。在一名个体中观察到了短暂的、未成功感染与长期免疫沉默期后成功感染的可能性。感染状态的确切判定需要长期评估。