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方法学对科特迪瓦艾滋病毒-1/艾滋病毒-2双重感染检测的影响。

Effect of methodology on detection of HIV-1/HIV-2 dual infections in Côte d'Ivoire.

作者信息

Peeters M, Fransen K, Gershy-Damet G M, Willems B, Koffi K, Coulibaly M, Piot P, Van der Groen G

机构信息

Department of Infection and Immunity, Institute of Tropical Medicine, Antwerp, Belgium.

出版信息

J Virol Methods. 1994 Jun;48(1):23-30. doi: 10.1016/0166-0934(94)90085-x.

Abstract

Dual seroreactivity to the human immunodeficiency virus (HIV) types 1 and 2 is common in Côte d'Ivoire. To assess whether dual infection is the reason for dual seroreactivity, different methods for detection of HIV-1 and HIV-2 viruses were compared. PCR on primary uncultured lymphocytes of 56 dually seropositive samples revealed the presence of both HIV-1 and HIV-2 proviral DNA in 23 (41%) cases. In 7 other dual seropositive persons, PCR was carried out on the primary lymphocytes as well as on lymphocytes after 3 and 6 weeks of cocultivation. More cultures, 5/7 (71%), were positive for both viruses at 3 weeks compared to 0/7 at 6 weeks post cultivation. Moreover, 2 out of 3 samples, where only HIV-1 was detected in uncultured cells, were positive for both viruses after 3 weeks of cultivation. These data indicate that the sensitivity of HIV-2 detection can be increased by stimulation of patients' lymphocytes. A higher number of dual seropositive individuals (10/23 (48%)) had antibodies able to neutralize simultaneously both HIV-1 and HIV-2 prototype viruses than did HIV-1 antibody-positive sera (5/21 (24%)) or HIV-2 antibody positive sera (3/18 (17%)). The prevalence of dual seropositives being infected with both viruses is highly dependent on the method used to detect infection. There is a need to standardize virological markers in order to gain a better insight into the relative proportions of HIV-1, HIV-2 and HIV-1/HIV-2 dually infected persons.

摘要

在科特迪瓦,对1型和2型人类免疫缺陷病毒(HIV)的双重血清反应性很常见。为了评估双重感染是否是双重血清反应性的原因,比较了检测HIV-1和HIV-2病毒的不同方法。对56份双重血清阳性样本的原代未培养淋巴细胞进行PCR检测,结果显示23例(41%)同时存在HIV-1和HIV-2前病毒DNA。在另外7名双重血清阳性者中,对原代淋巴细胞以及共培养3周和6周后的淋巴细胞进行了PCR检测。与培养6周后0/7的情况相比,更多的培养物(5/7,71%)在3周时对两种病毒均呈阳性。此外,在未培养细胞中仅检测到HIV-1的3份样本中,有2份在培养3周后对两种病毒均呈阳性。这些数据表明,通过刺激患者的淋巴细胞可以提高HIV-2检测的敏感性。与HIV-1抗体阳性血清(5/21,24%)或HIV-2抗体阳性血清(3/18,17%)相比,更多双重血清阳性个体(10/23,48%)的抗体能够同时中和HIV-1和HIV-2原型病毒。双重血清阳性者同时感染两种病毒的患病率高度依赖于用于检测感染的方法。需要对病毒学标志物进行标准化,以便更好地了解HIV-1、HIV-2和HIV-1/HIV-2双重感染人群的相对比例。

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