Viral Technology Laboratory, Advanced Technology Program, SAIC-Frederick, Inc., NCI-Frederick, Frederick, MD 21702, United States.
J Immunol Methods. 2010 Apr 30;356(1-2):39-46. doi: 10.1016/j.jim.2010.02.015. Epub 2010 Mar 4.
Detection of antibodies to Kaposi's sarcoma-associated herpesvirus (KSHV or Human herpesvirus 8) is a topic of ongoing controversy. KSHV expresses multiple antigens and host responses are highly variable. We have previously described an algorithm for determining KSHV infection based on K8.1 ELISA and LANA immunofluorescence assay (IFA). Here we describe the development of a recombinant ELISA for LANA and an improved testing strategy using ELISAs for LANA and K8.1. We assessed mammalian and baculovirus expression systems for the production of full-length recombinant LANA. We evaluated the performance of LANA ELISAs using human serum samples from several sources including blood donors and clinical patients diagnosed with Kaposi's sarcoma and compared them to LANA IFA. Both LANA ELISAs exhibited comparable sensitivity and specificity to LANA IFA but showed considerably greater reliability. The LANA ELISA can thus be used in conjunction with the previously described K8.1 ELISA to enable the highly sensitive and specific detection of antibodies to KSHV. Use of this testing strategy will provide a more accurate and reliable diagnostic assessment of KSHV status.
检测卡波济肉瘤相关疱疹病毒(KSHV 或人类疱疹病毒 8)的抗体一直存在争议。KSHV 表达多种抗原,宿主反应高度可变。我们之前描述了一种基于 K8.1 ELISA 和 LANA 免疫荧光检测(IFA)来确定 KSHV 感染的算法。在此,我们描述了一种用于 LANA 的重组 ELISA 的开发和使用 LANA 和 K8.1 ELISA 的改进检测策略。我们评估了哺乳动物和杆状病毒表达系统生产全长重组 LANA 的性能。我们使用来自多个来源的人血清样本评估了 LANA ELISA 的性能,包括献血者和临床诊断为卡波济肉瘤的患者,并将其与 LANA IFA 进行了比较。两种 LANA ELISA 与 LANA IFA 相比,均表现出相当的敏感性和特异性,但可靠性更高。因此,该 LANA ELISA 可以与之前描述的 K8.1 ELISA 一起使用,以实现对 KSHV 抗体的高度敏感和特异性检测。这种检测策略的使用将为 KSHV 状态提供更准确和可靠的诊断评估。