Burbelo Peter D, Leahy Hannah P, Groot Sandra, Bishop Lisa R, Miley Wendell, Iadarola Michael J, Whitby Denise, Kovacs Joseph A
Neurobiology and Pain Therapeutics Section, Laboratory of Sensory Biology, National Institute of Dental and Craniofacial Research, Bethesda, Maryland 20892-44101, USA.
Clin Vaccine Immunol. 2009 May;16(5):621-7. doi: 10.1128/CVI.00474-08. Epub 2009 Mar 4.
Improved diagnostic reagents and testing are currently needed for the serological detection of human herpesvirus 8 (HHV-8) infections. We evaluated the luciferase immunoprecipitation systems (LIPS) for profiling antibody responses to a panel of HHV-8 proteins for diagnosis of Kaposi sarcoma (KS)-infected individuals. Using a pilot serum set, LIPS detected robust antibody responses to several known antigens, and a screen of 14 additional HHV-8 proteins identified v-cyclin as a potentially new diagnostic antigen. In evaluating a training-serum set, a four-antigen panel (K8.1, v-cyclin, ORF65, and a LANA fragment) was found to provide sufficient information for diagnosis. Analysis of a validation serum set using the combined results from these four separate antigen tests showed 100% sensitivity and 100% specificity. Furthermore, a LIPS format using a mixture of the four antigens, which simplifies data collection and analysis, closely matched the diagnostic performance of the combined separate tests (R = 0.95). This four-antigen mixture format analyzed with the validation serum set also showed 100% sensitivity and 100% specificity but was not statistically different from two separate enzyme-linked immunosorbent assays (94% sensitivity and 100% specificity) using baculovirus-produced LANA and bacterially produced K8.1. Heat map analysis of KS patient antibody titers revealed marked heterogeneity in humoral responses to this four-antigen panel. Overall, the LIPS assay showed 97% sensitivity, and positive anti-v-cyclin antibodies were detected in approximately 75% of the KS sera. These results suggest that LIPS screening using an antigen mixture is a sensitive and high-throughput method for serological screening of HHV-8 infection in individuals with KS.
目前,人类疱疹病毒8型(HHV - 8)感染的血清学检测需要改进诊断试剂和检测方法。我们评估了荧光素酶免疫沉淀系统(LIPS),以分析针对一组HHV - 8蛋白的抗体反应,用于诊断卡波西肉瘤(KS)感染个体。使用一组试点血清,LIPS检测到对几种已知抗原的强烈抗体反应,对另外14种HHV - 8蛋白的筛选确定v - 细胞周期蛋白为一种潜在的新诊断抗原。在评估一组训练血清时,发现一个四抗原组合(K8.1、v - 细胞周期蛋白、ORF65和一个LANA片段)可为诊断提供足够信息。使用这四项单独抗原检测的综合结果对一组验证血清进行分析,显示敏感性为100%,特异性为100%。此外,使用四种抗原混合物的LIPS形式简化了数据收集和分析,其诊断性能与单独检测的组合结果密切匹配(R = 0.95)。用验证血清组分析的这种四抗原混合物形式也显示敏感性为100%,特异性为100%,但与使用杆状病毒产生的LANA和细菌产生的K8.1的两种单独酶联免疫吸附测定(敏感性94%,特异性100%)在统计学上无差异。对KS患者抗体滴度的热图分析显示,对该四抗原组合的体液反应存在明显异质性。总体而言,LIPS检测显示敏感性为97%,约75%的KS血清中检测到抗v - 细胞周期蛋白阳性抗体。这些结果表明,使用抗原混合物的LIPS筛选是一种用于对KS个体进行HHV - 8感染血清学筛选的灵敏且高通量的方法。