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Antibody responses to Epstein-Barr virus-determined nuclear antigen (EBNA)-1 and EBNA-2 in acute and chronic Epstein-Barr virus infection.

机译:在急性和慢性爱泼斯坦-巴尔病毒感染中,对爱泼斯坦-巴尔病毒确定的核抗原(EBNA)-1和EBNA-2的抗体反应。

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摘要

Five distinct Epstein-Barr virus (EBV)-determined nuclear antigens (EBNA-1 to EBNA-5) were recently identified. Antibody responses to these antigens could conceivably differ, and thus prove of serodiagnostic value, in EBV-associated disease processes. As a first step, murine or human cell lines transfected with appropriate EBV DNA fragments and stably expressing either EBNA-1 or EBNA-2 were used to determine the frequency and time of emergence of antibodies to these two antigens in the course of acute and chronic infectious mononucleosis (IM) and to assess their titers in so-called chronic active EBV infections. Following IM, antibodies to EBNA-2 arose first and, after reaching peak titers, declined again in time to lower persistent or even nondetectable levels. Antibodies to EBNA-1 emerged several weeks or months after anti-EBNA-2 and gradually attained the titers at which they persisted indefinitely. The ratios between the anti-EBNA-1 and anti-EBNA-2 titers therefore were generally well below 1.0 during the first 6-12 months after IM and turned to well above 1.0 during the second year. In clear cases of chronic IM, the inversion of this ratio was delayed or prevented. In the less well-defined chronic EBV infections, low ratios were observed in only some of the patients. Because many of these illnesses were not ushered in by a proven IM and often showed EBV-specific antibody profiles within the normally expected range, a causal role of the virus in these cases remains doubtful.
机译:最近发现了五种不同的由爱泼斯坦-巴尔病毒(EBV)确定的核抗原(EBNA-1至EBNA-5)。可以想象,在与EBV相关的疾病过程中,对这些抗原的抗体反应可能会有所不同,从而证明其具有血清诊断价值。第一步,使用转染有适当EBV DNA片段并稳定表达EBNA-1或EBNA-2的鼠或人细胞系,确定在急性和慢性过程中针对这两种抗原的抗体出现的频率和时间感染性单核细胞增多症(IM)并评估其在所谓的慢性活动性EBV感染中的效价。 IM后,首先出现针对EBNA-2的抗体,并在达到峰值滴度后及时下降,以降低持久性甚至不可检测的水平。 EBNA-1抗体在抗EBNA-2出现几周或几个月后出现,并逐渐达到无限期滴定的效价。因此,在IM后的前6-12个月内,抗EBNA-1和抗EBNA-2效价之间的比率通常远低于1.0,而在第二年则远高于1.0。在明确的慢性IM病例中,该比例的倒置被延迟或阻止。在定义不明确的慢性EBV感染中,仅部分患者观察到较低的比率。由于许多此类疾病不是由经过验证的IM引起的,并且通常显示EBV特异性抗体谱在正常预期范围内,因此在这些情况下病毒的致病作用仍然令人怀疑。

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