Serum IgA antibodies to Epstein-Barr virus (EBV) early lytic antigens are present in primary EBV infection

被引:11
|
作者
Bhaduri-McIntosh, Sumita
Landry, Marie L.
Nikiforow, Sarah
Rotenberg, Marisa
El-Guindy, Ayman
Miller, George
机构
[1] Yale Univ, Sch Med, Div Infect Dis, Dept Pediat, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Lab Med, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2007年 / 195卷 / 04期
关键词
D O I
10.1086/510916
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primary Epstein-Barr virus (EBV) infection is characterized by the presence of IgM antibodies to viral capsid antigen and the absence of antibodies to EB nuclear antigen. Here, using a flow cytometry-based assay, we investigated whether IgA antibodies are a marker for primary infection. Serum IgA antibodies in 15 individuals with primary EBV infection reacted with 15%-55.6% of HH514-16 Burkitt lymphoma cells expressing early lytic antigens (EAs), whereas IgA antibodies in serum samples from 15 healthy EBV-seropositive individuals reacted with 0.02%-2% of cells with EAs (P < .0001). IgA antibodies in primary infection were directed against the Bam Z Epstein-Barr replication activator (ZEBRA) (BZLF1) and diffuse EA (BMRF1) EAs. Thus, IgA antibodies to EBV EAs are produced during primary EBV infection and are likely to be stimulated as a result of lytic EBV replication in mucosal sites. Detection of IgA antibodies to EA may be developed into a diagnostic tool for primary EBV infection.
引用
收藏
页码:483 / 492
页数:10
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