Quantitative proviral DNA and antibody levels in the natural history of HTLV-I infection

被引:102
作者
Manns, A
Miley, WJ
Wilks, RJ
Morgan, OSC
Hanchard, B
Wharfe, G
Cranston, B
Maloney, E
Welles, SL
Blattner, WA
Waters, D
机构
[1] NCI, Viral Epidemiol Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[2] NCI, Frederick Canc Res & Dev Ctr, SAIC, Frederick, MD USA
[3] Univ Maryland, Inst Human Virol, Baltimore, MD 21201 USA
[4] Univ Minnesota, Div Epidemiol, Minneapolis, MN 55455 USA
[5] Univ W Indies, Trop Metab Res Unit, Dept Hematol, Kingston 7, Jamaica
[6] Univ W Indies, Dept Med, Kingston 7, Jamaica
[7] Univ W Indies, Dept Pathol, Kingston 7, Jamaica
关键词
D O I
10.1086/315088
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The pathogenesis of human T-cell lymphotropic virus type I (HTLV-I) in adult T-cell leukemia/lymphoma (ATL) and HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) is poorly understood. We prospectively followed up and evaluated the virologic correlates of infection in transfusion recipients after seroconversion, in asymptomatic carriers, and in ATL and HAM/TSP patients. Proviral DNA levels (copies/10(5) lymphocytes) were determined by real-time automated polymerase chain reaction and antibody titers by endpoint dilution by use of an HTLV-I enzyme-linked immunoassay, In early infection, proviral load was initially elevated (median, 212 copies/10(5) lymphocytes at time 1) and later decreased (median, 99 copies at time 2, and 27 copies at time 3), Corresponding antibody titers were low at time 1 (1 :2154), had significantly increased by time 2 (1 : 12312), and were stable by time 3 (1 :4694), These viral markers were significantly lower in asymptomatic carriers than in HAM/TSP or ATL patients. Therefore, proviral load and antibody titers may be useful as predictive markers of disease among carriers.
引用
收藏
页码:1487 / 1493
页数:7
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