Clearance of circulating Epstein-Barr virus DNA in children with acute malaria after antimalaria treatment

被引:52
作者
Donati, D
Espmark, E
Kironde, F
Mbidde, EK
Kamya, M
Lundkvist, Å
Wahlgren, M
Bejarano, MT
Falk, KI
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Ctr Infect Med, S-14186 Huddinge, Sweden
[2] Karolinska Inst, Swedish Inst Infect Dis Control, Stockholm, Sweden
[3] Karolinska Inst, Microbiol & Tumor Biol Ctr, Stockholm, Sweden
[4] Makerere Univ, Dept Biochem, Kampala, Uganda
[5] Makerere Univ, Fac Med, Kampala, Uganda
[6] Ugandan Canc Inst, Kampala, Uganda
关键词
D O I
10.1086/500839
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Children living in malaria-endemic regions have a high incidence of Burkitt lymphoma ( BL), the etiology of which involves Plasmodium falciparum malaria and Epstein-Barr virus (EBV) infections. In the present study, we compared EBV DNA loads in plasma and saliva samples from Ugandan children with acute malaria (M+) at the time of diagnosis and 14 days after antimalaria treatment, children without malaria ( M-), and children with BL. EBV DNA was detected, by real-time polymerase chain reaction, in 31% of the plasma and in 79% of the saliva samples from children in the M+ group. Antimalaria treatment led to clearance of plasma viral load in 85% of the cases but did not affect the levels in saliva. There was a significant difference in plasma EBV loads across the groups. The lowest levels were detected in samples from the M- group, increased levels were detected in samples from the M+ group, and levels reached the highest values in samples from children with BL. The same trend was evident in the frequency and levels of anti-BZLF1 antibodies, which is indicative of viral reactivation. In the M+ group, the positive plasma samples clustered around 7-9 years of age, the peak incidence of BL. The clearance of circulating EBV after antimalaria treatment suggests a direct relationship between active malaria infection and viral reactivation.
引用
收藏
页码:971 / 977
页数:7
相关论文
共 37 条
[31]   Amodiaquine, sulfadoxine/pyrimethamine, and combination therapy for treatment of uncomplicated falciparum malaria in Kampala, Uganda: a randomised trial [J].
Staedke, SG ;
Kamya, MR ;
Dorsey, G ;
Gasasira, A ;
Ndeezi, G ;
Charlebois, ED ;
Rosenthal, PJ .
LANCET, 2001, 358 (9279) :368-374
[32]   Toward standardization of Epstein-Barr virus DNA load monitoring: Unfractionated whole blood as preferred clinical specimen [J].
Stevens, SJC ;
Pronk, I ;
Middeldorp, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (04) :1211-1216
[34]  
Takeda T, 2000, ARTHRITIS RHEUM, V43, P1218, DOI 10.1002/1529-0131(200006)43:6<1218::AID-ANR4>3.0.CO
[35]  
2-2
[36]   T-CELL CONTROL OF EPSTEIN-BARR VIRUS-INFECTED B-CELLS IS LOST DURING P-FALCIPARUM MALARIA [J].
WHITTLE, HC ;
BROWN, J ;
MARSH, K ;
GREENWOOD, BM ;
SEIDELIN, P ;
TIGHE, H ;
WEDDERBURN, L .
NATURE, 1984, 312 (5993) :449-450
[37]  
WHITTLE HC, 1990, CLIN EXP IMMUNOL, V80, P213, DOI 10.1111/j.1365-2249.1990.tb05236.x