Lack of association between maternal antibody and protection of African infants from malaria infection

被引:78
作者
Riley, EM
Wagner, GE
Ofori, MF
Wheeler, JG
Akanmori, BD
Tetteh, K
McGuinness, D
Bennett, S
Nkrumah, FK
Anders, RF
Koram, KA
机构
[1] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
[2] Univ Edinburgh, Div Biol Sci, Inst Cell Anim & Populat Biol, Edinburgh EH9 3JT, Midlothian, Scotland
[3] Univ Ghana, Noguchi Mem Inst Med Res, Legon, Ghana
[4] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
基金
英国惠康基金;
关键词
D O I
10.1128/IAI.68.10.5856-5863.2000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Maternally derived antibodies are believed to protect infants against infection, but there is little direct evidence for a protective role of passively acquired antibodies against malaria. A longitudinal study of malaria infection in 143 infants was conducted in a region of southern Ghana where Plasmodium falciparum is endemic. Infants born in the high-transmission season were less likely to become infected in the first 20 weeks of life than children born in the low-transmission season. Plasma, obtained at birth, was tested for immunoglobulin G (IgG) and IgG subclasses to P. falciparum schizonts and recombinant circumsporozoite antigen, MSP-1(19), MSP-2, AMA-I, and Pf155 (also called ring-infected erytrocyte surface antigen). Antibody levels at birth were not associated with resistance to malaria infection. On the contrary, antibodies at birth were positively associated with infection, indicating that high levels of maternally derived antibodies represent a marker for intensity of exposure to malaria infection in infants, However, all five children who experienced high-density infections (>100 parasites/mu l of blood) were seronegative for MSP-1(19) at the time of infection.
引用
收藏
页码:5856 / 5863
页数:8
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