Increases in Levels of Schistosome-Specific Immunoglobulin E and CD23+ B Cells in a Cohort of Kenyan Children Undergoing Repeated Treatment and Reinfection with Schistosoma mansoni
Increases in Levels of Schistosome-Specific Immunoglobulin E and CD23+ B Cells in a Cohort of Kenyan Children Undergoing Repeated Treatment and Reinfection with Schistosoma mansoni
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DOI:
10.1086/653828
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发表时间:
2010-08-15
影响因子:
6.4
通讯作者:
Colley, Daniel G.
中科院分区:
文献类型:
--
作者:
Black, Carla L.;Muok, Erick M. O.;Colley, Daniel G.
Background. Age prevalence curves for areas in which schistosomiasis is endemic suggest that humans develop partial immunity to reinfection beginning in early adolescence. We conducted a 2-year longitudinal study to determine whether children infected with Schistosoma mansoni develop protection-related immune responses after treatment with praziquantel and whether the development of these immune responses is accelerated by frequent treatment after reinfection.Methods. Children (8-10 years old) were tested for S. mansoni every 4 months and treated with praziquantel when positive (arm A; n=68) or were tested and treated at the end of the 2-year follow-up period (arm B; n=49).Results. Children in arm A who remained free of infection during follow-up had significantly higher baseline levels of schistosome-specific immunoglobulin E (IgE) than did children with >= 2 repeat diagnoses of S. mansoni infection. Children with >= 2 repeat diagnoses of S. mansoni infection had significantly increased levels of anti-schistosome IgE and CD23(+) B cells after receiving >= 3 praziquantel treatments over the course of follow-up. No increase in either parameter was seen in children who received only the baseline praziquantel treatment.Conclusions. B cell activation and anti-schistosome IgE are associated with resistance to S. mansoni in children, and these immunological parameters can be increased by multiple rounds of infections and praziquantel-induced cures.