4.8 Article

Parasite Burden and Severity of Malaria in Tanzanian Children

期刊

NEW ENGLAND JOURNAL OF MEDICINE
卷 370, 期 19, 页码 1799-1808

出版社

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1303944

关键词

-

资金

  1. Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH)
  2. NIAID extramural program [R01AI52059]
  3. Fogarty International Center of the NIH [D43 TW005509]
  4. Foundation for the NIH through the Grand Challenges in Global Health Initiative - Bill and Melinda Gates Foundation [1364]

向作者/读者索取更多资源

BackgroundSevere Plasmodium falciparum malaria is a major cause of death in children. The contribution of the parasite burden to the pathogenesis of severe malaria has been controversial. MethodsWe documented P. falciparum infection and disease in Tanzanian children followed from birth for an average of 2 years and for as long as 4 years. ResultsOf the 882 children in our study, 102 had severe malaria, but only 3 had more than two episodes. More than half of first episodes of severe malaria occurred after a second infection. Although parasite levels were higher on average when children had severe rather than mild disease, most children (67 of 102) had high-density infection (>2500 parasites per 200 white cells) with only mild symptoms before severe malaria, after severe malaria, or both. The incidence of severe malaria decreased considerably after infancy, whereas the incidence of high-density infection was similar among all age groups. Infections before and after episodes of severe malaria were associated with similar parasite densities. Nonuse of bed nets, placental malaria at the time of a woman's second or subsequent delivery, high-transmission season, and absence of the sickle cell trait increased severe-malaria risk and parasite density during infections. ConclusionsResistance to severe malaria was not acquired after one or two mild infections. Although the parasite burden was higher on average during episodes of severe malaria, a high parasite burden was often insufficient to cause severe malaria even in children who later were susceptible. The diverging rates of severe disease and high-density infection after infancy, as well as the similar parasite burdens before and after severe malaria, indicate that naturally acquired resistance to severe malaria is not explained by improved control of parasite density. (Funded by the National Institute of Allergy and Infectious Diseases and others.) The pathogenesis of severe malaria due to Plasmodium falciparum remains controversial. In this study conducted over several years and involving 882 Tanzanian children, parasite burden was insufficient to explain the development of severe illness. Although almost 600,000 African children die each year from malaria,(1) most infections in children are mild.(2),(3) Fundamental questions about the pathogenesis of malaria remain unresolved, such as the relative contributions of parasite burden and host inflammation to severe disease.(4) In areas where transmission is stable, severe malaria is unlikely to occur after 5 years of age, presumably as a result of immunity,(5) and mathematical models suggest that protection against noncerebral severe malaria develops after one or two infections.(6) The mechanism of protective immunity is unclear; it might, for example, involve the reduction of parasite density or the blocking of ...

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据