Bousema J T, Drakeley C J, Kihonda J, Hendriks J C M, Akim N I J, Roeffen W, Sauerwein R W
Department of Medical Microbiology, University Medical Centre, Nijmegen, The Netherlands.
Parasite Immunol. 2007 Jun;29(6):309-17. doi: 10.1111/j.1365-3024.2007.00948.x.
Next to children, adults form a substantial part of the infectious reservoir that is responsible for the spread of malaria. In this longitudinal study, we determined sexual stage immune responses to Plasmodium falciparum and infectiousness to mosquitoes in adults from an area with intense malaria transmission. A cohort of 43 Tanzanian adults was followed for 18 months. Parasitological data were collected monthly; serum once every three months. Antibody prevalences were determined for sexual stage antigens Pfs230 and Pfs48/45 and circumsporozoite protein (NANP5)(n = 199). Functional transmission reducing activity (TRA) was assessed by standard membrane feeding assay (SMFA; n = 85). Cumulative parasite prevalence was 67.4% (29/43) for asexual stages and 34.9% (15/43) for gametocytes. Enrolment antibody prevalence was 95.3% (41/43) for NANP5, 18.9% (7/37) for Pfs230 and 7% (3/43) for Pfs48/45 epitope 3. TRA > 50% reduction was seen in 48.2% (41/85) and TRA > 90% reduction in 4.7% (4/85) of the samples. Our findings of low and inconsistent sexual stage immune responses are likely to be the result of a low exposure to gametocytes in this older age group. This may in turn be caused by effective asexual stage immunity. We conclude that the infectivity of older individuals is less likely to be affected by sexual stage immunity.
除儿童外,成年人构成了疟疾传播感染源的很大一部分。在这项纵向研究中,我们确定了来自疟疾高传播地区成年人对恶性疟原虫的性阶段免疫反应以及对蚊子的传染性。对43名坦桑尼亚成年人组成的队列进行了为期18个月的跟踪研究。每月收集寄生虫学数据;每三个月收集一次血清。测定了性阶段抗原Pfs230和Pfs48/45以及环子孢子蛋白(NANP5)的抗体流行率(n = 199)。通过标准膜饲法(SMFA;n = 85)评估功能性传播减少活性(TRA)。无性阶段的累积寄生虫流行率为67.4%(29/43),配子体为34.9%(15/43)。入组时NANP5的抗体流行率为95.3%(41/43),Pfs230为18.9%(7/37),Pfs48/45表位3为7%(3/43)。48.2%(41/85)的样本TRA降低>50%,4.7%(4/85)的样本TRA降低>90%。我们关于性阶段免疫反应较低且不一致的研究结果可能是由于该老年人群体中配子体暴露较少。这反过来可能是由有效的无性阶段免疫引起的。我们得出结论,老年人的传染性不太可能受到性阶段免疫的影响。