DNA基因表达研究尼日利亚西南部婴儿和儿童长期治疗疟疾的免疫机制

J. Thornthwaite, A. Olufemi, A. A. Ademola, O. T. Alli
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摘要

疟疾感染在尼日利亚和非洲大部分地区一直是一个非常严重的公共卫生问题。对于药物研究人员来说,开发能够永久治愈疟疾的抗疟疾疗法一直是一项艰巨的任务。在尼日利亚的Osogbo进行了一项新的专有混合配方(TriantimalTM),该配方用于儿童凝胶帽(n = 112)和水溶性,直径为18.51 nm的NutraNanoSphereTM封装TriantimalTM滴剂,用于婴儿(19.9个月±8.7个月,n = 15)。对入选受试者进行疟疾筛查,连续16天使用TriantimalTM治疗,并在第0、5、10、16、30、60和730天采集血清。此外,当收集血清时,其中31名儿童捐赠了褐色皮毛样本用于基因表达研究。60 d和730 d患儿的寄生虫阳性率分别为90.2%和85.1%。60天时,93.3%的婴儿无寄生虫。这些数据首次显示了在尼日利亚治愈疟疾的真正可能性。一次性、低剂量、长期治疗和天然成分的协同作用,最大限度地减少了寄生虫产生耐药性的能力,同时增强了免疫系统。事实上,DNA扩增数据表明,体液免疫、先天免疫和先天防御素免疫的所有方面都参与了对恶性疟原虫的长期免疫,这种免疫可称为一种“体内免疫”。
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DNA Gene Expression to Study Immunologic Mechanisms for the Long-Term Cure of Malaria in Babies and Children in South-Western Nigeria
Malaria infection has been a very serious public health problem in Nigeria and most parts of Africa. Development of antimalarial treatments capable of providing a permanent cure for malaria has been a herculean task for drug researchers. A trial of a novel, proprietary blend formulation (TriantimalTM) in gel caps for children (n = 112) and water-soluble, 18.51 nm diameter, NutraNanoSphereTM encapsulated TriantimalTM drops for babies (19.9 Months ± 8.7 SD, n = 15) was conducted in Osogbo, Nigeria. The enrolled subjects were screened for malaria, treated with TriantimalTM for 16 consecutive days and sera collected on days 0, 5, 10, 16, 30, 60, and 730. Also, 31 of the children donated buffy coat samples for the gene expression studies when sera were collected. The children showed 90.2% parasite-free at 60 days and 85.1% at 730 days. The babies revealed 93.3% parasite-free at 60 days. These data show for the first time a real possibility for a cure of malaria in Nigeria. The one-time, low dose, extended treatment and synergism of the natural components minimize the ability of the parasites to develop resistance, while boosting the immune system. Indeed, the DNA amplification data showed that all aspects of the humoral, innate, and innate defensin immunity are involved in the long-term immunity against P. falciparum in which may be termed a type of “in vivo immunization”.
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