J Clin Invest. 2014 Jan;124(1):140-4. doi: 10.1172/JCI70349.
Malaria, which is the result of Plasmodium falciparum infection, is a global health threat that resulted in 655,000 deaths and 216 million clinical cases in 2010 alone. Recent phase 3 trials with malaria vaccine candidate RTS,S/AS01 (RTS,S) in children has demonstrated modest efficacy against clinical and severe malaria. RTS,S targets the pre-erythrocytic phase of the disease and induces high antibody titers against the P. falciparum circumsporozoite protein (CSP) and a moderate CD4(+) T cell response. The individual contribution of these adaptive immune responses to protection from infection remains unknown. Here, we found that prophylactic administration of anti-CSP mAbs derived from an RTS,S-vaccinated recipient fully protected mice with humanized livers from i.v.- and mosquito bite–delivered P. falciparum sporozoite challenge. Titers of anti-CSP that conveyed full protection were within the range observed in human RTS,S vaccine recipients. Increasing anti-CSP titers resulted in a dose-dependent reduction of the liver parasite burden. These data indicate that RTS,S-induced antibodies are protective and provide sterilizing immunity against P. falciparum infection when reaching or exceeding a critical plasma concentration.
疟疾是由疟原虫感染引起的,是一种全球性的健康威胁,仅在 2010 年就导致了 65.5 万人死亡和 2.16 亿例临床病例。最近在儿童中进行的疟疾疫苗候选物 RTS,S/AS01(RTS,S)的 3 期临床试验显示,该疫苗对临床和严重疟疾具有一定的疗效。RTS,S 针对疾病的红细胞前期,并诱导针对疟原虫环子孢子蛋白(CSP)的高抗体滴度和适度的 CD4(+) T 细胞反应。这些适应性免疫反应对预防感染的个体贡献尚不清楚。在这里,我们发现,来自接种 RTS,S 的受者的抗-CSP mAb 的预防性给药完全保护了具有人源化肝脏的小鼠免受静脉内和蚊虫叮咬传播的疟原虫孢子挑战。赋予完全保护的抗-CSP 滴度在人类 RTS,S 疫苗接种者中观察到的范围内。抗-CSP 滴度的增加导致肝寄生虫负担呈剂量依赖性降低。这些数据表明,RTS,S 诱导的抗体具有保护作用,并在达到或超过临界血浆浓度时提供针对疟原虫感染的杀菌性免疫。