KEMRI-Wellcome Trust Collaborative Programme, P.O. Box 230, Kilifi, 80108, Kenya.
Institute of Immunology, Center for Infection Medicine, Freie Universtät Berlin, 14163, Berlin, Germany.
Malar J. 2021 Dec 2;20(1):452. doi: 10.1186/s12936-021-03961-2.
RTS,S/AS01, the leading malaria vaccine has been recommended by the WHO for widespread immunization of children at risk. RTS,S/AS01-induced anti-CSP IgG antibodies are associated with the vaccine efficacy. Here, the long-term kinetics of RTS,S/AS01-induced antibodies was investigated.
150 participants were randomly selected from the 447 children who participated in the RTS,S/AS01 phase IIb clinical trial in 2007 from Kilifi-Kenya. Cumulatively, the retrospective follow-up period was 93 months with annual plasma samples collection. The levels of anti-CSP IgM, total IgG, IgG1, IgG2, IgG3, and IgG4 antibodies were then determined using an enzyme-linked immunosorbent assay.
RTS,S/AS01 induced high levels of anti-CSP IgG antibodies which exhibited a rapid waning over 6.5 months post-vaccination, followed by a slower decay over the subsequent years. RTS,S/AS01-induced anti-CSP IgG antibodies remained elevated above the control group levels throughout the 7 years follow-up period. The anti-CSP IgG antibodies were mostly IgG1, IgG3, IgG2, and to a lesser extent IgG4. IgG2 predominated in later timepoints. RTS,S/AS01 also induced high levels of anti-CSP IgM antibodies which increased above the control group levels by month 3. The controls exhibited increasing levels of the anti-CSP IgM antibodies which caught up with the RTS,S/AS01 vaccinees levels by month 21. In contrast, there were no measurable anti-CSP IgG antibodies among the controls.
RTS,S/AS01-induced anti-CSP IgG antibodies kinetics are consistent with long-lived but waning vaccine efficacy. Natural exposure induces anti-CSP IgM antibodies in children, which increases with age, but does not induce substantial levels of anti-CSP IgG antibodies.
RTS,S/AS01 是一种领先的疟疾疫苗,已被世界卫生组织推荐用于广泛免疫有风险的儿童。RTS,S/AS01 诱导的抗 CSP IgG 抗体与疫苗效力相关。本研究旨在探究 RTS,S/AS01 诱导的抗体的长期动力学。
从 2007 年肯尼亚基利菲的 RTS,S/AS01 二期临床试验的 447 名儿童中随机选择 150 名参与者。回顾性随访期累计 93 个月,每年采集血浆样本。采用酶联免疫吸附试验测定抗 CSP IgM、总 IgG、IgG1、IgG2、IgG3 和 IgG4 抗体水平。
RTS,S/AS01 诱导高水平的抗 CSP IgG 抗体,接种后 6.5 个月迅速下降,随后几年缓慢下降。在 7 年的随访期间,RTS,S/AS01 诱导的抗 CSP IgG 抗体一直高于对照组水平。抗 CSP IgG 抗体主要为 IgG1、IgG3、IgG2,其次为 IgG4。IgG2 在后期占主导地位。RTS,S/AS01 还诱导高水平的抗 CSP IgM 抗体,在第 3 个月时高于对照组水平。对照组的抗 CSP IgM 抗体水平逐渐升高,在第 21 个月时与 RTS,S/AS01 疫苗组水平相当。相比之下,对照组中没有可检测到的抗 CSP IgG 抗体。
RTS,S/AS01 诱导的抗 CSP IgG 抗体动力学与长期但减弱的疫苗效力一致。自然暴露会使儿童体内产生抗 CSP IgM 抗体,且随年龄增长而增加,但不会诱导大量的抗 CSP IgG 抗体。