Duration of vaccine efficacy against malaria: 5th year of follow-up in children vaccinated with RTS,S/AS02 in Mozambique

被引:23
作者
Campo, Joseph J. [1 ,2 ]
Sacarlal, Jahit [2 ,3 ]
Aponte, John J. [1 ,2 ]
Aide, Pedro [1 ,4 ]
Nhabomba, Augusto J. [2 ]
Dobano, Carlota [1 ,2 ]
Alonso, Pedro L. [1 ,2 ]
机构
[1] Univ Barcelona, Hosp Clin, Barcelona Ctr Int Hlth Res CRESIB, Barcelona, Spain
[2] Ctr Invest Saude Manhica, Manhica, Mozambique
[3] Univ Eduardo Mondlane, Fac Med, Maputo, Mozambique
[4] Minist Saude, Inst Nacl Saude, Maputo, Mozambique
关键词
Plasmodium falciparum; RTS; S; Vaccine; Prevalence; Immunogenicity; PLASMODIUM-FALCIPARUM INFECTION; CIRCUMSPOROZOITE PROTEIN; DOUBLE-BLIND; SAFETY; PROTECTION; TRIAL; IMMUNOGENICITY; INFANTS; DISEASE;
D O I
10.1016/j.vaccine.2014.02.042
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A primary concern for the RTS,S malaria vaccine candidate is duration of protection. The ongoing Phase III trial reported evidence of waning efficacy within the first year following vaccination. Multiple Phase IIb trials demonstrated early waning of efficacy. The longest duration of protection for RTS,S recorded to date was in a trial of a cohort of 1605 Mozambican children age 1-4 yr at the time of immunization (Cl), which showed an overall efficacy against clinical malaria of 30.5% over 43 subsequent months of surveillance. A significant reduction in parasite prevalence in RTS,S vaccinees indicated that the vaccine continued to protect at the end of this period. Although follow-up for recording incident cases of clinical malaria was stopped at 45 months, we were interested in evidence of further durability of protection, and revisited the cohort at 63 months, recording the secondary trial endpoint, prevalence of asexual Plasmodium falciparum parasitemia, in the RTS,S and comparator vaccine groups as a proxy for efficacy. As a comparator, we also visited the contemporaneous cohort of 417 children (C2), which showed waning efficacy after 6 months of follow-up. We also assessed anti-circumsporozoite antibody titers. These results were compared with those of other Phase lib trials. Prevalence of parasitemia was not significantly lower in the RTS,S/AS02 group compared to comparator groups in Cl (57 [119%] Vs 62 [128%]; p = 0.696) or C2 (30 [226%] Vs 35 [276%]; p = 0.391), despite elevated antibody titers, suggesting that protection did not extend to 5 years after vaccination. This is in contrast to the earlier assessment of parasitemia in Cl, where a 34% lower prevalence of parasitemia was observed in the RTS,S/AS02 group at month 45. Comparison with other Phase II trials highlights a complex relationship between efficacy, age and transmission intensity. RTS,S/AS02 provided partial protection from clinical malaria for at least 3.5 years in Cl. Duration of protection may depend on environmental circumstances, such as changing malaria transmission, and special attention should be given in the Phase III trial to identifying factors that modify longevity of protection. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2209 / 2216
页数:8
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