Abstract
BackgroundMalaria transmission-blocking vaccines (TBVs) could help break the cycle of malaria transmission by conferring community rather than individual protection. When introducing new intervention strategies, uptake is dependent on acceptability, not just efficacy. In this exploratory study on acceptability of TBVs in Sierra Leone, it was hypothesized that TBVs would be largely acceptable to adults and health workers in areas with relatively few ongoing malaria interventions, and that (i) knowledge of malaria and vaccines, (ii) health behaviours associated with malaria and vaccines, and (iii) attitudes towards different vaccines types could lead to greater TBV acceptability.MethodsThis study used a mixed methods approach in Bo, Sierra Leone, to understand community knowledge, attitudes, and practices related to malaria and vaccination in general. This included: (i) a population-based cross-sectional survey (n=615 adults), (ii) 6 focus group discussions with parents, and (iii) 20 key informant interviews. The concept of a TBV was explained to participants before they were asked about their willingness to accept this vaccine modality as part of an integrated malaria elimination programme.ResultsThis study found that most adults would be willing to receive a TBV vaccine. Respondents noted mostly positive past experiences with adult and childhood vaccinations for other infectious diseases and high levels of engagement in other malaria prevention behaviors such as bed nets. Perceived barriers to TBV acceptance were largely focused on general community-level distribution of a vaccine, including personal fears of vaccination and possible costs. After an explanation of the TBV mechanism, nearly all focus group and interview participants believed that community members would accept the vaccine as part of an integrated malaria control approach. Both parents and health workers offered insight on how to successfully roll-out a future TBV vaccination programme.ConclusionsThe willingness of community members in Bo, Sierra Leone to accept a TBV as part of an integrated anti-malarial strategy suggests that the atypical mechanism of TBV action might not be an obstacle to future clinical trials. This study’s findings suggests that perceived general barriers to vaccination implementation, such as perceived personal fears and vaccine cost, must be addressed in future clinical and implementation research studies.
Highlights
Malaria transmission-blocking vaccines (TBVs) could help break the cycle of malaria transmission by conferring community rather than individual protection
A malaria transmission-blocking vaccine (TBV) targeting Anopheline mosquito midgut-specific alanyl aminopeptidase N (AnAPN1), a highly conserved luminal midgut surface glycoprotein involved in blood meal digestion, has recently completed a process development study in anticipation for subsequent manufacture for a first-in-human clinical trial [13,14,15]
It was hypothesized that knowledge of malaria transmission and engagement in malaria- and vaccine-related health behaviours would be associated with increased acceptability of a TBV
Summary
Malaria transmission-blocking vaccines (TBVs) could help break the cycle of malaria transmission by conferring community rather than individual protection. Phase 3 trials for the most advanced vaccine candidate (RTS,S/AS01 vaccine), which was given a positive scientific opinion in 2015 by the European Medicines Agency for the prevention of clinical malaria caused by Plasmodium falciparum in children, showed that four doses in children 5–17 years provided 36% protection over 4 years [2]. These modest results highlight the need for malaria elimination to be based on an integrated approach, aligned with local epidemiology, mosquito dynamics, and social and health system realities. These TBVs work to inhibit stages of parasite development within the mosquito, but they target sexual stages of Plasmodium rather than the mosquito midgut, as with AnAPN1 [12]
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