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. 2012 Jan;6(1):e1488.
doi: 10.1371/journal.pntd.0001488. Epub 2012 Jan 31.

Melioidosis vaccines: a systematic review and appraisal of the potential to exploit biodefense vaccines for public health purposes

Affiliations

Melioidosis vaccines: a systematic review and appraisal of the potential to exploit biodefense vaccines for public health purposes

Sharon J Peacock et al. PLoS Negl Trop Dis. 2012 Jan.

Erratum in

  • PLoS Negl Trop Dis. 2013 Feb;7(2). doi:10.1371/annotation/20664ec9-17e4-4ba6-8c65-481a70a5c4ad

Abstract

Background: Burkholderia pseudomallei is a Category B select agent and the cause of melioidosis. Research funding for vaccine development has largely considered protection within the biothreat context, but the resulting vaccines could be applicable to populations who are at risk of naturally acquired melioidosis. Here, we discuss target populations for vaccination, consider the cost-benefit of different vaccination strategies and review potential vaccine candidates.

Methods and findings: Melioidosis is highly endemic in Thailand and northern Australia, where a biodefense vaccine might be adopted for public health purposes. A cost-effectiveness analysis model was developed, which showed that a vaccine could be a cost-effective intervention in Thailand, particularly if used in high-risk populations such as diabetics. Cost-effectiveness was observed in a model in which only partial immunity was assumed. The review systematically summarized all melioidosis vaccine candidates and studies in animal models that had evaluated their protectiveness. Possible candidates included live attenuated, whole cell killed, sub-unit, plasmid DNA and dendritic cell vaccines. Live attenuated vaccines were not considered favorably because of possible reversion to virulence and hypothetical risk of latent infection, while the other candidates need further development and evaluation. Melioidosis is acquired by skin inoculation, inhalation and ingestion, but routes of animal inoculation in most published studies to date do not reflect all of this. We found a lack of studies using diabetic models, which will be central to any evaluation of a melioidosis vaccine for natural infection since diabetes is the most important risk factor.

Conclusion: Vaccines could represent one strand of a public health initiative to reduce the global incidence of melioidosis.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. The Markov model used to assess costs and health gains for a melioidosis vaccine.
M denotes a Markov node where individuals can transition into the subsequent states in each monthly cycle. In each cycle a susceptible patient can be infected and develop a melioidosis episode, from which they can recover and return to the susceptible state in the next cycle, or die. Patients can also die from natural causes according to their age specific mortality rates.
Figure 2
Figure 2. Cost-effectiveness of melioidosis vaccines as determined by incidence, cost, protective efficacy and protective duration.
It was assumed that policy makers in Thailand were willing to pay 3,000ドル for an additional QALY gained. Areas in blue indicate where the vaccine is considered cost-effective in the Thai context. The protective efficacy (PE) and protective duration (PD) of the vaccine were considered as homogenous for all routes of disease acquisition. Percentage reduction of PE in this figure was considered as a combination of reduction in both disease incidence and mortality rate.
Figure 3
Figure 3. Study flow diagram.

References

    1. Dance DAB. Melioidosis. Curr Opin Infect Dis. 2002;15:127–132. - PubMed
    1. Sarkar-Tyson M, Titball RW. Progress toward development of vaccines against melioidosis: A review. Clin Ther. 2010;32:1437–1445. - PubMed
    1. Currie BJ, Dance DA, Cheng AC. The global distribution of Burkholderia pseudomallei and melioidosis: an update. Trans R Soc Trop Med Hyg. 2008;102(Suppl 1):S1–4. - PubMed
    1. Limmathurotsakul D, Peacock SJ. Melioidosis: a clinical overview. Br Med Bull. 2011;99:125–39. - PubMed
    1. Limmathurotsakul D, Wongratanacheewin S, Teerawattanasook N, Wongsuvan G, Chaisuksant S, et al. Increasing incidence of human melioidosis in Northeast Thailand. Am J Trop Med Hyg. 2010;82:1113–1117. - PMC - PubMed

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