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Review
. 2018 May 11:9:1043.
doi: 10.3389/fimmu.2018.01043. eCollection 2018.

Peptide Vaccines for Leishmaniasis

Affiliations
Review

Peptide Vaccines for Leishmaniasis

Rory C F De Brito et al. Front Immunol. .

Abstract

Due to an increase in the incidence of leishmaniases worldwide, the development of new strategies such as prophylactic vaccines to prevent infection and decrease the disease have become a high priority. Classic vaccines against leishmaniases were based on live or attenuated parasites or their subunits. Nevertheless, the use of whole parasite or their subunits for vaccine production has numerous disadvantages. Therefore, the use of Leishmania peptides to design more specific vaccines against leishmaniases seems promising. Moreover, peptides have several benefits in comparison with other kinds of antigens, for instance, good stability, absence of potentially damaging materials, antigen low complexity, and low-cost to scale up. By contrast, peptides are poor immunogenic alone, and they need to be delivered correctly. In this context, several approaches described in this review are useful to solve these drawbacks. Approaches, such as, peptides in combination with potent adjuvants, cellular vaccinations, adenovirus, polyepitopes, or DNA vaccines have been used to develop peptide-based vaccines. Recent advancements in peptide vaccine design, chimeric, or polypeptide vaccines and nanovaccines based on particles attached or formulated with antigenic components or peptides have been increasingly employed to drive a specific immune response. In this review, we briefly summarize the old, current, and future stands on peptide-based vaccines, describing the disadvantages and benefits associated with them. We also propose possible approaches to overcome the related weaknesses of synthetic vaccines and suggest future guidelines for their development.

Keywords: chimeric vaccine; peptide-based vaccines; polypeptide vaccines; tegumentary leishmaniases; visceral leishmaniasis.

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Figures

Figure 1
Figure 1
Flowchart of various approaches used to identify promising immunogenic peptides of different Leishmania species.
Figure 2
Figure 2
Overview of approaches that can be used for peptide-based vaccines development against cutaneous and visceral leishmaniasis.

References

    1. Davies CR, Kaye P, Croft SL, Sundar S. Leishmaniasis: new approaches to disease control. BMJ (2003) 326(7385):377–82.10.1136/bmj.326.7385.377 - DOI - PMC - PubMed
    1. Alvar J, Velez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One (2012) 7(5):e35671.10.1371/journal.pone.0035671 - DOI - PMC - PubMed
    1. Global Burden of Disease Study 2013 Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: a systematic analysis for the global burden of disease study 2013. Lancet (2015) 386(9995):743–800.10.1016/S0140-6736(15)60692-4 - DOI - PMC - PubMed
    1. Desjeux P. Leishmaniasis: current situation and new perspectives. Comp Immunol Microbiol Infect Dis (2004) 27(5):305–18.10.1016/j.cimid.2004.03.004 - DOI - PubMed
    1. Maia-Elkhoury AN, Alves WA, Sousa-Gomes ML, Sena JM, Luna EA. Visceral leishmaniasis in Brazil: trends and challenges. Cad Saude Publica (2008) 24(12):2941–7.10.1590/S0102-311X2008001200024 - DOI - PubMed

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