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PerspectiveImmunology

Another Shot at a Malaria Vaccine

Science28 Oct 2011Vol 334, Issue 6055pp. 460-461DOI: 10.1126/science.1213934

Abstract

Malaria, an infectious disease caused by Plasmodium parasites that are transmitted by mosquito bite, has a devastating global impact, causing 300 to 500 million clinical cases and up to 800,000 deaths each year. Vaccine development for malaria is marked by many failures, some encouraging successes, and much hope. Recently, a malaria vaccine candidate (RTS,S/AS01) based on the major surface protein of the transmissible sporozoite form of the parasite advanced into phase three clinical trials in Africa, and preliminary data show 55% efficacy against malaria episodes and 35% efficacy against severe malaria (1). Although it is not yet known how long protection lasts, this vaccine constitutes a milestone for developing a more efficacious vaccine. A highly protective vaccine that prevents malaria infection will also prevent disease and further transmission by the mosquito and, hence, constitutes the potential “magic bullet” in our future armamentarium against malaria. Yet developing such a vaccine has been frustratingly difficult. On page 475 of this issue, Epstein et al. (2) report the results of a clinical trial with an injectable preparation of Plasmodium sporozoites, attenuated by exposure to DNA-damaging irradiation and intended to prevent infection. Their trial results mark an inflection point in malaria vaccine development.
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References and Notes

1
The RTS,S Clinical Trials Partnership, N. Engl. J. Med. 10.1056/NEJMoa1102287 (2011).
2
Epstein J. E., et al., Science 334, 475 (2011); 10.1126/sciene.1211548.
3
Hoffman S. L., et al., J. Infect. Dis. 185, 1155 (2002).
4
Overstreet M. G., Cockburn I. A., Chen Y. C., Zavala F., Immunol. Rev. 225, 272 (2008).
5
Zhang N., Bevan M. J., Immunity 35, 161 (2011).
6
Roestenberg M., et al., N. Engl. J. Med. 361, 468 (2009).
7
Butler N. S., et al., Cell Host Microbe 9, 451 (2011).
8
Seattle Biomedical Research Institute holds patents on the genetically attenuated parasite vaccine design.

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Science
Volume 334Issue 605528 October 2011
Pages: 460 - 461

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Stefan H. I. Kappe
Seattle Biomedical Research Institute, Seattle, WA 98109, USA.
Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Sebastian A. Mikolajczak
Seattle Biomedical Research Institute, Seattle, WA 98109, USA.

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Volume 334|Issue 6055
28 October 2011
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Cited by
  1. A Sporozoite- and Liver Stage-expressed Tryptophan-rich Protein Plays an Auxiliary Role in Plasmodium Liver Stage Development and Is a Potential Vaccine Candidate, Journal of Biological Chemistry, 290, 32, (19496-19511), (2015).https://doi.org/10.1074/jbc.M114.588129
    Crossref
  2. Epidemiological aspects of vivax and falciparum malaria: global spectrum, Asian Pacific Journal of Tropical Disease, 4, (S13-S26), (2014).https://doi.org/10.1016/S2222-1808(14)60410-2
    Crossref
  3. DNA Repair Mechanisms and Their Biological Roles in the Malaria Parasite Plasmodium falciparum, Microbiology and Molecular Biology Reviews, 78, 3, (469-486), (2014).https://doi.org/10.1128/MMBR.00059-13
    Crossref
  4. Genetic engineering of attenuated malaria parasites for vaccination, Current Opinion in Biotechnology, 23, 6, (908-916), (2012).https://doi.org/10.1016/j.copbio.2012.04.003
    Crossref
  5. Malaria vaccine development: persistent challenges, Current Opinion in Immunology, 24, 3, (324-331), (2012).https://doi.org/10.1016/j.coi.2012.03.009
    Crossref
  6. Still Seeking an Effective “One–Two” Malaria Vaccine Punch, Molecular Therapy, 20, 12, (2198-2200), (2012).https://doi.org/10.1038/mt.2012.241
    Crossref
  7. Whole parasite vaccination approaches for prevention of malaria infection, Trends in Immunology, 33, 5, (247-254), (2012).https://doi.org/10.1016/j.it.2012.02.001
    Crossref
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