A Review of Major Patents on Potential Malaria Vaccine Targets

Author:

Mariano Reysla Maria da Silveira1,Gonçalves Ana Alice Maia1ORCID,Oliveira Diana Souza de1,Ribeiro Helen Silva1ORCID,Pereira Diogo Fonseca Soares1,Santos Ingrid Soares1,Lair Daniel Ferreira1,Silva Augusto Ventura da1,Galdino Alexsandro Sobreira2ORCID,Chávez-Fumagalli Miguel Angel3ORCID,Silveira-Lemos Denise da4,Dutra Walderez Ornelas1ORCID,Giunchetti Rodolfo Cordeiro1ORCID

Affiliation:

1. Laboratory of Biology of Cell Interactions, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte CEP 31270-901, MG, Brazil

2. Laboratory of Biotechnology of Microorganisms, Federal University of São João Del-Rei, Divinópolis CEP 35501-296, MG, Brazil

3. Computational Biology and Chemistry Research Group, Vicerrectorado de Investigación, Universidad Católica de Santa María, Urb. San José S/N, Arequipa 04000, Peru

4. Campus Jaraguá, University José of Rosário Vellano, UNIFENAS, Belo Horizonte CEP 31270-901, MG, Brazil

Abstract

Malaria is a parasitic infection that is a great public health concern and is responsible for high mortality rates worldwide. Different strategies have been employed to improve disease control, demonstrating the ineffectiveness of controlling vectors, and parasite resistance to antimalarial drugs requires the development of an effective preventive vaccine. There are countless challenges to the development of such a vaccine directly related to the parasite’s complex life cycle. After more than four decades of basic research and clinical trials, the World Health Organization (WHO) has recommended the pre-erythrocytic Plasmodium falciparum (RTS, S) malaria vaccine for widespread use among children living in malaria-endemic areas. However, there is a consensus that major improvements are needed to develop a vaccine with a greater epidemiological impact in endemic areas. This review discusses novel strategies for malaria vaccine design taking the target stages within the parasite cycle into account. The design of the multi-component vaccine shows considerable potential, especially as it involves transmission-blocking vaccines (TBVs) that eliminate the parasite’s replication towards sporozoite stage parasites during a blood meal of female anopheline mosquitoes. Significant improvements have been made but additional efforts to achieve an efficient vaccine are required to improve control measures. Different strategies have been employed, thus demonstrating the ineffectiveness in controlling vectors, and parasite resistance to antimalarial drugs requires the development of a preventive vaccine. Despite having a vaccine in an advanced stage of development, such as the RTS, S malaria vaccine, the search for an effective vaccine against malaria is far from over. This review discusses novel strategies for malaria vaccine design taking into account the target stages within the parasite’s life cycle.

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

Reference77 articles.

1. World Health Organization (2018). WORLD MALARIA REPORT, WHO Library Cataloguing-in-Publication Data.

2. World Health Organization (2022). WORLD MALARIA REPORT, WHO Library Cataloguing-in-Publication Data.

3. An update on the search for a Plasmodium vivax vaccine;Herrera;Trends Parasitol.,2007

4. Update on malaria;Varo;Med. Clin.,2020

5. Nilsson, S.K., Childs, L.M., Buckee, C., and Marti, M. (2015). Targeting Human Transmission Biology for Malaria Elimination. PLoS Pathog., 11.

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