Malaria

P. falciparum Malaria: Developing a Synthetic Subunit Candidate Vaccine
Malaria is one of the most serious infectious diseases of humans, infecting 5–10% of the world’s population, with 300–600 million clinical cases and more than 2 million deaths annually. Moreover, malaria is a major social and economic burden in endemic areas. In recent years, malaria has spread at an alarming rate owing to the increasing resistance of the parasite to drugs, and the resistance of mosquitoes to insecticides. Therefore, new approaches to combat malaria are urgently needed, and a vaccine is predicted to have the greatest impact in addition to being the most cost-effective control measure.
Vaccine Development
One approach is to design a subunit vaccine that incorporates several malaria protein antigens for which there is evidence of protective immunity from epidemiological data or experimental animal challenge models. Development of such subunit vaccines is critically dependent on the availability of an antigen delivery system to drive suitable protein antigen-specific immune responses in humans. Vaccine formulations have to be highly effective, human-compatible and safe. Production of synthetic or recombinant proteins that stably mimic the native structure of the corresponding malaria antigens to induce effective humoral immune responses is a further major challenge.
Our research
We are addressing both problems by developing synthetic peptide structures that induce cross-reactive antibodies against the parent malaria proteins and by coupling them to the surface of immunopotentiating reconstituted influenza virosomes (IRIVs). In addition we are evaluating the use of so fare uncharacterized predicted proteins of Plasmodium falciparum as potential new candidate vaccine antigens.
Selected Publications
Swiss TPH: 30 years of R&D towards new drugs for tropical diseases. Chimia. 2023;77(9):570-640. OA
Abdikadir M.I, Tschopp R, Ali S.M, Zinsstag J, Pelikan K. Efficiency in transdisciplinary cooperation: the example of the Jigjiga One Health Initiative. trans-kom. 2023;16(1):58-73
Abukhattab S et al. Whole-genome sequencing for One Health surveillance of antimicrobial resistance in conflict zones: a case study of Salmonella spp. and Campylobacter spp. in the West Bank, Palestine. Appl Environ Microbiol. 2023(in press):e0065823. DOI: 10.1128/aem.00658-23
Aebi N.J et al. Facilitators and barriers of routine psychosocial distress assessment within a stepped and collaborative care model in a Swiss hospital setting. PLoS One. 2023;18(6):e0285395. DOI: 10.1371/journal.pone.0285395
Afriyie Osei D, Masiye F, Tediosi F, Fink G. Purchasing for high-quality care using national health insurance: evidence from Zambia. Health Policy Plan. 2023;38(6):681-688. DOI: 10.1093/heapol/czad022
Agyepong I et al. Lancet commission on synergies between universal health coverage, health security, and health promotion. Lancet. 2023;401(10392):1964-2012. DOI: 10.1016/S0140-6736(22)01930-4
Ahmad I et al. Systematic review and meta-analysis of tuberculosis in animals in Nigeria. Heliyon. 2023;9(6):e17215. DOI: 10.1016/j.heliyon.2023.e17215
Ahmed A et al. Guillain-Barre syndrome associated with COVID-19 infection: a case series. Clin Case Rep. 2023;11(2):e6988. DOI: 10.1002/ccr3.6988
Ahmed A, El-Sadig S.M, Siddig E.E. Guillain-Barre syndrome associated with hepatitis E virus infection: a case report. Clin Case Rep. 2023;11(9):e7863. DOI: 10.1002/ccr3.7863
Ahmed A, Hagelnur A.A, Eltigani H.F, Siddig E.E. Cutaneous tuberculosis of the foot clinically mimicking mycetoma: a case report. Clin Case Rep. 2023;11(5):e7295. DOI: 10.1002/ccr3.7295