Document Type
Article
Publication Date
9-17-2021
Abstract
Introduction: Human onchocerciasis caused by the filarial nematode parasite Onchocerca volvulus remains a major cause of debilitating disease infecting millions primarily in Sub-Saharan Africa. The development of a prophylactic vaccine, along with mass drug administration, would facilitate meeting the goal of onchocerciasis elimination by 2030.
Areas covered: Models used to study immunity to Onchocerca include natural infection of cattle with Onchocerca ochengi and O. volvulus infective third-stage larvae implanted within diffusion chambers in mice. A vaccine, comprised of two adjuvanted recombinant antigens, induced protective immunity in genetically diverse mice suggesting that it will function similarly in diverse human populations. These antigens were recognized by immune humans and also induced protective immunity against Brugia malayi. We describe the development of a fusion protein composed of the two vaccine antigens with the plan to test the vaccine in cows and non-human primates as a prelude to the initiation of phase 1 clinical trials.
Expert opinion: The adjuvanted O. volvulus vaccine composed of two antigens Ov-103 and Ov-RAL-2 was shown to be consistently effective at inducing protective immunity using multiple immune mechanisms. The vaccine is ready for further evaluation in other animal models before moving to clinical trials in humans.
Recommended Citation
Abraham, David; Graham-Brown, John; Carter, Darrick; Gray, Sean A.; Hess, Jessica A.; Makepeace, Benjamin L.; and Lustigman, Sara, "Development of a recombinant vaccine against human onchocerciasis." (2021). Department of Microbiology and Immunology Faculty Papers. Paper 142.
https://jdc.jefferson.edu/mifp/142
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
PubMed ID
34488533
Language
English
Comments
This article is the authors’ final published version in Expert Review of Vaccines, Volume 20, Issue 11, September 2021, Pages 1459-1470.
The published version is available at https://doi.org/10.1080/14760584.2021.1977125. Copyright © Abraham et al.