Immunisation with transgenic L. tarentolae expressing gamma glutamyl cysteine synthetase from pathogenic Leishmania species protected against L. major and L. donovani infection in a murine model
Topuz Ata, Derya and Hussain, Muattaz and Jones, Michael and Best, Jonathan and Wiese, Martin and Carter, Katharine Christine (2023) Immunisation with transgenic L. tarentolae expressing gamma glutamyl cysteine synthetase from pathogenic Leishmania species protected against L. major and L. donovani infection in a murine model. Microorganisms, 11 (5). 1322. ISSN 2076-2607 (https://doi.org/10.3390/microorganisms11051322)
Preview |
Text.
Filename: Topuz_Ata_etal_Microorganisms_2023_Immunisation_with_transgenic_L_tarentolae_expressing_gamma_glutamyl_cysteine_synthetase.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
Leishmaniasis is a protozoan disease responsible for significant morbidity and mortality. There is no recommended vaccine to protect against infection. In this study, transgenic Leishmania tarentolae expressing gamma glutamyl cysteine synthetase (γGCS) from three pathogenic species were produced and their ability to protect against infection determined using models of cutaneous and visceral leishmaniasis. The ability of IL-2-producing PODS® to act as an adjuvant was also determined in L. donovani studies. Two doses of the live vaccine caused a significant reduction in L. major (p < 0.001) and L. donovani (p < 0.05) parasite burdens compared to their respective controls. In contrast, immunisation with wild type L. tarentolae, using the same immunisation protocol, had no effect on parasite burdens compared to infection controls. Joint treatment with IL-2-producing PODS® enhanced the protective effect of the live vaccine in L. donovani studies. Protection was associated with a Th1 response in L. major and a mixed Th1/Th2 response in L. donovani, based on specific IgG1 and IgG2a antibody and cytokine production from in vitro proliferation assays using antigen-stimulated splenocytes. The results of this study provide further proof that γGCS should be considered a candidate vaccine for leishmaniasis.
ORCID iDs
Topuz Ata, Derya, Hussain, Muattaz ORCID: https://orcid.org/0000-0002-1979-3384, Jones, Michael, Best, Jonathan, Wiese, Martin ORCID: https://orcid.org/0000-0003-4493-0835 and Carter, Katharine Christine;-
-
Item type: Article ID code: 85544 Dates: DateEvent17 May 2023Published15 May 2023Accepted6 March 2023SubmittedSubjects: Science > Microbiology > Immunology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 17 May 2023 13:29 Last modified: 11 Nov 2024 13:50 URI: https://strathprints.strath.ac.uk/id/eprint/85544