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GRA7 provides protective immunity in cocktail DNA vaccines against Toxoplasma gondii
Abstract
SUMMARY: In a previous study, single‐gene vaccination with GRA1, GRA7 or ROP2 was shown to elicit partial protection against Toxoplasma gondii. In this study, the contribution of each antigen in the evoked humoral and cellular immune responses was evaluated after vaccination with plasmid mixtures containing GRA1, GRA7 and ROP2. Cocktail DNA vaccinated mice developed high antibody titers against the antigens from two‐gene DNA vaccine cocktails, but lower titres when immunized with the three‐gene cocktail. High numbers of IFN‐γ secreting splenocytes were generated predominantly against GRA7. Brain cyst burden was reduced by 81% in mice vaccinated with the three‐gene mixture and they were completely protected against acute toxoplasmosis. Similar high levels of brain cyst reductions were obtained after vaccination with cocktails composed of GRA1 and GRA7 (89% reduction), or GRA7 and ROP2 (79% reduction), but not with the cocktail composed of GRA1 and ROP2. In low dose single‐gene vaccinations, IFN‐γ and strong protection could only be elicited by GRA7. Hence, the presence of GRA7 in the DNA vaccine formulation was important for optimal protection and this was correlated with GRA7‐specific IFN‐γ production. We propose GRA7 as a main component in cocktail DNA vaccines for vaccination against T. gondii.
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“The presence of GRA7 in a DNA vaccine triggered strong antibody responses and higher levels of IFN-γ, indicating that GRA7 should be a main component of vaccines against T. gondii (Jongert et al., 2007).”
From Protective efficacy of Toxoplasma gondii GRA12 or GRA7 recombinant proteins encapsulated in PLGA nanoparticles against acute Toxoplasma gondii infection in mice (2023) · cites this paper as Jongert et al., 2007
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Sun, H.-C., Deng, P.-M., Fu, Y., Deng, J.-H., Xie, R.-H., Huang, J., Qi, M., & Shi, T.-Y. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1209755 · Cited by 22
Metadata
- Authors
- JONGERT, E., DE CRAEYE, S., DEWIT, J., & HUYGEN, K.
- Affiliations
- Institut Scientifique de Santé Publique (BE)
- Corresponding author
- JONGERT, E.
- ORCID
- HUYGEN, K.
- Venue
- Parasite Immunology
- Publisher
- Wiley
- Published
- 2007-08-23
- Volume
- 29
- Issue
- 9
- Pages
- 445-453
- ISSN
- 0141-9838 (ISSN-L)
- 1365-3024
- OpenAlex
- W2019087904
- Cited by
- 74
- References
- 0
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 7 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 1 · 2019: 2 · 2018: 3 · 2017: 4 · 2015: 3 · 2014: 5 · 2013: 5 · 2012: 5
- FWCI
- 5.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Parasite Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fonds Wetenschappelijk Onderzoek
- Vlaamse regering
- Topics
- Life Sciences › Immunology and Microbiology › Parasitology › Toxoplasma gondii Research Studies
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Coccidia and coccidiosis research
- Life Sciences › Immunology and Microbiology › Parasitology › Parasitic infections in humans and animals
- Keywords
- Toxoplasma gondii, GRA7, GRA1, ROP2, protective immunity, interferon-gamma, humoral immune response, cell-mediated immunity, brain cyst burden, acute toxoplasmosis
- MeSH terms
- Animals, Antibodies, Protozoan, Antigens, Protozoan, Female, Interferon-gamma, Membrane Proteins, Mice, Inbred C3H, Toxoplasma, Toxoplasmosis, Animal, Protozoan Proteins, Protozoan Vaccines, Vaccines, DNA, Mice
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