<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fang Y</submitter><funding>High Level Scientific and Technological Talents Project of Lvliang City</funding><funding>National Natural Science Foundation of China</funding><funding>Ningxia Agricultural Science and Technology Independent Innovation Special Project - Scientific and Technological Innovation Guidance Project</funding><funding>Scientific Research Start Funds for Advanced Talent in Ningxia Province</funding><pagination>521</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12374472</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>Toxoplasma gondii (T. gondii) is a globally prevalent zoonotic parasite causing severe health and economic impacts. Despite decades of research, no commercial vaccine provides comprehensive protection against both acute and chronic toxoplasmosis. DNA vaccines represent a promising strategy, but their application is hindered by low delivery efficiency and limited immunogenicity. Here, we developed and evaluated pVAX1-TgIMC1-loaded PLGA and chitosan (CS) nanospheres as potential vaccine candidates. Immunization studies in mice showed that pVAX1-TgIMC1/PLGA and pVAX1-TgIMC1/CS nanospheres induced robust humoral and cellular immune responses, significantly enhancing specific IgG levels and cytokine production IFN-γ and IL-17 compared to the naked DNA vaccine. Both nanospheres also promoted dendritic cell maturation and T-cell activation, resulting in reduced parasite burdens in cardiac tissues post-challenge. Notably, the PLGA nanospheres exhibited superior protection against acute toxoplasmosis, while CS nanospheres provided additional advantages in antigen stability and delivery. The nanospheres were non-toxic, as confirmed by biochemical markers and histopathological analysis. These findings highlight pVAX1-TgIMC1/PLGA and pVAX1-TgIMC1/CS nanospheres as promising candidates for T. gondii vaccine development, warranting further optimization and validation in broader animal models.</pubmed_abstract><journal>BMC veterinary research</journal><pubmed_title>Research on inner membrane complex protein 1: a novel nanovaccines against Toxoplasma gondii.</pubmed_title><pmcid>PMC12374472</pmcid><funding_grant_id>2024BEH04076</funding_grant_id><funding_grant_id>NSFC, 72203117</funding_grant_id><funding_grant_id>2023RC-2-5</funding_grant_id><funding_grant_id>NKYG-25-22</funding_grant_id><pubmed_authors>Fang Y</pubmed_authors><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Zhou P</pubmed_authors><pubmed_authors>Qi W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Yu Z</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Research on inner membrane complex protein 1: a novel nanovaccines against Toxoplasma gondii.</name><description>Toxoplasma gondii (T. gondii) is a globally prevalent zoonotic parasite causing severe health and economic impacts. Despite decades of research, no commercial vaccine provides comprehensive protection against both acute and chronic toxoplasmosis. DNA vaccines represent a promising strategy, but their application is hindered by low delivery efficiency and limited immunogenicity. Here, we developed and evaluated pVAX1-TgIMC1-loaded PLGA and chitosan (CS) nanospheres as potential vaccine candidates. Immunization studies in mice showed that pVAX1-TgIMC1/PLGA and pVAX1-TgIMC1/CS nanospheres induced robust humoral and cellular immune responses, significantly enhancing specific IgG levels and cytokine production IFN-γ and IL-17 compared to the naked DNA vaccine. Both nanospheres also promoted dendritic cell maturation and T-cell activation, resulting in reduced parasite burdens in cardiac tissues post-challenge. Notably, the PLGA nanospheres exhibited superior protection against acute toxoplasmosis, while CS nanospheres provided additional advantages in antigen stability and delivery. The nanospheres were non-toxic, as confirmed by biochemical markers and histopathological analysis. These findings highlight pVAX1-TgIMC1/PLGA and pVAX1-TgIMC1/CS nanospheres as promising candidates for T. gondii vaccine development, warranting further optimization and validation in broader animal models.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-08T10:46:21.67Z</modification><creation>2026-04-07T23:47:23.681Z</creation></dates><accession>S-EPMC12374472</accession><cross_references><pubmed>40849645</pubmed><doi>10.1186/s12917-025-04961-z</doi></cross_references></HashMap>