<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zuo Z</submitter><funding>Natural Science Foundation of Beijing Municipality</funding><funding>National Natural Science Foundation of China</funding><pagination>10389</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8129140</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Vaccines based on live attenuated Chlamydia elementary bodies (EBs) can cause disease in vaccinated animals and the comparably safer inactivated whole EBs are only marginally protective. Recent studies show that a vaccine formulation comprising UV-inactivated EBs (EB) and appropriate mucosal delivery systems and/or adjuvants induced significant protective immunity. We tested the hypothesis that intranasal delivery of UV-inactivated C. psittaci EB formulated in Vibrio cholerae ghosts (VCG)-chitosan nanoparticles will induce protective immunity against intranasal challenge in SPF chickens. We first compared the impact of VCG and CpG adjuvants on protective immunity following IN mucosal and IM systemic delivery of EB formulated in chitosan hydrogel/microspheres. Immunologic analysis revealed </pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Intranasal immunization with inactivated chlamydial elementary bodies formulated in VCG-chitosan nanoparticles induces robust immunity against intranasal Chlamydia psittaci challenge.</pubmed_title><pmcid>PMC8129140</pmcid><funding_grant_id>No.31672517</funding_grant_id><funding_grant_id>No.6172019</funding_grant_id><pubmed_authors>Zou Y</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>He C</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Zuo Z</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Eko FO</pubmed_authors><pubmed_authors>Li Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intranasal immunization with inactivated chlamydial elementary bodies formulated in VCG-chitosan nanoparticles induces robust immunity against intranasal Chlamydia psittaci challenge.</name><description>Vaccines based on live attenuated Chlamydia elementary bodies (EBs) can cause disease in vaccinated animals and the comparably safer inactivated whole EBs are only marginally protective. Recent studies show that a vaccine formulation comprising UV-inactivated EBs (EB) and appropriate mucosal delivery systems and/or adjuvants induced significant protective immunity. We tested the hypothesis that intranasal delivery of UV-inactivated C. psittaci EB formulated in Vibrio cholerae ghosts (VCG)-chitosan nanoparticles will induce protective immunity against intranasal challenge in SPF chickens. We first compared the impact of VCG and CpG adjuvants on protective immunity following IN mucosal and IM systemic delivery of EB formulated in chitosan hydrogel/microspheres. Immunologic analysis revealed </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2025-04-05T14:33:46.545Z</modification><creation>2025-04-05T14:33:46.545Z</creation></dates><accession>S-EPMC8129140</accession><cross_references><pubmed>34001988</pubmed><doi>10.1038/s41598-021-89940-8</doi></cross_references></HashMap>