<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Han R</submitter><funding>National Key Research and Development Program of China</funding><funding>National Science Foundation</funding><pagination>686</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11209252</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(6)</volume><pubmed_abstract>Respiratory syncytial virus (RSV) is a leading cause of severe lower respiratory tract disease of infants and older people. There is an urgent need for safe and effective vaccines against RSV infection. In this study, we analyzed the effects of the immune response and protection with the RSV recombinant G protein extracellular domain (G&lt;sup>ecto&lt;/sup>) combined with various adjuvants as novel subunit vaccines in mice. All groups receiving RSV G&lt;sup>ecto&lt;/sup> combined with adjuvants exhibited robust humoral and cellular immunity compared to those receiving an adjuvant alone or inactivated RSV vaccine. The greatest effect was observed in mice receiving G&lt;sup>ecto&lt;/sup> combined with a CpG ODN + Alum salt adjuvant, resulting in the highest production of neutralizing antibodies against both R</pubmed_abstract><journal>Vaccines</journal><pubmed_title>Immune Responses and Protection Profiles in Mice Induced by Subunit Vaccine Candidates Based on the Extracellular Domain Antigen of Respiratory Syncytial Virus G Protein Combined with Different Adjuvants.</pubmed_title><pmcid>PMC11209252</pmcid><funding_grant_id>2022YFC2304100 and 2022YFC2303401</funding_grant_id><funding_grant_id>82041041</funding_grant_id><pubmed_authors>Bing J</pubmed_authors><pubmed_authors>Han R</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Shan X</pubmed_authors><pubmed_authors>Tan W</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Sun S</pubmed_authors><pubmed_authors>Cheng X</pubmed_authors><pubmed_authors>Deng Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immune Responses and Protection Profiles in Mice Induced by Subunit Vaccine Candidates Based on the Extracellular Domain Antigen of Respiratory Syncytial Virus G Protein Combined with Different Adjuvants.</name><description>Respiratory syncytial virus (RSV) is a leading cause of severe lower respiratory tract disease of infants and older people. There is an urgent need for safe and effective vaccines against RSV infection. In this study, we analyzed the effects of the immune response and protection with the RSV recombinant G protein extracellular domain (G&lt;sup>ecto&lt;/sup>) combined with various adjuvants as novel subunit vaccines in mice. All groups receiving RSV G&lt;sup>ecto&lt;/sup> combined with adjuvants exhibited robust humoral and cellular immunity compared to those receiving an adjuvant alone or inactivated RSV vaccine. The greatest effect was observed in mice receiving G&lt;sup>ecto&lt;/sup> combined with a CpG ODN + Alum salt adjuvant, resulting in the highest production of neutralizing antibodies against both R</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-04-08T18:59:47.425Z</modification><creation>2025-02-19T00:17:13.886Z</creation></dates><accession>S-EPMC11209252</accession><cross_references><pubmed>38932414</pubmed><doi>10.3390/vaccines12060686</doi></cross_references></HashMap>