<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>105(30)</volume><submitter>Mosca F</submitter><pubmed_abstract>Oil-in-water emulsions are potent human adjuvants used for effective pandemic influenza vaccines; however, their mechanism of action is still unknown. By combining microarray and immunofluorescence analysis, we monitored the effects of the adjuvants MF59 oil-in-water emulsion, CpG, and alum in the mouse muscle. MF59 induced a time-dependent change in the expression of 891 genes, whereas CpG and alum regulated 387 and 312 genes, respectively. All adjuvants modulated a common set of 168 genes and promoted antigen-presenting cell recruitment. MF59 was the stronger inducer of cytokines, cytokine receptors, adhesion molecules involved in leukocyte migration, and antigen-presentation genes. In addition, MF59 triggered a more rapid influx of CD11b+ blood cells compared with other adjuvants. The early biomarkers selected by microarray, JunB and Ptx3, were used to identify skeletal muscle as a direct target of MF59. We propose that oil-in-water emulsions are the most efficient human vaccine adjuvants, because they induce an early and strong immunocompetent environment at the injection site by targeting muscle cells.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>10501-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2483233</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular and cellular signatures of human vaccine adjuvants.</pubmed_title><pmcid>PMC2483233</pmcid><pubmed_authors>Bagnoli F</pubmed_authors><pubmed_authors>Iavarone C</pubmed_authors><pubmed_authors>Muzzi A</pubmed_authors><pubmed_authors>De Gregorio E</pubmed_authors><pubmed_authors>Tritto E</pubmed_authors><pubmed_authors>Monaci E</pubmed_authors><pubmed_authors>Mosca F</pubmed_authors><pubmed_authors>O'Hagan D</pubmed_authors><pubmed_authors>Rappuoli R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular and cellular signatures of human vaccine adjuvants.</name><description>Oil-in-water emulsions are potent human adjuvants used for effective pandemic influenza vaccines; however, their mechanism of action is still unknown. By combining microarray and immunofluorescence analysis, we monitored the effects of the adjuvants MF59 oil-in-water emulsion, CpG, and alum in the mouse muscle. MF59 induced a time-dependent change in the expression of 891 genes, whereas CpG and alum regulated 387 and 312 genes, respectively. All adjuvants modulated a common set of 168 genes and promoted antigen-presenting cell recruitment. MF59 was the stronger inducer of cytokines, cytokine receptors, adhesion molecules involved in leukocyte migration, and antigen-presentation genes. In addition, MF59 triggered a more rapid influx of CD11b+ blood cells compared with other adjuvants. The early biomarkers selected by microarray, JunB and Ptx3, were used to identify skeletal muscle as a direct target of MF59. We propose that oil-in-water emulsions are the most efficient human vaccine adjuvants, because they induce an early and strong immunocompetent environment at the injection site by targeting muscle cells.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Jul</publication><modification>2024-11-12T11:36:45.671Z</modification><creation>2019-03-27T00:15:56Z</creation></dates><accession>S-EPMC2483233</accession><cross_references><pubmed>18650390</pubmed><doi>10.1073/pnas.0804699105</doi></cross_references></HashMap>