{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["de la Fuente J"],"funding":["Innovación y Universidades","Facing tick vaccinomics strategies from a systems biology perspective","Grupo Sabio","Ministerio de Ciencia"],"pagination":["1995"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9784196"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["10(12)"],"pubmed_abstract":["<i>Anaplasma phagocytophilum</i> Major surface protein 4 (MSP4) plays a role during infection and multiplication in host neutrophils and tick vector cells. Recently, vaccination trials with the <i>A. phagocytophilum</i> antigen MSP4 in sheep showed only partial protection against pathogen infection. However, in rabbits immunized with MSP4, this recombinant antigen was protective. Differences between rabbit and sheep antibody responses are probably associated with the recognition of non-protective epitopes by IgG of immunized lambs. To address this question, we applied quantum vaccinomics to identify and characterize MSP4 protective epitopes by a microarray epitope mapping using sera from vaccinated rabbits and sheep. The identified candidate protective epitopes or immunological quantum wer"],"journal":["Vaccines"],"pubmed_title":["A Quantum Vaccinomics Approach for the Design and Production of MSP4 Chimeric Antigen for the Control of <i>Anaplasma phagocytophilum</i> Infections."],"pmcid":["PMC9784196"],"funding_grant_id":["IJC2020-042710-I","2020-GRIN-29072","UCLM-CSIC-JCLM"],"pubmed_authors":["de la Fuente J","Fernandez-Melgar R","Alberdi P","Garcia-Alvarez O","Contreras M","Moraga-Fernandez A","Diaz-Sanchez S"],"additional_accession":[]},"is_claimable":false,"name":"A Quantum Vaccinomics Approach for the Design and Production of MSP4 Chimeric Antigen for the Control of <i>Anaplasma phagocytophilum</i> Infections.","description":"<i>Anaplasma phagocytophilum</i> Major surface protein 4 (MSP4) plays a role during infection and multiplication in host neutrophils and tick vector cells. Recently, vaccination trials with the <i>A. phagocytophilum</i> antigen MSP4 in sheep showed only partial protection against pathogen infection. However, in rabbits immunized with MSP4, this recombinant antigen was protective. Differences between rabbit and sheep antibody responses are probably associated with the recognition of non-protective epitopes by IgG of immunized lambs. To address this question, we applied quantum vaccinomics to identify and characterize MSP4 protective epitopes by a microarray epitope mapping using sera from vaccinated rabbits and sheep. The identified candidate protective epitopes or immunological quantum wer","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Nov","modification":"2026-06-22T03:19:55.661Z","creation":"2025-04-21T14:17:12.393Z"},"accession":"S-EPMC9784196","cross_references":{"pubmed":["36560405"],"doi":["10.3390/vaccines10121995"]}}