Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2000-2-24
pubmed:abstractText
We have investigated noninvasive immunization to plague. Recombinant subunit antigens, F1 and V from Yersinia pestis, were coencapsulated in biodegradable poly(L100 LD(50's) inhalational challenge with virulent Y. pestis. These data expand on previous findings from our laboratories, providing further insight into the mechanics of safeguarding mice from plague through nasal immunization. Further, these results demonstrate that in a murine model, solid protection from pneumonic plague can be engendered by two intranasal administrations of appropriately formulated recombinant proteins.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Bacterial, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Bacterial, http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Vaccines, http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G, http://linkedlifedata.com/resource/pubmed/chemical/LcrV protein, Yersinia, http://linkedlifedata.com/resource/pubmed/chemical/Polyesters, http://linkedlifedata.com/resource/pubmed/chemical/Pore Forming Cytotoxic Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Vaccines, Synthetic, http://linkedlifedata.com/resource/pubmed/chemical/caf1 protein, Yersinia pestis, http://linkedlifedata.com/resource/pubmed/chemical/poly(lactide)
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0168-3659
pubmed:author
pubmed:issnType
Print
pubmed:day
3
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
191-200
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10640592-Administration, Intranasal, pubmed-meshheading:10640592-Animals, pubmed-meshheading:10640592-Antibodies, Bacterial, pubmed-meshheading:10640592-Antigens, Bacterial, pubmed-meshheading:10640592-Bacterial Proteins, pubmed-meshheading:10640592-Bacterial Vaccines, pubmed-meshheading:10640592-Biocompatible Materials, pubmed-meshheading:10640592-Dose-Response Relationship, Immunologic, pubmed-meshheading:10640592-Female, pubmed-meshheading:10640592-Immunity, Cellular, pubmed-meshheading:10640592-Immunoglobulin G, pubmed-meshheading:10640592-Mice, pubmed-meshheading:10640592-Mice, Inbred BALB C, pubmed-meshheading:10640592-Microspheres, pubmed-meshheading:10640592-Nasal Mucosa, pubmed-meshheading:10640592-Plague, pubmed-meshheading:10640592-Polyesters, pubmed-meshheading:10640592-Pore Forming Cytotoxic Proteins, pubmed-meshheading:10640592-Vaccines, Synthetic, pubmed-meshheading:10640592-Yersinia pestis
pubmed:year
2000
pubmed:articleTitle
Generation of protective immune responses to plague by mucosal administration of microsphere coencapsulated recombinant subunits.
pubmed:affiliation
Department of Pharmaceutical and Biological Sciences, Aston University, Birmingham, UK.
pubmed:publicationType
Journal Article