rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
1993-1-29
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pubmed:abstractText |
OspA is a protective antigen of the Lyme disease spirochete Borrelia burgdorferi. Expression of the full-length B. burgdorferi B31 OspA gene in Escherichia coli produces a protein that is processed posttranslationally by signal peptidase II and contains an attached lipid moiety. The recombinant OspA lipoprotein has been purified by detergent extraction and ion-exchange chromatography. Priming and boosting with OspA lipoprotein, either with no adjuvant or adsorbed to alum, elicited a strong, dose-dependent immunoglobulin G response. Serum from vaccinated mice inhibited spirochetal growth in vitro. Mice immunized twice with as little as 0.4 micrograms of OspA lipoprotein were protected against an intradermal challenge with 10(4) infectious spirochetes. The ability of the purified recombinant lipoprotein to induce a strong protective response in the absence of toxic adjuvants makes it an excellent candidate antigen for a human vaccine against Lyme disease. By contrast, no serum immunoglobulin G or growth inhibitory response to OspA nonlipoprotein was seen at any dose. The difference in immunogenicities of the lipoprotein and nonlipoprotein forms of OspA is not due to any difference in the antigenicities of the two proteins. These results suggest that posttranslational lipid attachment is a critical determinant of the immunogenicity of the OspA protein.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/8418068-1349173,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8418068-1372297,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8418068-1541551,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8418068-1608951,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/8418068-7439930
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Bacterial Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Outer Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Lipids,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/OspA protein,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/globomycin
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0019-9567
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
61
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
81-90
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:8418068-Animals,
pubmed-meshheading:8418068-Mice,
pubmed-meshheading:8418068-Anti-Bacterial Agents,
pubmed-meshheading:8418068-Lipids,
pubmed-meshheading:8418068-Peptides,
pubmed-meshheading:8418068-Vaccination,
pubmed-meshheading:8418068-Lipoproteins,
pubmed-meshheading:8418068-Base Sequence,
pubmed-meshheading:8418068-Amino Acid Sequence,
pubmed-meshheading:8418068-Bacterial Vaccines,
pubmed-meshheading:8418068-Chromatography, Ion Exchange,
pubmed-meshheading:8418068-Chromatography, Gel,
pubmed-meshheading:8418068-Immunoglobulin G,
pubmed-meshheading:8418068-Mice, Inbred BALB C,
pubmed-meshheading:8418068-Mice, Inbred C3H,
pubmed-meshheading:8418068-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:8418068-Molecular Sequence Data,
pubmed-meshheading:8418068-Cross Reactions,
pubmed-meshheading:8418068-Antigens, Surface,
pubmed-meshheading:8418068-Cloning, Molecular,
pubmed-meshheading:8418068-Dose-Response Relationship, Immunologic,
pubmed-meshheading:8418068-Protein Processing, Post-Translational
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