Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/2872
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dc.contributor.authorMartínez-Alonso, Carlos-
dc.contributor.authorKleine, B.-
dc.contributor.authorSprenger, R.-
dc.contributor.authorBessler, W. G-
dc.date.accessioned2008-02-06T11:26:35Z-
dc.date.available2008-02-06T11:26:35Z-
dc.date.issued1987-05-
dc.identifier.citationImmunology 1987 May; 61(1): 29–34.en_US
dc.identifier.urihttp://hdl.handle.net/10261/2872-
dc.description.abstractThe reactivity of 38 murine strains to a synthetic analogue of bacterial lipoprotein, tripalmitoyl-pentapeptide (TPP), was tested and compared with the reactivity to lipopolysaccharide (LPS). These strains include common laboratory mice and H-2 recombinant inbred lines, as well as some newly bred lines originating from animals recently captured in different regions of Europe. All animals analysed were reactive to TPP and polyclonally activated to proliferation and immunoglobulin synthesis. Large differences in mitogen reactivities of various H-2 recombinant inbred strains suggest that MHC or closely linked gene products influence the reactivity to the LPS and TPP mitogens. By analysing the frequencies of precursor cells reactive to TPP or LPS and the isotype patterns obtained after stimulation, we demonstrated that both mitogens activate individual B cells in different ways.en_US
dc.format.extent997404 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherBritish Society for Immunologyen_US
dc.rightsclosedAccessen_US
dc.titlePolyclonal B-cell activation by a synthetic analogue of bacterial lipoprotein is functionally different from activation by bacterial lipopolysaccharideen_US
dc.typeartículoen_US
dc.description.peerreviewedPeer revieweden_US
dc.identifier.pmid3495485-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
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