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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003083naa a2200325 4500
001oai:DiVA.org:uu-95523
003SwePub
008070308s2007 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-955232 URI
024a https://doi.org/10.1111/j.1365-3083.2007.01953.x2 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Carlsson, Fredriku Uppsala universitet,Institutionen för genetik och patologi4 aut
2451 0a IgE enhances specific antibody and T cell responses in mice overexpressing CD23
264 1b Wiley,c 2007
338 a print2 rdacarrier
520 a IgE administered with its specific antigen in vivo induces enhanced proliferation of specific T cells as well as enhanced production of specific antibodies. Both effects are dependent on the low-affinity receptor for IgE (CD23) and the underlying mechanism is thought to be increased antigen presentation following uptake of IgE/antigen complexes via CD23+ B cells. By contrast, CD23 negatively regulates antibody responses to antigens administered with alum, i.e. without IgE. This effect has been observed as low IgG1 and IgE responses in transgenic mice overexpressing CD23 (CD23Tg). The present study was designed to test whether IgE could enhance antibody and T-cell responses in CD23Tg animals or whether CD23's downregulatory effect precludes IgE-mediated enhancement. IgE-anti-TNP administered with OVA-TNP enhances the OVA-specific antibody responses in wild-type (wt) and CD23Tg mice equally well. Interestingly, the total magnitude of antibody responses to IgE + OVA-TNP and to uncomplexed OVA-TNP, as well as to sheep erythrocytes and keyhole limpet haemocyanine, were lower in the CD23Tg mice. IgE induced proliferation of OVA-specific CD4+ T cells to the same degree in wt and CD23Tg mice. The effect on T cells was dependent on CD23+ B cells as demonstrated in in vitro proliferation assays. In conclusion, CD23 does indeed have dual immunoregulatory effects in the same animal. The receptor mediates enhancement of antibody and T-cell responses to IgE-complexed antigen, most likely via increased presentation of complexed antigen, while it negatively regulates the total antibody response to a variety of antigens.
653 a MEDICINE
653 a MEDICIN
700a Hjelm, Fredriku Uppsala universitet,Institutionen för genetik och patologi4 aut
700a Conrad, Daniel H.4 aut
700a Heyman, Birgittau Uppsala universitet,Institutionen för genetik och patologi4 aut0 (Swepub:uu)birgheym
710a Uppsala universitetb Institutionen för genetik och patologi4 org
773t Scandinavian Journal of Immunologyd : Wileyg 66:2-3, s. 261-270q 66:2-3<261-270x 0300-9475x 1365-3083
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1365-3083.2007.01953.x
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-95523
8564 8u https://doi.org/10.1111/j.1365-3083.2007.01953.x

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