دورية أكاديمية

Selective antibody intervention of toll-like receptor 4 activation through Fc γ receptor tethering

التفاصيل البيبلوغرافية
العنوان: Selective antibody intervention of toll-like receptor 4 activation through Fc γ receptor tethering
المؤلفون: Shang, Limin, Daubeuf, Bruno, Triantafilou, Martha, Olden, Robin, Depis, Fabien, Raby, Anne-Catherine, Herren, Suzanne, Dos Santos, Anaelle, Malinge, Pauline, Dunn-Siegrist, Irene, Benmkaddem, Sanae, Geinoz, Antoine, Magistrelli, Giovanni, Rousseau, Francois, Buatois, Vanessa, Salgado-Pires, Susana, Reith, Walter, Monteiro, Renato, Pugin, Jerome, Leger, Olivier, Ferlin, Walter, Kosco-Vilbois, Marie, Triantafilou, Kathy, Elson, Greg
بيانات النشر: American Society for Biochemistry and Molecular Biology
سنة النشر: 2014
المجموعة: Cardiff University: ORCA (Online Research @ Cardiff)
مصطلحات موضوعية: R Medicine (General)
الوصف: Inflammation is mediated mainly by leukocytes that express both Toll-like receptor 4 (TLR4) and Fc γ receptors (FcγR). Dysregulated activation of leukocytes via exogenous and endogenous ligands of TLR4 results in a large number of inflammatory disorders that underlie a variety of human diseases. Thus, differentially blocking inflammatory cells while sparing structural cells, which are FcγR-negative, represents an elegant strategy when targeting the underlying causes of human diseases. Here, we report a novel tethering mechanism of the Fv and Fc portions of anti-TLR4 blocking antibodies that achieves increased potency on inflammatory cells. In the presence of ligand (e.g. lipopolysaccharide (LPS)), TLR4 traffics into glycolipoprotein microdomains, forming concentrated protein platforms that include FcγRs. This clustering produces a microenvironment allowing anti-TLR4 antibodies to co-engage TLR4 and FcγRs, increasing their avidity and thus substantially increasing their inhibitory potency. Tethering of antibodies to both TLR4 and FcγRs proves valuable in ameliorating inflammation in vivo. This novel mechanism of action therefore has the potential to enable selective intervention of relevant cell types in TLR4-driven diseases.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: Shang, Limin, Daubeuf, Bruno, Triantafilou, Martha https://orca.cardiff.ac.uk/view/cardiffauthors/A2173080.htmlTest orcid:0000-0002-8489-2602 orcid:0000-0002-8489-2602, Olden, Robin https://orca.cardiff.ac.uk/view/cardiffauthors/A211918X.htmlTest, Depis, Fabien, Raby, Anne-Catherine https://orca.cardiff.ac.uk/view/cardiffauthors/A030669E.htmlTest orcid:0000-0002-5354-5835 orcid:0000-0002-5354-5835, Herren, Suzanne, Dos Santos, Anaelle, Malinge, Pauline, Dunn-Siegrist, Irene, Benmkaddem, Sanae, Geinoz, Antoine, Magistrelli, Giovanni, Rousseau, Francois, Buatois, Vanessa, Salgado-Pires, Susana, Reith, Walter, Monteiro, Renato, Pugin, Jerome, Leger, Olivier, Ferlin, Walter, Kosco-Vilbois, Marie, Triantafilou, Kathy https://orca.cardiff.ac.uk/view/cardiffauthors/A217309Y.htmlTest orcid:0000-0002-7473-6278 orcid:0000-0002-7473-6278 and Elson, Greg 2014. Selective antibody intervention of toll-like receptor 4 activation through Fc γ receptor tethering. Journal of Biological Chemistry 289 (22) , pp. 15309-15318. 10.1074/jbc.M113.537936 https://doi.org/10.1074/jbc.M113.537936Test
DOI: 10.1074/jbc.M113.537936
الإتاحة: https://doi.org/10.1074/jbc.M113.537936Test
https://orca.cardiff.ac.uk/id/eprint/67673Test/
رقم الانضمام: edsbas.9528328C
قاعدة البيانات: BASE