| Literature DB >> 34417258 |
Rahel Frick1,2, Lene S Høydahl1,2,3, Jan Petersen4,5, M Fleur du Pré1,3, Shraddha Kumari6, Grete Berntsen6, Alisa E Dewan1,3, Jeliazko R Jeliazkov7, Kristin S Gunnarsen1,2, Terje Frigstad6, Erik S Vik6, Carmen Llerena4, Knut E A Lundin1,3,8, Sheraz Yaqub9,10, Jørgen Jahnsen10,11, Jeffrey J Gray7,12,13, Jamie Rossjohn4,5,14, Ludvig M Sollid1,3, Inger Sandlie1,2, Geir Åge Løset15,2,6.
Abstract
Antibodies specific for peptides bound to human leukocyte antigen (HLA) molecules are valuable tools for studies of antigen presentation and may have therapeutic potential. Here, we generated human T cell receptor (TCR)-like antibodies toward the immunodominant signature gluten epitope DQ2.5-glia-α2 in celiac disease (CeD). Phage display selection combined with secondary targeted engineering was used to obtain highly specific antibodies with picomolar affinity. The crystal structure of a Fab fragment of the lead antibody 3.C11 in complex with HLA-DQ2.5:DQ2.5-glia-α2 revealed a binding geometry and interaction mode highly similar to prototypic TCRs specific for the same complex. Assessment of CeD biopsy material confirmed disease specificity and reinforced the notion that abundant plasma cells present antigen in the inflamed CeD gut. Furthermore, 3.C11 specifically inhibited activation and proliferation of gluten-specific CD4+ T cells in vitro and in HLA-DQ2.5 humanized mice, suggesting a potential for targeted intervention without compromising systemic immunity.Entities:
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Year: 2021 PMID: 34417258 PMCID: PMC8670751 DOI: 10.1126/sciimmunol.abg4925
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468