| Literature DB >> 21213105 |
Ruth K Moysey1, Yi Li, Samantha J Paston, Emma E Baston, Malkit S Sami, Brian J Cameron, Jessie Gavarret, Penio Todorov, Annelise Vuidepot, Steven M Dunn, Nicholas J Pumphrey, Katherine J Adams, Fang Yuan, Rebecca E Dennis, Deborah H Sutton, Andy D Johnson, Joanna E Brewer, Rebecca Ashfield, Nikolai M Lissin, Bent K Jakobsen.
Abstract
Using directed mutagenesis and phage display on a soluble fragment of the human immunoglobulin super-family receptor ILT2 (synonyms: LIR1, MIR7, CD85j), we have selected a range of mutants with binding affinities enhanced by up to 168,000-fold towards the conserved region of major histocompatibility complex (MHC) class I molecules. Produced in a dimeric form, either by chemical cross-linking with bivalent polyethylene glycol (PEG) derivatives or as a genetic fusion with human IgG Fc-fragment, the mutants exhibited a further increase in ligand-binding strength due to the avidity effect, with resident half-times (t(1/2)) on the surface of MHC I-positive cells of many hours. The novel compounds antagonized the interaction of CD8 co-receptor with MHC I in vitro without affecting the peptide-specific binding of T-cell receptors (TCRs). In both cytokine-release assays and cell-killing experiments the engineered receptors inhibited the activation of CD8(+) cytotoxic T lymphocytes (CTLs) in the presence of their target cells, with subnanomolar potency and in a dose-dependent manner. As a selective inhibitor of CD8(+) CTL responses, the engineered high affinity ILT2 receptor presents a new tool for studying the activation mechanism of different subsets of CTLs and could have potential for the development of novel autoimmunity therapies.Entities:
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Year: 2011 PMID: 21213105 PMCID: PMC4875079 DOI: 10.1007/s13238-010-0144-5
Source DB: PubMed Journal: Protein Cell ISSN: 1674-800X Impact factor: 14.870