| Literature DB >> 33951750 |
Huan Cao1, Andreas Neerincx2, Bernard de Bono3, Ursula Lakner4, Catherine Huntington5, John Elvin5, Emma Gudgin6, Clare Pridans6, Mark A Vickers1, Brian Huntly6, John Trowsdale2, Alexander D Barrow7.
Abstract
Sialic acid-binding immunoglobulin-like lectin (Siglec)-15 has recently been identified as a critical tumour checkpoint, augmenting the expression and function of programmed death-ligand 1. We raised a monoclonal antibody, A9E8, specific for Siglec-15 using phage display. A9E8 stained myeloid leukaemia cell lines and peripheral cluster of differentiation (CD)33+ blasts and CD34+ leukaemia stem cells from patients with acute myeloid leukaemia (AML). By contrast, there was minimal expression on healthy donor leucocytes or CD34+ stem cells from non-AML donors, suggesting targeting Siglec-15 may have significant therapeutic advantages over its fellow Siglec CD33. After binding, A9E8 was rapidly internalised (half-life of 180 s) into K562 cells. Antibodies to Siglec-15 therefore hold therapeutic potential for AML treatment.Entities:
Keywords: Siglec-15; acute myeloid leukaemia; antibody; endocytosis; phage display
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Year: 2021 PMID: 33951750 DOI: 10.1111/bjh.17496
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998