Genome-wide CRISPR screens reveal a specific ligand for the glycan-binding immune checkpoint receptor Siglec-7

Proc Natl Acad Sci U S A. 2021 Feb 2;118(5):e2015024118. doi: 10.1073/pnas.2015024118.

Abstract

Glyco-immune checkpoint receptors, molecules that inhibit immune cell activity following binding to glycosylated cell-surface antigens, are emerging as attractive targets for cancer immunotherapy. Defining biologically relevant ligands that bind and activate such receptors, however, has historically been a significant challenge. Here, we present a CRISPRi genomic screening strategy that allowed unbiased identification of the key genes required for cell-surface presentation of glycan ligands on leukemia cells that bind the glyco-immune checkpoint receptors Siglec-7 and Siglec-9. This approach revealed a selective interaction between Siglec-7 and the mucin-type glycoprotein CD43. Further work identified a specific N-terminal glycopeptide region of CD43 containing clusters of disialylated O-glycan tetrasaccharides that form specific Siglec-7 binding motifs. Knockout or blockade of CD43 in leukemia cells relieves Siglec-7-mediated inhibition of immune killing activity. This work identifies a potential target for immune checkpoint blockade therapy and represents a generalizable approach to dissection of glycan-receptor interactions in living cells.

Keywords: Tumor Immunology; CRISPR Screening; Glycobiology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Motifs
  • Antigens, Differentiation, Myelomonocytic / chemistry
  • Antigens, Differentiation, Myelomonocytic / metabolism*
  • Cell Line, Tumor
  • Cell Membrane / metabolism
  • Clustered Regularly Interspaced Short Palindromic Repeats / genetics*
  • Genome, Human*
  • Glycopeptides / metabolism
  • Humans
  • Immunological Synapses / metabolism
  • Killer Cells, Natural / metabolism
  • Lectins / chemistry
  • Lectins / metabolism*
  • Leukosialin / chemistry
  • Leukosialin / metabolism
  • Ligands
  • Polysaccharides / metabolism*
  • Protein Binding

Substances

  • Antigens, Differentiation, Myelomonocytic
  • Glycopeptides
  • Lectins
  • Leukosialin
  • Ligands
  • Polysaccharides
  • SIGLEC7 protein, human