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Novel CD33 antibodies unravel localization, biology and therapeutic implications of CD33 isoforms.

Mohammed O GbadamosiVivek M ShastriTiffany HylkemaIoannis PapageorgiouLaura PardoChristopher R CogleAndria DotyMichael R LokenSoheil MeshinchiJatinder Kaur Lamba
Published in: Future oncology (London, England) (2020)
The aim of this study was to establish the therapeutic relevance of the CD33D2 isoform by developing novel antibodies targeting the IgC domain of CD33. Two novel IgC-targeting antibodies, HL2541 and 5C11-2, were developed, and CD33 isoforms were assessed using multiple assays in cells overexpressing either CD33FL or CD33D2 isoforms, unmodified acute myeloid leukemia (AML) cell lines and primary AML specimens representing different genotypes for the CD33 splicing single nucleotide polymorphism. CD33D2 was recognized on cells overexpressing CD33D2 and unmodified AML cell lines; however, minimal/no cell surface detection of CD33D2 was observed in primary AML specimens. Both isoforms were detected intracellularly using novel antibodies. Minimal cell surface expression of CD33D2 on primary AML/progenitor cells warrants further studies on anti-CD33D2 immunotherapeutics.
Keyphrases
  • acute myeloid leukemia
  • nk cells
  • allogeneic hematopoietic stem cell transplantation
  • poor prognosis
  • acute lymphoblastic leukemia
  • cell proliferation
  • binding protein
  • fine needle aspiration