Peter E. van Bommel

ORCID: 0009-0006-1250-3213
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About
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Research Areas
  • Phagocytosis and Immune Regulation
  • Immunotherapy and Immune Responses
  • Glycosylation and Glycoproteins Research
  • Erythrocyte Function and Pathophysiology
  • CAR-T cell therapy research
  • Cell Adhesion Molecules Research
  • Immune Cell Function and Interaction
  • Immune cells in cancer
  • Monoclonal and Polyclonal Antibodies Research
  • RNA Interference and Gene Delivery

University Medical Center Groningen
2017

University of Groningen
2017

Here, we report on a novel bispecific antibody-derivative, designated RTX-CD47, with unique capacity for CD20-directed inhibition of CD47-SIRPα "don't eat me" signaling. RTX-CD47 comprises CD20-targeting scFv antibody fragment derived from rituximab fused in tandem to CD47-blocking scFv. Single agent treatment triggered significant phagocytic removal CD20pos/CD47pos malignant B-cells, but not CD20neg/CD47pos cells, and required no pro-phagocytic FcR-mediated Importantly, synergistically...

10.1080/2162402x.2017.1386361 article EN OncoImmunology 2017-10-04

10.4267/2042/62150 article EN Atlas of Genetics and Cytogenetics in Oncology and Haematology 2017-04-01

TNFR superfamily (TNFRSF) members have important immunoregulatory functions and are of clear interest for cancer immunotherapy. Various TNFRSF agonists been clinically evaluated, but met with limited efficacy and/or toxicity. Recent insights indicate that 'first-generation' lack as they do not effectively cross-link their corresponding receptor. Reversely, ubiquitous receptor(s) cross-linking by CD40 Fas agonistic antibodies resulted in dose-limiting liver To overcome these issues, we...

10.1038/s41598-017-13530-w article EN cc-by Scientific Reports 2017-10-10
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