| Literature DB >> 30410017 |
S Michael Chin1, Christopher R Kimberlin2, Zygy Roe-Zurz2,3, Pamela Zhang2, Allison Xu2, Sindy Liao-Chan2, Debasish Sen2, Andrew R Nager2, Nicole Schirle Oakdale2, Colleen Brown2, Feng Wang2,4, Yuting Yang5, Kevin Lindquist2, Yik Andy Yeung2, Shahram Salek-Ardakani2, Javier Chaparro-Riggers6.
Abstract
4-1BB (CD137, TNFRSF9) is an inducible costimulatory receptor expressed on activated T cells. Clinical trials of two agonist antibodies, utomilumab (PF-05082566) and urelumab (BMS-663513), are ongoing in multiple cancer indications, and both antibodies demonstrate distinct activities in the clinic. To understand these differences, we solved structures of the human 4-1BB/4-1BBL complex, the 4-1BBL trimer alone, and 4-1BB bound to utomilumab or urelumab. The 4-1BB/4-1BBL complex displays a unique interaction between receptor and ligand when compared with other TNF family members. Furthermore, our ligand-only structure differs from previously published data. Utomilumab, a ligand-blocking antibody, binds 4-1BB between CRDs 3 and 4. In contrast, urelumab binds 4-1BB CRD-1, away from the ligand binding site. Finally, cell-based assays demonstrate utomilumab is a milder agonist than urelumab. Collectively, our data provide a deeper understanding of the 4-1BB signaling complex, providing a template for future development of next generation 4-1BB targeted biologics.Entities:
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Year: 2018 PMID: 30410017 PMCID: PMC6224509 DOI: 10.1038/s41467-018-07136-7
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919