Diamino Allose Phosphates: Novel, Potent, and Highly Stable Toll-like Receptor 4 Agonists

  • Juhienah K. Khalaf
  • , Laura S. Bess
  • , Lois M. Walsh
  • , Janine M. Ward
  • , Craig L. Johnson
  • , Mark T. Livesay
  • , Konner J. Jackson
  • , Jay T. Evans
  • , Kendal T. Ryter
  • , Hélène G. Bazin-Lee

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Most known synthetic toll-like receptor 4 (TLR4) agonists are carbohydrate-based lipid-A mimetics containing several fatty acyl chains, including a labile 3-O-acyl chain linked to the C-3 position of the non-reducing sugar known to undergo cleavage impacting stability and resulting in loss of activity. To overcome this inherent instability, we rationally designed a new class of chemically more stable synthetic TLR4 ligands that elicit robust innate and adaptive immune responses. This new class utilized a diamino allose phosphate (DAP) scaffold containing a nonhydrolyzable 3-amide bond instead of the classical 3-ester. Accordingly, the DAPs have significantly improved thermostability in aqueous formulations and potency relative to other known natural and synthetic TLR4 ligands. Furthermore, the DAP analogues function as potent vaccine adjuvants to enhance influenza-specific antibodies in mice and provide protection against lethal influenza virus challenges. This novel set of TLR4 ligands show promise as next-generation vaccine adjuvants and stand-alone immunomodulators.

Original languageEnglish
Pages (from-to)13900-13917
Number of pages18
JournalJournal of Medicinal Chemistry
Volume66
Issue number20
DOIs
StatePublished - Oct 26 2023

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