Chemical Synthesis of Marine-Derived Sulfoglycolipids, a New Class of Molecular Adjuvants

Mar Drugs. 2017 Sep 20;15(9):288. doi: 10.3390/md15090288.

Abstract

Vaccines play a primary role in the protection of human health by preventing infectious and chronic diseases. Recently we have reported 1,2-O-distearoyl-3-O-β-d-sulfoquinovosylglycerol (β-SQDG18), here named Sulfavant A (1), which shows promising properties as a new molecular adjuvant in in vitro and in vivo tests. In the present manuscript, we provide full details about a synthetic strategy for the preparation of 1, including a discussion of chemical determinants of the activity and the major technical hurdles we faced during the study. Synthesis of Sulfavant A (1) is achieved by a versatile procedure based on a trichloroacetimidate methodology and peracetate sugar precursors. The final design opens possibilities for the preparation of a series of interesting analogs for further pharmacological optimization and development, including derivatives containing different saturated and polyunsaturated fatty acids (e.g., 17 and 22).

Keywords: Sulfavant A; adjuvant; dendritic cells; glycolipids; immunogenic lipid; immunology; innate immunity; sulfolipid; vaccine.

MeSH terms

  • Adjuvants, Immunologic / chemical synthesis*
  • Adjuvants, Immunologic / chemistry
  • Adjuvants, Immunologic / pharmacology
  • Adjuvants, Pharmaceutic
  • Animals
  • Aquatic Organisms*
  • Dendritic Cells / drug effects
  • Glycolipids / chemical synthesis*
  • Glycolipids / chemistry
  • Glycolipids / pharmacology
  • Vaccines

Substances

  • Adjuvants, Immunologic
  • Adjuvants, Pharmaceutic
  • Glycolipids
  • Vaccines
  • sulfoglycolipids