Glycosylation-modified antigens as a tolerance-inducing vaccine platform prevent anaphylaxis in a pre-clinical model of food allergy

Shijie Cao, Chitavi D. Maulloo, Michal M. Raczy, Matthew Sabados, Anna J. Slezak, Mindy Nguyen, Ani Solanki, Rachel P. Wallace, Ha Na Shim, D. Scott Wilson, Jeffrey A. Hubbell

Research output: Contribution to journalArticlepeer-review

Abstract

The only FDA-approved oral immunotherapy for a food allergy provides protection against accidental exposure to peanuts. However, this therapy often causes discomfort or side effects and requires long-term commitment. Better preventive and therapeutic solutions are urgently needed. We develop a tolerance-inducing vaccine technology that utilizes glycosylation-modified antigens to induce antigen-specific non-responsiveness. The glycosylation-modified antigens are administered intravenously (i.v.) or subcutaneously (s.c.) and traffic to the liver or lymph nodes, respectively, leading to preferential internalization by antigen-presenting cells, educating the immune system to respond in an innocuous way. In a mouse model of cow's milk allergy, treatment with glycosylation-modified β-lactoglobulin (BLG) is effective in preventing the onset of allergy. In addition, s.c. administration of glycosylation-modified BLG shows superior safety and potential in treating existing allergies in combination with anti-CD20 co-therapy. This platform provides an antigen-specific immunomodulatory strategy to prevent and treat food allergies.

Original languageEnglish (US)
Article number101346
JournalCell Reports Medicine
Volume5
Issue number1
DOIs
StatePublished - Jan 16 2024

Keywords

  • antigen delivery
  • food allergy
  • glycosylation
  • immune tolerance
  • subcutaneous immunotherapy

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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