Pentamers not found in the universal proteome can enhance antigen specific immune responses and adjuvant vaccines

  • Ami Patel
  • , Jessica C. Dong
  • , Brett Trost
  • , Jason S. Richardson
  • , Sarah Tohme
  • , Shawn Babiuk
  • , Anthony Kusalik
  • , Sam K.P. Kung
  • , Gary P. Kobinger

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

Certain short peptides do not occur in humans and are rare or non-existent in the universal proteome. Antigens that contain rare amino acid sequences are in general highly immunogenic and may activate different arms of the immune system. We first generated a list of rare, semi-common, and common 5-mer peptides using bioinformatics tools to analyze the UniProtKB database. Experimental observations indicated that rare and semi-common 5-mers generated stronger cellular responses in comparison with common-occurring sequences. We hypothesized that the biological process responsible for this enhanced immunogenicity could be used to positively modulate immune responses with potential application for vaccine development. Initially, twelve rare 5-mers, 9-mers, and 13-mers were incorporated in frame at the end of an H5N1 hemagglutinin (HA) antigen and expressed from a DNA vaccine. The presence of some 5-mer peptides induced improved immune responses. Adding one 5-mer peptide exogenously also offered improved clinical outcome and/or survival against a lethal H5N1 or H1N1 influenza virus challenge in BALB/c mice and ferrets, respectively. Interestingly, enhanced anti-HBsAg antibody production by up to 25-fold in combination with a commercial Hepatitis B vaccine (Engerix-B, GSK) was also observed in BALB/c mice. Mechanistically, NK cell activation and dependency was observed with enhancing peptides ex vivo and in NK-depleted mice. Overall, the data suggest that rare or non-existent oligopeptides can be developed as immunomodulators and supports the further evaluation of some 5-mer peptides as potential vaccine adjuvants.

Original languageEnglish (US)
Article numbere43802
JournalPloS one
Volume7
Issue number8
DOIs
StatePublished - Aug 24 2012
Externally publishedYes

ASJC Scopus subject areas

  • General

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