Potent adaptive immune responses induced against HIV-1 gp140 and influenza virus HA by a polyanionic carbomer

George Krashias, Anna Katharina Simon, Frank Wegmann, Wai Ling Kok, Ling Pei Ho, David Stevens, John Skehel, Jonathan L. Heeney, Amin E. Moghaddam, Quentin J. Sattentau*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Carbopol is a polyanionic carbomer gel used in man for a variety of topical applications and drug delivery purposes. Here we show that subcutaneous administration of carbopol with glycoprotein antigens elicits unusually strong specific adaptive immune responses in mice. Recombinant soluble HIV-1 envelope glycoprotein (Env)-based antigen formulated in carbopol was at least as potent at stimulating Env-specific B and T cell responses as Freund's Complete Adjuvant, and significantly more potent than aluminium salts. The antigen-specific T cell immune response elicited both Th1 and Th2 cytokines including high titers of IFN-γ, IL-2 and IL-4, and drove a Th1 isotype-switched antibody response. Mice immunized with a low dose of purified influenza HA in carbopol generated high titers of anti-HA antibodies and were protected from lethal challenge and disease with live virus. Similarly, immunization of mice with the melanoma cell line B16F10 formulated in carbopol significantly delayed tumor growth. We propose that carbopol, or related cross-linked polyacrylic acid analogues, may have promise for use as systemic vaccine adjuvants in man.

Original languageEnglish
Pages (from-to)2482-2489
Number of pages8
JournalVaccine
Volume28
Issue number13
DOIs
Publication statusPublished - 16 Mar 2010

ASJC Scopus subject areas

  • Molecular Medicine
  • General Immunology and Microbiology
  • General Veterinary
  • Public Health, Environmental and Occupational Health
  • Infectious Diseases

Keywords

  • Adjuvant
  • Antibody
  • HIV-1
  • Influenza A
  • Th1 response
  • Vaccine

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