Vaccines And Adjuvants

Alum adjuvant: some of the tricks of the oldest adjuvant

  • 1Laboratory of Immunoregulation and Mucosal Immunology, University Hospital Ghent, Ghent, Belgium
  • 2Department of Pulmonary Medicine, Erasmus MC, Rotterdam, The Netherlands
  • Correspondence
    Mirjam Kool m.kool{at}erasmusmc.nl
  • Journal of Medical Microbiology 2012; 61(Pt 7):927–934 · https://doi.org/10.1099/jmm.0.038943-0

    View at publisher PubMed

    Abstract

    Alum has been the most widely used adjuvant for over 80 years. Although there have been searches for alternative adjuvants, aluminium-containing adjuvants will continue to be used for many years due to their good track record of safety, low cost and adjuvanticity with a variety of antigens. For infections that can be prevented by induction of serum antibodies, aluminium-containing adjuvants formulated under optimal conditions are the adjuvants of choice. There are also some limitations of aluminium-containing adjuvants, which include local reactions, augmentation of IgE antibody responses, ineffectiveness for some antigens and inability to augment cell-mediated immune responses, especially cytotoxic T-cell responses. In this review, we describe the current knowledge regarding the mechanisms (both cellular and molecular) by which alum employs its adjuvant effect, although the final mechanism is not yet well-defined. Furthermore, we discuss how alum’s adjuvanticity could be improved.

    This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

    Abbreviations:
    DAMPs
    damage-associated molecular patterns
    DCs
    dendritic cells
    DTP
    Diphtheria–Tetanus–Pertussis
    HBV
    hepatitis B virus
    HIB
    Haemophilus influenzae B
    HPV
    human papilloma virus
    NLR
    NOD-like receptor
    PAMPs
    pathogen-associated molecular patterns
    PGE2
    prostaglandin E2
    TCR
    T-cell receptor
    TLR
    Toll-like receptor
    UA
    uric acid