Effective Combination Adjuvants Engage Both TLR and Inflammasome Pathways To Promote Potent Adaptive Immune Responses

J Immunol. 2018 Jul 1;201(1):98-112. doi: 10.4049/jimmunol.1701604. Epub 2018 May 16.

Abstract

The involvement of innate receptors that recognize pathogen- and danger-associated molecular patterns is critical to programming an effective adaptive immune response to vaccination. The synthetic TLR4 agonist glucopyranosyl lipid adjuvant (GLA) synergizes with the squalene oil-in-water emulsion (SE) formulation to induce strong adaptive responses. Although TLR4 signaling through MyD88 and TIR domain-containing adapter inducing IFN-β are essential for GLA-SE activity, the mechanisms underlying the synergistic activity of GLA and SE are not fully understood. In this article, we demonstrate that the inflammasome activation and the subsequent release of IL-1β are central effectors of the action of GLA-SE, as infiltration of innate cells into the draining lymph nodes and production of IFN-γ are reduced in ASC-/- animals. Importantly, the early proliferation of Ag-specific CD4+ T cells was completely ablated after immunization in ASC-/- animals. Moreover, numbers of Ag-specific CD4+ T and B cells as well as production of IFN-γ, TNF-α, and IL-2 and Ab titers were considerably reduced in ASC-/-, NLRP3-/-, and IL-1R-/- mice compared with wild-type mice and were completely ablated in TLR4-/- animals. Also, extracellular ATP, a known trigger of the inflammasome, augments Ag-specific CD4+ T cell responses, as hydrolyzing it with apyrase diminished adaptive responses induced by GLA-SE. These data thus demonstrate that GLA-SE adjuvanticity acts through TLR4 signaling and NLRP3 inflammasome activation to promote robust Th1 and B cell responses to vaccine Ags. The findings suggest that engagement of both TLR and inflammasome activators may be a general paradigm for induction of robust CD4 T cell immunity with combination adjuvants such as GLA-SE.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism
  • Adenosine Triphosphate / metabolism
  • Adjuvants, Immunologic / pharmacology*
  • Animals
  • Antigens / immunology*
  • B-Lymphocytes / immunology*
  • CARD Signaling Adaptor Proteins / genetics
  • Female
  • Glucosides / immunology
  • Immunity, Humoral
  • Inflammasomes / immunology*
  • Interferon-beta / immunology
  • Interferon-gamma / immunology
  • Interleukin-1beta / metabolism
  • Interleukin-2 / immunology
  • Lipid A / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Differentiation Factor 88 / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein / genetics
  • Receptors, Interleukin-1 Type I / genetics
  • Squalene / immunology
  • Th1 Cells / immunology*
  • Toll-Like Receptor 4 / agonists
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology*
  • Tumor Necrosis Factor-alpha / immunology
  • Vaccination
  • Vaccines / immunology*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Adjuvants, Immunologic
  • Antigens
  • CARD Signaling Adaptor Proteins
  • Glucosides
  • IFNG protein, mouse
  • IL1B protein, mouse
  • IL1R1 protein, mouse
  • Inflammasomes
  • Interleukin-1beta
  • Interleukin-2
  • Lipid A
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Nlrp3 protein, mouse
  • Pycard protein, mouse
  • Receptors, Interleukin-1 Type I
  • TICAM-1 protein, mouse
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Vaccines
  • glucopyranosyl lipid-A
  • Interferon-beta
  • Squalene
  • Interferon-gamma
  • Adenosine Triphosphate