Modified High-Molecular-Weight Hyaluronan Promotes Allergen-Specific Immune Tolerance.

نویسندگان

  • John A Gebe
  • Koshika Yadava
  • Shannon M Ruppert
  • Payton Marshall
  • Paul Hill
  • Ben A Falk
  • Johanna M Sweere
  • Hongwei Han
  • Gernot Kaber
  • Ingrid A Harten
  • Carlos Medina
  • Katalin Mikecz
  • Steven F Ziegler
  • Swathi Balaji
  • Sundeep G Keswani
  • Vinicio A de Jesus Perez
  • Manish J Butte
  • Kari Nadeau
  • William A Altemeier
  • Neil Fanger
  • Paul L Bollyky
چکیده

The extracellular matrix in asthmatic lungs contains abundant low-molecular-weight hyaluronan, and this is known to promote antigen presentation and allergic responses. Conversely, high-molecular-weight hyaluronan (HMW-HA), typical of uninflamed tissues, is known to suppress inflammation. We investigated whether HMW-HA can be adapted to promote tolerance to airway allergens. HMW-HA was thiolated to prevent its catabolism and was tethered to allergens via thiol linkages. This platform, which we call "XHA," delivers antigenic payloads in the context of antiinflammatory costimulation. Allergen/XHA was administered intranasally to mice that had been sensitized previously to these allergens. XHA prevents allergic airway inflammation in mice sensitized previously to either ovalbumin or cockroach proteins. Allergen/XHA treatment reduced inflammatory cell counts, airway hyperresponsiveness, allergen-specific IgE, and T helper type 2 cell cytokine production in comparison with allergen alone. These effects were allergen specific and IL-10 dependent. They were durable for weeks after the last challenge, providing a substantial advantage over the current desensitization protocols. Mechanistically, XHA promoted CD44-dependent inhibition of nuclear factor-κB signaling, diminished dendritic cell maturation, and reduced the induction of allergen-specific CD4 T-helper responses. XHA and other potential strategies that target CD44 are promising alternatives for the treatment of asthma and allergic sinusitis.

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عنوان ژورنال:
  • American journal of respiratory cell and molecular biology

دوره 56 1  شماره 

صفحات  -

تاریخ انتشار 2017