Regulatory T cell specificity directs tolerance versus allergy against aeroantigens in humans

• Petra Bacher ^[3] ; Frederik Heinrich ^[1] ; Ulrik Stervbo ^[2]
  1. [1] German Rheumatism Research Centre

     German Rheumatism Research Centre

     Berlin, Stadt, Alemania

     
  2. [2] Ruhr University Bochum

     Ruhr University Bochum

     Kreisfreie Stadt Bochum, Alemania

     
  3. [3] University Medicine Berlin

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• Localización: Cell, ISSN 0092-8674, Vol. 167, Nº. 4, 2016, págs. 1067-1078
• Idioma: inglés
• Texto completo no disponible (Saber más ...)
• Resumen

  • FOXP3+ regulatory T cells (Tregs) maintain tolerance against self-antigens and innocuous environmental antigens. However, it is still unknown whether Treg-mediated tolerance is antigen specific and how Treg specificity contributes to the selective loss of tolerance, as observed in human immunopathologies such as allergies. Here, we used antigen-reactive T cell enrichment to identify antigen-specific human Tregs. We demonstrate dominant Treg-mediated tolerance against particulate aeroallergens, such as pollen, house dust mites, and fungal spores. Surprisingly, we found no evidence of functional impairment of Treg responses in allergic donors. Rather, major allergenic proteins, known to rapidly dissociate from inhaled allergenic particles, have a generally reduced capability to generate Treg responses. Most strikingly, in individual allergic donors, Th2 cells and Tregs always target disparate proteins. Thus, our data highlight the importance of Treg antigen-specificity for tolerance in humans and identify antigen-specific escape from Treg control as an important mechanism enabling antigen-specific loss of tolerance in human allergy.