Clinical and Translational Allergy (Oct 2021)

Heterogeneity of magnitude, allergen immunodominance, and cytokine polarization of cockroach allergen‐specific T cell responses in allergic sensitized children

  • Ricardo daSilva Antunes,
  • Aaron Sutherland,
  • April Frazier,
  • Veronique Schulten,
  • Anna Pomés,
  • Jill Glesner,
  • Agustin Calatroni,
  • Matthew C. Altman,
  • Robert A. Wood,
  • George T. O'Connor,
  • Jacqueline A. Pongracic,
  • Gurjit K. Khurana Hershey,
  • Carolyn M. Kercsmar,
  • Rebecca S. Gruchalla,
  • Michelle Gill,
  • Andrew H. Liu,
  • Edward Zoratti,
  • Meyer Kattan,
  • Paula J. Busse,
  • Leonard B. Bacharier,
  • Stephen J. Teach,
  • Lisa M. Wheatley,
  • Alkis Togias,
  • William W. Busse,
  • Daniel J. Jackson,
  • Alessandro Sette

DOI
https://doi.org/10.1002/clt2.12073
Journal volume & issue
Vol. 11, no. 8
pp. n/a – n/a

Abstract

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Abstract Background Characterization of allergic responses to cockroach (CR), a common aeroallergen associated with asthma, has focused mainly on IgE reactivity, but little is known about T cell responses, particularly in children. We conducted a functional evaluation of CR allergen‐specific T cell reactivity in a cohort of CR allergic children with asthma. Methods Peripheral blood mononuclear cells (PBMCs) were obtained from 71 children, with mild‐to‐moderate asthma who were enrolled in a CR immunotherapy (IT) clinical trial, prior to treatment initiation. PBMC were stimulated with peptide pools derived from 11 CR allergens, and CD4+ T cell responses assessed by intracellular cytokine staining. Results Highly heterogeneous responses in T cell reactivity were observed among participants, both in terms of the magnitude of cytokine response and allergen immunodominance. Reactivity against Bla g 9 and Bla g 5 was most frequent. The phenotype of the T cell response was dominated by IL‐4 production and a Th2 polarized profile in 54.9% of participants, but IFNγ production and Th1 polarization was observed in 25.3% of the participants. The numbers of regulatory CD4+ T cells were also highly variable and the magnitude of effector responses and Th2 polarization were positively correlated with serum IgE levels specific to a clinical CR extract. Conclusions Our results demonstrate that in children with mild‐to‐moderate asthma, CR‐specific T cell responses display a wide range of magnitude, allergen dominance, and polarization. These results will enable examination of whether any of the variables measured are affected by IT and/or are predictive of clinical outcomes.

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