TY - JOUR
T1 - Heterogeneity of magnitude, allergen immunodominance, and cytokine polarization of cockroach allergen-specific T cell responses in allergic sensitized children
AU - da Silva Antunes, Ricardo
AU - Sutherland, Aaron
AU - Frazier, April
AU - Schulten, Veronique
AU - Pomés, Anna
AU - Glesner, Jill
AU - Calatroni, Agustin
AU - Altman, Matthew C.
AU - Wood, Robert A.
AU - O'Connor, George T.
AU - Pongracic, Jacqueline A.
AU - Khurana Hershey, Gurjit K.
AU - Kercsmar, Carolyn M.
AU - Gruchalla, Rebecca S.
AU - Gill, Michelle
AU - Liu, Andrew H.
AU - Zoratti, Edward
AU - Kattan, Meyer
AU - Busse, Paula J.
AU - Bacharier, Leonard B.
AU - Teach, Stephen J.
AU - Wheatley, Lisa M.
AU - Togias, Alkis
AU - Busse, William W.
AU - Jackson, Daniel J.
AU - Sette, Alessandro
N1 - Funding Information:
We wish to acknowledge all subjects for their participation and donate their blood and time for this study. The authors wish to thank all the personnel from the clinical sites involved in this work and Rho, particularly Amanda Farrell, Stephanie Wellford, Jessica Baucom, and Kelly Penke for their incessant efforts, supervision, and coordination. This project has been funded in whole or in part with Federal funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services, under grants 1UM1AI114271‐01, UM2AI117870, and 5UM1AI114271‐03. Additional support was provided by the National Center for Research Resources, and National Center for Advancing Translational Sciences, National Institutes of Health, under grants NCATS/NIH UL1TR001079, NCATS/NIH UL1TR001422, NCATS/NIH UL1TR001876, NIH/CTSA 5UL1TR001425‐03, and NIAID/NIH U19AI135731. Dr. Lisa M. Wheatley and Alkis Togias co‐authorship of this publication does not necessarily constitute endorsement by the National Institute of Allergy and Infectious Diseases, the National Institutes of Health or any other agency of the United States government.
Funding Information:
We wish to acknowledge all subjects for their participation and donate their blood and time for this study. The authors wish to thank all the personnel from the clinical sites involved in this work and Rho, particularly Amanda Farrell, Stephanie Wellford, Jessica Baucom, and Kelly Penke for their incessant efforts, supervision, and coordination. This project has been funded in whole or in part with Federal funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services, under grants 1UM1AI114271-01, UM2AI117870, and 5UM1AI114271-03. Additional support was provided by the National Center for Research Resources, and National Center for Advancing Translational Sciences, National Institutes of Health, under grants NCATS/NIH UL1TR001079, NCATS/NIH UL1TR001422, NCATS/NIH UL1TR001876, NIH/CTSA 5UL1TR001425-03, and NIAID/NIH U19AI135731. Dr. Lisa M. Wheatley and Alkis Togias co-authorship of this publication does not necessarily constitute endorsement by the National Institute of Allergy and Infectious Diseases, the National Institutes of Health or any other agency of the United States government.
Publisher Copyright:
© 2021 The Authors. Clinical and Translational Allergy published by John Wiley & Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology.
PY - 2021/10
Y1 - 2021/10
N2 - 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.
AB - 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.
KW - T cell
KW - allergens
KW - asthma
KW - clinical immunology
KW - cockroach
UR - http://www.scopus.com/inward/record.url?scp=85117914921&partnerID=8YFLogxK
U2 - 10.1002/clt2.12073
DO - 10.1002/clt2.12073
M3 - Article
C2 - 34691392
AN - SCOPUS:85117914921
SN - 2045-7022
VL - 11
JO - Clinical and Translational Allergy
JF - Clinical and Translational Allergy
IS - 8
M1 - e12073
ER -