TY - JOUR
T1 - Differential T follicular helper cell phenotypes distinguish IgE-mediated milk allergy from eosinophilic esophagitis in children
AU - Lozano-Ojalvo, Daniel
AU - Chen, Xin
AU - Kazmi, Wajiha
AU - Menchén-Martínez, David
AU - Pérez-Rodríguez, Leticia
AU - Fernandes-Braga, Weslley
AU - Tyler, Scott
AU - Benkov, Keith
AU - Pittman, Nanci
AU - Lai, Joanne
AU - Sampson, Hugh A.
AU - Curotto de Lafaille, Maria
AU - Dunkin, David
AU - Berin, M. Cecilia
N1 - Publisher Copyright:
© 2024 American Academy of Allergy, Asthma & Immunology
PY - 2025/3
Y1 - 2025/3
N2 - Background: IgE-mediated food allergy and eosinophilic esophagitis (EoE) are diseases commonly triggered by milk. Milk-responsive CD4+ T cells producing type 2 cytokines are present in both diseases, yet the clinical manifestation of disease in milk allergy (MA) and EoE are distinct. Objective: We sought to identify differences in CD4+ T cells between EoE and MA that may be responsible for distinct disease manifestations. Method: The total and milk-specific CD4+ T-cell phenotype of children with MA, children with EoE (active or in remission), and controls was measured using spectral flow cytometry of peripheral blood (all groups) or esophageal biopsies (EoE and control). Results: Circulating milk-responsive T cells could be identified in active EoE and MA. An increased frequency of TH2A cells was also noted in MA and EoE. In circulating T cells, type 2 cytokine production was elevated in MA, but not EoE. Within the milk-responsive T follicular helper (TFH) subset, a dichotomy of phenotype was noted: TFH13 cells predominated in MA, while IL-10–producing TFH cells predominated in EoE. In the esophagus, CD4+ T cells were constitutively activated and expressed not only type 2 cytokines, but also IL-10 and IL-21 in active EoE. IgG4 was produced from CD38+ plasma cells in close proximity to CD4+ T cells. In vitro activation studies demonstrated that IL-10 and IL-21 elicited strong IgG4 responses in B lymphocytes, while IL-4 and IL-13 promoted IgE production. Conclusions: Our studies demonstrate a dichotomy of TFH responses that may be the basis for different clinical manifestations to milk in EoE and MA.
AB - Background: IgE-mediated food allergy and eosinophilic esophagitis (EoE) are diseases commonly triggered by milk. Milk-responsive CD4+ T cells producing type 2 cytokines are present in both diseases, yet the clinical manifestation of disease in milk allergy (MA) and EoE are distinct. Objective: We sought to identify differences in CD4+ T cells between EoE and MA that may be responsible for distinct disease manifestations. Method: The total and milk-specific CD4+ T-cell phenotype of children with MA, children with EoE (active or in remission), and controls was measured using spectral flow cytometry of peripheral blood (all groups) or esophageal biopsies (EoE and control). Results: Circulating milk-responsive T cells could be identified in active EoE and MA. An increased frequency of TH2A cells was also noted in MA and EoE. In circulating T cells, type 2 cytokine production was elevated in MA, but not EoE. Within the milk-responsive T follicular helper (TFH) subset, a dichotomy of phenotype was noted: TFH13 cells predominated in MA, while IL-10–producing TFH cells predominated in EoE. In the esophagus, CD4+ T cells were constitutively activated and expressed not only type 2 cytokines, but also IL-10 and IL-21 in active EoE. IgG4 was produced from CD38+ plasma cells in close proximity to CD4+ T cells. In vitro activation studies demonstrated that IL-10 and IL-21 elicited strong IgG4 responses in B lymphocytes, while IL-4 and IL-13 promoted IgE production. Conclusions: Our studies demonstrate a dichotomy of TFH responses that may be the basis for different clinical manifestations to milk in EoE and MA.
KW - Eosinophilic esophagitis
KW - T follicular helper
KW - T2A
KW - food allergy
KW - milk allergy
UR - https://www.scopus.com/pages/publications/85209583971
U2 - 10.1016/j.jaci.2024.09.024
DO - 10.1016/j.jaci.2024.09.024
M3 - Article
C2 - 39389123
AN - SCOPUS:85209583971
SN - 0091-6749
VL - 155
SP - 909
EP - 922
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 3
ER -