Differential T follicular helper cell phenotypes distinguish IgE-mediated milk allergy from eosinophilic esophagitis in children

Daniel Lozano-Ojalvo, Xin Chen, Wajiha Kazmi, David Menchén-Martínez, Leticia Pérez-Rodríguez, Weslley Fernandes-Braga, Scott Tyler, Keith Benkov, Nanci Pittman, Joanne Lai, Hugh A. Sampson, Maria Curotto de Lafaille, David Dunkin, M. Cecilia Berin*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)909-922
Number of pages14
JournalJournal of Allergy and Clinical Immunology
Volume155
Issue number3
DOIs
StatePublished - Mar 2025

Funding

Funding was provided by grant R01 AI151707 from the National Institute of Allergy and Infectious Diseases (to M.C.B. and M.C.d.L.) and pilot grants from the Mindich Child Health and Development Institute (one to M.C.B. and D.D. and one to D.L.-O.). D.L.-O. was partially funded by a postdoctoral fellowship from the Spanish Fundaci\u00F3n Alfonso Mart\u00EDn Escudero.Disclosure of potential conflict of interest: H. A. Sampson reports funding to his institution from National Institutes of Health/National Institute of Allergy and Infectious Diseases grants and has received consulting fees from DBV Technologies SA, N-FOLD Therapeutics, Alpina Biotechnology, and Siolta Therapeutics unrelated to this work and stock options from DBV Technologies SA and N-FOLD Therapeutics. M. Curotto de Lafaille received consulting fees from Genentech, unrelated to this work. The rest of the authors declare that they have no conflicts of interest.

Keywords

  • Eosinophilic esophagitis
  • T follicular helper
  • T2A
  • food allergy
  • milk allergy

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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