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Identification of specifically reduced Th2 cell subsets in allergic rhinitis patients after sublingual immunotherapy
Author(s) -
Ihara F.,
Sakurai D.,
Yonekura S.,
Iinuma T.,
Yagi R.,
Sakurai T.,
Ito T.,
Matsuura A.,
Morimoto Y.,
Arai T.,
Suzuki S.,
Katayama K.,
Nakayama T.,
Okamoto Y.
Publication year - 2018
Publication title -
allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.363
H-Index - 173
eISSN - 1398-9995
pISSN - 0105-4538
DOI - 10.1111/all.13436
Subject(s) - house dust mite , peripheral blood mononuclear cell , slit , immunology , flow cytometry , medicine , pathogenesis , allergy , t cell , cytokine , allergen , biology , immune system , in vitro , biochemistry , genetics
Background Although Th2 cells are well known to play important roles in allergic diseases including allergic rhinitis ( AR ), the factors that induce and sustain the pathogenesis of AR remain unclear. The recent development of sublingual immunotherapy ( SLIT ) is expected to allow changes to the underlying pathogenesis of AR . However, which Th2 cell subsets are important in house dust mite‐induced AR ( HDM ‐ AR ), the influence of SLIT on the pathogenic Th2 cells, and the association of Th2 cell subsets with SLIT efficacy have not been clarified. Methods The cytokine production and frequency of HDM ‐reactive T‐cell subsets in peripheral blood mononuclear cells ( PBMC s) were evaluated using flow cytometry in 89 HDM ‐ AR patients (placebo [n = 43] and HDM 300 IR [n = 46]) who participated in a placebo‐controlled study of SLIT with HDM tablets. All patients provided samples both before treatment as a baseline and at the end of the 52‐week study. The PBMC s were stained with CellTrace™ Violet ( CTV ) before culture with HDM extract, and HDM ‐reactive T cells were detected as the proliferated cells with diminished CTV . Results HDM ‐reactive IL ‐5 + IL ‐13 + CD 27 − CD 161 + CD 4 + cells and ST 2 + CD 45 RO + CD 4 + cells were observed in the peripheral blood from each patient with HDM ‐ AR ; these cells significantly decreased after SLIT in the group treated with active tablets. HDM ‐reactive ST 2 + CD 45 RO + CD 4 + cells were significantly lower in active‐responders. Conclusion Allergen‐reactive ST 2 + CD 45 RO + CD 4 + cells or those combined with IL ‐5 + IL ‐13 + CD 27 − CD 161 + CD 4 + cells may be useful as markers indicating the successful treatment of SLIT . These cells may play a crucial role in the pathogenesis of AR as pathogenic memory Th2 cells.