Depletion of CD4+CD25+T cells switches the whey-allergic response from immunoglobulin E- to immunoglobulin free light chain-dependent

B.C.A.M. Van Esch, B. Schouten, B.R.J. Blokhuis, G.A. Hofman, L. Boon, J. Garssen, L.M.J. Knippels, L.E.M. Willemsen, F.A. Redegeld

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background Symptoms of allergy are largely attributed to an IgE-mediated hypersensitivity response. However, a considerable number of patients also exhibit clinical features of allergy without detectable systemic IgE. Previous work showed that Ig-free light chains (IgLC) may act as an alternate mechanism to induce allergic responses. CD4+CD25+T cells are crucial in the initiation and regulation of allergic responses and compromised function might affect the response to allergens. Objective To examine the contribution of CD4+CD25+T cells and IgLC towards the whey-allergic response. Methods Mice were sensitized orally with whey using cholera toxin as an adjuvant. CD25+T cells were depleted in vivo using a CD25 mAb. The acute allergic skin response to whey and ex vivo colon reactivity was measured in the presence or absence of F991, a specific inhibitor of IgLC. Serum whey-specific antibodies and IgLC in serum and mesenteric lymph node (MLN) supernatants were measured. Depletion of CD4+CD25+T cells was confirmed in the spleen. Results Anti-CD25 treatment strongly reduced whey-specific antibody levels and resulted in a partial depletion of effector T cells and a major depletion of Foxp3+regulatory T cells. Surprisingly, despite the abolished specific IgE response, the acute allergic skin response to whey was not affected. IgLC levels were enhanced in the serum and MLN supernatants of CD25-depleted sensitized mice. F991 inhibited the acute skin response and colon hyperreactivity in anti-CD25-treated mice, indicating that these responses were mainly IgLC dependent. Conclusions Depletion of CD4+CD25+T cells resulted in a switch from an IgE- to an IgLC-dependent acute skin response and functional hyperresponsiveness of the colon. Our data suggest that CD25+T cells play a crucial role in balancing cow's milk allergy between IgE and IgE-independent responses and both mechanisms might play a role in allergic responses to the same allergen. © 2010 Blackwell Publishing Ltd.
Original languageEnglish
Pages (from-to)1414-1421
Number of pages8
JournalClinical and Experimental Allergy
Volume40
Issue number9
DOIs
Publication statusPublished - 1 Sept 2010

Keywords

  • atopic disease
  • CD25 depletion
  • cow's milk allergy
  • effector T cells
  • food allergy
  • Ig-free light chain
  • IgE
  • regulatory T cells
  • antibody
  • cholera toxin
  • immunoglobulin E
  • transcription factor FOXP3
  • animal experiment
  • animal model
  • animal tissue
  • article
  • CD25+ T lymphocyte
  • CD4+ CD25+ T lymphocyte
  • controlled study
  • ex vivo study
  • female
  • immune response
  • in vivo study
  • mesentery lymph node
  • milk allergy
  • mouse
  • nonhuman
  • priority journal
  • regulatory T lymphocyte
  • skin allergy
  • spleen
  • supernatant
  • T cell depletion
  • whey

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