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B cells establish, but do not maintain, long-lived murine anti-peanut IgE(a).

AbstractBACKGROUND:
Peanut allergy (PNA) has been reported to be transferred to tolerant recipients through organ and bone marrow (BM) transplantation. The roles T and B cells play in establishing, and the roles B cell subsets play in maintaining lifelong anti-peanut IgE levels are unknown.
OBJECTIVES:
To determine the cellular requirements for the transfer of murine PNA and to determine the role CD20(+) cells play in maintaining long-lived anti-peanut IgE levels.
METHODS:
We developed a novel adoptive transfer model to investigate the cellular requirements for transferring murine PNA. We also treated peanut-allergic (PA) mice with anti-CD20 antibody and measured IgE levels throughout treatment.
RESULTS:
Purified B220(+) cells from PA splenocytes and purified CD4(+) cells from naïve (NA) splenocytes are the minimal requirements for the adoptive transfer of PNA. Prolonged treatment of allergic mice with anti-CD20 antibody results in significant depletion of B cell subsets but does not affect anti-peanut IgE levels, symptoms, or numbers of IgE antibody secreting cells (ASCs) in the BM. Adoptive transfer of BM and spleen cells from allergic donors treated with anti-CD20 antibody does not result in the transfer of PNA in NA recipients, demonstrating that anti-CD20 antibody treatment depletes B cells capable of differentiating into peanut-specific IgE ASCs.
CONCLUSIONS AND CLINICAL RELEVANCE:
Peanut allergy can be established in a NA hosts with B220(+) cells from PA donors and CD4(+) cells from peanut-NA donors. However, long-term depletion of B220(+) cells with anti-CD20 antibody does not affect anti-peanut IgE levels. These results highlight a novel role for B cells in the development of PNA and provide evidence that long-lived anti-peanut IgE levels may be maintained by long-lived ASCs.
AuthorsD M Moutsoglou, S C Dreskin
JournalClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology (Clin Exp Allergy) Vol. 46 Issue 4 Pg. 640-53 (Apr 2016) ISSN: 1365-2222 [Electronic] England
PMID27021119 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© 2016 John Wiley & Sons Ltd.
Chemical References
  • Allergens
  • Biomarkers
  • Chemokine CCL2
  • Immunoglobulin E
  • Leukocyte Common Antigens
Topics
  • Adoptive Transfer
  • Allergens (immunology)
  • Animals
  • Arachis (adverse effects)
  • B-Lymphocyte Subsets (immunology, metabolism)
  • B-Lymphocytes (immunology, metabolism)
  • Biomarkers
  • Chemokine CCL2 (metabolism)
  • Disease Models, Animal
  • Immunoglobulin E (immunology)
  • Immunophenotyping
  • Leukocyte Common Antigens (metabolism)
  • Mast Cells (immunology, metabolism)
  • Mice
  • Peanut Hypersensitivity (immunology, metabolism)

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