Abstract | BACKGROUND:
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.
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Authors | D M Moutsoglou, S C Dreskin |
Journal | Clinical 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 |
PMID | 27021119
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | © 2016 John Wiley & Sons Ltd. |
Chemical References |
- Allergens
- Biomarkers
- Chemokine CCL2
- Immunoglobulin E
- Leukocyte Common Antigens
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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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