Allergen Drives Class Switching to IgE in the Nasal Mucosa in Allergic Rhinitis

IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance of these B cells in the nasal mucosa in allergic rhinitis. It is generally accepted that expression of activation-induced cytidine deaminase a...

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Published inThe Journal of immunology (1950) Vol. 174; no. 8; pp. 5024 - 5032
Main Authors Takhar, Pooja, Smurthwaite, Lyn, Coker, Heather A, Fear, David J, Banfield, Graham K, Carr, Victoria A, Durham, Stephen R, Gould, Hannah J
Format Journal Article
LanguageEnglish
Published United States Am Assoc Immnol 15.04.2005
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Online AccessGet full text
ISSN0022-1767
1550-6606
DOI10.4049/jimmunol.174.8.5024

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Abstract IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance of these B cells in the nasal mucosa in allergic rhinitis. It is generally accepted that expression of activation-induced cytidine deaminase and class switch recombination (CSR) occur in lymphoid tissue, implying that IgE-committed B cells must migrate through the circulation to the nasal mucosa. Our detection of mRNA for activation-induced cytidine, multiple germline gene transcripts, and ε circle transcripts in the nasal mucosa of allergic, in contrast to nonallergic control subjects, however, indicates that local CSR occurs in allergic rhinitis. The germline gene transcripts and ε circle transcripts in grass pollen-allergic subjects are up-regulated during the season and also when biopsies from allergic subjects are incubated with the allergen ex vivo. These results demonstrate that allergen stimulates local CSR to IgE, revealing a potential target for topical therapies in allergic rhinitis.
AbstractList IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance of these B cells in the nasal mucosa in allergic rhinitis. It is generally accepted that expression of activation-induced cytidine deaminase and class switch recombination (CSR) occur in lymphoid tissue, implying that IgE-committed B cells must migrate through the circulation to the nasal mucosa. Our detection of mRNA for activation-induced cytidine, multiple germline gene transcripts, and epsilon circle transcripts in the nasal mucosa of allergic, in contrast to nonallergic control subjects, however, indicates that local CSR occurs in allergic rhinitis. The germline gene transcripts and epsilon circle transcripts in grass pollen-allergic subjects are up-regulated during the season and also when biopsies from allergic subjects are incubated with the allergen ex vivo. These results demonstrate that allergen stimulates local CSR to IgE, revealing a potential target for topical therapies in allergic rhinitis.
IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance of these B cells in the nasal mucosa in allergic rhinitis. It is generally accepted that expression of activation-induced cytidine deaminase and class switch recombination (CSR) occur in lymphoid tissue, implying that IgE-committed B cells must migrate through the circulation to the nasal mucosa. Our detection of mRNA for activation-induced cytidine, multiple germline gene transcripts, and epsilon circle transcripts in the nasal mucosa of allergic, in contrast to nonallergic control subjects, however, indicates that local CSR occurs in allergic rhinitis. The germline gene transcripts and epsilon circle transcripts in grass pollen-allergic subjects are up-regulated during the season and also when biopsies from allergic subjects are incubated with the allergen ex vivo. These results demonstrate that allergen stimulates local CSR to IgE, revealing a potential target for topical therapies in allergic rhinitis.IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance of these B cells in the nasal mucosa in allergic rhinitis. It is generally accepted that expression of activation-induced cytidine deaminase and class switch recombination (CSR) occur in lymphoid tissue, implying that IgE-committed B cells must migrate through the circulation to the nasal mucosa. Our detection of mRNA for activation-induced cytidine, multiple germline gene transcripts, and epsilon circle transcripts in the nasal mucosa of allergic, in contrast to nonallergic control subjects, however, indicates that local CSR occurs in allergic rhinitis. The germline gene transcripts and epsilon circle transcripts in grass pollen-allergic subjects are up-regulated during the season and also when biopsies from allergic subjects are incubated with the allergen ex vivo. These results demonstrate that allergen stimulates local CSR to IgE, revealing a potential target for topical therapies in allergic rhinitis.
IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance of these B cells in the nasal mucosa in allergic rhinitis. It is generally accepted that expression of activation-induced cytidine deaminase and class switch recombination (CSR) occur in lymphoid tissue, implying that IgE-committed B cells must migrate through the circulation to the nasal mucosa. Our detection of mRNA for activation-induced cytidine, multiple germline gene transcripts, and ε circle transcripts in the nasal mucosa of allergic, in contrast to nonallergic control subjects, however, indicates that local CSR occurs in allergic rhinitis. The germline gene transcripts and ε circle transcripts in grass pollen-allergic subjects are up-regulated during the season and also when biopsies from allergic subjects are incubated with the allergen ex vivo. These results demonstrate that allergen stimulates local CSR to IgE, revealing a potential target for topical therapies in allergic rhinitis.
Author Banfield, Graham K
Carr, Victoria A
Smurthwaite, Lyn
Durham, Stephen R
Fear, David J
Coker, Heather A
Gould, Hannah J
Takhar, Pooja
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Snippet IgE-expressing B cells are over 1000 times more frequent in the nasal B cell than the peripheral blood B cell population. We have investigated the provenance...
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SubjectTerms Adult
Allergens - administration & dosage
B-Lymphocytes - enzymology
B-Lymphocytes - immunology
B-Lymphocytes - pathology
Base Sequence
Case-Control Studies
Cytidine Deaminase
Cytosine Deaminase - genetics
Cytosine Deaminase - metabolism
DNA, Complementary - genetics
Female
Humans
Immunoglobulin Class Switching
Immunoglobulin E - genetics
In Vitro Techniques
Male
Middle Aged
Molecular Sequence Data
Nasal Mucosa - enzymology
Nasal Mucosa - immunology
Nasal Mucosa - pathology
Rhinitis, Allergic, Perennial - enzymology
Rhinitis, Allergic, Perennial - genetics
Rhinitis, Allergic, Perennial - immunology
Rhinitis, Allergic, Perennial - pathology
Rhinitis, Allergic, Seasonal - enzymology
Rhinitis, Allergic, Seasonal - genetics
Rhinitis, Allergic, Seasonal - immunology
Rhinitis, Allergic, Seasonal - pathology
RNA, Messenger - genetics
RNA, Messenger - metabolism
Sequence Homology, Nucleic Acid
Title Allergen Drives Class Switching to IgE in the Nasal Mucosa in Allergic Rhinitis
URI http://www.jimmunol.org/cgi/content/abstract/174/8/5024
https://www.ncbi.nlm.nih.gov/pubmed/15814733
https://www.proquest.com/docview/17872236
https://www.proquest.com/docview/67713654
Volume 174
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