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 in | The Journal of immunology (1950) Vol. 174; no. 8; pp. 5024 - 5032 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Am Assoc Immnol
15.04.2005
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Subjects | |
Online Access | Get full text |
ISSN | 0022-1767 1550-6606 |
DOI | 10.4049/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. |
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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 |
Author_xml | – sequence: 1 fullname: Takhar, Pooja – sequence: 2 fullname: Smurthwaite, Lyn – sequence: 3 fullname: Coker, Heather A – sequence: 4 fullname: Fear, David J – sequence: 5 fullname: Banfield, Graham K – sequence: 6 fullname: Carr, Victoria A – sequence: 7 fullname: Durham, Stephen R – sequence: 8 fullname: Gould, Hannah J |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15814733$$D View this record in MEDLINE/PubMed |
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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 |
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