Frequency of Th17 CD20+ cells in the peripheral blood of rheumatoid arthritis patients is higher compared to healthy subjects

Introduction Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies, to alleviate RA is unclear. This study examined the proportions of IL-17-secreting lymphocytes in the blood of healthy subjects a...

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Published inArthritis research & therapy Vol. 13; no. 6; p. R208
Main Authors Eggleton, Paul, Bremer, Edwin, Tarr, Joanna M, de Bruyn, Marco, Helfrich, Wijnand, Kendall, Alexandra, Haigh, Richard C, Viner, Nick J, Winyard, Paul G
Format Journal Article
LanguageEnglish
Published London BioMed Central 01.01.2011
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ISSN1478-6354
1478-6362
1478-6354
1478-6362
DOI10.1186/ar3541

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Abstract Introduction Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies, to alleviate RA is unclear. This study examined the proportions of IL-17-secreting lymphocytes in the blood of healthy subjects and RA patients and determined if Th17 cells belong to a CD20+ subset of T cells. Methods Fluorescence-activated cell sorting and confocal microscopy verified CD3, CD4/CD8 and CD20-staining of T cells. IL-17 secretion was determined using a commercial assay. Results In healthy subjects and RA patients blood, the median percentage of total CD20+ lymphocytes was similar (7.5%; n = 6 and 10.3%; n = 9, respectively) and comprised predominantly of B cells (~ 86%). However, 2-4% of CD3+ T cells from both healthy subjects ( n = 7) and RA ( n = 8) individuals co-expressed CD20. The peripheral blood of healthy subjects contained few IL-17-secreting CD20+ T cells (< 0.1%; n = 6). In contrast, in RA blood a median and interquartile range % of, 24.2%; IQR 28.5 of IL-17-secreting T cells were CD20+ ( n = 9; p = 0.02). Conclusions In the blood of RA patients, a greater proportion of Th17 cells are of a CD20+ phenotype compared to healthy individuals. These cells may represent an additional target for anti-CD20 therapies.
AbstractList Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies, to alleviate RA is unclear. This study examined the proportions of IL-17-secreting lymphocytes in the blood of healthy subjects and RA patients and determined if Th17 cells belong to a CD20+ subset of T cells. Fluorescence-activated cell sorting and confocal microscopy verified CD3, CD4/CD8 and CD20-staining of T cells. IL-17 secretion was determined using a commercial assay. In healthy subjects and RA patients blood, the median percentage of total CD20+ lymphocytes was similar (7.5%; n = 6 and 10.3%; n = 9, respectively) and comprised predominantly of B cells (~ 86%). However, 2-4% of CD3+ T cells from both healthy subjects (n = 7) and RA (n = 8) individuals co-expressed CD20. The peripheral blood of healthy subjects contained few IL-17-secreting CD20+ T cells (< 0.1%; n = 6). In contrast, in RA blood a median and interquartile range % of, 24.2%; IQR 28.5 of IL-17-secreting T cells were CD20+ (n = 9; p = 0.02). In the blood of RA patients, a greater proportion of Th17 cells are of a CD20+ phenotype compared to healthy individuals. These cells may represent an additional target for anti-CD20 therapies.
Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies, to alleviate RA is unclear. This study examined the proportions of IL-17-secreting lymphocytes in the blood of healthy subjects and RA patients and determined if Th17 cells belong to a CD20+ subset of T cells.INTRODUCTIONRheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies, to alleviate RA is unclear. This study examined the proportions of IL-17-secreting lymphocytes in the blood of healthy subjects and RA patients and determined if Th17 cells belong to a CD20+ subset of T cells.Fluorescence-activated cell sorting and confocal microscopy verified CD3, CD4/CD8 and CD20-staining of T cells. IL-17 secretion was determined using a commercial assay.METHODSFluorescence-activated cell sorting and confocal microscopy verified CD3, CD4/CD8 and CD20-staining of T cells. IL-17 secretion was determined using a commercial assay.In healthy subjects and RA patients blood, the median percentage of total CD20+ lymphocytes was similar (7.5%; n = 6 and 10.3%; n = 9, respectively) and comprised predominantly of B cells (~ 86%). However, 2-4% of CD3+ T cells from both healthy subjects (n = 7) and RA (n = 8) individuals co-expressed CD20. The peripheral blood of healthy subjects contained few IL-17-secreting CD20+ T cells (< 0.1%; n = 6). In contrast, in RA blood a median and interquartile range % of, 24.2%; IQR 28.5 of IL-17-secreting T cells were CD20+ (n = 9; p = 0.02).RESULTSIn healthy subjects and RA patients blood, the median percentage of total CD20+ lymphocytes was similar (7.5%; n = 6 and 10.3%; n = 9, respectively) and comprised predominantly of B cells (~ 86%). However, 2-4% of CD3+ T cells from both healthy subjects (n = 7) and RA (n = 8) individuals co-expressed CD20. The peripheral blood of healthy subjects contained few IL-17-secreting CD20+ T cells (< 0.1%; n = 6). In contrast, in RA blood a median and interquartile range % of, 24.2%; IQR 28.5 of IL-17-secreting T cells were CD20+ (n = 9; p = 0.02).In the blood of RA patients, a greater proportion of Th17 cells are of a CD20+ phenotype compared to healthy individuals. These cells may represent an additional target for anti-CD20 therapies.CONCLUSIONSIn the blood of RA patients, a greater proportion of Th17 cells are of a CD20+ phenotype compared to healthy individuals. These cells may represent an additional target for anti-CD20 therapies.
Introduction Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies, to alleviate RA is unclear. This study examined the proportions of IL-17-secreting lymphocytes in the blood of healthy subjects and RA patients and determined if Th17 cells belong to a CD20+ subset of T cells. Methods Fluorescence-activated cell sorting and confocal microscopy verified CD3, CD4/CD8 and CD20-staining of T cells. IL-17 secretion was determined using a commercial assay. Results In healthy subjects and RA patients blood, the median percentage of total CD20+ lymphocytes was similar (7.5%; n = 6 and 10.3%; n = 9, respectively) and comprised predominantly of B cells (~ 86%). However, 2-4% of CD3+ T cells from both healthy subjects ( n = 7) and RA ( n = 8) individuals co-expressed CD20. The peripheral blood of healthy subjects contained few IL-17-secreting CD20+ T cells (< 0.1%; n = 6). In contrast, in RA blood a median and interquartile range % of, 24.2%; IQR 28.5 of IL-17-secreting T cells were CD20+ ( n = 9; p = 0.02). Conclusions In the blood of RA patients, a greater proportion of Th17 cells are of a CD20+ phenotype compared to healthy individuals. These cells may represent an additional target for anti-CD20 therapies.
ArticleNumber R208
Author Haigh, Richard C
Helfrich, Wijnand
Kendall, Alexandra
Bremer, Edwin
de Bruyn, Marco
Winyard, Paul G
Eggleton, Paul
Tarr, Joanna M
Viner, Nick J
AuthorAffiliation 1 Peninsula Medical School, University of Exeter, Heavitree Road, Exeter EX1 2LU, UK
2 Department of Surgery, University Medical Center Groningen, Surgical Research Laboratory, Hanzeplein 1, Groningen 9713 EZ, The Netherlands
3 Department of Rheumatology, Royal Devon and Exeter Foundation Trust Hospital, Exeter EX2 5DW, UK
4 Department of Rheumatology, Torbay Hospital, Torquay TQ2 7AA, UK
AuthorAffiliation_xml – name: 3 Department of Rheumatology, Royal Devon and Exeter Foundation Trust Hospital, Exeter EX2 5DW, UK
– name: 2 Department of Surgery, University Medical Center Groningen, Surgical Research Laboratory, Hanzeplein 1, Groningen 9713 EZ, The Netherlands
– name: 1 Peninsula Medical School, University of Exeter, Heavitree Road, Exeter EX1 2LU, UK
– name: 4 Department of Rheumatology, Torbay Hospital, Torquay TQ2 7AA, UK
Author_xml – sequence: 1
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  surname: Eggleton
  fullname: Eggleton, Paul
  email: paul.eggleton@pms.ac.uk
  organization: Peninsula Medical School, University of Exeter
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  givenname: Edwin
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  surname: Winyard
  fullname: Winyard, Paul G
  email: paul.winyard@pms.ac.uk
  organization: Peninsula Medical School, University of Exeter
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22171710$$D View this record in MEDLINE/PubMed
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Issue 6
Keywords Median Percentage
Synovial Fluid
Rheumatoid Arthritis
Th17 Cell
Rheumatoid Arthritis Patient
Language English
License This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Snippet Introduction Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20...
Rheumatoid arthritis (RA) is considered a T cell driven autoimmune disease, therefore, the ability of B cell depleting biologics, e.g., anti-CD20 antibodies,...
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StartPage R208
SubjectTerms Adult
Aged
Aged, 80 and over
Antigens, CD20 - immunology
Antigens, CD20 - metabolism
Arthritis, Rheumatoid - blood
Arthritis, Rheumatoid - immunology
B-Lymphocytes - immunology
B-Lymphocytes - metabolism
CD3 Complex - immunology
CD3 Complex - metabolism
Flow Cytometry
Humans
Immunophenotyping
Interleukin-17 - immunology
Interleukin-17 - metabolism
Leukocytes, Mononuclear - immunology
Leukocytes, Mononuclear - metabolism
Lymphocyte Count
Medicine
Medicine & Public Health
Microscopy, Confocal
Middle Aged
Orthopedics
Research Article
Rheumatology
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
Th17 Cells - immunology
Th17 Cells - metabolism
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Title Frequency of Th17 CD20+ cells in the peripheral blood of rheumatoid arthritis patients is higher compared to healthy subjects
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