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 in | Arthritis research & therapy Vol. 13; no. 6; p. R208 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
BioMed Central
01.01.2011
|
| Subjects | |
| Online Access | Get full text |
| ISSN | 1478-6354 1478-6362 1478-6354 1478-6362 |
| DOI | 10.1186/ar3541 |
Cover
| 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 givenname: Paul surname: Eggleton fullname: Eggleton, Paul email: paul.eggleton@pms.ac.uk organization: Peninsula Medical School, University of Exeter – sequence: 2 givenname: Edwin surname: Bremer fullname: Bremer, Edwin organization: Department of Surgery, University Medical Center Groningen, Surgical Research Laboratory – sequence: 3 givenname: Joanna M surname: Tarr fullname: Tarr, Joanna M organization: Peninsula Medical School, University of Exeter – sequence: 4 givenname: Marco surname: de Bruyn fullname: de Bruyn, Marco organization: Department of Surgery, University Medical Center Groningen, Surgical Research Laboratory – sequence: 5 givenname: Wijnand surname: Helfrich fullname: Helfrich, Wijnand organization: Department of Surgery, University Medical Center Groningen, Surgical Research Laboratory – sequence: 6 givenname: Alexandra surname: Kendall fullname: Kendall, Alexandra organization: Peninsula Medical School, University of Exeter – sequence: 7 givenname: Richard C surname: Haigh fullname: Haigh, Richard C organization: Peninsula Medical School, University of Exeter, Department of Rheumatology, Royal Devon and Exeter Foundation Trust Hospital – sequence: 8 givenname: Nick J surname: Viner fullname: Viner, Nick J organization: Peninsula Medical School, University of Exeter, Department of Rheumatology, Torbay Hospital – sequence: 9 givenname: Paul G 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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| Keywords | Median Percentage Synovial Fluid Rheumatoid Arthritis Th17 Cell Rheumatoid Arthritis Patient |
| Language | English |
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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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| 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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