Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

KLRG1 and its role in Rheumatoid Arthritis

Thompson, Charlotte 2019. KLRG1 and its role in Rheumatoid Arthritis. MD Thesis, Cardiff University.
Item availability restricted.

[img] PDF - Accepted Post-Print Version
Restricted to Repository staff only until 19 August 2020 due to copyright restrictions.

Download (4MB)
[img] PDF - Supplemental Material
Restricted to Repository staff only

Download (545kB)


Introduction: Rheumatoid arthritis (RA) is an autoimmune disease that causes chronic joint inflammation. A homeostatic disequilibrium of the immune system is implicated in the failure of systemic tolerance. A part of this disequilibrium may be the rise of CD3+CD8+CD28- T cells in RA. Their role in the pathogenesis of RA remains unknown. Methods: Analysis of peripheral blood samples from RA patients using flow cytometry were compared to healthy controls (RA patients n=50, healthy controls n=25). Results: CD3+CD8+CD28- cells are higher in RA. Further subdivision of this group revealed that CD3+CD8+CD28- cells are higher in Early RA as well as Established RA. This subset of CD3+CD8+CD28- cells also correlated with disease duration in Early RA patients. The cell surface receptor KLRG1, is expressed by a high percentage of CD3+CD8+CD28- cells. As well as being associated with clinical and serological markers in RA, CD3+CD8+CD28-KLRG1+ cells are higher in the Early RA patients who had a poor response to therapy at six months. CD3+CD8+CD28-KLRG1+ cells were found to produce more IL-10 than KLRG1- cells. The percentage of CD3+CD8+CD28- and CD3+CD8+CD28-KLRG1+ cells is higher in CMV positive than CMV negative RA patients but CMV distribution is similar across the responders and non-responders to treatment in Early RA. CMV positive CD3+CD8+CD28-KLRG1+ cells produce more IL-10 than KLRG1- cells. Conclusion: The higher percentage of CD3+CD8+CD28-KLRG1+ cells is associated clinical and serological markers as well as poor response to treatment in Early RA patients. This reinforces the importance of this subtype of T regs in the course of RA. However, the precise reason is unclear and requires further investigation.

Item Type: Thesis (MD)
Date Type: Completion
Status: Unpublished
Schools: Medicine
Date of First Compliant Deposit: 20 August 2019
Last Modified: 04 Apr 2020 01:28

Actions (repository staff only)

Edit Item Edit Item


Downloads per month over past year

View more statistics