Research output: Contribution to journal › Article › peer-review
P. Wehr, H. Purvis, S. C. Law, R. Thomas
Original language | English |
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Pages (from-to) | 12-27 |
Number of pages | 16 |
Journal | Clinical and Experimental Immunology |
Volume | 196 |
Issue number | 1 |
Early online date | 27 Dec 2018 |
DOIs | |
Accepted/In press | 10 Dec 2018 |
E-pub ahead of print | 27 Dec 2018 |
Published | 18 Mar 2019 |
Additional links |
Dendritic cells (DCs) are the key professional antigen-presenting cells which bridge innate and adaptive immune responses, inducing the priming and differentiation of naive to effector CD4+ T cells, the cross-priming of CD8+ T cells and the promotion of B cell antibody responses. DCs also play a critical role in the maintenance of immune homeostasis and tolerance. DC–T cell interactions underpin the generation of an autoimmune response in rheumatoid arthritis (RA). Here we describe the function of DCs and review evidence for DC and T cell involvement in RA pathogenesis, in particular through the presentation of self-peptide by DCs that triggers differentiation and activation of autoreactive T cells. Finally, we discuss the emerging field of targeting the DC–T cell interaction for antigen-specific immunotherapy of RA.
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