TY - JOUR
T1 - Synovial VLA-1+ T cells display an oligoclonal and partly distinct repertoire in rheumatoid and psoriatic arthritis
AU - Goldstein, Itamar
AU - Simon, Amos J.
AU - Horin, Shomron Ben
AU - Matzri, Sarit
AU - Koltakov, Alexander
AU - Langevitz, Pnina
AU - Rechavi, Gideon
AU - Amariglio, Ninette
AU - Bank, Ilan
N1 - Funding Information:
This work was supported in part by an investigator initiated research grant from Biogen Idec to I.B. G.R. holds the Djerasi Chair for Oncology (Sackler School of Medicine, Tel Aviv University). Part of this work was performed in partial fulfillment of the requirements of the MSc of S. Matzri at the Sackler School of Medicine (Tel Aviv University).
PY - 2008/7
Y1 - 2008/7
N2 - VLA-1 integrin expressing T cells are more frequent in inflammatory synovial fluids (SF) compared to peripheral blood. Recent studies suggest that VLA-1 expression mainly marks IFNγ+ T cells while excluding both IL-4+ and regulatory FoxP3+ T cells. To further characterize the TCR repertoire of the potentially pathogenic VLA-1+ IFNγ+ T cells, isolated from SF of adult patients with rheumatoid and psoriatic arthritis, we determined the complementarity determining region (CDR)3 spectratypes. Here we show in a cohort of 9 patients that VLA-1+ T cells display a perturbed repertoire that, moreover, differs from that of VLA-1- synovial T cells and even VLA-1+ PB T cells. Importantly, random sequencing of the CDR3 region of the TCR variable β (BV) 6.1 gene of both VLA-1+ and VLA-1- synovial T cells, in one patient, revealed that their sequences were by and large different (29 out of 33 clones). Thus, our results imply that VLA-1+ T cells that infiltrate into inflamed joints represent a partly distinct and highly oligoclonal population of Th1 cells, probably selected by unique antigens.
AB - VLA-1 integrin expressing T cells are more frequent in inflammatory synovial fluids (SF) compared to peripheral blood. Recent studies suggest that VLA-1 expression mainly marks IFNγ+ T cells while excluding both IL-4+ and regulatory FoxP3+ T cells. To further characterize the TCR repertoire of the potentially pathogenic VLA-1+ IFNγ+ T cells, isolated from SF of adult patients with rheumatoid and psoriatic arthritis, we determined the complementarity determining region (CDR)3 spectratypes. Here we show in a cohort of 9 patients that VLA-1+ T cells display a perturbed repertoire that, moreover, differs from that of VLA-1- synovial T cells and even VLA-1+ PB T cells. Importantly, random sequencing of the CDR3 region of the TCR variable β (BV) 6.1 gene of both VLA-1+ and VLA-1- synovial T cells, in one patient, revealed that their sequences were by and large different (29 out of 33 clones). Thus, our results imply that VLA-1+ T cells that infiltrate into inflamed joints represent a partly distinct and highly oligoclonal population of Th1 cells, probably selected by unique antigens.
KW - CDR3 length diversity
KW - Effector and memory T cells
KW - Inflammatory arthritis
KW - Integrin
KW - T cell receptor (TCR)
KW - TCR repertoire
KW - Very late activation antigen (VLA-1)
UR - https://www.scopus.com/pages/publications/49949152116
U2 - 10.1016/j.clim.2008.02.014
DO - 10.1016/j.clim.2008.02.014
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C2 - 18456562
AN - SCOPUS:49949152116
SN - 1521-6616
VL - 128
SP - 75
EP - 84
JO - Clinical Immunology
JF - Clinical Immunology
IS - 1
ER -