Clinicopathological value of programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) expression in synovium of patients with rheumatoid arthritis

The etiology of rheumatoid arthritis (RA) is thought to involve dysfunction of the programmed cell death 1/programmed cell death ligand 1 (PD-1/PD-L1) pathway; PD-1 negatively regulates autoimmunity by interacting with its ligand, PD-L1. We therefore investigated PD-1/PD-L1 expression in synovial ti...

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Veröffentlicht in:Clinical and experimental medicine 2018-11, Vol.18 (4), p.487-494
Hauptverfasser: Matsuda, Kotaro, Miyoshi, Hiroaki, Hiraoka, Koji, Hamada, Tetsuya, Yoshida, Shiro, Ishibashi, Yukinao, Haraguchi, Toshiaki, Shiba, Naoto, Ohshima, Koichi
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Sprache:eng
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Zusammenfassung:The etiology of rheumatoid arthritis (RA) is thought to involve dysfunction of the programmed cell death 1/programmed cell death ligand 1 (PD-1/PD-L1) pathway; PD-1 negatively regulates autoimmunity by interacting with its ligand, PD-L1. We therefore investigated PD-1/PD-L1 expression in synovial tissue of patients with RA. We immunohistochemically stained synovial specimens from 51 patients with RA and assessed the association between PD-1/PD-L1 expression and rheumatoid factor (RF), the total count of infiltrating T cells, C-reactive protein (CRP), and Krenn’s synovitis score. PD-1 expression on infiltrating lymphocytes was detected in 34/51 RA cases (66.7%), while PD-1 expression was very mildly correlated only with the number of total infiltrating T cells ( R 2  = 0.1011, P  = 0.0230). On the other hand, PD-L1 expression on synovial lining cells was observed in 37/51 RA cases (72.5%). Furthermore, a higher PD-L1 expression was significantly associated with RF positive state ( P  = 0.0454), and the correlations between PD-L1 expression and the number of infiltrating T cells ( R 2  = 0.5571, P  
ISSN:1591-8890
1591-9528
DOI:10.1007/s10238-018-0515-4