Gut derived ILC3 have been demonstrated to participate in AS pathogenesis. CX3CR1+ mononuclear phagocytes (MNP) have been demonstrated to modulate ILC3 function in the gut. The aim of this study was to study the role of pro-inflammatory CX3CR1+ CD59+ MNP in modulating ILC3 function in AS patients.
Ciccia, F., Guggino, G., Zeng, M., Thomas, R., Ranganathan, V., Rahman, A., et al. (2018). Pro-inflammatory CX3CR1+ CD59+ TL1A+ IL-23+ monocytes are expanded in patients with Ankylosing Spondylitis and modulate ILC3 immune functions. ARTHRITIS & RHEUMATOLOGY [10.1002/art.40582].
Pro-inflammatory CX3CR1+ CD59+ TL1A+ IL-23+ monocytes are expanded in patients with Ankylosing Spondylitis and modulate ILC3 immune functions
Ciccia, Francesco;Guggino, Giuliana;Alessandro, Riccardo;Saieva, Laura;Di Liberto, Diana;Dieli, Francesco;
2018-01-01
Abstract
Gut derived ILC3 have been demonstrated to participate in AS pathogenesis. CX3CR1+ mononuclear phagocytes (MNP) have been demonstrated to modulate ILC3 function in the gut. The aim of this study was to study the role of pro-inflammatory CX3CR1+ CD59+ MNP in modulating ILC3 function in AS patients.File in questo prodotto:
File | Dimensione | Formato | |
---|---|---|---|
Ciccia_et_al-2018-Arthritis_%26_Rheumatology-2.pdf
accesso aperto
Dimensione
1.41 MB
Formato
Adobe PDF
|
1.41 MB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.