FRI0305 PREDICTIVE VALUE OF INNATE LYMPHOID CELLS IN SYSTEMIC SCLEROSIS

Background Systemic sclerosis (SSc) is a chronic autoimmune disease with a high morbidity and mortality. Activation of the immune system is a characteristic feature of SSc. Numerous studies have suggested that type 2 and type 3 cytokines are key drivers of progressive fibrosis. Recently, innate lymphoid cells (ILC) are emerging as an important cellular source of type 2 and type 3 cytokines triggering fibrotic tissue remodeling independently of the adaptive immune system. ILCs are characterized by the absence of conventional lineage markers. Similar to T cells, they are categorized into three groups (ILC1, ILC2, ILC3), according to distinct pattern of cytokine production and the requirement of specific transcription factors guiding their development and function. Increased levels of ILC2 were found in patients with SSc. However, the contributive role of ILC2 and ILC3 in pathogenesis of SSc is not completely understood. Objectives We aim in our study to evaluate the predictive role of ILC2 and ILC3 in SSc patients. Methods We conducted an observational retrospective study on 52 patients with SSc fulfilling the 2013 ACR/EULAR classification criteria. Yearly clinical, laboratory and investigational data according to EUSTAR recommendations were collected. Blood samples collected between 15.09.2014 and 15.01.2015 were analyzed by flow cytometry and ILC2 and ILC3 counts were measured. The predictive value of ILC2 and ILC3 during a 2-year follow-up was analyzed using SPSS 21.0. ILC3 counts were also analyzed in skin sections (10 patients with SSc and 10 healthy controls) by immunofluorescence (IF) staining using two complementary panels of markers. Cytokine production of skin resident ILC3s was additionally analyzed by IF staining. Results 52 patients were included in the study, 78% female, 63% limited cutaneous SSc with a mean follow-up time of 2.85 ± 1.28 years. At baseline we have shown that circulating ILC2s are significantly increased compared to gender and age-matched healthy controls. Increased numbers of ILC2s significantly correlated with worsening of mRSS calculated by five point increase in mRSS or 25% increase from baseline (p Conclusion Here, we provide first evidence for a role of ILC2s as potential prognostic marker of disease progression in SSc. Circulating ILC3 counts were not elevated in SSc. However, ILC3s showed strong cytokine production in the fibrotic skin of SSc patients. The functional impact has to be further evaluated. Disclosure of Interests: Alina Soare: None declared, Stefanie Weber: None declared, Markus Luber: None declared, Simon Rauber: None declared, Thomas Wohlfahrt: None declared, Georg Schett: None declared, Jorg Distler: None declared, Andreas Ramming Grant/research support from: Novartis