Lung Transplantation under a Janus Kinase Inhibitor in Three Patients with SAVI Syndrome.
Kenza Rhzioual BerradaAlexandre BelotBénédicte NevenCamille OhlmannFrançois TroncGillian I RiceGuillaume ThouveninJean-Christophe DubusJulie MazenqMarie-Louise FrémondNathalie StremlerSéverine Soummer-FeuilletVincent CottinPhilippe ReixPublished in: Journal of clinical immunology (2023)
Stimulator of interferon genes (STING)-associated vasculopathy with onset in infancy (SAVI) is a very rare autoinflammatory disease related to STING1 mutation. SAVI is mainly characterized by fever attacks and skin and respiratory manifestations such as interstitial lung disease or alveolar hemorrhage. Respiratory involvement occurs in 80% of cases and might progress to severe lung fibrosis and require lung transplantation (LT). Three patients with SAVI who underwent LT have been reported to date. Two of the three patients died months or years after LT due to multiple organ failure or sepsis. However, the diagnosis of SAVI was made after LT, thus preventing the use of targeted therapy, such as the Janus kinase 1 and 2 inhibitor (JAK1/2i) ruxolitinib, which might be beneficial for the respiratory status of these patients. We aimed to report our experience in managing three patients who were followed in three large lung transplantation centers in France and who benefited from ruxolitinib before undergoing LT. We describe posttransplant complications that occurred as well as outcomes.
Keyphrases
- end stage renal disease
- interstitial lung disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- systemic sclerosis
- peritoneal dialysis
- extracorporeal membrane oxygenation
- type diabetes
- intensive care unit
- rheumatoid arthritis
- acute kidney injury
- gene expression
- patient reported outcomes
- immune response
- genome wide
- early onset
- dendritic cells
- metabolic syndrome
- protein kinase