Inflammatory monocytes promote pre-engraftment syndrome and tocilizumab can therapeutically limit pathology in patients.
Linlin JinZimin SunHuilan LiuXiaoyu ZhuYonggang ZhouBinqing FuXiaohu ZhengKaidi SongBaolin TangYun WuJiang ZhuRui SunZhigang TianHaiming WeiPublished in: Nature communications (2021)
Unrelated cord blood transplantation (UCBT) is an effective treatment for hematopoietic disorders. However, this attractive approach is frequently accompanied by pre-engraftment syndrome (PES), severe cases of PES are associated with enhanced mortality and morbidity, but the pathogenesis of PES remains unclear. Here we show that GM-CSF produced by cord blood-derived inflammatory monocytes drives PES pathology, and that monocytes are the main source of IL-6 during PES. Further, we report the outcome of a single arm, single-center clinical study of tocilizumab in the treatment of steroid-refractory severe PES patients (www.chictr.org.cn ChiCTR1800015472). The study met the primary outcome measure since none of the patients was nonrelapse death during the 100 days follow-up. The study also met key secondary outcomes measures of neutrophil engraftment and hematopoiesis. These findings offer a therapeutic strategy with which to tackle PES and improve nonrelapse mortality.
Keyphrases
- cord blood
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- rheumatoid arthritis
- peritoneal dialysis
- clinical trial
- dendritic cells
- bone marrow
- prognostic factors
- oxidative stress
- stem cells
- squamous cell carcinoma
- coronary artery disease
- adipose tissue
- peripheral blood
- metabolic syndrome
- patient reported outcomes
- mesenchymal stem cells
- combination therapy
- weight loss
- rheumatoid arthritis patients