12 January 2021>: Original Paper
Suppression of Allograft Fibrosis by Regulation of Mammalian Target of Rapamycin-Related Protein Expression in Kidney-Transplanted Recipients Treated with Everolimus and Reduced Tacrolimus
Shun Nishioka ABCDE , Takeshi Ishimura ACDE* , Takahito Endo B , Naoki Yokoyama BC , Satoshi Ogawa BCD , Masato Fujisawa EDOI: 10.12659/AOT.926476
Ann Transplant 2021; 26:e926476
Figure 6 Change in eGFR and FI after kidney transplantation stratified by immunosuppressive protocol and degree of mTOR signal enhancement. The mTOR signal score is defined as the sum of the score in phosphorylated mTOR and phosphorylated p70S6K, and phosphorylated 4EBP staining. Group 1: EVR+ with mTOR signal score decreased from 3 months to 3 years (n=18); group 2: EVR+ with mTOR signaling score increased from 3 months to 3 years (n=14); group 3: EVR− with mTOR signaling score decreased from 3 months to 3 years (n=8); group 4: EVR− with mTOR signaling score increased from 3 months to 3 years (n=20). (A) Decreases in eGFR from 3 months to 3 years after KTx (ΔeGFR=eGFR at 3 years–eGFR at 3 months) in the groups 1 and 2 (EVR+ with mTOR signal score decrease or increase) were significantly lower than those in groups 3 and 4 (EVR− with mTOR signal score decrease or increase) (P<0.01). (B) The progression of fibrosis (ΔFI=FI at 3 years–FI at 3 months) in group 1 (EVR+ with mTOR signal score decrease) was significantly milder than in the other 3 groups (P<0.001). mTOR – mammalian target of rapamycin; eGFR – estimated-glomerular filtration rate (ml/min/1.73 m2); FI – fibrosis index (%); KTx – kidney transplantation; EVR – everolimus.