PMID- 34124342 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220423 IS - 2373-8731 (Print) IS - 2373-8731 (Electronic) IS - 2373-8731 (Linking) VI - 7 IP - 7 DP - 2021 Jul TI - Impact of Subclinical and Clinical Kidney Allograft Rejection Within 1 Year Posttransplantation Among Compatible Transplant With Steroid Withdrawal Protocol. PG - e706 LID - 10.1097/TXD.0000000000001132 [doi] LID - e706 AB - Early acute kidney rejection remains an important clinical issue. METHODS: The current study included 552 recipients who had 1-2 surveillance or indication biopsy within the 1 y posttransplant. We evaluated the impact of type of allograft inflammation on allograft outcome. They were divided into 5 groups: no inflammation (NI: 95), subclinical inflammation (SCI: 244), subclinical T cell-mediated rejection (TCMR) (SC-TCMR: 110), clinical TCMR (C-TCMR: 83), and antibody-mediated rejection (AMR: 20). Estimated glomerular filtration rate (eGFR) over time using linear mixed model, cumulative chronic allograft scores/interstitial fibrosis and tubular atrophy (IFTA) >/=2 at 12 mo, and survival estimates were compared between groups. RESULTS: The common types of rejections were C-TCMR (15%), SC-TCMR (19.9%), and AMR (3.6%) of patients. Eighteen of 20 patients with AMR had mixed rejection with TCMR. Key findings were as follows: (i) posttransplant renal function: eGFR was lower for patients with C-TCMR and AMR (P < 0.0001) compared with NI, SCI, and SC-TCMR groups. There was an increase in delta-creatinine from 3 to 12 mo and cumulative allograft chronicity scores at 12 mo (P < 0.001) according to the type of allograft inflammation. (ii) Allograft histology: the odds of IFTA >/=2 was higher for SC-TCMR (3.7 [1.3-10.4]; P = 0.04) but was not significant for C-TCMR (3.1 [1.0-9.4]; P = 0.26), and AMR (2.5 [0.5-12.8]; P = 0.84) compared with NI group, and (iii) graft loss: C-TCMR accounted for the largest number of graft losses and impending graft losses on long-term follow-up. Graft loss among patient with AMR was numerically higher but was not statistically significant. CONCLUSIONS: The type of kidney allograft inflammation predicted posttransplant eGFR, cumulative chronic allograft score/IFTA >/=2 at 12 mo, and graft loss. CI - Copyright (c) 2021 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. FAU - Owoyemi, Itunu AU - Owoyemi I AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Tandukar, Srijan AU - Tandukar S AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Jorgensen, Dana R AU - Jorgensen DR AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Wu, Christine M AU - Wu CM AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Sood, Puneet AU - Sood P AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Puttarajappa, Chethan AU - Puttarajappa C AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Sharma, Akhil AU - Sharma A AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Shah, Nirav A AU - Shah NA AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Randhawa, Parmjeet AU - Randhawa P AD - Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA. FAU - Molinari, Michele AU - Molinari M AD - Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA. FAU - Tevar, Amit D AU - Tevar AD AD - Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA. FAU - Mehta, Rajil B AU - Mehta RB AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. FAU - Hariharan, Sundaram AU - Hariharan S AD - Department of Medicine, Thomas E Starzl Transplantation Institute, Pittsburgh, PA. LA - eng PT - Journal Article DEP - 20210608 PL - United States TA - Transplant Direct JT - Transplantation direct JID - 101651609 PMC - PMC8191698 COIS- The authors declare no funding or conflicts of interest. EDAT- 2021/06/15 06:00 MHDA- 2021/06/15 06:01 PMCR- 2021/06/08 CRDT- 2021/06/14 09:53 PHST- 2020/12/17 00:00 [received] PHST- 2021/01/07 00:00 [revised] PHST- 2021/01/09 00:00 [accepted] PHST- 2021/06/14 09:53 [entrez] PHST- 2021/06/15 06:00 [pubmed] PHST- 2021/06/15 06:01 [medline] PHST- 2021/06/08 00:00 [pmc-release] AID - 10.1097/TXD.0000000000001132 [doi] PST - epublish SO - Transplant Direct. 2021 Jun 8;7(7):e706. doi: 10.1097/TXD.0000000000001132. eCollection 2021 Jul.