TY - JOUR
T1 - i-IFTA and chronic active T cell–mediated rejection
T2 - A tale of 2 (DeKAF) cohorts
AU - Helgeson, Erika S.
AU - Mannon, Roslyn
AU - Grande, Joseph
AU - Gaston, Robert S.
AU - Cecka, Michael J.
AU - Kasiske, Bertram L.
AU - Rush, David
AU - Gourishankar, Sita
AU - Cosio, Fernando
AU - Hunsicker, Lawrence
AU - Connett, John
AU - Matas, Arthur J.
N1 - Funding Information:
We thank Astellas, Bristol‐Myers Squibb, Novartis, Pfizer, and Sanofi‐Aventis for unrestricted grants that supported this research. We thank Stephanie Taylor for editorial assistance and preparation of the manuscript.
Funding Information:
We thank Astellas, Bristol-Myers Squibb, Novartis, Pfizer, and Sanofi-Aventis for unrestricted grants that supported this research. We thank Stephanie Taylor for editorial assistance and preparation of the manuscript.
Publisher Copyright:
© 2020 The American Society of Transplantation and the American Society of Transplant Surgeons
PY - 2021/5
Y1 - 2021/5
N2 - Inflammation in areas of fibrosis (i-IFTA) in posttransplant biopsies is part of the diagnostic criteria for chronic active TCMR (CA TCMR -- i-IFTA ≥ 2, ti ≥ 2, t ≥ 2). We evaluated i-IFTA and CA TCMR in the DeKAF indication biopsy cohorts: prospective (n = 585, mean time to biopsy = 1.7 years); cross-sectional (n = 458, mean time to biopsy = 7.8 years). Grouped by i-IFTA scores, the 3-year postbiopsy DC-GS is similar across cohorts. Although a previous acute rejection episode (AR) was more common in those with i-IFTA on biopsy, the majority of those with i-IFTA had not had previous AR. There was no association between type of previous AR (AMR, TCMR) and presence of i-IFTA. In both cohorts, i-IFTA was associated with markers of both cellular (increased Banff i, t, ti) and humoral (increased g, ptc, C4d, DSA) activity. Biopsies with i-IFTA = 1 and i-IFTA ≥ 2 with concurrent t ≥ 2 and ti ≥ 2 had similar DC-GS. These results suggest that (a) i-IFTA≥1 should be considered a threshold for diagnoses incorporating i-IFTA, ti, and t; (b) given that i-IFTA ≥ 2,t ≥ 2, ti ≥ 2 can occur in the absence of preceding TCMR and that the component histologic scores (i-IFTA,t,ti) each indicate an acute change (albeit i-IFTA on the nonspecific background of IFTA), the diagnostic category “CA TCMR” should be reconsidered.
AB - Inflammation in areas of fibrosis (i-IFTA) in posttransplant biopsies is part of the diagnostic criteria for chronic active TCMR (CA TCMR -- i-IFTA ≥ 2, ti ≥ 2, t ≥ 2). We evaluated i-IFTA and CA TCMR in the DeKAF indication biopsy cohorts: prospective (n = 585, mean time to biopsy = 1.7 years); cross-sectional (n = 458, mean time to biopsy = 7.8 years). Grouped by i-IFTA scores, the 3-year postbiopsy DC-GS is similar across cohorts. Although a previous acute rejection episode (AR) was more common in those with i-IFTA on biopsy, the majority of those with i-IFTA had not had previous AR. There was no association between type of previous AR (AMR, TCMR) and presence of i-IFTA. In both cohorts, i-IFTA was associated with markers of both cellular (increased Banff i, t, ti) and humoral (increased g, ptc, C4d, DSA) activity. Biopsies with i-IFTA = 1 and i-IFTA ≥ 2 with concurrent t ≥ 2 and ti ≥ 2 had similar DC-GS. These results suggest that (a) i-IFTA≥1 should be considered a threshold for diagnoses incorporating i-IFTA, ti, and t; (b) given that i-IFTA ≥ 2,t ≥ 2, ti ≥ 2 can occur in the absence of preceding TCMR and that the component histologic scores (i-IFTA,t,ti) each indicate an acute change (albeit i-IFTA on the nonspecific background of IFTA), the diagnostic category “CA TCMR” should be reconsidered.
KW - classification systems: Banff classification
KW - clinical research / practice
KW - fibrosis
KW - graft survival
KW - interstitial fibrosis and tubular atrophy
KW - kidney transplantation / nephrology
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U2 - 10.1111/ajt.16352
DO - 10.1111/ajt.16352
M3 - Article
C2 - 33052625
AN - SCOPUS:85096659139
SN - 1600-6135
VL - 21
SP - 1866
EP - 1877
JO - American Journal of Transplantation
JF - American Journal of Transplantation
IS - 5
ER -