T cell–mediated rejection is a major determinant of inflammation in scarred areas in kidney allografts

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Abstract

Inflammation in fibrosis areas (i-IF/TA) of kidney allografts is associated with allograft loss; however, its diagnostic significance remains to be determined. We investigated the clinicohistologic phenotype and determinants of i-IF/TA in a prospective cohort of 1539 kidney recipients undergoing evaluation of i-IF/TA and tubulitis in atrophic tubules (t-IF/TA) on protocol allograft biopsies performed at 1 year posttransplantation. We considered donor, recipient, and transplant characteristics, immunosuppression, and histological diagnoses in 2260 indication biopsies performed within the first year posttransplantation. Nine hundred forty-six (61.5%) patients presented interstitial fibrosis/tubular atrophy (IF/TA Banff grade > 0) at 1 year posttransplant, among whom 394 (41.6%) showed i-IF/TA. i-IF/TA correlated with concurrent t-IF/TA (P

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Lefaucheur, C., Gosset, C., Rabant, M., Viglietti, D., Verine, J., Aubert, O., … Loupy, A. (2018). T cell–mediated rejection is a major determinant of inflammation in scarred areas in kidney allografts. American Journal of Transplantation, 18(2), 377–390. https://doi.org/10.1111/ajt.14565

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