Kidney allograft biopsy findings after COVID-19.

biopsy clinical research / practice complication: infectious infection and infectious agents - viral kidney (allograft) function / dysfunction kidney transplantation / nephrology

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
12 2021
Historique:
revised: 26 07 2021
received: 22 04 2021
accepted: 11 08 2021
pubmed: 18 8 2021
medline: 15 12 2021
entrez: 17 8 2021
Statut: ppublish

Résumé

COVID-19 has been associated with acute kidney injury and published reports of native kidney biopsies have reported diverse pathologies. Case series directed specifically to kidney allograft biopsy findings in the setting of COVID-19 are lacking. We evaluated 18 kidney transplant recipients who were infected with SARS-CoV-2 and underwent allograft biopsy. Patients had a median age of 55 years, six were female, and five were Black. Fifteen patients developed COVID-19 pneumonia, of which five required mechanical ventilation. Notably, five of 11 (45%) biopsies obtained within 1 month of positive SARS-CoV-2 PCR showed acute rejection (four with arteritis, three of which were not associated with reduced immunosuppression). The remaining six biopsies revealed podocytopathy (n = 2, collapsing glomerulopathy and lupus podocytopathy), acute tubular injury (n = 2), infarction (n = 1), and transplant glomerulopathy (n = 1). Biopsies performed >1 month after positive SARS-CoV-2 PCR revealed collapsing glomerulopathy (n = 1), acute tubular injury (n = 1), and nonspecific histologic findings (n = 5). No direct viral infection of the kidney allograft was detected by immunohistochemistry, in situ hybridization, or electron microscopy. On follow-up, two patients died and most patients showed persistent allograft dysfunction. In conclusion, we demonstrate diverse causes of kidney allograft dysfunction after COVID-19, the most common being acute rejection with arteritis.

Identifiants

pubmed: 34403563
doi: 10.1111/ajt.16804
pmc: PMC8441660
pii: S1600-6135(22)08850-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4032-4042

Informations de copyright

© 2021 The American Society of Transplantation and the American Society of Transplant Surgeons.

Références

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Auteurs

Emily Daniel (E)

Department of Medicine, Division of Nephrology, Columbia University Irving Medical Center, New York, New York, USA.

Miroslav Sekulic (M)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

Satoru Kudose (S)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

Christine Kubin (C)

Department of Pharmacy, New York Presbyterian Hospital, New York, New York, USA.

Xiaoyi Ye (X)

Department of Medicine, Nephrology, Hartford Hospital, Hartford, Connecticut, USA.

Katayoon Shayan (K)

Department of Pathology, Rady Children's Specialists of San Diego, California, USA.

Ankita Patel (A)

Department of Medicine, Nephrology, Hackensack University Medical Center, Hackensack, New Jersey, USA.

David J Cohen (DJ)

Department of Medicine, Division of Nephrology, Columbia University Irving Medical Center, New York, New York, USA.

Lloyd E Ratner (L)

Department of Surgery, Renal and Pancreatic Transplantation, Columbia University Irving Medical Center, New York, New York, USA.

Dominick Santoriello (D)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

M Barry Stokes (M)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

Glen S Markowitz (GS)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

Marcus R Pereira (MR)

Department of Medicine, Division of Infectious Disease, Columbia University Irving Medical Center, New York, New York, USA.

Vivette D D'Agati (VD)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

Ibrahim Batal (I)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.

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Classifications MeSH