De novo lupus-like glomerulonephritis after pediatric non-kidney organ transplantation.


Journal

Pediatric nephrology (Berlin, Germany)
ISSN: 1432-198X
Titre abrégé: Pediatr Nephrol
Pays: Germany
ID NLM: 8708728

Informations de publication

Date de publication:
01 2022
Historique:
received: 30 03 2021
accepted: 15 06 2021
revised: 08 06 2021
pubmed: 23 7 2021
medline: 30 3 2022
entrez: 22 7 2021
Statut: ppublish

Résumé

We propose a novel clinically significant finding, de novo lupus-like glomerulonephritis (DNLLGN), in patients with autoantibodies and kidney abnormalities in pediatric liver transplant (LT) and intestinal inclusive transplants (ITx). We describe the clinical, serologic, and histopathologic presentation and kidney outcomes in eight patients from our center found to have DNLLGN on kidney biopsy. Pediatric recipients of non-kidney solid organ transplants developed an unusual de novo immune complex glomerulonephritis with morphologic similarity to lupus nephritis. Six had isolated LT (0.9% of all pediatric LT at our center) and two had ITx (2.1% of all ITx). Five (63%) presented with nephrotic syndrome. Five patients had autoantibodies. Patients underwent kidney biopsy at a mean of 11.5 years in LT and 2.8 years in ITx after the index transplant. Biopsies demonstrated changes similar to focal or diffuse active lupus. Follow-up eGFR at a mean of 6 years after biopsy showed a mean decrease of 30 ml/min/1.73 m DNLLGN has not been previously recognized in this clinical setting, yet 8 kidney biopsies from pediatric recipients of LT and ITx at our center in 25 years demonstrated this finding. DNLLGN appears to be an under-reported phenomenon of clinical significance. A higher resolution version of the Graphical abstract is available as Supplementary information.

Sections du résumé

BACKGROUND
We propose a novel clinically significant finding, de novo lupus-like glomerulonephritis (DNLLGN), in patients with autoantibodies and kidney abnormalities in pediatric liver transplant (LT) and intestinal inclusive transplants (ITx).
METHODS
We describe the clinical, serologic, and histopathologic presentation and kidney outcomes in eight patients from our center found to have DNLLGN on kidney biopsy.
RESULTS
Pediatric recipients of non-kidney solid organ transplants developed an unusual de novo immune complex glomerulonephritis with morphologic similarity to lupus nephritis. Six had isolated LT (0.9% of all pediatric LT at our center) and two had ITx (2.1% of all ITx). Five (63%) presented with nephrotic syndrome. Five patients had autoantibodies. Patients underwent kidney biopsy at a mean of 11.5 years in LT and 2.8 years in ITx after the index transplant. Biopsies demonstrated changes similar to focal or diffuse active lupus. Follow-up eGFR at a mean of 6 years after biopsy showed a mean decrease of 30 ml/min/1.73 m
CONCLUSIONS
DNLLGN has not been previously recognized in this clinical setting, yet 8 kidney biopsies from pediatric recipients of LT and ITx at our center in 25 years demonstrated this finding. DNLLGN appears to be an under-reported phenomenon of clinical significance. A higher resolution version of the Graphical abstract is available as Supplementary information.

Identifiants

pubmed: 34292379
doi: 10.1007/s00467-021-05194-6
pii: 10.1007/s00467-021-05194-6
pmc: PMC8674157
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

153-161

Informations de copyright

© 2021. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

Références

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Auteurs

Cristina M Farkas-Skiles (CM)

Department of Pediatrics, Division of Nephrology, University of California Los Angeles Medical Center, Los Angeles, CA, USA. farkas.cristina@gmail.com.

Robert B Ettenger (RB)

Department of Pediatrics, Division of Nephrology, University of California Los Angeles Medical Center, Los Angeles, CA, USA.

Jonathan E Zuckerman (JE)

Department of Pathology, University of California Los Angeles Medical Center, Los Angeles, CA, USA.

Meghan Pearl (M)

Department of Pediatrics, Division of Nephrology, University of California Los Angeles Medical Center, Los Angeles, CA, USA.

Robert S Venick (RS)

Department of Pediatrics, Division of Gastroenterology, University of California Los Angeles Medical Center, Los Angeles, CA, USA.

Patricia L Weng (PL)

Department of Pediatrics, Division of Nephrology, University of California Los Angeles Medical Center, Los Angeles, CA, USA.

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