The association between human leukocyte antigen eplet mismatches, de novo donor-specific antibodies, and the risk of acute rejection in pediatric kidney transplant recipients.


Journal

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

Informations de publication

Date de publication:
06 2020
Historique:
received: 27 05 2019
accepted: 03 01 2020
revised: 16 12 2019
pubmed: 18 2 2020
medline: 5 5 2021
entrez: 18 2 2020
Statut: ppublish

Résumé

The longitudinal relationship between HLA class I and II eplet mismatches, de novo donor-specific antibodies (dnDSA) development, and acute rejection after transplantation in childhood is unknown. Eplet mismatches at HLA class I and II loci were calculated retrospectively for each donor/recipient pair transplanted between 2005 and 2015 at a single Australian center. Logistic regression analyses were conducted to determine the association between the number of eplet mismatches, dnDSA, and acute rejection. The cohort comprised 59 children (aged 0-18 years) who received their first kidney allograft and were followed for median (interquartile range) 4.5 (± 2.6) years. Overall, 32% (19/59) developed dnDSA (class I 3% (2/59), class II 14% (8/59), 15% class I and II (9/59)), and 24% (14/59) developed biopsy-proven acute rejection. Every unit increase in class I and II eplet mismatches corresponded to an increase in risk of class I (odds ratio (OR) 1.22, 95% CI 1.07-1.39, p < 0.01) and class II (OR 1.06, 95% CI 1.01-1.11, p = 0.02) dnDSA development. Compared with recipients without dnDSA, class I and II dnDSA were associated with direction of effect towards increased risk of acute cellular rejection (class I: OR 5.87, 95% CI 0.99-34.94, p = 0.05; class II: OR 12.00, 95% CI 1.25-115.36, p = 0.03) and acute antibody-mediated rejection (class I: OR 25.67, 95% CI 3.54-186.10, p < 0.01; class II: OR 9.71, 95% CI 1.64-57.72, p = 0.01). Increasing numbers of HLA class I or II eplet mismatches were associated with the development of dnDSA. Children who developed dnDSA were also more likely to develop acute rejection compared with children without dnDSA.

Sections du résumé

BACKGROUND
The longitudinal relationship between HLA class I and II eplet mismatches, de novo donor-specific antibodies (dnDSA) development, and acute rejection after transplantation in childhood is unknown.
METHODS
Eplet mismatches at HLA class I and II loci were calculated retrospectively for each donor/recipient pair transplanted between 2005 and 2015 at a single Australian center. Logistic regression analyses were conducted to determine the association between the number of eplet mismatches, dnDSA, and acute rejection.
RESULTS
The cohort comprised 59 children (aged 0-18 years) who received their first kidney allograft and were followed for median (interquartile range) 4.5 (± 2.6) years. Overall, 32% (19/59) developed dnDSA (class I 3% (2/59), class II 14% (8/59), 15% class I and II (9/59)), and 24% (14/59) developed biopsy-proven acute rejection. Every unit increase in class I and II eplet mismatches corresponded to an increase in risk of class I (odds ratio (OR) 1.22, 95% CI 1.07-1.39, p < 0.01) and class II (OR 1.06, 95% CI 1.01-1.11, p = 0.02) dnDSA development. Compared with recipients without dnDSA, class I and II dnDSA were associated with direction of effect towards increased risk of acute cellular rejection (class I: OR 5.87, 95% CI 0.99-34.94, p = 0.05; class II: OR 12.00, 95% CI 1.25-115.36, p = 0.03) and acute antibody-mediated rejection (class I: OR 25.67, 95% CI 3.54-186.10, p < 0.01; class II: OR 9.71, 95% CI 1.64-57.72, p = 0.01).
CONCLUSIONS
Increasing numbers of HLA class I or II eplet mismatches were associated with the development of dnDSA. Children who developed dnDSA were also more likely to develop acute rejection compared with children without dnDSA.

Identifiants

pubmed: 32065279
doi: 10.1007/s00467-020-04474-x
pii: 10.1007/s00467-020-04474-x
doi:

Substances chimiques

HLA Antigens 0
Isoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1061-1068

Références

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Auteurs

Ankit Sharma (A)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia. ankit.sharma@health.nsw.gov.au.
School of Public Health, Sydney Medical School, The University of Sydney, Sydney, Australia. ankit.sharma@health.nsw.gov.au.

Anne Taverniti (A)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.

Nicole Graf (N)

Department of Histopathology, Children's Hospital at Westmead, Sydney, Australia.

Armando Teixeira-Pinto (A)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.
School of Public Health, Sydney Medical School, The University of Sydney, Sydney, Australia.

Joshua R Lewis (JR)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.
School of Medical and Health Sciences, Edith Cowan University, Joondalup, Australia.
School of Medicine and Pharmacology, University of Western Australia, Perth, Australia.

Wai H Lim (WH)

School of Medicine and Pharmacology, University of Western Australia, Perth, Australia.
Department of Renal Medicine, Sir Charles Gairdner Hospital, Perth, Australia.

Stephen I Alexander (SI)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.

Anne Durkan (A)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.

Jonathan C Craig (JC)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.
School of Public Health, Sydney Medical School, The University of Sydney, Sydney, Australia.
College of Medicine and Public Health, Flinders University, Adelaide, Australia.

Germaine Wong (G)

Centre for Kidney Research, Children's Hospital at Westmead, Sydney, Australia.
School of Public Health, Sydney Medical School, The University of Sydney, Sydney, Australia.

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