Pancreatic autoantibodies and CD14+CD16+ monocytes subset are associated with the impairment of ß-cell function after simultaneous pancreas-kidney transplantation.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 02 02 2018
accepted: 05 02 2019
entrez: 23 2 2019
pubmed: 23 2 2019
medline: 22 11 2019
Statut: epublish

Résumé

Pancreatic autoantibodies (AAb) has been associated with a worse pancreas graft survival after simultaneous pancreas-kidney transplantation (SPK). However, due to the variable time for AAb to become positive and the lack of early biomarkers suggesting such autoimmune activation, the mechanisms leading ß-cell destruction remain uncertain. The present study aimed to evaluate the association between post-transplant AAb and the functional impairment of the pancreatic ß-cell and also the association of such AAb with inflammation after SPK. In a longitudinal study, we analyzed the impact of post-transplant glutamic acid decarboxylase (GAD-65) and the insulinoma-associated autoantigen 2 (IA-2) AAb on pancreas graft function. Serum Hb1Ac and C-peptide (C-pep) were longitudinally compared between a group with positive posttransplant AAb (AAb+; n = 40) and another matched group with negative AAb (AAb-; n = 40) until the fifth year following seroconversion. In the cross-sectional analysis, we further evaluated the systemic signatures of inflammation by measuring pro-inflammatory CD14+CD16+ monocytes by flow-cytometry and interleukin 17-A serum levels in 38 SPK recipients and ten healthy controls. In the longitudinal study, patients with AAb+ showed higher levels of Hb1Ac (p<0.001) and lower C-pep levels (p<0.001) compared to those who remained AAb- throughout the follow-up. In the cross-sectional study, AAb+ patients showed a higher percentage of CD14+CD16+ monocytes compared with those with AAb- and the healthy controls (6.70±4.19% versus 4.0±1.84% and 3.44±0.93%; p = 0.026 and 0.009 respectively). Also, CD14+CD16+ monocytes correlated with Hb1Ac and C-pep serum levels. Multivariate logistic regression showed that posttransplant AAb+ was independently associated with a higher percentage of pro-inflammatory monocytes (adjusted-OR 1.59, 95%CI 1.05-2.40, p = 0.027). The group of patients with positive AAb also showed higher levels of IL17A as compared with the other groups (either healthy control or the negative AAb subjects). In conclusion, pancreatic AAb+ after SPK were not only associated with higher Hb1Ac and lower c-peptide serum levels but also with an increased percentage of CD14+CD16+ monocytes and higher levels of circulating IL17-A.

Identifiants

pubmed: 30794611
doi: 10.1371/journal.pone.0212547
pii: PONE-D-18-03611
pmc: PMC6386378
doi:

Substances chimiques

Autoantibodies 0
Autoantigens 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0212547

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Cristian Rodelo-Haad (C)

Maimonides Biomedical Research Institute of Cordoba (IMIBIC)/Reina Sofia University Hospital/University of Cordoba, Cordoba, Spain.
Nephrology Unit. Reina Sofia University Hospital, Cordoba, Spain.
RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.

Maria Luisa Agüera (ML)

Maimonides Biomedical Research Institute of Cordoba (IMIBIC)/Reina Sofia University Hospital/University of Cordoba, Cordoba, Spain.
Nephrology Unit. Reina Sofia University Hospital, Cordoba, Spain.
RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.

Andres Carmona (A)

Nephrology Unit. Reina Sofia University Hospital, Cordoba, Spain.
RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.

Maria Dolores Navarro (MD)

Maimonides Biomedical Research Institute of Cordoba (IMIBIC)/Reina Sofia University Hospital/University of Cordoba, Cordoba, Spain.
Nephrology Unit. Reina Sofia University Hospital, Cordoba, Spain.
RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.

Julia Carracedo (J)

RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.
Departamento de Genética, Fisiología y Microbiología, Facultad de Biología, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain.

Alberto Rodriguez-Benot (A)

Maimonides Biomedical Research Institute of Cordoba (IMIBIC)/Reina Sofia University Hospital/University of Cordoba, Cordoba, Spain.
Nephrology Unit. Reina Sofia University Hospital, Cordoba, Spain.
RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.

Pedro Aljama (P)

Maimonides Biomedical Research Institute of Cordoba (IMIBIC)/Reina Sofia University Hospital/University of Cordoba, Cordoba, Spain.
Nephrology Unit. Reina Sofia University Hospital, Cordoba, Spain.
RETICs Red Renal (Instituto de Salud Carlos III), Madrid, Spain.

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