Evaluating the Prognostic Value of Islet Autoantibody Monitoring in Islet Transplant Recipients with Long-Standing Type 1 Diabetes Mellitus.

GADA allogenic islet cell transplantation autoantibodies pancreas type 1 diabetes mellitus

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
19 Jun 2021
Historique:
received: 30 04 2021
revised: 15 06 2021
accepted: 17 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

(1) Background: The correlation between titers of islet autoantibodies (IAbs) and the loss of transplanted islets remains controversial. We sought to evaluate the prognostic utility of monitoring IAbs in diabetic patients after islet transplantation (ITx); (2) Methods: Twelve patients with Type 1 diabetes mellitus and severe hypoglycemia underwent ITx. Serum concentration of glutamic acid decarboxylase (GAD), insulinoma antigen 2 (IA-2), and zinc transport 8 (ZnT8) autoantibodies was assessed before ITx and 0, 7, and 75 days and every 3 months post-operatively; (3) Results: IA-2A (IA-2 antibody) and ZnT8A (ZnT8 antibody) levels were not detectable before or after ITx in all patients (median follow-up of 53 months (range 24-61)). Prior to ITx, GAD antibody (GADA) was undetectable in 67% (8/12) of patients. Of those, 75% (6/8) converted to GADA+ after ITx. In 67% (4/6) of patients with GADA+ seroconversion, GADA level peaked within 3 months after ITx and subsequently declined. All patients with GADA+ seroconversion maintained long-term partial or complete islet function (insulin independence) after 1 or 2 ITx. There was no correlation between the presence of IAb-associated HLA haplotypes and the presence of IAbs before or after ITx; (4) Conclusions: There is no association between serum GADA trends and ITx outcomes. IA-2A and ZnT8A were not detectable in any of our patients before or after ITx.

Identifiants

pubmed: 34205321
pii: jcm10122708
doi: 10.3390/jcm10122708
pmc: PMC8233942
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : University of Chicago Diabetes Research and Training Center US Public Health Service Grant
ID : P30DK020595
Organisme : Dompe Pharmaceutical
ID : NA

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Auteurs

Roi Anteby (R)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.
Harvard School of Public Health, Boston, MA 02115, USA.

Aaron Lucander (A)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Department of Surgery, University of Alabama at Birmingham, Birmingham, AL 35233, USA.

Piotr J Bachul (PJ)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Jordan Pyda (J)

Department of Surgery, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.

Damian Grybowski (D)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Lindsay Basto (L)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Gabriela S Generette (GS)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Laurencia Perea (L)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Karolina Golab (K)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Ling-Jia Wang (LJ)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Martin Tibudan (M)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Celeste Thomas (C)

Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.

John Fung (J)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Piotr Witkowski (P)

Department of Surgery, The University of Chicago, Chicago, IL 60637, USA.

Classifications MeSH