Cytokine Profiles Associated With Angiotensin II Type 1 Receptor Antibodies.

angiotensin II type 1 receptor antibody cytokine human leukocyte antigen donor-specific antibody pediatric nephrology transplantation

Journal

Kidney international reports
ISSN: 2468-0249
Titre abrégé: Kidney Int Rep
Pays: United States
ID NLM: 101684752

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 16 11 2018
revised: 13 12 2018
accepted: 17 12 2018
entrez: 19 4 2019
pubmed: 19 4 2019
medline: 19 4 2019
Statut: epublish

Résumé

Angiotensin II type 1 receptor antibody (AT1R-Ab), is a non-human leukocyte antigen (HLA) antibody implicated in poor renal allograft outcomes, although its actions may be mediated through a different pathway than HLA donor-specific antibodies (DSAs). Our aim was to examine serum cytokine profiles associated with AT1R-Ab and distinguish them from those associated with HLA DSA in serially collected blood samples from a cohort of pediatric renal transplant recipients. Blood samples from 65 pediatric renal transplant recipients drawn during the first 3 months posttransplant, at 6, 12, and 24 months posttransplant, and during suspected episodes of kidney transplant rejection were tested for AT1R-Ab, HLA DSA, and a panel of 6 cytokines (tumor necrosis factor [TNF]-α, interferon [IFN]-γ, interleukin [IL]-8, IL-1β, IL-6, and IL-17). Associations between antibodies and cytokines were evaluated. AT1R-Ab, but not HLA DSA, was associated with elevations in TNF-α, IFN-γ, IL-8, IL-1β, IL-6, and IL-17. This relationship remained significant even after controlling for relevant clinical factors and was consistent across all time points. In contrast to HLA DSA, AT1R-Ab was associated with elevations in vascular inflammatory cytokines in the first 2 years posttransplant. This profile of vascular cytokines may be informative for clinical monitoring and designing future studies to delineate the distinct pathophysiology of AT1R-Ab-mediated allograft injury in kidney transplantation.

Identifiants

pubmed: 30997435
doi: 10.1016/j.ekir.2018.12.011
pii: S2468-0249(18)30354-1
pmc: PMC6451195
doi:

Types de publication

Journal Article

Langues

eng

Pagination

541-550

Subventions

Organisme : NIAID NIH HHS
ID : P01 AI120944
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI135201
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK104687
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001881
Pays : United States

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Auteurs

Meghan H Pearl (MH)

Department of Pediatrics, Division of Pediatric Nephrology, University of California, Los Angeles, Los Angeles, California, USA.

Jonathan Grotts (J)

Department of Medicine Statistics Core, University of California, Los Angeles, Los Angeles, California, USA.

Maura Rossetti (M)

Department of Pathology and Laboratory Medicine University of California, Los Angeles, Los Angeles, California, USA.

Qiuheng Zhang (Q)

Department of Pathology and Laboratory Medicine University of California, Los Angeles, Los Angeles, California, USA.

David W Gjertson (DW)

Department of Pathology and Laboratory Medicine University of California, Los Angeles, Los Angeles, California, USA.

Patricia Weng (P)

Department of Pediatrics, Division of Pediatric Nephrology, University of California, Los Angeles, Los Angeles, California, USA.

David Elashoff (D)

Department of Medicine Statistics Core, University of California, Los Angeles, Los Angeles, California, USA.

Elaine F Reed (EF)

Department of Pathology and Laboratory Medicine University of California, Los Angeles, Los Angeles, California, USA.

Eileen Tsai Chambers (E)

Department of Pediatrics, Division of Pediatric Nephrology, Duke University, Durham, North Carolina, USA.

Classifications MeSH