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
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
541-550Subventions
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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