4.6 Article

Cytokine Profiles Associated With Angiotensin II Type 1 Receptor Antibodies

期刊

KIDNEY INTERNATIONAL REPORTS
卷 4, 期 4, 页码 541-550

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ekir.2018.12.011

关键词

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

资金

  1. Ruth L. Kirschstein National Research Service Award UCLA Translational Research Grant in Pediatric Nephrology Program [T32 DK104687]
  2. National Kidney Foundation
  3. American Society of Nephrology
  4. Casey Lee Ball Foundation
  5. Today's and Tomorrow's Children Fund
  6. Duke Health Scholars Award
  7. National Institute of Allergy and Infectious Diseases [R01AI13520]
  8. National Institutes of Health [PO1 AI120944, 5U19AI128913, 1U01AI124319]
  9. National Center for Advancing Translational Sciences [UL1 TR000124]

向作者/读者索取更多资源

Introduction: 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. Methods: Blood samples from 65 pediatric renal transplant recipients drawn during the first 3 months post-transplant, 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]-alpha, interferon [IFN]-gamma, interleukin [IL]-8, IL-1 beta, IL-6, and IL-17). Associations between antibodies and cytokines were evaluated. Results: AT1R-Ab, but not HLA DSA, was associated with elevations in TNF-alpha, IFN-gamma, IL-8, IL-1 beta, 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. Conclusions: 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.

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