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Author Notes:

Correspondence: Allan D. Kirk, MD, PhD, Box 3704, Duke University Medical Center, Durham, NC 27710, allan.kirk@duke.edu

Author contributions: DJA, DJL, FL, MS, EAS, JBJ, CPL, and ADK contributed to design of the study. DJA, DJL, FL, EAS, JBJ, and ADK performed the study. Data analysis was performed by DJA and DJL. Manuscript preparation and editing was performed by DJA, DJL, CPL, and ADK.

The authors would like to thank the research support staff of the Emory Transplant Center and the veterinary staff at the Yerkes National Primate Research Center for their efforts on our behalf.

Disclosures: Dr. Larsen has received funding from Bristol-Myers-Squibb for clinical trials and preclinical studies. The remaining authors of this manuscript have no conflicts of interest to disclose as described by Clinical Transplantation.

Subjects:

Research Funding:

Funding for this research was provided by a grant from the NIH, 1U01AI079223, U01AI084150 and 2U19AI051731-11.

Further grant support of the Yerkes National Primate Research Center was provided by the National Center for Research Resources P51RR165 and is currently supported by the Office of Research Infrastructure Programs/OD P51OD11132.

Dr. Anderson was partially supported by the ASTS-Genentech Scientist Scholarship.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Surgery
  • Transplantation
  • costimulation
  • methotrexate
  • non-human primate
  • Prolongs allograft survival
  • Long-term acceptance
  • Versus host disease
  • Rheumatoid arthritis
  • Monoclonal antibody
  • Phase III
  • Therapy
  • Belatacept
  • Rejection
  • Cyclosporine

Corticosteroids and methotrexate as adjuvants to costimulation blockade in non-human primate renal transplantation

Tools:

Journal Title:

Clinical Transplantation

Volume:

Volume 33, Number 6

Publisher:

, Pages e13568-e13568

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Belatacept, the CD28-B7 costimulation pathway inhibitor, has been approved as a calcineurin inhibitor (CNI) alternative in kidney transplantation. Although costimulation blockade (CoB) allows for CNI avoidance, it is associated with increased rates of early rejection, prompting a search for agents to pair with belatacept. Methotrexate (MTX) is an antimetabolite that has been found to be complimentary with abatacept, a lower affinity CD28-B7-specific analogue of belatacept, in the treatment of rheumatoid arthritis (RA). We examined whether this synergy would extend to prevention of kidney allograft rejection. Rhesus macaques underwent kidney transplantation treated with abatacept maintenance therapy with either a steroid taper, MTX, or both. The combination of abatacept maintenance with steroids prolonged graft survival compared to untreated historical controls and previous reports of abatacept monotherapy. The addition of MTX did not provide additional benefit. These data demonstrate that abatacept with adjuvant therapy may delay the onset of acute rejection, but fail to show synergy between abatacept and MTX beyond that of steroids. These findings indicate that MTX is unlikely to be a suitable adjuvant to CoB in kidney transplantation, but also suggest that with further modification, a CoB regimen used for advanced RA may suffice for RA patients requiring kidney transplantation.

Copyright information:

© 2019 John Wiley & Sons, Inc. All rights reserved.

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