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31st International Congress of The Transplantation Society (TTS 2026) | Sydney, Australia | September 20-23, 2026
Innovation through Collaboration

Biogen - Breakfast Symposium

Microvascular Inflammation: A Defining Characteristic of Antibody‑Mediated Rejection in Kidney Transplantation

Wednesday, September 23, 2026

07:00-08:00 Parkside 1&2

Microvascular inflammation (MVI) is a hallmark of antibody-mediated rejection (AMR) and an important predictor of long-term allograft outcomes in kidney transplantation. This symposium examines the clinical significance of MVI, including its association with graft injury and loss1, and reviews the impact of current standard treatments and investigational therapies on MVI. The session highlights CD38⁺ cells as central drivers of antibody-dependent and -independent mechanisms of MVI, with a focus on the role of activated CD38⁺ natural killer (NK) cells2,3. These findings provide rationale for CD38-targeted therapies as a potential strategy to modify the underlying biology of AMR and MVI. We examine clinical evidence supporting this approach, including data from the Phase 2 felzartamab study and subsequent open-label extension evaluating the effects of targeting CD38 on AMR activity, biomarkers, and molecular features of disease over time.

Biogen 291974

Agenda

  1. Welcome
  2. Microvascular Inflammation and Long-Term Outcomes: Current Evidence and Unmet Needs
  3. Key Pathological Drivers of Antibody-Mediated Rejection and Microvascular Inflammation
  4. Targeting CD38+ Immune Cells in Antibody-Mediated Rejection and Microvascular Inflammation
  5. Q&A

Disclaimers and References

Disclaimers:

Felzartamab is investigational and is not approved for use in any country. The safety profile and efficacy has not yet been established.

BIOGEN is a registered trademark of Biogen MA Inc. Biogen Australia Pty Ltd, Macquarie Park, NSW. ABN 30 095 760 115. Date of preparation: July 2026. © 2026 Biogen. All rights reserved.

References:

  1. Sablik M, et al. N Engl J Med. 2025;392(8):763-776.
  2. Heeger PS, et al. Nat Rev Nephrol.2024;20(4):218-232
  3. Pontrelli P, et al. Front Immunol. 2020;11:1454

Steven Chadban, BMed, PhD, FRACP, FAHMS

University of Sydney Sydney, Australia

Dr. Chadban is Head of Renal Medicine at Royal Prince Alfred Hospital and Professor of Medicine at the University of Sydney. As a clinician-scientist, he leads research spanning basic science, clinical trials, and transplant outcomes and has published over 400 peer-reviewed papers (34,000+ citations; H-index 98). Dr. Chadban is Past-President of the Transplantation Society of Australia and New Zealand, past chair of ANZDATA, advises Government on Transplantation and CKD, and is co-chair of the 2020 KDIGO Clinical Guidelines for assessment and management of candidates for Kidney Transplantation. 

Katharina Mayer, MD, PhD

Medical University of Vienna Vienna, Austria

Dr. Mayer received her medical degree from the Medical University of Vienna. She was trained in Immunology and completed her PhD at the Institute of Immunology at the Medical University of Vienna. Since joining the Division of Nephrology and Dialysis at the same institution, her research has focused on transplant immunology, especially antibody-mediated kidney transplant rejection and the immunological monitoring of kidney transplant recipients.