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Risk-adapted HLA delisting and imlifidase enable deceased-donor kidney transplantation for highly sensitized candidatesNew guide helps transplant kidneys for hardest-to-match patients

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Key Takeaway
Consider risk-adapted HLA delisting and imlifidase to manage immunological risks in highly sensitized kidney candidates.

This expert consensus provides a practical framework for managing highly sensitized adult candidates on the waitlist for deceased-donor kidney transplantation. The scope of the guideline includes clinical decision-making when compatibility-preserving pathways have been exhausted or are unlikely to succeed.

The guidelines synthesize recommendations for several critical stages of care, including candidate selection, risk-adapted HLA delisting, and the assessment of organ offers. It also provides guidance on perioperative immunosuppression, prophylaxis for infection, post-transplant monitoring, and the management of antibody-mediated rejection. The inclusion of imlifidase is specifically addressed to manage immunological risks in these high-risk patients.

A noted limitation is that the use of imlifidase in living-donor transplantation is considered an off-label scenario and is addressed separately from this guidance. The recommendations are intended for use in experienced transplant centers where clinicians can balance transplant opportunities against significant immunological risks. Clinical application should be tailored to the specific complexities of highly sensitized patients.

For people with end-stage kidney disease who are highly sensitized, finding a matching donor kidney can feel impossible. Their immune systems attack almost any organ offered. But a new expert consensus guideline offers a practical path forward.

The guide, from experienced transplant centers, outlines a step-by-step approach. It covers how to select candidates, assess organ offers, and use a drug called imlifidase to reduce the risk of rejection. It also details perioperative care, infection prevention, and monitoring after transplant.

This is not a clinical trial with hard numbers. It is a consensus report from experts, meant to balance opportunity against risk. The goal is to help transplant teams make decisions for patients who have exhausted other options.

Importantly, the guide notes that using imlifidase in living-donor transplants is still an off-label scenario. That means it is not yet formally approved for that use. The recommendations are intended for experienced centers only.

What this means for you:
New expert guide offers a practical roadmap for kidney transplant in highly sensitized patients.

Common questions

Who is this new guideline for?

This guideline is for highly sensitized adult patients with end-stage kidney disease who are waiting for a deceased-donor kidney transplant. It is intended for use at experienced transplant centers after other compatibility-preserving options have been exhausted.

What is imlifidase and how is it used?

Imlifidase is a drug that can reduce the risk of antibody-mediated rejection in highly sensitized kidney transplant recipients. The guideline describes its use in deceased-donor transplantation. However, using imlifidase in living-donor transplants is still considered off-label.

Does this guideline provide new clinical trial data?

No. This is an expert consensus guideline, not a clinical trial. It does not report new data on outcomes like survival or rejection rates. Instead, it offers practical recommendations based on expert opinion for candidate selection, organ assessment, and post-transplant care.

Study Details

Study typeGuideline
EvidenceLevel 5
PublishedJun 2026
View Original Abstract ↓
Kidney transplantation is the preferred treatment for suitable patients with end-stage renal disease; however, access to transplantation declines dramatically with increasing HLA sensitization. While the acceptable mismatch (AM) program by Eurotransplant improves transplantability for highly sensitized candidates, a clinically relevant subgroup with extremely low donor frequency or ineligible for AM remains disadvantaged. In carefully selected cases, the controlled delisting of unacceptable HLA antigens and the use of peri-transplant desensitization (e.g., imlifidase) may enable transplantation. In order to provide better guidance, this German expert consensus report was compiled by the Kidney and Immunology Commissions of the German Transplantation Society and the Organ Transplantation Commission of the German Society for Immunogenetics. Within the German legal framework of urgency and chances for success, the report proposes a practical guide for candidate selection, multidisciplinary governance, risk-adapted HLA delisting, assessment of organ offers, use of imlifidase, perioperative immunosuppression, prophylaxis for infection, post-transplant monitoring, and management of antibody-mediated rejection. These recommendations are intended for experienced transplant centers and aim to balance transplant opportunity against immunological risk in highly sensitized kidney transplant candidates. The primary scope of this article is highly sensitized adult wait-listed candidates considered for deceased-donor kidney transplantation after compatibility-preserving pathways have been exhausted or are unlikely to succeed; HLA-incompatible living-donor transplantation with imlifidase is addressed separately as a potential off-label scenario for selected highly sensitized patients.
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