ReviewClinical transplantation and research2026
Re-engineering CD154 blockade for transplantation: Fc-free design to separate thrombotic risk from therapeutic function.
Review in Clinical transplantation and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Costimulation blockade of the CD40-CD154 pathway is among the most effective strategies for preventing allograft rejection, yet development of first-generation anti-CD154 antibodies was discontinued after thromboembolic complications. Higher-order immune complexes of soluble CD154 and anti-CD154 immunoglobulin G cross-link Fcγ receptor IIa (FcγRIIa) on platelets and activate them, localizing the liability to the fragment crystallizable region (Fc) rather than to the CD154-binding arm of the antibody. Engineering strategies address this by excluding the Fc altogether or silencing Fc function. Fc-free antagonists structurally preclude FcγRIIa cross-linking but forfeit neonatal Fc receptor (FcRn)-mediated recycling and size protection from glomerular filtration. Such antagonists must therefore recover both functions by other means. Size-based carriers recover only the second: conjugation of polyethylene glycol (PEG) to an anti-CD154 Fab' extends its half-life from hours to weeks, as in dapirolizumab pegol, but leaves FcRn recycling unaddressed, while uncertainties remain regarding long-term PEG exposure. Albumin recovers both through FcRn-dependent recycling and its own molecular size, without engaging Fcγ receptors. Dazodalibep, an Fc-free albumin-fusion CD154 antagonist, was administered with belatacept to kidney transplant recipients in a single-arm phase 2a trial without thrombotic events, but the prespecified composite efficacy endpoint was not met.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.