Absence of IL-6 Receptor Blockade Effect on the Outcomes of Transplant Glomerulopathy in the Absence of Anti-HLA Donor-specific Antibodies

Alberto Mella(Department of Medical Sciences), Antonio Lavacca(Department of Medical Sciences), Diana Teodora Dodoi(Department of Medical Sciences), Roberto Presta(Department of Medical Sciences), Fabrizio Fop(Department of Medical Sciences), Marco Campagna(Department of Medical Sciences), Ana Maria Manzione(Department of Medical Sciences), Caterina Dolla(Department of Medical Sciences), Ester Gallo(Department of Medical Sciences), Isabella Abbasciano(Department of Medical Sciences), Chiara Gai(University of Turin), Giovanni Camussi(University of Turin), Antonella Barreca(Department of Medical Sciences), Cristiana Caorsi(Department of Medical Sciences), Gloria Giovinazzo(Department of Medical Sciences), Luigi Biancone(Department of Medical Sciences)
Transplantation Direct
May 16, 2024
Cited by 4Open Access
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Abstract

Background. Transplant glomerulopathy (TG) is the hallmark of chronic antibody-mediated rejection but often occurs without anti-HLA donor-specific antibodies (DSAs) in the assumption that other DSAs may be the effectors of the tissue injury. Recently, we reported a positive effect of interleukin-6 (IL-6) receptor blocker tocilizumab (TCZ) in TG/DSA + . In the present study, we investigate the effect of TCZ in a cohort of TG cases without detectable anti-HLA DSAs. Methods. Single-center retrospective analysis of TG cases without anti-HLA DSAs (TG/DSA) treated with TCZ for chronic antibody-mediated rejection as first-line therapy evaluated through clinical, protocol biopsies, and gene expression analyses was included. Results. Differently from TG/DSA + , TG/DSA – showed a progressive reduction in the estimated glomerular filtration rate at 12 mo and after that with no significant modification in microvascular inflammation or C4d + . No upregulation in tight junction protein-1, aldo-keto reductase family 1 member C3, and calcium/calmodulin-dependent serine protein kinase, documented in TG/DSA + , was noted in post-TCZ biopsies. The reduction of microvascular inflammation was associated with natural killer-cell reduction in TG/DSA + , whereas TG/DSA – tends to maintain or increase periglomerular/interstitial infiltration. Conclusions. In the absence of anti-HLA DSAs, TG behavior seems not to be modified by IL-6 receptor blockade. These results are at variance with observational studies and previous trials with IL-6 inhibitors in TG associated with anti-HLA DSAs. These data may fuel the hypothesis of different mechanisms underlying TGs (including the potentially different roles of natural killer cells) and suggest carefully selecting patients with TG for clinical trials or off-label treatment based on their antidonor serologic status.


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