Biopsy-Proven T-Cell Mediated Rejection After Belatacept Rescue Conversion: A Multicenter Retrospective Study

After kidney transplantation, conversion to belatacept is a promising alternative in patients with poor graft function or intolerance to calcineurin inhibitors. The risk of acute rejection has not been well described under these conditions. Here we present a retrospective multicenter study investigating the occurrence of acute rejection after conversion in 901 patients (2011-2021). The incidence of cellular and humoral rejection was 5.2% and 0.9%, respectively. T-cell mediated rejection (TCMR) occurred after a median of 2.6 months after conversion. Out of 47 patients with TCMR, death-censored graft survival was 70.1%, 55.1% and 50.8% at 1 year, 3 years and 5 years post-rejection, respectively. Eight patients died after rejection, mainly from infectious diseases. We compared these 47 patients with a cohort of kidney transplant recipients who were converted to belatacept between 2011 and 2017 and did not develop rejection (n = 238). In multivariate analysis, shorter time between KT and conversion, and the absence of anti-thymocyte globulin induction after KT were associated with the occurrence of TCMR after belatacept conversion. The occurrence of rejection after conversion to belatacept appeared to be less frequent than with <i>de novo</i> use. Nevertheless, the risk of graft loss could be significant in patients with already low renal function.

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Journal
Transplant International
Published
2024-12-06
DOI
https://doi.org/10.3389/ti.2024.13544
Citations
4
Primary Topic
Renal Transplantation Outcomes and Treatments
Type
article
Field-Weighted Citation Impact
2.03
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article

Biopsy-Proven T-Cell Mediated Rejection After Belatacept Rescue Conversion: A Multicenter Retrospective Study

Nicolas Bouvier, Charlotte Laurent, Arnaud François, Jérôme Olagne et al.
4 citations
Transplant International
Renal Transplantation Outcomes and Treatments
2.03
article

Biopsy-Proven T-Cell Mediated Rejection After Belatacept Rescue Conversion: A Multicenter Retrospective Study

Nicolas Bouvier, Charlotte Laurent, Arnaud François, Jérôme Olagne, Dominique Bertrand, Dany Anglicheau, Nathalie Chavarot, Léonard Golbin, Clarisse Grèze, Dominique Guerrot, Mathilde Lemoine, Philippe Gatault, Clément Danthu, Antoine Thierry, Maïté Jaureguy, Yannick Le Meur, Charlotte Colosio, É. Thervet, Agnès Duveau
article en
4 citations

Abstract

After kidney transplantation, conversion to belatacept is a promising alternative in patients with poor graft function or intolerance to calcineurin inhibitors. The risk of acute rejection has not been well described under these conditions. Here we present a retrospective multicenter study investigating the occurrence of acute rejection after conversion in 901 patients (2011-2021). The incidence of cellular and humoral rejection was 5.2% and 0.9%, respectively. T-cell mediated rejection (TCMR) occurred after a median of 2.6 months after conversion. Out of 47 patients with TCMR, death-censored graft survival was 70.1%, 55.1% and 50.8% at 1 year, 3 years and 5 years post-rejection, respectively. Eight patients died after rejection, mainly from infectious diseases. We compared these 47 patients with a cohort of kidney transplant recipients who were converted to belatacept between 2011 and 2017 and did not develop rejection (n = 238). In multivariate analysis, shorter time between KT and conversion, and the absence of anti-thymocyte globulin induction after KT were associated with the occurrence of TCMR after belatacept conversion. The occurrence of rejection after conversion to belatacept appeared to be less frequent than with <i>de novo</i> use. Nevertheless, the risk of graft loss could be significant in patients with already low renal function.

Transplant InternationalVol. 37
Hôpital Necker-Enfants Malades (FR), Assistance Publique – Hôpitaux de Paris (FR), Université de Rouen Normandie (FR), Université de Strasbourg (FR)
No poverty, Good health and well-being
Openalex Percentile: Top 13%
Renal Transplantation Outcomes and Treatments
2.03
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