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Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection
Piñeiro, Gaston Julio; Sousa Amorim, Erika de; Solé, Manel; Ríos, José; Lozano Molero, Miguel; Cofán Pujol, Federico; Ventura Aguiar, Pedro; Cucchiari, David; Revuelta, Ignacio; Cid Vidal, Joan; Palou, Eduard; Campistol Plana, Josep M.; Oppenheimer Salinas, Federico; Rovira, Jordi; Diekmann, Fritz
BACKGROUND: Chronic active antibody-mediated rejection (c-aABMR) is an important cause of allograft failure and graft loss in long-term kidney transplants. METHODS: To determine the efficacy and safety of combined therapy with rituximab, plasma exchange (PE) and intravenous immunoglobulins (IVIG), a cohort of patients with transplant glomerulopathy (TG) that met criteria of active cABMR, according to BANFF'17 classification, was identified. RESULTS: We identified 62 patients with active c-aABMR and TG (cg ≥ 1). Twenty-three patients were treated with the combination therapy and, 39 patients did not receive treatment and were considered the control group. There were no significant differences in the graft survival between the two groups. The number of graft losses at 12 and 24 months and the decline of eGFR were not different and independent of the treatment. A decrease of eGFR≥13 ml/min between 6 months before and c-aABMR diagnosis, was an independent risk factor for graft loss at 24 months (OR = 5; P = 0.01). Infections that required hospitalization during the first year after c-aABMR diagnosis were significantly more frequent in treated patients (OR = 4.22; P = 0.013), with a ratio infection/patient-year of 0.65 and 0.20 respectively. CONCLUSIONS: Treatment with rituximab, PE, and IVIG in kidney transplants with c-aABMR did not improve graft survival and was associated with a significant increase in severe infectious complications.
-Trasplantament renal
-Infeccions
-Terapèutica
-Utilització de medicaments
-Kidney transplantation
-Infections
-Therapeutics
-Drug utilization
cc-by (c) Piñeiro, Gaston Julio et al., 2018
http://creativecommons.org/licenses/by/3.0/es
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Article - Published version
BioMed Central
         

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