plasma exchange (PE) with or without rituximab, with or without intravenous immunoglobulins (Iv-Ig). However, if used, the optimal dose of rituximab is still unknown. Furthermore, an increased risk of infection has been reported in kidney-transplant patients receiving rituximab, mainly when combined with polyclonal antibodies. Here, we compared the efficacy and safety of low-dose (375 mg/m²/week for 2 weeks) to high-dose (375 mg/m²/ week for 3–5 weeks, median 4) rituximab given for AMR after kidney transplantation (read more).
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