BACKGROUND
Rituximab induces long-lasting B cell depletion in the peripheral blood and increases the levels of proinflammatory
cytokines associated with regulatory B cell depletion. Previous reports showed that B cell-related
cytokine release after administration of
rituximab may induce acute cellular rejection (ACR) and delayed-onset
neutropenia. The present study was conducted to investigate the correlation between acute rejection and delayed-onset
neutropenia in ABO-incompatible renal transplant recipients who underwent administration of
rituximab for 1 year after
transplantation. MATERIAL AND METHODS From June 2006 to July 2015, 47 patients with
chronic renal failure received ABO-incompatible renal transplant with
rituximab induction at Osaka City University Hospital. All 47 patients underwent
plasmapheresis due to removal of anti-A/B
antibodies and administration of
rituximab, and their transplants were carried out successfully. We investigated the correlation between ACR and delayed-onset
neutropenia in ABO-incompatible renal transplant recipients who underwent administration of
rituximab for 1 year after
transplantation. RESULTS Fourteen patients (29.8%) experienced ACR (group A), and 33 recipients did not develop ACR (group B). The frequency of delayed-onset
neutropenia was higher in group A than in group B (p=0.0503). Multivariate logistic regression analysis revealed that the frequency of ACR correlated significantly with the prevalence of delayed-onset
neutropenia. CONCLUSIONS Our results indicated that ACR in ABO-incompatible renal transplant recipients receiving
rituximab was associated with delayed-onset
neutropenia.