摘要

We hypothesized that diagnoses may be associated with alloantibody responder' status and examined associations between disease states and alloimmunization. Patients with 1 alloantibody and non-alloimmunized controls were analysed. Pearson's coefficients were calculated to determine associations between alloimmunization and diseases; significant correlations were selected to construct a network. Inflammatory disorders and diseases requiring chronic transfusion support were associated with responder status. Mitigation steps may be considered in patients with these disorders.

  • 出版日期2017-7