“…7 Regarding Rh and K antibodies, we observed that in the majority of responding patients, 1 to 2 incompatible units (RBCs or PLTs) were sufficient to induce antibodies, confirming the relative high immunogenicity of these antigens (D. Evers, R.A. Middelburg, S. Zalpuri, et al, submitted for publication). 29 Residual non-D-matched RBC in PLT products have been reported to be the offender of anti-D in mainly immunosuppressed hematooncology patients, with reports of 0% to 14%, [30][31][32] while non-D antibodies have been scarcely reported. [33][34][35] In this study seven non-D antibodies (five anti-E, one anti-e and anti-K) were formed by six EM patients after cognate antigen exposure through (nonmatched) PLT transfusions.…”