Oko Andrzej, Wyrwicz Lucjan S, Glyda Maciej, Idasiak-Piechocka Ilona, Bińczak-Kuleta Agnieszka, Kaczmarczyk Mariusz, Drozd Arleta, Ciechanowicz Andrzej, Czekalski Stanisław
Katedra i Klinika Nefrologii, Transplantologii i Chorób Wewnetrznych, Uniwersytetu Medycznego im. Karola Marcinkowskiego ul. Przybyszewskiego 49, 60-355 Poznań.
Ann Acad Med Stetin. 2009;55(2):22-6.
CD52 is a small glycopeptide leukocyte antigen present on selected subpopulations of human cells. From the clinical point of view this protein is an important target for therapeutic interventions aimed at leukocyte depletion in hematological malignancies and post-transplant immunosuppression. Recently, two variants of CD52--rs1071849 (A119G; Asn40Ser) and rs17645 (A123G; I1e41Met)--were discovered. We now report on the distribution of these variants in kidney graft recipients and controls. Our bioinformatics findings suggest that CD52 polymorphism may affect the efficiency of GPI anchor formation and thus may indirectly alter the response to anti-CD52 agents.