High occurence of DRB1 11 in chronic lymphocytic leukaemia families
Ioannis Theodorou, Laboratoire Central d'Immunologie Cellulaire et Tissulaire, Hôpital Pitié Salpêtrière Bâtiment CERVI, 83 Bd. De l'Hôpital 75013 Paris, France. E-mail: [email protected]
Abstract
Summary. Recently, linkage analysis of a series of familial chronic lymphocytic leukaemia (CLL) showed that affected sibling pairs did not share common major histocompatibilty complex haplotypes. We analysed Class I and II antigens in 11 Italian families with familial CLL. Although there was no association of disease status with any particular human leucocyte antigen, there was an overrepresentation of DRB1 11 alleles in these families (P = 0·009). A similar trend was also observed in a second series of nine French families (P = 0·002). Larger studies are needed to determine whether non-inherited paternal or maternal DRB1 antigens play a role in familial CLL development.
