Working together to block alloimmunization.

The discovery of ABO(H) blood group antigens resulted in the birth of transfusion medicine and allowed for the first time the use of a laboratory test that could predict immunologic outcomes prior to transfusion. Although ABO(H) antibody testing continues to represent one of the first and most common examples of personalized medicine, it was not until many years later that the existence of non-ABO(H) blood group antigens relevant in transfusion became apparent. One of the earliest descriptions of a non-ABO(H) reaction occurred following a hemolytic transfusion in the mother of a stillborn child following infusion of otherwise ABO(H)-compatible blood donated by the father. Additional investigation demonstrated that nearly 20% of individuals fail to express the Rh factor, a non-ABO(H) antigen also targeted on rhesus macaque RBCs following injection into rabbits. Ensuing studies confirmed that the presence or absence of Rh factor directly correlated with the majority of ABO(H)compatible transfusion reactions. Subsequent reports demonstrated that the development of anti-Rh (RhD) antibodies might not only be responsible for ABO(H)independent transfusion reactions, but may similarly underlie the development of hemolytic disease of the fetus and newborn (HDFN). Circulation of fetal RhD RBCs released during pregnancy or parturition appeared to stimulate anti-RhD antibody formation, putting subsequent RhD pregnancies at risk for developing HDFN. Although these studies provided key insight into factors that appeared to influence RBC alloimmunization during pregnancy, subsequent studies provided a rationale behind strategies designed to prevent RBC alloimmunization during pregnancy and thus HDFN. Although pregnancy with a RhD fetus clearly put RhD mothers at risk for developing anti-RhD alloantibodies, ABO(H) incompatibility between a mother and fetus independently reduced the likelihood of antiRhD antibody formation. The ability of anti-A and/or anti-B antibodies to inhibit anti-RhD antibody development appeared to be consistent with an observation by Theobald Smith many years earlier that administration of passive antibody can prevent immunization following exposure to a target antigen. These combined results suggested that naturally occurring antiABO(H) antibodies likely engage RhD fetal RBCs and prevent RhD alloimmunization. As the conception of human life is rarely predicated on a partner’s blood group status, avoidance of RhD exposure, as routinely occurs in the setting of RBC transfusion, was not a practical intervention to prevent Rh alloimmunization during pregnancy. Given the ability of anti-ABO(H) antibodies, which are predominantly immunoglobulin M (IgM), to inhibit RhD alloimmunization, early efforts sought to generate IgM anti-D antibodies to intentionally prevent RhD alloimmunization in RhD pregnant females. However, unlike anti-ABO(H) antibodies, IgM anti-RhD failed to similarly inhibit RhD alloantibody formation. As a result, subsequent studies used polyclonal IgG anti-RhD antibodies primarily isolated from women previously sensitized through pregnancy. Injection of polyclonal IgG anti-RhD significantly inhibited anti-RhD alloantibody formation in RhD males and likewise reduced RhD alloimmunization during pregnancy. In pregnancy alone, anti-RhD immunoprophylaxis reduced the likelihood of RhD alloimmunization nearly 50-fold, all but eliminating HDFN secondary to RhD alloimmunization. For .20 years, these studies exemplified the power of a multidisciplinary approach when seeking to not only understand but also develop a strategy to prevent a devastating disease. Although anti-RhD immunoprophylaxis continues to enjoy considerable success, several key drawbacks still exist. As the efficacy of RhD immunoprophylaxis reduced the incidence of RhD alloimmunization, the natural source of anti-RhD generated during pregnancy likewise decreased. As a result, manufacturing centers enrolled RhD-negative men and intentionally immunized these individuals