The serology of HLA is of high importance in transplantation as well as transfusion medicine, in diseases which are HLA-associated and in forensic medicine. Serological problems are present, since the leucocyte antibodies from different samples vary in respect of their properties in spite of the same specificity. In addition, the antibodies from different samples which react wih the same cell type, e. g. granulocytes, may reveal various specificities. Therefore, presently available methods are described which enable us to discriminate these antibodies. Crosslinkage of Fc-receptors of type I on monocytes and macrophages with HLA-antigens through HLA-antibodies has been recently observed. From this finding a simple and sensitive new technique was developed which detects non-cytotoxic and cytotoxic HLA-antibodies. The mechanism of crosslinkage of molecules corresponds to the phenomenon of immune phagocytosis inhibition' in regard to cell function. This type of inhibition probably is generated in -fetal cells of the placenta and the fetus, if the mother produces HLA-antibodies against it. This is interpreted to be shelter of the fetus against an immunologically aggressive mother. The hypothesis is put forward that immune phagocytosis inhibition in the cells of the reticulo-endothelial system, due to inhibitory HLA-antibodies in commercial immunoglobulins, is the mechanism of effective treatment of the autoimmune thrombocytopenia with these immunoglobulins. Among antibodies specific for non-HLA-antigens we distinguish clinically insignificant, at low temperature active autoantibodies to various types of leucocytes from pathogenetically relevant granulocyte antibodies which cause autoimmune neutropenia or neonatal alloimmune neutropehia. Leucocyte antibodies are described which can induce a severe non-cardiogenic pulmonary oedema after transfusion. In most instances, these antibodies were detected in donor blood components.