Using a specific serum anti-soluble T lymphocytes receptor for sheep erythrocytes (E) and SDS-PAGE, we detected radioactive bands of molecular weight 58,000 in immunoprecipitates of supernatant of heated human lymphocytes (SHL), in the supernatant of PHA stimulated lymphocyte cultures (SLC), normal human serum (NHS), and serum from cancer and uremia patients, labelled with 131I. By Sephadex G-200 chromatography, in addition to this fraction, we detected molecules of molecular weight higher than 150,000 which interact with the anti-soluble receptor serum (anti-RS), in serum from cancer and uremia patients. These molecules were detected in NHS or SHL after concentration or by prolonged exposure of SDS-PAGE with some labelled and immunoprecipitated SHL samples. The soluble receptors of molecular weights 58,000 (RS1) and more than 150,000 (RS2) were fully identical when analyzed by immunodiffusion with anti-RS serum. When submitted to immunoelectrophoresis, RS1 showed electrophoretic migration similar to that of albumin, while RS2 showed a pattern close to that of alpha 2-globulin. However, RS2 did not show antigenic relationship with IgM and was not an immune complex with IgG. Even though the presence of RS in human saliva has not yet been reported, molecules that interact with anti-RS serum have been detected in human saliva and are fully identical to molecules found in supernatant of heated human T lymphocytes and NHS. The RS molecules present in human saliva have a molecular weight and electrophoretic migration similar to those of RS1 from SLC and from human serum and have no antigenic relationship with human albumin.
Ninety-nine Tükuna Indians, inhabitants of the high Amazon, were typed for the HLA antigens. The method used was the microlymphocytotoxicity technique recommended by the NIH. At the same time, cross-matching was performed between the lymphocytes of the 99 Indians and the sera of 240 other multiparous Indians. Later the multiparous sera were cross-matched with a selected panel of Caucasoid individuals. The results showed that the most frequent antigens for th HLA-A locus were A2, Aw24 and Aw31. As for the HLA-B locus, B5, Bw39 and B40 were most frequent. The haplotypes HLA-Aw31-Bw39, and A2-B5 were in linkage disequilibrium. The results of the cross-matching showed 21.3% sera with positive reactions against Indian cells. Ten sera presented antibodies against known HLA antigens; five of them were monospecific, four had two specificities, and one showed three specificities. It was not possible to arrive at any conclusion about the 41 remaining sera. Six sera had positive reactions only with Indians cells.
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