Immunoglobulin V region sequences of two human antiplatelet monoclonal autoantibodies derived from B cells of normal origin

• Published in: Journal of autoimmunity Vol. 7; no. 4; pp. 521 - 535
• Main Authors: DENOMME, G. A, MAHMOUD MAHMOUDI, CAIRNS, E, BELL, D. A
• Format: Journal Article
• Language: English
• Published: London Elsevier 01.08.1994
• Subjects: Amino Acid Sequence; Animals; Antibodies, Antiphospholipid - genetics; Antibodies, Antiphospholipid - immunology; Antibodies, Monoclonal - genetics; Antibodies, Monoclonal - immunology; Antibody Specificity; Antigens, Human Platelet - immunology; Autoantibodies - genetics; Autoantibodies - immunology; B-Lymphocytes - immunology; Base Sequence; Biological and medical sciences; Blood Platelets - immunology; Cell Line; Child; Experimental and animal immunopathology. Animal models; Gene Rearrangement, B-Lymphocyte; Genes, Immunoglobulin; Humans; Hybridomas - immunology; Immunoglobulin Heavy Chains - genetics; Immunoglobulin Heavy Chains - immunology; Immunoglobulin kappa-Chains - genetics; Immunoglobulin kappa-Chains - immunology; Immunoglobulin M - genetics; Immunoglobulin M - immunology; Immunoglobulin Variable Region - genetics; Immunoglobulin Variable Region - immunology; Immunopathology; Male; Medical sciences; Mice; Molecular Sequence Data; Palatine Tonsil - cytology; Phospholipids - immunology; Platelet Membrane Glycoproteins - immunology; Polymerase Chain Reaction; Human; Immunoglobulins; Platelet; Gene; Variable region; Autoantibody; Genetics; B-Lymphocyte; Monoclonal antibody; Molecular biology; In vitro; Aminoacid sequence
• ISSN: 0896-8411; 1095-9157

Autoimmune thrombocytopenia has been attributed to the presence of antiplatelet autoantibodies which mediate platelet destruction. The derivation of these autoantibodies is presently unknown. While normal B cells do not produce these autoantibodies in vivo, it has been demonstrated in vitro by somatic cell hybridization that the B lymphocytes of nonthrombocytopenic individuals have the potential to produce antiplatelet autoantibodies. Antigen specificities of these antibodies are similar to those seen in autoimmune thrombocytopenic purpura and the lupus anticoagulant syndrome. The immunoglobulin V region genes encoding two such human monoclonal antiplatelet antibodies, an anti-GP IIb (STO 171) and an anti-phospholipid antibody (STO 103) derived from tonsillar lymphocytes of a non-thrombocytopenic male, have now been sequenced. These antiplatelet antibodies were found to be encoded by unmutated germline VH and VK genes. The third complementarity determining region (CDR3) of the genes encoding both of these antibodies have unique D regions with evidence of N-nucleotide additions, and the light chain genes show VK-JK junctional diversity. STO 103 is encoded by the VH4 V71-2 germline gene and a truncated JH4 gene. The light chain gene showed closest homology with the VK4 Humk18 gene and JK2 gene. STO 171 showed closest homology with the VH4.18 germline gene and had a complete germline JH6 gene. The light chain of STO 171 is encoded by the VK3 Humkv325 germline gene, which is also used by some rheumatoid factors and cold agglutinins, and a JK4 gene. Although these antibodies were not derived from circulating B cells or found to be actively producing antibody at the time they were harvested, it is possible that naturally occurring antibody producing B cells, similar to those represented here, are recruited for the development of pathogenic autoantibodies in immune thrombocytopenia.