A common anti-cardiolipin antibody idiotype in autoimmune disease: identification using a mouse monoclonal antibody directed against a naturally-occurring anti …

M Sutjita, A Hohmann, R Comacchio… - Clinical and …, 1989 - ncbi.nlm.nih.gov
M Sutjita, A Hohmann, R Comacchio, ML Boey, J Bradley
Clinical and experimental immunology, 1989ncbi.nlm.nih.gov
We have recently produced a series of human monoclonal antibodies reacting with
cardiolipin. One of these, H3, a polyspecific IgM/k derived from a normal individual, was
used to raise mouse monoclonal antibody to its idiotype. Two anti-idiotypic antibodies, S2. 9
(IgG2b) and S2. 10 (IgM) were selected for their specific reaction with H3. S2. 9 did not react
with five other human monoclonal antibodies of IgM/k class despite the fact that these
shared some antigen-binding characteristics with H3. S2. 9 was able to block the binding of …
Abstract
We have recently produced a series of human monoclonal antibodies reacting with cardiolipin. One of these, H3, a polyspecific IgM/k derived from a normal individual, was used to raise mouse monoclonal antibody to its idiotype. Two anti-idiotypic antibodies, S2. 9 (IgG2b) and S2. 10 (IgM) were selected for their specific reaction with H3. S2. 9 did not react with five other human monoclonal antibodies of IgM/k class despite the fact that these shared some antigen-binding characteristics with H3. S2. 9 was able to block the binding of H3 to all of its cross-reactive antigens including cardiolipin, while S2. 10 was not. S2. 9 was equally efficient in blocking the binding of H3 to three of its cross-reactive antigens, cardiolipin, diphtheria and tetanus toxoids; greater than 90% inhibition could be achieved at an equimolar ratio of H3 to S2. 9. The anti-idiotype S2. 9 was used to demonstrate the presence of the H3 idiotype in serum. This idiotype was found in amounts greater than that seen in 42 normal individuals, in 30 of 36 patients with systemic lupus erythematosus (SLE), eight of 20 patients with rheumatoid arthritis (RA), 8 of 20 patients with Felty's syndrome as well as 10 of 23 patients with syphilis. Not one of nine patients with drug-induced lupus syndrome had abnormal levels. In patients with SLE and Felty's syndrome there was a good correlation between the amount of anti-cardiolipin antibodies and the amount of H3 idiotype (rs= 0.70 and 0.69 respectively). No such correlation was found in syphilitics or in patients with RA. In patients with SLE the H3 idiotype was present on IgM and IgG anti-cardiolipin antibodies. In 15 of 16 SLE sera with high levels of cardiolipin antibody, S2. 9 blocked binding of serum antibodies to cardiolipin by 13-72%, with a mean value of 49%. One patient had a high level of anti-cardiolipin antibody which could not be blocked by S2. 9. These results indicate that a mouse monoclonal antibody which reacts with an idiotope in the antigen-binding region of a naturally-occurring phospholipid antibody also defines a common idiotype of anti-cardiolipin antibodies in patients with autoimmune disease.
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