Polyspecificity of monoclonal lupus autoantibodies produced by human-human hybridomas.
Polyspecificity of monoclonal lupus autoantibodies produced by human-human hybridomas.
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人-人杂交瘤产生的单克隆狼疮自身抗体的多特异性。
DOI:
10.1056/nejm198302243080802
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发表时间:
1983
期刊:
影响因子:
--
通讯作者:
Schwartz,RS
中科院分区:
文献类型:
--
作者:
Shoenfeld,Y;Rauch,J;Massicotte,H;Datta,SK;Andre-Schwartz,J;Stollar,BD;Schwartz,RS
We studied the serologic properties of monoclonal autoantibodies that were produced by hybridomas derived from lymphocytes of patients with systemic lupus erythematosus. The hybridomas were made by fusion of a human lymphoblastoid cell line, GM 4672 (derived from a patient with multiple myeloma), with peripheral-blood or splenic lymphocytes from six patients with lupus. Thirty monoclonal autoantibodies, selected for their ability to react with denatured DNA, were analyzed. Eighteen of them reacted with three or more additional polynucleotides, including native DNA, left-handed double-helical DNA (Z-DNA), poly(I), and poly(dT). Ten reacted both with nucleic acids and the phospholipid cardiolipin. The multiple binding reactions of the monoclonal autoantibodies may be explained by the presence of appropriately spaced phosphodiester groups in both the polynucleotides and the phospholipid. The sharing of antigenic groups by polymers of different natures may contribute to the apparent diversity of serologic reactions in systemic lupus erythematosus. These findings suggest that DNA itself need not be the immunogenic stimulus for autoantibody formation in this disease. (N Engl J Med. 1983; 308:414–20.)
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