Warren R W, Sailstad D M, Caster S A, Pisetsky D S
Arthritis Rheum. 1984 May;27(5):545-51. doi: 10.1002/art.1780270510.
The binding properties of B6-lpr/lpr anti-DNA monoclonal antibodies were characterized to evaluate the influence of genetic background on the diversity and specificity of lpr-induced autoantibody responses. Six anti-DNA antibodies were produced from fusions with B6-lpr/lpr mice, while another was obtained from a fusion with a B6-+/+ mouse immunized with lipopolysaccharide. Each antibody bound single-stranded DNA in preference to double-stranded DNA, with variation of over 300-fold in relative binding activities. In terms of binding to a panel of synthetic polynucleotides, each antibody exhibited a unique antigenic specificity. This binding, however, was not dependent on recognition of a unique base or sugar moiety, since individual antibodies bound polymers of dissimilar composition. These results suggest a diversity of binding reactions for B6-lpr/lpr anti-DNA antibodies, with a clonal repertoire similar to that of mice from autoimmune backgrounds.
对B6-lpr/lpr抗DNA单克隆抗体的结合特性进行了表征,以评估遗传背景对lpr诱导的自身抗体反应的多样性和特异性的影响。从与B6-lpr/lpr小鼠融合产生了六种抗DNA抗体,而另一种则来自与用脂多糖免疫的B6-+/+小鼠的融合。每种抗体优先结合单链DNA而非双链DNA,相对结合活性变化超过300倍。就与一组合成多核苷酸的结合而言,每种抗体都表现出独特的抗原特异性。然而,这种结合并不依赖于对独特碱基或糖部分的识别,因为单个抗体结合不同组成的聚合物。这些结果表明B6-lpr/lpr抗DNA抗体的结合反应具有多样性,其克隆库与自身免疫背景小鼠的相似。