Demaison C, Ravirajan C T, Isenberg D A, Zouali M
Unité d'Immunogénétique Cellulaire, Institut Pasteur, Paris, France.
Immunology. 1995 Nov;86(3):487-94.
We have analysed the heavy and light chain variable region genes of two monoclonal antibodies, specific for the Sm antigen (RSP1; IgG kappa) and for cardiolipin (RSP4; IgM lambda), derived from a patient with active systemic lupus erythematosus (SLE). We have established that the variable region genes of the RSP1 autoantibody are somatic mutants of two germ line genes from the VH4 and V kappa 1 gene families. RSP4 antibody uses gene segments closely related to a VH3 gene member and to a V lambda 1 gene. The presence and distribution of the somatic mutations on both monoclonal autoantibodies are compatible with an antigen-driven immune process. These data suggest that in SLE a common antigenic stimulus may govern the autoantibody response against a wide spectrum of unrelated antigens, including native DNA, cardiolipin or Sm antigens, and provide further evidence that disease-associated autoantibodies are generated through antigen-selected somatic mutations.
我们分析了来自一名活动性系统性红斑狼疮(SLE)患者的两种单克隆抗体的重链和轻链可变区基因,这两种抗体分别对Sm抗原(RSP1;IgG κ)和心磷脂(RSP4;IgM λ)具有特异性。我们确定,RSP1自身抗体的可变区基因是VH4和Vκ1基因家族中两个种系基因的体细胞突变体。RSP4抗体使用与一个VH3基因成员和一个Vλ1基因密切相关的基因片段。两种单克隆自身抗体上体细胞突变的存在和分布与抗原驱动的免疫过程相符。这些数据表明,在SLE中,一种共同的抗原刺激可能控制针对多种不相关抗原的自身抗体反应,包括天然DNA、心磷脂或Sm抗原,并进一步证明疾病相关的自身抗体是通过抗原选择的体细胞突变产生的。