Repertoire cloning of lupus anti-DNA autoantibodies

被引:78
作者
Roben, P
Barbas, SM
Sandoval, L
Lecerf, JM
Stollar, BD
Solomon, A
Silverman, GJ
机构
[1] UNIV CALIF SAN DIEGO, DEPT MED 0663, SAM & ROSE STEIN INST RES AGING, LA JOLLA, CA 92093 USA
[2] UNIV CALIF SAN DIEGO, DEPT MED, THEODORE GILDRED CANC CTR, LA JOLLA, CA 92093 USA
[3] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
[4] TUFTS UNIV, DEPT BIOCHEM, BOSTON, MA 02111 USA
[5] UNIV TENNESSEE, MED CTR, HUMAN IMMUNOL & CANC PROGRAM, KNOXVILLE, TN 37920 USA
关键词
lupus; repertoire; autoantibody; anti-DNA; phage display;
D O I
10.1172/JCI119111
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To investigate the autoantibody repertoire associated with SLE, we have created phage display IgG Fab libraries from two clinically active SLE patients and from the healthy identical twin of one of these patients. The libraries from the lupus discordant twins were found to both include unusually large representations of the V(H)5 gene family. By panning with DNA, the SLE libraries each yielded IgG anti-doublestranded (ds) DNA autoantibodies, which are characteristic of lupus disease. These included a V(H)5 autoantibody from the affected twin, that has a targeted cluster of mutations that potentially improves binding affinity. The recovered IgG anti-dsDNA autoantibodies expressed the same idiotypes associated with the in vivo. IgG anti-dsDNA response of the respective SLE donor. Heavy-light chain shuffling experiments demonstrated a case in which the in vitro creation of anti-dsDNA binding activity required restrictive pairing of a heavy chain with V-lambda light chains similar to those in circulating anti-dsDNA autoantibodies. By contrast, IgG anti-ds autoantibodies could not be recovered from the library from the healthy twin, or from shuffled libraries with heavy chains from the healthy twin. These repertoire analyses illustrate how inheritance and somatic processes interplay to produce lupus-associated IgG autoantibodies.
引用
收藏
页码:2827 / 2837
页数:11
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