Characteristics and pathogenic role of anti-β2-glycoprotein I single-chain Fv domains:: induction of experimental antiphospholipid syndrome

被引:23
作者
Blank, M
Waisman, A
Mozes, E
Koike, T
Shoenfeld, Y [1 ]
机构
[1] Tel Aviv Univ, Dept Med B, Autoimmune Dis Res Unit, Sackler Fac Med,Chaim Sheba Med Ctr, IL-52621 Tel Hashomer, Israel
[2] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[3] Hokkaido Univ, Sch Med, Dept Med 2, Sapporo, Hokkaido 060, Japan
关键词
anti-beta(2)-glycoprotein I; anti-cardiolipin antibodies; anti-phospholipid syndrome; single-chain Fv; autoimmunity;
D O I
10.1093/intimm/11.12.1917
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antiphospholipid syndrome is characterized by the presence crf high titers of anti-beta(2)-glycoprotein I (beta(2)GPI) antibodies, lupus anticoagulant associated with thromboembolic phenomena, thrombocytopenia and recurrent fetal loss. Single-chain Fv (scFv) were prepared from four anti-beta(2)GPI mAb, CAM, GAL, CAR and 2C4C2, and one anti-ssDNA, Ail five scFv showed the same antigen binding properties as the original mAb, Replacement of the pathogenic CAM VH domain with the non-pathogenic CAL VH or anti-ssDNA VH decreased the binding affinity of the scFv to beta(2)GPI and completely abrogated the anticoagulant activity. Exchanging the CAM VH With anti-DNA VH resulted in a shift from anti-beta(2)GPI to anti-ssDNA binding of the scFv. Replacement of the CAM VL with CAL VL did not affect the binding and activity. BALB/c mice were immunized with the anti-beta(2)GPI scFv, and the scFv resulting from the substitution of the heavy (H) and light (L) chains. The mice which were immunized with CAM, 2C4C2 and CAR scFv developed clinical manifestations of experimental anti-phospholipid syndrome. Elevated titers of mouse anti-cardiolipin (aCL), anti-beta(2)GPI, associated with lupus anticoagulant activity, thrombocytopenia, prolonged activated partial thromboplastin time and a high percentage of fetal resorptions were detected, in the CAVI scFv group and in the scFv composed of CAM VH groups. High titers of aCL, anti-beta(2)GPI, anti-ss/dsDNA and anti-histone associated with lupus findings were observed in the sera of the 2C4C2 scFv-immunized mice. Immunization with CAL scFv did not lead to any clinical findings. The current study shows that scFv of pathogenic antibodies are capable of inducing the same clinical manifestations as the whole antibody molecule upon active immunization. Replacement of H/L chains point to the importance of the VH domains in the pathogenic potential of anti-beta(2)GPI.
引用
收藏
页码:1917 / 1926
页数:10
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