A limited lupus anti-spliceosomal response targets a cross-reactive, proline rich motif

被引:16
作者
Arbuckle, MR
Schilling, AR
Harley, JB
James, JA
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Oklahoma Med Res Fdn, Dept Pathol,Arthrit & Immunol Program, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Oklahoma Med Res Fdn, Dept Med,Arthrit & Immunol Program, Oklahoma City, OK 73104 USA
关键词
autoantibodies; epitope mapping; spliceosome; systemic lupus erythematosus;
D O I
10.1006/jaut.1998.0227
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by the production of large amounts of characteristic autoantibodies. Anti-Sm and anti-nRNP (also known as anti-spliceosome) autoantibodies are among these. Previous epitope mapping of anti-spliceosomal antibodies has identified multiple antigenic determinants within this complex immune response. In this report we describe an SLE patient with a relatively simple, long-lasting anti-spliceosomal response. In the earliest serum sample tested the autoimmune response appeared restricted to the similar peptides PPPG-MR(P,G)P of Sm B/B', PAPGMRPP of nRNP C, and PPPGMIPP of nRNP A. Unlike all the other tested lupus patients with anti-spliceosomal autoantibodies, in this patient these proline-rich epitopes remained the primary target for humoral autoimmunity in subsequent serum samples collected over many years, Absorption of anti-PAPGMRPP antibodies also removed binding to PPPGMR(P,G)P and PPPGMIPP. Isolated antibodies to PAPGMRPP were capable of binding Sm B/B', nRNP C and nRNP A by Western blot. For this particular SLE patient the autoimmune response observed against these three proteins is a single cross-reactive response against a similar proline-rich motif. Also, this patient has failed to undergo the B cell epitope spreading, typically observed in the naturally arising autoimmune response against the spliceosome in human lupus patients. (C) 1998 Academic Press
引用
收藏
页码:431 / 438
页数:8
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