Neuromyelitis optica and anti-aquaporin-4 antibodies measured by an enzyme-linked immunosorbent assay

被引:93
作者
Hayakawa, Sei [1 ]
Mori, Masahiro [1 ]
Okuta, Akiko [2 ]
Kamegawa, Akiko [3 ,4 ]
Fujiyoshi, Yoshinori [4 ,5 ]
Yoshiyama, Yasumasa [6 ]
Mitsuoka, Kaoru [5 ]
Ishibashi, Kenichi [7 ]
Sasaki, Sei [8 ]
Hattori, Takamichi [1 ]
Kuwabara, Satoshi [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Neurol, Chou Ku, Chiba 2608670, Japan
[2] JBIC, JBIRC, Tokyo, Japan
[3] Japan Sci & Technol Agcy, CREST, Kyoto, Japan
[4] Kyoto Univ, Fac Sci, Dept Biophys, Kyoto, Japan
[5] Natl Inst Adv Ind Sci & Technol, JBIRC, Tokyo, Japan
[6] Chiba E Natl Hosp, Clin Res Ctr, Dept Neurol, Chiba, Japan
[7] Meiji Pharmaceut Univ, Dept Med Physiol, Tokyo, Japan
[8] Tokyo Med & Dent Univ, Dept Nephrol, Tokyo, Japan
关键词
neuromyelitis optica; multiple sclerosis; aquaporin-4; anti-aquaporin-4; antibody; ELISA;
D O I
10.1016/j.jneuroim.2008.03.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NMO-IgG, a disease-specific autoantibody for neuromyelitis optica, recognizes aquaporin-4 (AQP4) and has been examined by indirect immunofluorescence assay. We developed an enzyme-linked immunosorbent assay (ELISA) to detect anti-AQP4 antibodies by establishing methods for expression in a baculovirus system and purification of recombinant AQP4 as antigen. Elevated anti-AQP4 antibody titers in serum were found in 15 (71%) of 21 patients with neuromyelitis optica, 4.3% of 46 patients with multiple sclerosis, none of 51 normal controls, and 2.6% of 115 patients with other neurological diseases. The ELISA system can be substituted for the conventional NMO-IgG assay. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:181 / 187
页数:7
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