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Lack of KIR4.1 autoantibodies in Japanese patients with MS and NMO.


ABSTRACT: To examine anti-KIR4.1 antibodies by 2 different assays in Japanese patients with multiple sclerosis (MS) or neuromyelitis optica (NMO).One hundred sixty serum samples from 57 patients with MS, 40 patients with NMO/NMO spectrum disorder (NMOSD), and 50 healthy controls (all were Japanese) were tested with ELISA using a synthetic peptide of the first extracellular portion of human KIR4.1. In addition, we attempted to detect anti-KIR4.1 immunoglobulin G in the serum by the luciferase immunoprecipitation systems (LIPS) with the full length of human KIR4.1 produced in a human cell line, which is highly sensitive to single or multiple epitopes.We failed to detect antibodies to the peptide fragment KIR4.1(83-120) in any case of MS and NMO/NMOSD using ELISA. Antibodies to the recombinant full length of KIR4.1 protein were detected in only 2 patients with MS and none in the patients with NMO/NMOSD by the LIPS assay.We developed 2 different methods (ELISA and LIPS) to measure autoantibodies to KIR4.1 in serum. We detected anti-KIR4.1 immunoglobulin G at a very low frequency in Japanese patients with MS or NMO/NMOSD. Serologic testing for human KIR4.1-specific antibodies is unlikely to improve the diagnosis of MS or NMO/NMOSD in Japanese patients.

SUBMITTER: Higuchi O 

PROVIDER: S-EPMC4959509 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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Lack of KIR4.1 autoantibodies in Japanese patients with MS and NMO.

Higuchi Osamu O   Nakane Shunya S   Sakai Waka W   Maeda Yasuhiro Y   Niino Masaaki M   Takahashi Toshiyuki T   Fukazawa Toshiyuki T   Kikuchi Seiji S   Fujihara Kazuo K   Matsuo Hidenori H  

Neurology(R) neuroimmunology & neuroinflammation 20160722 5


<h4>Objectives</h4>To examine anti-KIR4.1 antibodies by 2 different assays in Japanese patients with multiple sclerosis (MS) or neuromyelitis optica (NMO).<h4>Methods</h4>One hundred sixty serum samples from 57 patients with MS, 40 patients with NMO/NMO spectrum disorder (NMOSD), and 50 healthy controls (all were Japanese) were tested with ELISA using a synthetic peptide of the first extracellular portion of human KIR4.1. In addition, we attempted to detect anti-KIR4.1 immunoglobulin G in the se  ...[more]

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