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Neurofascin-155 IgG4 in chronic inflammatory demyelinating polyneuropathy

Identifieur interne : 003094 ( Ncbi/Checkpoint ); précédent : 003093; suivant : 003095

Neurofascin-155 IgG4 in chronic inflammatory demyelinating polyneuropathy

Auteurs : Jérôme J. Devaux ; Yumako Miura ; Yuki Fukami ; Takayuki Inoue ; Constance Manso ; Maya Belghazi ; Kenji Sekiguchi ; Norito Kokubun ; Hiroo Ichikawa ; Anna Hiu Yi Wong ; Nobuhiro Yuki

Source :

RBID : PMC:4793783

Descripteurs français

English descriptors

Abstract

Objective:

We report the clinical and serologic features of Japanese patients with chronic inflammatory demyelinating polyneuropathy (CIDP) displaying anti-neurofascin-155 (NF155) immunoglobulin G4 (IgG4) antibodies.

Methods:

In sera from 533 patients with CIDP, anti-NF155 IgG4 antibodies were detected by ELISA. Binding of IgG antibodies to central and peripheral nerves was tested.

Results:

Anti-NF155 IgG4 antibodies were identified in 38 patients (7%) with CIDP, but not in disease controls or normal participants. These patients were younger at onset as compared to 100 anti-NF155–negative patients with CIDP. Twenty-eight patients (74%) presented with sensory ataxia, 16 (42%) showed tremor, 5 (13%) presented with cerebellar ataxia associated with nystagmus, 3 (8%) had demyelinating lesions in the CNS, and 20 of 25 (80%) had poor response to IV immunoglobulin. The clinical features of the antibody-positive patients were statistically more frequent as compared to negative patients with CIDP (n = 100). Anti-NF155 IgG antibodies targeted similarly central and peripheral paranodes.

Conclusion:

Anti-NF155 IgG4 antibodies were associated with a subgroup of patients with CIDP showing a younger age at onset, ataxia, tremor, CNS demyelination, and a poor response to IV immunoglobulin. The autoantibodies may serve as a biomarker to improve patients' diagnosis and guide treatments.


Url:
DOI: 10.1212/WNL.0000000000002418
PubMed: 26843559
PubMed Central: 4793783


Affiliations:


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PMC:4793783

Le document en format XML

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<term>Aged, 80 and over</term>
<term>Autoantibodies (blood)</term>
<term>Autoantibodies (immunology)</term>
<term>Biomarkers (blood)</term>
<term>Cell Adhesion Molecules (blood)</term>
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<term>Humans</term>
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<term>Immunoglobulin G (immunology)</term>
<term>Incidence</term>
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<term>Male</term>
<term>Middle Aged</term>
<term>Nerve Growth Factors (blood)</term>
<term>Nerve Growth Factors (immunology)</term>
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<term>Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (diagnosis)</term>
<term>Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (epidemiology)</term>
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<term>Autoanticorps (sang)</term>
<term>Enfant</term>
<term>Facteurs de croissance nerveuse (immunologie)</term>
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<term>Femelle</term>
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<div type="abstract" xml:lang="en">
<sec>
<title>Objective:</title>
<p>We report the clinical and serologic features of Japanese patients with chronic inflammatory demyelinating polyneuropathy (CIDP) displaying anti-neurofascin-155 (NF155) immunoglobulin G4 (IgG4) antibodies.</p>
</sec>
<sec>
<title>Methods:</title>
<p>In sera from 533 patients with CIDP, anti-NF155 IgG4 antibodies were detected by ELISA. Binding of IgG antibodies to central and peripheral nerves was tested.</p>
</sec>
<sec>
<title>Results:</title>
<p>Anti-NF155 IgG4 antibodies were identified in 38 patients (7%) with CIDP, but not in disease controls or normal participants. These patients were younger at onset as compared to 100 anti-NF155–negative patients with CIDP. Twenty-eight patients (74%) presented with sensory ataxia, 16 (42%) showed tremor, 5 (13%) presented with cerebellar ataxia associated with nystagmus, 3 (8%) had demyelinating lesions in the CNS, and 20 of 25 (80%) had poor response to IV immunoglobulin. The clinical features of the antibody-positive patients were statistically more frequent as compared to negative patients with CIDP (n = 100). Anti-NF155 IgG antibodies targeted similarly central and peripheral paranodes.</p>
</sec>
<sec>
<title>Conclusion:</title>
<p>Anti-NF155 IgG4 antibodies were associated with a subgroup of patients with CIDP showing a younger age at onset, ataxia, tremor, CNS demyelination, and a poor response to IV immunoglobulin. The autoantibodies may serve as a biomarker to improve patients' diagnosis and guide treatments.</p>
</sec>
</div>
</front>
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<name sortKey="Belghazi, Maya" sort="Belghazi, Maya" uniqKey="Belghazi M" first="Maya" last="Belghazi">Maya Belghazi</name>
<name sortKey="Devaux, Jerome J" sort="Devaux, Jerome J" uniqKey="Devaux J" first="Jérôme J." last="Devaux">Jérôme J. Devaux</name>
<name sortKey="Fukami, Yuki" sort="Fukami, Yuki" uniqKey="Fukami Y" first="Yuki" last="Fukami">Yuki Fukami</name>
<name sortKey="Ichikawa, Hiroo" sort="Ichikawa, Hiroo" uniqKey="Ichikawa H" first="Hiroo" last="Ichikawa">Hiroo Ichikawa</name>
<name sortKey="Inoue, Takayuki" sort="Inoue, Takayuki" uniqKey="Inoue T" first="Takayuki" last="Inoue">Takayuki Inoue</name>
<name sortKey="Kokubun, Norito" sort="Kokubun, Norito" uniqKey="Kokubun N" first="Norito" last="Kokubun">Norito Kokubun</name>
<name sortKey="Manso, Constance" sort="Manso, Constance" uniqKey="Manso C" first="Constance" last="Manso">Constance Manso</name>
<name sortKey="Miura, Yumako" sort="Miura, Yumako" uniqKey="Miura Y" first="Yumako" last="Miura">Yumako Miura</name>
<name sortKey="Sekiguchi, Kenji" sort="Sekiguchi, Kenji" uniqKey="Sekiguchi K" first="Kenji" last="Sekiguchi">Kenji Sekiguchi</name>
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<name sortKey="Yuki, Nobuhiro" sort="Yuki, Nobuhiro" uniqKey="Yuki N" first="Nobuhiro" last="Yuki">Nobuhiro Yuki</name>
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