Autoimmune cerebellar ataxia associated with anti-leucine-rich glioma-inactivated protein 1 antibodies: Two pediatric cases

To report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies. The clinical features of the two patients were described retrospectively. The indirect immunofluorescence using transfected cells (cell-based assay, CBA)...

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Published inJournal of neuroimmunology Vol. 370; p. 577918
Main Authors Weihua, Zhang, Haitao, Ren, Jie, Deng, Changhong, Ren, Ji, Zhou, Anna, Zhou, Hongzhi, Guan, Xiaotun, Ren
Format Journal Article
LanguageEnglish
Published Elsevier B.V 15.09.2022
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Abstract To report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies. The clinical features of the two patients were described retrospectively. The indirect immunofluorescence using transfected cells (cell-based assay, CBA) and the rat cerebellum (tissue-based assay, TBA) with the multi-antigen co-plate biochip mosaic techniques were used to detect the antibodies. Clinical and laboratory characteristics were described. Two males were included. The onset ages were 2.7y and 4y, respectively. Patient 1 manifested as isolated acute cerebellar ataxia. Patient 2 had extra-cerebellar symptoms, including seizures, encephalopathy, faciobrachial dystonic seizures(FBDs), and significant cerebellar ataxia. The hyponatremia and tumors were not found. Both of them responded well to the immunotherapy. The autoimmune cerebellar ataxia might be a new phenotype of LGI1-Abs autoimmunity in children.
AbstractList To report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies. The clinical features of the two patients were described retrospectively. The indirect immunofluorescence using transfected cells (cell-based assay, CBA) and the rat cerebellum (tissue-based assay, TBA) with the multi-antigen co-plate biochip mosaic techniques were used to detect the antibodies. Clinical and laboratory characteristics were described. Two males were included. The onset ages were 2.7y and 4y, respectively. Patient 1 manifested as isolated acute cerebellar ataxia. Patient 2 had extra-cerebellar symptoms, including seizures, encephalopathy, faciobrachial dystonic seizures(FBDs), and significant cerebellar ataxia. The hyponatremia and tumors were not found. Both of them responded well to the immunotherapy. The autoimmune cerebellar ataxia might be a new phenotype of LGI1-Abs autoimmunity in children.
To report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies.OBJECTIVESTo report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies.The clinical features of the two patients were described retrospectively. The indirect immunofluorescence using transfected cells (cell-based assay, CBA) and the rat cerebellum (tissue-based assay, TBA) with the multi-antigen co-plate biochip mosaic techniques were used to detect the antibodies. Clinical and laboratory characteristics were described.METHODSThe clinical features of the two patients were described retrospectively. The indirect immunofluorescence using transfected cells (cell-based assay, CBA) and the rat cerebellum (tissue-based assay, TBA) with the multi-antigen co-plate biochip mosaic techniques were used to detect the antibodies. Clinical and laboratory characteristics were described.Two males were included. The onset ages were 2.7y and 4y, respectively. Patient 1 manifested as isolated acute cerebellar ataxia. Patient 2 had extra-cerebellar symptoms, including seizures, encephalopathy, faciobrachial dystonic seizures(FBDs), and significant cerebellar ataxia. The hyponatremia and tumors were not found. Both of them responded well to the immunotherapy.RESULTSTwo males were included. The onset ages were 2.7y and 4y, respectively. Patient 1 manifested as isolated acute cerebellar ataxia. Patient 2 had extra-cerebellar symptoms, including seizures, encephalopathy, faciobrachial dystonic seizures(FBDs), and significant cerebellar ataxia. The hyponatremia and tumors were not found. Both of them responded well to the immunotherapy.The autoimmune cerebellar ataxia might be a new phenotype of LGI1-Abs autoimmunity in children.CONCLUSIONSThe autoimmune cerebellar ataxia might be a new phenotype of LGI1-Abs autoimmunity in children.
ArticleNumber 577918
Author Ji, Zhou
Changhong, Ren
Weihua, Zhang
Jie, Deng
Anna, Zhou
Haitao, Ren
Xiaotun, Ren
Hongzhi, Guan
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  email: renxiaotun@bch.com.cn
  organization: Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Centre for Children's Health, Beijing, China
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Cites_doi 10.1016/j.neuron.2006.01.033
10.3389/fneur.2020.618109
10.1136/jnnp-2017-315720
10.1186/s12974-015-0358-9
10.1002/ana.25310
10.1007/s12311-019-01048-y
10.1212/NXI.0000000000000371
10.1007/s12311-014-0628-6
10.14802/jmd.20040
10.1016/j.ejpn.2017.08.004
10.1007/s12311-015-0664-x
10.3390/ijms21103701
10.1523/JNEUROSCI.3506-13.2013
10.1016/j.yebeh.2021.108159
10.1093/brain/awq213
10.1111/nan.12132
10.1093/brain/aww012
10.1002/ana.24979
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Keywords LGI1
Autoimmune
Child
Leucine-rich glioma-inactivated protein 1
Cerebellar ataxia
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References Jarius, Wildemann (bb0035) 2015; 12
Irani, Alexander, Waters (bb0020) 2010; 133
Su, Xie, Zhou, Shen, Hu (bb0105) 2015; 14
Shao, Fan, Luo (bb0095) 2021; 11
López-Chiriboga, Klein, Zekeridou (bb0050) 2018; 84
Schulte, Thumfart, Klocker (bb0090) 2006; 49
Dade, Berzero, Izquierdo (bb0010) 2020; 21
Navarro, Kas, Apartis (bb0065) 2016; 139
Steriade, Day, Lee (bb0100) 2014; 40
Weihua, Haitao, Fang (bb0110) 2019; 18
Lin, Liu, Chen (bb0045) 2021; 122
Ohkawa, Fukata, Yamasaki (bb0070) 2013; 33
Joubert, Gobert, Thomas (bb0040) 2017; 4
Gadoth, Pittock, Dubey (bb0015) 2017; 82
Qiao, Wu, Liu (bb0080) 2021; 17
Schimmel, Fruhwald, Bien (bb0085) 2018; 22
Jarius, Wildemann (bb0025) 2015; 12
Mitoma, Adhikari, Aeschlimann (bb0055) 2016; 15
Binks, Klein, Waters, Pittock, Irani (bb0005) 2018; 89
Jarius, Wildemann (bb0030) 2015; 12
Petit-Pedrol, Sell, Planagumà, Mannara, Radosevic, Haselmann, Ceanga, Sabater, Spatola, Soto, Gasull, Dalmau, Geis (bb0075) 2018 Nov 1; 141
Mitoma, Manto, Hadjivassiliou (bb0060) 2021; 14
Schulte (10.1016/j.jneuroim.2022.577918_bb0090) 2006; 49
Steriade (10.1016/j.jneuroim.2022.577918_bb0100) 2014; 40
Weihua (10.1016/j.jneuroim.2022.577918_bb0110) 2019; 18
Qiao (10.1016/j.jneuroim.2022.577918_bb0080) 2021; 17
Joubert (10.1016/j.jneuroim.2022.577918_bb0040) 2017; 4
Lin (10.1016/j.jneuroim.2022.577918_bb0045) 2021; 122
Navarro (10.1016/j.jneuroim.2022.577918_bb0065) 2016; 139
Jarius (10.1016/j.jneuroim.2022.577918_bb0030) 2015; 12
Jarius (10.1016/j.jneuroim.2022.577918_bb0035) 2015; 12
Binks (10.1016/j.jneuroim.2022.577918_bb0005) 2018; 89
Shao (10.1016/j.jneuroim.2022.577918_bb0095) 2021; 11
Gadoth (10.1016/j.jneuroim.2022.577918_bb0015) 2017; 82
Su (10.1016/j.jneuroim.2022.577918_bb0105) 2015; 14
Dade (10.1016/j.jneuroim.2022.577918_bb0010) 2020; 21
Petit-Pedrol (10.1016/j.jneuroim.2022.577918_bb0075) 2018; 141
Schimmel (10.1016/j.jneuroim.2022.577918_bb0085) 2018; 22
Irani (10.1016/j.jneuroim.2022.577918_bb0020) 2010; 133
López-Chiriboga (10.1016/j.jneuroim.2022.577918_bb0050) 2018; 84
Ohkawa (10.1016/j.jneuroim.2022.577918_bb0070) 2013; 33
Mitoma (10.1016/j.jneuroim.2022.577918_bb0060) 2021; 14
Jarius (10.1016/j.jneuroim.2022.577918_bb0025) 2015; 12
Mitoma (10.1016/j.jneuroim.2022.577918_bb0055) 2016; 15
References_xml – volume: 89
  start-page: 526
  year: 2018
  end-page: 534
  ident: bb0005
  article-title: LGI1, CASPR2 and related antibodies: a molecular evolution of the phenotypes
  publication-title: J. Neurol. Neurosurg. Psychiatry
– volume: 11
  year: 2021
  ident: bb0095
  article-title: Brain magnetic resonance imaging characteristics of anti-leucine-rich glioma-inactivated 1 encephalitis and their clinical relevance: a single-center study in China
  publication-title: Front. Neurol.
– volume: 133
  start-page: 2734
  year: 2010
  end-page: 2748
  ident: bb0020
  article-title: Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia
  publication-title: Brain
– volume: 82
  start-page: 79
  year: 2017
  end-page: 92
  ident: bb0015
  article-title: Expanded phenotypes and outcomes among 256 LGI1/CASPR2-IgG-positive patients
  publication-title: Ann. Neurol.
– volume: 49
  start-page: 697
  year: 2006
  end-page: 706
  ident: bb0090
  article-title: The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1
  publication-title: Neuron.
– volume: 17
  start-page: 203
  year: 2021
  end-page: 212
  ident: bb0080
  article-title: Clinical features and long-term outcomes of anti-leucine-rich glioma-inactivated 1 encephalitis
  publication-title: Multi Center Study.
– volume: 18
  start-page: 1137
  year: 2019
  end-page: 1142
  ident: bb0110
  article-title: Neurochondrin antibody serum positivity in three cases of autoimmune cerebellar Ataxia
  publication-title: Cerebellum.
– volume: 14
  start-page: 10
  year: 2021
  end-page: 28
  ident: bb0060
  article-title: Immune-mediated cerebellar ataxias: clinical diagnosis and treatment based on immunological and physiological mechanisms
  publication-title: J. Mov. Disord.
– volume: 22
  start-page: 190
  year: 2018
  end-page: 193
  ident: bb0085
  article-title: Limbic encephalitis with LGI1 antibodies in a 14-year-old boy
  publication-title: Eur. J. Paediatr. Neurol.
– volume: 33
  start-page: 18161
  year: 2013
  end-page: 18174
  ident: bb0070
  article-title: Autoantibodies to epilepsy-related LGI1 in limbic encephalitis neutralize LGI1-ADAM22 interaction and reduce synaptic AMPA receptors
  publication-title: J. Neurosci.
– volume: 15
  start-page: 213
  year: 2016
  end-page: 232
  ident: bb0055
  article-title: Consensus paper: neuroimmune mechanisms of cerebellar ataxias
  publication-title: Cerebellum.
– volume: 84
  start-page: 473
  year: 2018
  end-page: 480
  ident: bb0050
  article-title: LGI1 and CASPR2 neurological autoimmunity in children
  publication-title: Ann. Neurol.
– volume: 4
  year: 2017
  ident: bb0040
  article-title: Autoimmune episodic ataxia in patients with anti-CASPR2 antibody-associated encephalitis
  publication-title: Neurol. Neuroimmunol. Neuroinflamm.
– volume: 40
  start-page: 645
  year: 2014
  end-page: 649
  ident: bb0100
  article-title: LGI1 autoantibodies associated with cerebellar degeneration
  publication-title: Neuropathol. Appl. Neurobiol.
– volume: 12
  year: 2015
  ident: bb0030
  article-title: ‘Medusa head ataxia’: the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: anti-PKC-gamma, anti-GluR-delta2, anti-ca/ARHGAP26 and anti-VGCC
  publication-title: J. Neuroinflammation
– volume: 12
  year: 2015
  ident: bb0025
  article-title: ‘Medusa head ataxia’: the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 1: anti-mGluR1, anti-Homer-3, anti-Sj/ITPR1 and anti-CARP VIII
  publication-title: J. Neuroinflammation
– volume: 14
  start-page: 12
  year: 2015
  end-page: 14
  ident: bb0105
  article-title: LGI1 is involved in the development of mouse brain
  publication-title: Cerebellum
– volume: 141
  start-page: 3144
  year: 2018 Nov 1
  end-page: 3159
  ident: bb0075
  article-title: LGI1 antibodies alter Kv1.1 and AMPA receptors changing synaptic excitability, plasticity and memory
  publication-title: Brain.
– volume: 21
  start-page: 3701
  year: 2020
  ident: bb0010
  article-title: Neurological syndromes associated with anti-GAD antibodies
  publication-title: Int. J. Mol. Sci.
– volume: 122
  year: 2021
  ident: bb0045
  article-title: Long-term seizure outcomes in patients with anti-leucine-rich glioma-inactivated 1 encephalitis
  publication-title: Epilepsy Behav.
– volume: 139
  start-page: 1079
  year: 2016
  end-page: 1093
  ident: bb0065
  article-title: Motor cortex and hippocampus are the two main cortical targets in LGI1-antibody encephalitis
  publication-title: Brain.
– volume: 12
  year: 2015
  ident: bb0035
  article-title: ‘Medusa head ataxia’: the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 3: anti-Yo/CDR2, anti-Nb/AP3B2, PCA-2, anti-Tr/DNER, other antibodies, diagnostic pitfalls, summary and outlook
  publication-title: J. Neuroinflammation
– volume: 49
  start-page: 697
  issue: 5
  year: 2006
  ident: 10.1016/j.jneuroim.2022.577918_bb0090
  article-title: The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1
  publication-title: Neuron.
  doi: 10.1016/j.neuron.2006.01.033
– volume: 11
  year: 2021
  ident: 10.1016/j.jneuroim.2022.577918_bb0095
  article-title: Brain magnetic resonance imaging characteristics of anti-leucine-rich glioma-inactivated 1 encephalitis and their clinical relevance: a single-center study in China
  publication-title: Front. Neurol.
  doi: 10.3389/fneur.2020.618109
– volume: 89
  start-page: 526
  issue: 5
  year: 2018
  ident: 10.1016/j.jneuroim.2022.577918_bb0005
  article-title: LGI1, CASPR2 and related antibodies: a molecular evolution of the phenotypes
  publication-title: J. Neurol. Neurosurg. Psychiatry
  doi: 10.1136/jnnp-2017-315720
– volume: 12
  issue: 1
  year: 2015
  ident: 10.1016/j.jneuroim.2022.577918_bb0035
  article-title: ‘Medusa head ataxia’: the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 3: anti-Yo/CDR2, anti-Nb/AP3B2, PCA-2, anti-Tr/DNER, other antibodies, diagnostic pitfalls, summary and outlook
  publication-title: J. Neuroinflammation
  doi: 10.1186/s12974-015-0358-9
– volume: 84
  start-page: 473
  issue: 3
  year: 2018
  ident: 10.1016/j.jneuroim.2022.577918_bb0050
  article-title: LGI1 and CASPR2 neurological autoimmunity in children
  publication-title: Ann. Neurol.
  doi: 10.1002/ana.25310
– volume: 18
  start-page: 1137
  issue: 6
  year: 2019
  ident: 10.1016/j.jneuroim.2022.577918_bb0110
  article-title: Neurochondrin antibody serum positivity in three cases of autoimmune cerebellar Ataxia
  publication-title: Cerebellum.
  doi: 10.1007/s12311-019-01048-y
– volume: 4
  issue: 4
  year: 2017
  ident: 10.1016/j.jneuroim.2022.577918_bb0040
  article-title: Autoimmune episodic ataxia in patients with anti-CASPR2 antibody-associated encephalitis
  publication-title: Neurol. Neuroimmunol. Neuroinflamm.
  doi: 10.1212/NXI.0000000000000371
– volume: 14
  start-page: 12
  issue: 1
  year: 2015
  ident: 10.1016/j.jneuroim.2022.577918_bb0105
  article-title: LGI1 is involved in the development of mouse brain
  publication-title: Cerebellum
  doi: 10.1007/s12311-014-0628-6
– volume: 17
  start-page: 203
  year: 2021
  ident: 10.1016/j.jneuroim.2022.577918_bb0080
  article-title: Clinical features and long-term outcomes of anti-leucine-rich glioma-inactivated 1 encephalitis
  publication-title: Multi Center Study.
– volume: 14
  start-page: 10
  issue: 1
  year: 2021
  ident: 10.1016/j.jneuroim.2022.577918_bb0060
  article-title: Immune-mediated cerebellar ataxias: clinical diagnosis and treatment based on immunological and physiological mechanisms
  publication-title: J. Mov. Disord.
  doi: 10.14802/jmd.20040
– volume: 22
  start-page: 190
  issue: 1
  year: 2018
  ident: 10.1016/j.jneuroim.2022.577918_bb0085
  article-title: Limbic encephalitis with LGI1 antibodies in a 14-year-old boy
  publication-title: Eur. J. Paediatr. Neurol.
  doi: 10.1016/j.ejpn.2017.08.004
– volume: 15
  start-page: 213
  issue: 2
  year: 2016
  ident: 10.1016/j.jneuroim.2022.577918_bb0055
  article-title: Consensus paper: neuroimmune mechanisms of cerebellar ataxias
  publication-title: Cerebellum.
  doi: 10.1007/s12311-015-0664-x
– volume: 21
  start-page: 3701
  issue: 10
  year: 2020
  ident: 10.1016/j.jneuroim.2022.577918_bb0010
  article-title: Neurological syndromes associated with anti-GAD antibodies
  publication-title: Int. J. Mol. Sci.
  doi: 10.3390/ijms21103701
– volume: 33
  start-page: 18161
  issue: 46
  year: 2013
  ident: 10.1016/j.jneuroim.2022.577918_bb0070
  article-title: Autoantibodies to epilepsy-related LGI1 in limbic encephalitis neutralize LGI1-ADAM22 interaction and reduce synaptic AMPA receptors
  publication-title: J. Neurosci.
  doi: 10.1523/JNEUROSCI.3506-13.2013
– volume: 12
  issue: 1
  year: 2015
  ident: 10.1016/j.jneuroim.2022.577918_bb0030
  article-title: ‘Medusa head ataxia’: the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: anti-PKC-gamma, anti-GluR-delta2, anti-ca/ARHGAP26 and anti-VGCC
  publication-title: J. Neuroinflammation
  doi: 10.1186/s12974-015-0358-9
– volume: 122
  year: 2021
  ident: 10.1016/j.jneuroim.2022.577918_bb0045
  article-title: Long-term seizure outcomes in patients with anti-leucine-rich glioma-inactivated 1 encephalitis
  publication-title: Epilepsy Behav.
  doi: 10.1016/j.yebeh.2021.108159
– volume: 12
  issue: 1
  year: 2015
  ident: 10.1016/j.jneuroim.2022.577918_bb0025
  article-title: ‘Medusa head ataxia’: the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 1: anti-mGluR1, anti-Homer-3, anti-Sj/ITPR1 and anti-CARP VIII
  publication-title: J. Neuroinflammation
  doi: 10.1186/s12974-015-0358-9
– volume: 133
  start-page: 2734
  issue: 9
  year: 2010
  ident: 10.1016/j.jneuroim.2022.577918_bb0020
  article-title: Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia
  publication-title: Brain
  doi: 10.1093/brain/awq213
– volume: 40
  start-page: 645
  issue: 5
  year: 2014
  ident: 10.1016/j.jneuroim.2022.577918_bb0100
  article-title: LGI1 autoantibodies associated with cerebellar degeneration
  publication-title: Neuropathol. Appl. Neurobiol.
  doi: 10.1111/nan.12132
– volume: 139
  start-page: 1079
  issue: 4
  year: 2016
  ident: 10.1016/j.jneuroim.2022.577918_bb0065
  article-title: Motor cortex and hippocampus are the two main cortical targets in LGI1-antibody encephalitis
  publication-title: Brain.
  doi: 10.1093/brain/aww012
– volume: 82
  start-page: 79
  issue: 1
  year: 2017
  ident: 10.1016/j.jneuroim.2022.577918_bb0015
  article-title: Expanded phenotypes and outcomes among 256 LGI1/CASPR2-IgG-positive patients
  publication-title: Ann. Neurol.
  doi: 10.1002/ana.24979
– volume: 141
  start-page: 3144
  issue: 11
  year: 2018
  ident: 10.1016/j.jneuroim.2022.577918_bb0075
  article-title: LGI1 antibodies alter Kv1.1 and AMPA receptors changing synaptic excitability, plasticity and memory
  publication-title: Brain.
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Snippet To report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies. The clinical...
To report two pediatric cases of autoimmune cerebellar ataxia associated with the anti-Leucine-rich glioma-inactivated protein 1 (LGI1)antibodies.OBJECTIVESTo...
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SubjectTerms Autoimmune
Cerebellar ataxia
Child
Leucine-rich glioma-inactivated protein 1
LGI1
Title Autoimmune cerebellar ataxia associated with anti-leucine-rich glioma-inactivated protein 1 antibodies: Two pediatric cases
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0165572822001138
https://dx.doi.org/10.1016/j.jneuroim.2022.577918
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