An effective immunotherapy regimen for VGKC antibody-positive limbic encephalitis

BackgroundVoltage-gated potassium channel antibody-positive limbic encephalitis (VGKC+LE) frequently improves with immunotherapy, although the optimum regimen is unknown. The effectiveness of a combination immunomodulatory regimen was tested in consecutive VGKC+LE patients.MethodsThis was an open-la...

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Veröffentlicht in:Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2010-10, Vol.81 (10), p.1167-1169
Hauptverfasser: Wong, S H, Saunders, M D, Larner, A J, Das, K, Hart, I K
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container_issue 10
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container_title Journal of neurology, neurosurgery and psychiatry
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creator Wong, S H
Saunders, M D
Larner, A J
Das, K
Hart, I K
description BackgroundVoltage-gated potassium channel antibody-positive limbic encephalitis (VGKC+LE) frequently improves with immunotherapy, although the optimum regimen is unknown. The effectiveness of a combination immunomodulatory regimen was tested in consecutive VGKC+LE patients.MethodsThis was an open-label prospective study of nine VGKC+LE patients. All patients had plasma exchange (50 ml/kg), intravenous immunoglobulin (2 g/kg) and intravenous methylprednisolone (1 g×3), followed by maintenance oral prednisolone (1 mg/kg/day). Mycophenolate (2 g/day) was used in the first three patients. Assessments included serial clinical, cognitive, brain MRI and VGKC antibody testing.ResultsWithin 1 week, seizures and hyponatraemia remitted in all affected patients. Cognitive function improved in all patients within 3 months. MRI appearances improved substantially within 9 months, with remission of inflammation in the majority of patients. All achieved immunological remission with normal VGKC antibody titres within 1–4 months. Major adverse events of therapy included one septicaemia and one thrombosis on plasma exchange and one death from sepsis after incidental bowel surgery. One patient remains in remission after 40 months of follow up, 26 months after being off all treatment.ConclusionsOur immunotherapy regimen was effective for the treatment of the clinical, cognitive and immunological features of VGKC+LE. Radiological improvement was seen in the majority. Pending randomised controlled trials, this regimen is proposed for the treatment of VGKC+LE.
doi_str_mv 10.1136/jnnp.2009.178293
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The effectiveness of a combination immunomodulatory regimen was tested in consecutive VGKC+LE patients.MethodsThis was an open-label prospective study of nine VGKC+LE patients. All patients had plasma exchange (50 ml/kg), intravenous immunoglobulin (2 g/kg) and intravenous methylprednisolone (1 g×3), followed by maintenance oral prednisolone (1 mg/kg/day). Mycophenolate (2 g/day) was used in the first three patients. Assessments included serial clinical, cognitive, brain MRI and VGKC antibody testing.ResultsWithin 1 week, seizures and hyponatraemia remitted in all affected patients. Cognitive function improved in all patients within 3 months. MRI appearances improved substantially within 9 months, with remission of inflammation in the majority of patients. All achieved immunological remission with normal VGKC antibody titres within 1–4 months. Major adverse events of therapy included one septicaemia and one thrombosis on plasma exchange and one death from sepsis after incidental bowel surgery. One patient remains in remission after 40 months of follow up, 26 months after being off all treatment.ConclusionsOur immunotherapy regimen was effective for the treatment of the clinical, cognitive and immunological features of VGKC+LE. Radiological improvement was seen in the majority. Pending randomised controlled trials, this regimen is proposed for the treatment of VGKC+LE.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp.2009.178293</identifier><identifier>PMID: 20660916</identifier><identifier>CODEN: JNNPAU</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>ACE ; ACE-R ; Addenbrookes Cognitive Examination ; Addenbrookes Cognitive Examination-Revised ; Aged ; Anti-Inflammatory Agents - administration &amp; dosage ; Biological and medical sciences ; Cognition Disorders - complications ; Cognition Disorders - drug therapy ; Cognitive ability ; Drug Therapy, Combination ; Female ; Human viral diseases ; Humans ; Immunoglobulins ; Immunoglobulins - administration &amp; dosage ; Immunologic Factors - administration &amp; dosage ; Immunology ; Immunosuppressive Agents - therapeutic use ; Immunotherapy ; Infectious diseases ; intravenous immunoglobulins ; IVIg ; limbic encephalitis ; Limbic Encephalitis - complications ; Limbic Encephalitis - drug therapy ; Limbic Encephalitis - immunology ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Memory ; Methylprednisolone - administration &amp; dosage ; Middle Aged ; Mycophenolic Acid - analogs &amp; derivatives ; Mycophenolic Acid - therapeutic use ; Neurology ; Patients ; PEX ; Plasma ; plasma exchange ; Potassium Channels, Voltage-Gated - immunology ; Prednisolone - therapeutic use ; Serotyping ; Staphylococcus infections ; Steroids ; VGKC+LE ; Viral diseases ; Viral diseases of the nervous system ; Voltage-gated potassium channel antibody ; voltage-gated potassium channel antibody-positive limbic encephalitis</subject><ispartof>Journal of neurology, neurosurgery and psychiatry, 2010-10, Vol.81 (10), p.1167-1169</ispartof><rights>2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright: 2010 (c) 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b528t-23462d9d8e52cb82882d39fa826c0a066f125bd3fc1347d4c5021a4c83f1c8fd3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jnnp.bmj.com/content/81/10/1167.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jnnp.bmj.com/content/81/10/1167.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77569,77600</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23265475$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20660916$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wong, S H</creatorcontrib><creatorcontrib>Saunders, M D</creatorcontrib><creatorcontrib>Larner, A J</creatorcontrib><creatorcontrib>Das, K</creatorcontrib><creatorcontrib>Hart, I K</creatorcontrib><title>An effective immunotherapy regimen for VGKC antibody-positive limbic encephalitis</title><title>Journal of neurology, neurosurgery and psychiatry</title><addtitle>J Neurol Neurosurg Psychiatry</addtitle><description>BackgroundVoltage-gated potassium channel antibody-positive limbic encephalitis (VGKC+LE) frequently improves with immunotherapy, although the optimum regimen is unknown. The effectiveness of a combination immunomodulatory regimen was tested in consecutive VGKC+LE patients.MethodsThis was an open-label prospective study of nine VGKC+LE patients. All patients had plasma exchange (50 ml/kg), intravenous immunoglobulin (2 g/kg) and intravenous methylprednisolone (1 g×3), followed by maintenance oral prednisolone (1 mg/kg/day). Mycophenolate (2 g/day) was used in the first three patients. Assessments included serial clinical, cognitive, brain MRI and VGKC antibody testing.ResultsWithin 1 week, seizures and hyponatraemia remitted in all affected patients. Cognitive function improved in all patients within 3 months. MRI appearances improved substantially within 9 months, with remission of inflammation in the majority of patients. All achieved immunological remission with normal VGKC antibody titres within 1–4 months. Major adverse events of therapy included one septicaemia and one thrombosis on plasma exchange and one death from sepsis after incidental bowel surgery. One patient remains in remission after 40 months of follow up, 26 months after being off all treatment.ConclusionsOur immunotherapy regimen was effective for the treatment of the clinical, cognitive and immunological features of VGKC+LE. Radiological improvement was seen in the majority. Pending randomised controlled trials, this regimen is proposed for the treatment of VGKC+LE.</description><subject>ACE</subject><subject>ACE-R</subject><subject>Addenbrookes Cognitive Examination</subject><subject>Addenbrookes Cognitive Examination-Revised</subject><subject>Aged</subject><subject>Anti-Inflammatory Agents - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Cognition Disorders - complications</subject><subject>Cognition Disorders - drug therapy</subject><subject>Cognitive ability</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Immunoglobulins - administration &amp; dosage</subject><subject>Immunologic Factors - administration &amp; dosage</subject><subject>Immunology</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Immunotherapy</subject><subject>Infectious diseases</subject><subject>intravenous immunoglobulins</subject><subject>IVIg</subject><subject>limbic encephalitis</subject><subject>Limbic Encephalitis - complications</subject><subject>Limbic Encephalitis - drug therapy</subject><subject>Limbic Encephalitis - immunology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Methylprednisolone - administration &amp; dosage</subject><subject>Middle Aged</subject><subject>Mycophenolic Acid - analogs &amp; derivatives</subject><subject>Mycophenolic Acid - therapeutic use</subject><subject>Neurology</subject><subject>Patients</subject><subject>PEX</subject><subject>Plasma</subject><subject>plasma exchange</subject><subject>Potassium Channels, Voltage-Gated - immunology</subject><subject>Prednisolone - therapeutic use</subject><subject>Serotyping</subject><subject>Staphylococcus infections</subject><subject>Steroids</subject><subject>VGKC+LE</subject><subject>Viral diseases</subject><subject>Viral diseases of the nervous system</subject><subject>Voltage-gated potassium channel antibody</subject><subject>voltage-gated potassium channel antibody-positive limbic encephalitis</subject><issn>0022-3050</issn><issn>1468-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0U1v1DAQBmALUdGlcOeEIiHEocribzvHNoJCqYCqUHGzHMemXhIn2Ali_329ZCkSl_piyX5mNPYLwDME1wgR_noTwrjGEFZrJCSuyAOwQpTLkhD47SFYQYhxSSCDh-BxShu4W7J6BA4x5BxWiK_A5UkorHPWTP6XLXzfz2GYbmzU47aI9rvvbSjcEIvrsw91ocPkm6HdluOQ_J-CzveNN4UNxo43usuH6Qk4cLpL9ul-PwJf3775Ur8rLz6dva9PLsqGYTmVmFCO26qVlmHTSCwlbknltMTcQJ3ncwizpiXOIEJFSw2DGGlqJHHISNeSI_Bq6TvG4eds06R6n4ztOh3sMCclOMaCQILul4xRiASXWb74T26GOYb8DJU_GGHKaCWygosycUgpWqfG6HsdtwpBtctF7XJRu1zUkksueb5vPDe9be8K_gaRwcs90MnozkUdjE__HMGcUcGyKxfn02R_393r-ENxQQRTH69rxa_qy_OrU64-Z3-8-Kbf3D_mLb3YsdI</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Wong, S H</creator><creator>Saunders, M D</creator><creator>Larner, A J</creator><creator>Das, K</creator><creator>Hart, I K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope></search><sort><creationdate>20101001</creationdate><title>An effective immunotherapy regimen for VGKC antibody-positive limbic encephalitis</title><author>Wong, S H ; 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dosage</topic><topic>Middle Aged</topic><topic>Mycophenolic Acid - analogs &amp; derivatives</topic><topic>Mycophenolic Acid - therapeutic use</topic><topic>Neurology</topic><topic>Patients</topic><topic>PEX</topic><topic>Plasma</topic><topic>plasma exchange</topic><topic>Potassium Channels, Voltage-Gated - immunology</topic><topic>Prednisolone - therapeutic use</topic><topic>Serotyping</topic><topic>Staphylococcus infections</topic><topic>Steroids</topic><topic>VGKC+LE</topic><topic>Viral diseases</topic><topic>Viral diseases of the nervous system</topic><topic>Voltage-gated potassium channel antibody</topic><topic>voltage-gated potassium channel antibody-positive limbic encephalitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, S H</creatorcontrib><creatorcontrib>Saunders, M D</creatorcontrib><creatorcontrib>Larner, A J</creatorcontrib><creatorcontrib>Das, K</creatorcontrib><creatorcontrib>Hart, I K</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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The effectiveness of a combination immunomodulatory regimen was tested in consecutive VGKC+LE patients.MethodsThis was an open-label prospective study of nine VGKC+LE patients. All patients had plasma exchange (50 ml/kg), intravenous immunoglobulin (2 g/kg) and intravenous methylprednisolone (1 g×3), followed by maintenance oral prednisolone (1 mg/kg/day). Mycophenolate (2 g/day) was used in the first three patients. Assessments included serial clinical, cognitive, brain MRI and VGKC antibody testing.ResultsWithin 1 week, seizures and hyponatraemia remitted in all affected patients. Cognitive function improved in all patients within 3 months. MRI appearances improved substantially within 9 months, with remission of inflammation in the majority of patients. All achieved immunological remission with normal VGKC antibody titres within 1–4 months. Major adverse events of therapy included one septicaemia and one thrombosis on plasma exchange and one death from sepsis after incidental bowel surgery. One patient remains in remission after 40 months of follow up, 26 months after being off all treatment.ConclusionsOur immunotherapy regimen was effective for the treatment of the clinical, cognitive and immunological features of VGKC+LE. Radiological improvement was seen in the majority. Pending randomised controlled trials, this regimen is proposed for the treatment of VGKC+LE.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><pmid>20660916</pmid><doi>10.1136/jnnp.2009.178293</doi><tpages>3</tpages></addata></record>
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subjects ACE
ACE-R
Addenbrookes Cognitive Examination
Addenbrookes Cognitive Examination-Revised
Aged
Anti-Inflammatory Agents - administration & dosage
Biological and medical sciences
Cognition Disorders - complications
Cognition Disorders - drug therapy
Cognitive ability
Drug Therapy, Combination
Female
Human viral diseases
Humans
Immunoglobulins
Immunoglobulins - administration & dosage
Immunologic Factors - administration & dosage
Immunology
Immunosuppressive Agents - therapeutic use
Immunotherapy
Infectious diseases
intravenous immunoglobulins
IVIg
limbic encephalitis
Limbic Encephalitis - complications
Limbic Encephalitis - drug therapy
Limbic Encephalitis - immunology
Magnetic Resonance Imaging
Male
Medical sciences
Memory
Methylprednisolone - administration & dosage
Middle Aged
Mycophenolic Acid - analogs & derivatives
Mycophenolic Acid - therapeutic use
Neurology
Patients
PEX
Plasma
plasma exchange
Potassium Channels, Voltage-Gated - immunology
Prednisolone - therapeutic use
Serotyping
Staphylococcus infections
Steroids
VGKC+LE
Viral diseases
Viral diseases of the nervous system
Voltage-gated potassium channel antibody
voltage-gated potassium channel antibody-positive limbic encephalitis
title An effective immunotherapy regimen for VGKC antibody-positive limbic encephalitis
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