Tofacitinib treatment for refractory autoimmune encephalitis
To treat intractable cases of autoimmune encephalitis, the need for novel immunotherapy that penetrates the blood‐brain barrier (BBB) is increasing. Tofacitinib is a Janus kinase (JAK) inhibitor used to treat refractory immune‐mediated diseases that effectively penetrates the BBB. Accordingly, tofac...
Gespeichert in:
Veröffentlicht in: | Epilepsia (Copenhagen) 2021-04, Vol.62 (4), p.e53-e59 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e59 |
---|---|
container_issue | 4 |
container_start_page | e53 |
container_title | Epilepsia (Copenhagen) |
container_volume | 62 |
creator | Jang, Yoonhyuk Lee, Woo‐Jin Lee, Han Sang Chu, Kon Lee, Sang Kun Lee, Soon‐Tae |
description | To treat intractable cases of autoimmune encephalitis, the need for novel immunotherapy that penetrates the blood‐brain barrier (BBB) is increasing. Tofacitinib is a Janus kinase (JAK) inhibitor used to treat refractory immune‐mediated diseases that effectively penetrates the BBB. Accordingly, tofacitinib could be a new option for patients with refractory autoimmune encephalitis. Patients treated with tofacitinib were selected from Seoul National University Hospital cohort for autoimmune encephalitis from April 2019 until July 2020. We retrospectively analyzed the efficacy of tofacitinib in patients with autoimmune encephalitis who showed insufficient responses to multimodal conventional immunotherapies. Tofacitinib was administered orally at a dose of 5 mg twice daily. A total of eight patients were treated with tofacitinib; two had good responses (clinical global impression‐improvement score [CGI‐I] = 1 or 2), three had partial responses (CGI‐I = 3), and three showed no significant improvements (CGI‐I = 4) in response to tofacitinib. The two good responders showed the improvement of chronic autoimmune meningoencephalitis and the cessation of the new‐onset refractory status epilepticus in anti‐myelin oligodendrocyte glycoprotein (MOG)–associated disorder, which was previously intractable to anesthetics and the other immunotherapies. No patients had serious side effects. Our findings suggest the potential of tofacitinib as a therapeutic option for central nervous system autoimmune diseases. |
doi_str_mv | 10.1111/epi.16848 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_wiley_primary_10_1111_epi_16848_EPI16848</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2510322839</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3538-24996e43285c258c6cf09d59b8d21692a8570c0582e1c133ddf45ceade8533583</originalsourceid><addsrcrecordid>eNp10E9LwzAYBvAgis7pwS8gBS966JY_TZqCFxlTBwM9zHPI0reY0TYzaZF9ezM7PQjmkssvz5v3QeiK4AmJZwpbOyFCZvIIjQinMiVE5MdohDFhacElPkPnIWwwxrnI2Sk6Y0xwQXIyQvcrV2ljO9vaddJ50F0DbZdUziceKq9N5_wu0X3nbNP0LSTQGti-6zo-CRfopNJ1gMvDPUZvj_PV7DldvjwtZg_L1DDOZEqzohCQMSq5oVwaYSpclLxYy5ISUVAteY4N5pICMYSxsqwybkCXIDljXLIxuh1yt9599BA61dhgoK51C64PKg4QlBOWFZHe_KEb1_s2_k5FgRmlku3V3aCMdyHERdXW20b7nSJY7StVsVL1XWm014fEft1A-St_OoxgOoBPW8Pu_yQ1f10MkV8Tb36Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2510322839</pqid></control><display><type>article</type><title>Tofacitinib treatment for refractory autoimmune encephalitis</title><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library All Journals</source><source>Alma/SFX Local Collection</source><creator>Jang, Yoonhyuk ; Lee, Woo‐Jin ; Lee, Han Sang ; Chu, Kon ; Lee, Sang Kun ; Lee, Soon‐Tae</creator><creatorcontrib>Jang, Yoonhyuk ; Lee, Woo‐Jin ; Lee, Han Sang ; Chu, Kon ; Lee, Sang Kun ; Lee, Soon‐Tae</creatorcontrib><description>To treat intractable cases of autoimmune encephalitis, the need for novel immunotherapy that penetrates the blood‐brain barrier (BBB) is increasing. Tofacitinib is a Janus kinase (JAK) inhibitor used to treat refractory immune‐mediated diseases that effectively penetrates the BBB. Accordingly, tofacitinib could be a new option for patients with refractory autoimmune encephalitis. Patients treated with tofacitinib were selected from Seoul National University Hospital cohort for autoimmune encephalitis from April 2019 until July 2020. We retrospectively analyzed the efficacy of tofacitinib in patients with autoimmune encephalitis who showed insufficient responses to multimodal conventional immunotherapies. Tofacitinib was administered orally at a dose of 5 mg twice daily. A total of eight patients were treated with tofacitinib; two had good responses (clinical global impression‐improvement score [CGI‐I] = 1 or 2), three had partial responses (CGI‐I = 3), and three showed no significant improvements (CGI‐I = 4) in response to tofacitinib. The two good responders showed the improvement of chronic autoimmune meningoencephalitis and the cessation of the new‐onset refractory status epilepticus in anti‐myelin oligodendrocyte glycoprotein (MOG)–associated disorder, which was previously intractable to anesthetics and the other immunotherapies. No patients had serious side effects. Our findings suggest the potential of tofacitinib as a therapeutic option for central nervous system autoimmune diseases.</description><identifier>ISSN: 0013-9580</identifier><identifier>EISSN: 1528-1167</identifier><identifier>DOI: 10.1111/epi.16848</identifier><identifier>PMID: 33656171</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Anesthetics ; Autoimmune diseases ; autoimmune encephalitis ; autoimmune meningitis ; Blood-brain barrier ; Central nervous system ; Dosage ; Encephalitis ; Enzyme inhibitors ; Epilepsy ; Immunotherapy ; Janus kinase ; Meningoencephalitis ; Myelin ; new‐onset refractory status epilepticus ; Oligodendrocyte-myelin glycoprotein ; Oral administration ; Patients ; tofacitinib</subject><ispartof>Epilepsia (Copenhagen), 2021-04, Vol.62 (4), p.e53-e59</ispartof><rights>2021 International League Against Epilepsy</rights><rights>2021 International League Against Epilepsy.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-24996e43285c258c6cf09d59b8d21692a8570c0582e1c133ddf45ceade8533583</citedby><cites>FETCH-LOGICAL-c3538-24996e43285c258c6cf09d59b8d21692a8570c0582e1c133ddf45ceade8533583</cites><orcidid>0000-0003-4767-7564 ; 0000-0001-5863-0302 ; 0000-0003-1908-0699</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fepi.16848$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fepi.16848$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33656171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jang, Yoonhyuk</creatorcontrib><creatorcontrib>Lee, Woo‐Jin</creatorcontrib><creatorcontrib>Lee, Han Sang</creatorcontrib><creatorcontrib>Chu, Kon</creatorcontrib><creatorcontrib>Lee, Sang Kun</creatorcontrib><creatorcontrib>Lee, Soon‐Tae</creatorcontrib><title>Tofacitinib treatment for refractory autoimmune encephalitis</title><title>Epilepsia (Copenhagen)</title><addtitle>Epilepsia</addtitle><description>To treat intractable cases of autoimmune encephalitis, the need for novel immunotherapy that penetrates the blood‐brain barrier (BBB) is increasing. Tofacitinib is a Janus kinase (JAK) inhibitor used to treat refractory immune‐mediated diseases that effectively penetrates the BBB. Accordingly, tofacitinib could be a new option for patients with refractory autoimmune encephalitis. Patients treated with tofacitinib were selected from Seoul National University Hospital cohort for autoimmune encephalitis from April 2019 until July 2020. We retrospectively analyzed the efficacy of tofacitinib in patients with autoimmune encephalitis who showed insufficient responses to multimodal conventional immunotherapies. Tofacitinib was administered orally at a dose of 5 mg twice daily. A total of eight patients were treated with tofacitinib; two had good responses (clinical global impression‐improvement score [CGI‐I] = 1 or 2), three had partial responses (CGI‐I = 3), and three showed no significant improvements (CGI‐I = 4) in response to tofacitinib. The two good responders showed the improvement of chronic autoimmune meningoencephalitis and the cessation of the new‐onset refractory status epilepticus in anti‐myelin oligodendrocyte glycoprotein (MOG)–associated disorder, which was previously intractable to anesthetics and the other immunotherapies. No patients had serious side effects. Our findings suggest the potential of tofacitinib as a therapeutic option for central nervous system autoimmune diseases.</description><subject>Anesthetics</subject><subject>Autoimmune diseases</subject><subject>autoimmune encephalitis</subject><subject>autoimmune meningitis</subject><subject>Blood-brain barrier</subject><subject>Central nervous system</subject><subject>Dosage</subject><subject>Encephalitis</subject><subject>Enzyme inhibitors</subject><subject>Epilepsy</subject><subject>Immunotherapy</subject><subject>Janus kinase</subject><subject>Meningoencephalitis</subject><subject>Myelin</subject><subject>new‐onset refractory status epilepticus</subject><subject>Oligodendrocyte-myelin glycoprotein</subject><subject>Oral administration</subject><subject>Patients</subject><subject>tofacitinib</subject><issn>0013-9580</issn><issn>1528-1167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp10E9LwzAYBvAgis7pwS8gBS966JY_TZqCFxlTBwM9zHPI0reY0TYzaZF9ezM7PQjmkssvz5v3QeiK4AmJZwpbOyFCZvIIjQinMiVE5MdohDFhacElPkPnIWwwxrnI2Sk6Y0xwQXIyQvcrV2ljO9vaddJ50F0DbZdUziceKq9N5_wu0X3nbNP0LSTQGti-6zo-CRfopNJ1gMvDPUZvj_PV7DldvjwtZg_L1DDOZEqzohCQMSq5oVwaYSpclLxYy5ISUVAteY4N5pICMYSxsqwybkCXIDljXLIxuh1yt9599BA61dhgoK51C64PKg4QlBOWFZHe_KEb1_s2_k5FgRmlku3V3aCMdyHERdXW20b7nSJY7StVsVL1XWm014fEft1A-St_OoxgOoBPW8Pu_yQ1f10MkV8Tb36Q</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Jang, Yoonhyuk</creator><creator>Lee, Woo‐Jin</creator><creator>Lee, Han Sang</creator><creator>Chu, Kon</creator><creator>Lee, Sang Kun</creator><creator>Lee, Soon‐Tae</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4767-7564</orcidid><orcidid>https://orcid.org/0000-0001-5863-0302</orcidid><orcidid>https://orcid.org/0000-0003-1908-0699</orcidid></search><sort><creationdate>202104</creationdate><title>Tofacitinib treatment for refractory autoimmune encephalitis</title><author>Jang, Yoonhyuk ; Lee, Woo‐Jin ; Lee, Han Sang ; Chu, Kon ; Lee, Sang Kun ; Lee, Soon‐Tae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-24996e43285c258c6cf09d59b8d21692a8570c0582e1c133ddf45ceade8533583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anesthetics</topic><topic>Autoimmune diseases</topic><topic>autoimmune encephalitis</topic><topic>autoimmune meningitis</topic><topic>Blood-brain barrier</topic><topic>Central nervous system</topic><topic>Dosage</topic><topic>Encephalitis</topic><topic>Enzyme inhibitors</topic><topic>Epilepsy</topic><topic>Immunotherapy</topic><topic>Janus kinase</topic><topic>Meningoencephalitis</topic><topic>Myelin</topic><topic>new‐onset refractory status epilepticus</topic><topic>Oligodendrocyte-myelin glycoprotein</topic><topic>Oral administration</topic><topic>Patients</topic><topic>tofacitinib</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jang, Yoonhyuk</creatorcontrib><creatorcontrib>Lee, Woo‐Jin</creatorcontrib><creatorcontrib>Lee, Han Sang</creatorcontrib><creatorcontrib>Chu, Kon</creatorcontrib><creatorcontrib>Lee, Sang Kun</creatorcontrib><creatorcontrib>Lee, Soon‐Tae</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Epilepsia (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jang, Yoonhyuk</au><au>Lee, Woo‐Jin</au><au>Lee, Han Sang</au><au>Chu, Kon</au><au>Lee, Sang Kun</au><au>Lee, Soon‐Tae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tofacitinib treatment for refractory autoimmune encephalitis</atitle><jtitle>Epilepsia (Copenhagen)</jtitle><addtitle>Epilepsia</addtitle><date>2021-04</date><risdate>2021</risdate><volume>62</volume><issue>4</issue><spage>e53</spage><epage>e59</epage><pages>e53-e59</pages><issn>0013-9580</issn><eissn>1528-1167</eissn><abstract>To treat intractable cases of autoimmune encephalitis, the need for novel immunotherapy that penetrates the blood‐brain barrier (BBB) is increasing. Tofacitinib is a Janus kinase (JAK) inhibitor used to treat refractory immune‐mediated diseases that effectively penetrates the BBB. Accordingly, tofacitinib could be a new option for patients with refractory autoimmune encephalitis. Patients treated with tofacitinib were selected from Seoul National University Hospital cohort for autoimmune encephalitis from April 2019 until July 2020. We retrospectively analyzed the efficacy of tofacitinib in patients with autoimmune encephalitis who showed insufficient responses to multimodal conventional immunotherapies. Tofacitinib was administered orally at a dose of 5 mg twice daily. A total of eight patients were treated with tofacitinib; two had good responses (clinical global impression‐improvement score [CGI‐I] = 1 or 2), three had partial responses (CGI‐I = 3), and three showed no significant improvements (CGI‐I = 4) in response to tofacitinib. The two good responders showed the improvement of chronic autoimmune meningoencephalitis and the cessation of the new‐onset refractory status epilepticus in anti‐myelin oligodendrocyte glycoprotein (MOG)–associated disorder, which was previously intractable to anesthetics and the other immunotherapies. No patients had serious side effects. Our findings suggest the potential of tofacitinib as a therapeutic option for central nervous system autoimmune diseases.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33656171</pmid><doi>10.1111/epi.16848</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4767-7564</orcidid><orcidid>https://orcid.org/0000-0001-5863-0302</orcidid><orcidid>https://orcid.org/0000-0003-1908-0699</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0013-9580 |
ispartof | Epilepsia (Copenhagen), 2021-04, Vol.62 (4), p.e53-e59 |
issn | 0013-9580 1528-1167 |
language | eng |
recordid | cdi_wiley_primary_10_1111_epi_16848_EPI16848 |
source | EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals; Alma/SFX Local Collection |
subjects | Anesthetics Autoimmune diseases autoimmune encephalitis autoimmune meningitis Blood-brain barrier Central nervous system Dosage Encephalitis Enzyme inhibitors Epilepsy Immunotherapy Janus kinase Meningoencephalitis Myelin new‐onset refractory status epilepticus Oligodendrocyte-myelin glycoprotein Oral administration Patients tofacitinib |
title | Tofacitinib treatment for refractory autoimmune encephalitis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T23%3A57%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tofacitinib%20treatment%20for%20refractory%20autoimmune%20encephalitis&rft.jtitle=Epilepsia%20(Copenhagen)&rft.au=Jang,%20Yoonhyuk&rft.date=2021-04&rft.volume=62&rft.issue=4&rft.spage=e53&rft.epage=e59&rft.pages=e53-e59&rft.issn=0013-9580&rft.eissn=1528-1167&rft_id=info:doi/10.1111/epi.16848&rft_dat=%3Cproquest_cross%3E2510322839%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2510322839&rft_id=info:pmid/33656171&rfr_iscdi=true |