Rituximab treatment in seronegative autoimmune autonomic neuropathy and autoimmune autonomic ganglionopathy: Case-report and literature review
Autoimmune autonomic ganglionopathy (AAG) is a rare disease with no well-established treatment. Until recently, AAG could be seropositive (50 to 60% of patients) or seronegative for ganglionic (α3-type) nicotinic acetylcholine receptor (Gα3NAChR) antibodies. In early 2018, the two forms of the disea...
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description | Autoimmune autonomic ganglionopathy (AAG) is a rare disease with no well-established treatment. Until recently, AAG could be seropositive (50 to 60% of patients) or seronegative for ganglionic (α3-type) nicotinic acetylcholine receptor (Gα3NAChR) antibodies. In early 2018, the two forms of the disease were distinguished, separating seropositive from seronegative ones, designating this latter form “seronegative autoimmune autonomic neuropathy” (SAAN). Most described treatments are plasma exchange (PE) and intravenous immunoglobulin (IVIG). However in some cases with no or small benefit, other immunomodulatory therapies, such as rituximab have been reported. We report the case of a 24-year-old female patient successfully treated for SAAN with rituximab and steroids after IVIG and PE failure. We also provide a review of case-reports reporting rituximab treatment for both SAAN and AAG.
To identify articles reporting SAAN and AAG treatment with rituximab, we searched the PubMed database using the terms “autoimmune autonomic ganglionopathy”, “autoimmune autonomic neuropathy” or “seronegative autoimmune autonomic neuropathy” and “rituximab”.
Including our patient, nine cases have been described in the literature (4 SAAN and 5 AAG). Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases, used alone or in association with other etiologic treatments.
Our study suggests rituximab (alone or in association with other treatments) could provide efficacy in both SAAN and AAG when PE and/or IVIG are not effective enough.
•We provide a review of case-reports reporting rituximab treatment for seronegative autoimmune autonomic neuropathy (SAAN) and autoimmune autonomic ganglionopathy (AAG).•Nine cases have been described in the literature (4 SAAN and 5 AAG).•Rituximab was used alone or in association with other etiologic treatments.•Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases.•Our study suggests efficacy of rituximab in both SAAN and AAG when PE and/or IVIG are not effective enough. |
doi_str_mv | 10.1016/j.jneuroim.2018.11.009 |
format | Article |
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To identify articles reporting SAAN and AAG treatment with rituximab, we searched the PubMed database using the terms “autoimmune autonomic ganglionopathy”, “autoimmune autonomic neuropathy” or “seronegative autoimmune autonomic neuropathy” and “rituximab”.
Including our patient, nine cases have been described in the literature (4 SAAN and 5 AAG). Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases, used alone or in association with other etiologic treatments.
Our study suggests rituximab (alone or in association with other treatments) could provide efficacy in both SAAN and AAG when PE and/or IVIG are not effective enough.
•We provide a review of case-reports reporting rituximab treatment for seronegative autoimmune autonomic neuropathy (SAAN) and autoimmune autonomic ganglionopathy (AAG).•Nine cases have been described in the literature (4 SAAN and 5 AAG).•Rituximab was used alone or in association with other etiologic treatments.•Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases.•Our study suggests efficacy of rituximab in both SAAN and AAG when PE and/or IVIG are not effective enough.</description><identifier>ISSN: 0165-5728</identifier><identifier>EISSN: 1872-8421</identifier><identifier>DOI: 10.1016/j.jneuroim.2018.11.009</identifier><identifier>PMID: 30468952</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acute autonomic and sensory neuropathy ; Autoimmune autonomic ganglionopathy ; Emerging diseases ; Human health and pathology ; Immunomodulatory therapy ; Infectious diseases ; Life Sciences ; Rituximab ; Seronegative autoimmune autonomic neuropathy</subject><ispartof>Journal of neuroimmunology, 2019-01, Vol.326, p.28-32</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-b2225e25c2ab0f39ec92ab9ac113ca99c6b8fc9bb1a2c18fac152e1cbe6311ce3</citedby><cites>FETCH-LOGICAL-c402t-b2225e25c2ab0f39ec92ab9ac113ca99c6b8fc9bb1a2c18fac152e1cbe6311ce3</cites><orcidid>0000-0001-9391-7800 ; 0000-0003-2729-9420</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jneuroim.2018.11.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30468952$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02883130$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Bouxin, M.</creatorcontrib><creatorcontrib>Schvartz, B.</creatorcontrib><creatorcontrib>Mestrallet, S.</creatorcontrib><creatorcontrib>Debrumetz, A.</creatorcontrib><creatorcontrib>Hentzien, M.</creatorcontrib><creatorcontrib>Tabary, T.</creatorcontrib><creatorcontrib>Cohen, R.</creatorcontrib><creatorcontrib>Nicolas, G.</creatorcontrib><creatorcontrib>Bani-Sadr, F.</creatorcontrib><title>Rituximab treatment in seronegative autoimmune autonomic neuropathy and autoimmune autonomic ganglionopathy: Case-report and literature review</title><title>Journal of neuroimmunology</title><addtitle>J Neuroimmunol</addtitle><description>Autoimmune autonomic ganglionopathy (AAG) is a rare disease with no well-established treatment. Until recently, AAG could be seropositive (50 to 60% of patients) or seronegative for ganglionic (α3-type) nicotinic acetylcholine receptor (Gα3NAChR) antibodies. In early 2018, the two forms of the disease were distinguished, separating seropositive from seronegative ones, designating this latter form “seronegative autoimmune autonomic neuropathy” (SAAN). Most described treatments are plasma exchange (PE) and intravenous immunoglobulin (IVIG). However in some cases with no or small benefit, other immunomodulatory therapies, such as rituximab have been reported. We report the case of a 24-year-old female patient successfully treated for SAAN with rituximab and steroids after IVIG and PE failure. We also provide a review of case-reports reporting rituximab treatment for both SAAN and AAG.
To identify articles reporting SAAN and AAG treatment with rituximab, we searched the PubMed database using the terms “autoimmune autonomic ganglionopathy”, “autoimmune autonomic neuropathy” or “seronegative autoimmune autonomic neuropathy” and “rituximab”.
Including our patient, nine cases have been described in the literature (4 SAAN and 5 AAG). Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases, used alone or in association with other etiologic treatments.
Our study suggests rituximab (alone or in association with other treatments) could provide efficacy in both SAAN and AAG when PE and/or IVIG are not effective enough.
•We provide a review of case-reports reporting rituximab treatment for seronegative autoimmune autonomic neuropathy (SAAN) and autoimmune autonomic ganglionopathy (AAG).•Nine cases have been described in the literature (4 SAAN and 5 AAG).•Rituximab was used alone or in association with other etiologic treatments.•Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases.•Our study suggests efficacy of rituximab in both SAAN and AAG when PE and/or IVIG are not effective enough.</description><subject>Acute autonomic and sensory neuropathy</subject><subject>Autoimmune autonomic ganglionopathy</subject><subject>Emerging diseases</subject><subject>Human health and pathology</subject><subject>Immunomodulatory therapy</subject><subject>Infectious diseases</subject><subject>Life Sciences</subject><subject>Rituximab</subject><subject>Seronegative autoimmune autonomic neuropathy</subject><issn>0165-5728</issn><issn>1872-8421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi1ERZfCK1Q5wiHBYydZmxPVCijSSkhVe7Yc72TrVWIvtrOlL8Ez4920PSFx8nj8_fPL8xNyCbQCCu2nXbVzOAVvx4pREBVARal8RRYglqwUNYPXZJHBpmyWTJyTtzHuKIWG1_INOee0boVs2IL8ubFp-m1H3RUpoE4julRYV0QM3uFWJ3vAQk8pG42Tm0vnR2uKk_1ep_vHQrvNv5mtdtvB5suJ-1ysdMQy4N6HdBINNmHQaQpYBDxYfHhHzno9RHz_dF6Qu29fb1fX5frn9x-rq3VpaspS2THGGmSNYbqjPZdoZK6kNgDcaClN24neyK4DzQyIPj80DMF02HIAg_yCfJzn3utB7UP-f3hUXlt1fbVWxx5lQnDg9ACZ_TCz--B_TRiTGm00OAzaoZ-iYsCX9bIWUmS0nVETfIwB-5fZQNUxN7VTz7mpY24KQOXcsvDyyWPqRty8yJ6DysCXGcC8lbypoKKx6AxubECT1Mbb_3n8BZ32slA</recordid><startdate>20190115</startdate><enddate>20190115</enddate><creator>Bouxin, M.</creator><creator>Schvartz, B.</creator><creator>Mestrallet, S.</creator><creator>Debrumetz, A.</creator><creator>Hentzien, M.</creator><creator>Tabary, T.</creator><creator>Cohen, R.</creator><creator>Nicolas, G.</creator><creator>Bani-Sadr, F.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-9391-7800</orcidid><orcidid>https://orcid.org/0000-0003-2729-9420</orcidid></search><sort><creationdate>20190115</creationdate><title>Rituximab treatment in seronegative autoimmune autonomic neuropathy and autoimmune autonomic ganglionopathy: Case-report and literature review</title><author>Bouxin, M. ; Schvartz, B. ; Mestrallet, S. ; Debrumetz, A. ; Hentzien, M. ; Tabary, T. ; Cohen, R. ; Nicolas, G. ; Bani-Sadr, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-b2225e25c2ab0f39ec92ab9ac113ca99c6b8fc9bb1a2c18fac152e1cbe6311ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acute autonomic and sensory neuropathy</topic><topic>Autoimmune autonomic ganglionopathy</topic><topic>Emerging diseases</topic><topic>Human health and pathology</topic><topic>Immunomodulatory therapy</topic><topic>Infectious diseases</topic><topic>Life Sciences</topic><topic>Rituximab</topic><topic>Seronegative autoimmune autonomic neuropathy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bouxin, M.</creatorcontrib><creatorcontrib>Schvartz, B.</creatorcontrib><creatorcontrib>Mestrallet, S.</creatorcontrib><creatorcontrib>Debrumetz, A.</creatorcontrib><creatorcontrib>Hentzien, M.</creatorcontrib><creatorcontrib>Tabary, T.</creatorcontrib><creatorcontrib>Cohen, R.</creatorcontrib><creatorcontrib>Nicolas, G.</creatorcontrib><creatorcontrib>Bani-Sadr, F.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of neuroimmunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bouxin, M.</au><au>Schvartz, B.</au><au>Mestrallet, S.</au><au>Debrumetz, A.</au><au>Hentzien, M.</au><au>Tabary, T.</au><au>Cohen, R.</au><au>Nicolas, G.</au><au>Bani-Sadr, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rituximab treatment in seronegative autoimmune autonomic neuropathy and autoimmune autonomic ganglionopathy: Case-report and literature review</atitle><jtitle>Journal of neuroimmunology</jtitle><addtitle>J Neuroimmunol</addtitle><date>2019-01-15</date><risdate>2019</risdate><volume>326</volume><spage>28</spage><epage>32</epage><pages>28-32</pages><issn>0165-5728</issn><eissn>1872-8421</eissn><abstract>Autoimmune autonomic ganglionopathy (AAG) is a rare disease with no well-established treatment. Until recently, AAG could be seropositive (50 to 60% of patients) or seronegative for ganglionic (α3-type) nicotinic acetylcholine receptor (Gα3NAChR) antibodies. In early 2018, the two forms of the disease were distinguished, separating seropositive from seronegative ones, designating this latter form “seronegative autoimmune autonomic neuropathy” (SAAN). Most described treatments are plasma exchange (PE) and intravenous immunoglobulin (IVIG). However in some cases with no or small benefit, other immunomodulatory therapies, such as rituximab have been reported. We report the case of a 24-year-old female patient successfully treated for SAAN with rituximab and steroids after IVIG and PE failure. We also provide a review of case-reports reporting rituximab treatment for both SAAN and AAG.
To identify articles reporting SAAN and AAG treatment with rituximab, we searched the PubMed database using the terms “autoimmune autonomic ganglionopathy”, “autoimmune autonomic neuropathy” or “seronegative autoimmune autonomic neuropathy” and “rituximab”.
Including our patient, nine cases have been described in the literature (4 SAAN and 5 AAG). Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases, used alone or in association with other etiologic treatments.
Our study suggests rituximab (alone or in association with other treatments) could provide efficacy in both SAAN and AAG when PE and/or IVIG are not effective enough.
•We provide a review of case-reports reporting rituximab treatment for seronegative autoimmune autonomic neuropathy (SAAN) and autoimmune autonomic ganglionopathy (AAG).•Nine cases have been described in the literature (4 SAAN and 5 AAG).•Rituximab was used alone or in association with other etiologic treatments.•Rituximab had a significant positive effect in 2 out of 4 SAAN and all 5 AAG cases.•Our study suggests efficacy of rituximab in both SAAN and AAG when PE and/or IVIG are not effective enough.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30468952</pmid><doi>10.1016/j.jneuroim.2018.11.009</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-9391-7800</orcidid><orcidid>https://orcid.org/0000-0003-2729-9420</orcidid></addata></record> |
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subjects | Acute autonomic and sensory neuropathy Autoimmune autonomic ganglionopathy Emerging diseases Human health and pathology Immunomodulatory therapy Infectious diseases Life Sciences Rituximab Seronegative autoimmune autonomic neuropathy |
title | Rituximab treatment in seronegative autoimmune autonomic neuropathy and autoimmune autonomic ganglionopathy: Case-report and literature review |
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