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Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature

BACKGROUND: Only 15 patients of autoimmune encephalitis with metabotropic glutamate receptor 5 (mGluR5) antibodies have been reported worldwide since 2011, mostly from western countries. Patients with different genetic backgrounds are necessary to further clarify the clinical phenotype and prognosis...

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Autores principales: Guo, Kundian, Liu, Xu, Gong, Xue, Li, Aiqing, Liu, Yue, Li, Xingjie, Zhou, Dong, Hong, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070949/
https://www.ncbi.nlm.nih.gov/pubmed/37025999
http://dx.doi.org/10.3389/fimmu.2023.1146536
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author Guo, Kundian
Liu, Xu
Gong, Xue
Li, Aiqing
Liu, Yue
Li, Xingjie
Zhou, Dong
Hong, Zhen
author_facet Guo, Kundian
Liu, Xu
Gong, Xue
Li, Aiqing
Liu, Yue
Li, Xingjie
Zhou, Dong
Hong, Zhen
author_sort Guo, Kundian
collection PubMed
description BACKGROUND: Only 15 patients of autoimmune encephalitis with metabotropic glutamate receptor 5 (mGluR5) antibodies have been reported worldwide since 2011, mostly from western countries. Patients with different genetic backgrounds are necessary to further clarify the clinical phenotype and prognosis of this rare disease. OBJECTIVE: We initially describe a case series from China to confirm the previous findings, expand the clinical phenotype, and identify the prognostic factors of autoimmune encephalitis with mGluR5 antibodies. METHODS: Observational data with follow-up were prospectively collected from autoimmune encephalitis patients with mGluR5 antibodies. Clinical information and outcomes on current and previously reported cases were combined and analyzed. RESULTS: We identified five patients (median age 35 years); two were female. The main clinical manifestations were behavioral/personality changes (five of five, 100%) and cognitive disorders (four of five, 80%), accompanied with other neurologic symptoms. Hypoventilation occurred in two (40%) patients, which was life-threatening. One patient had meningoencephalitis, suggesting a new phenotype in anti-mGluR5 encephalitis. All patients received immunotherapy. At the last follow-up (median 18 months), two (40%) patients showed complete recovery, two (40%) patients showed partial recovery, and one (20%) patient died. One (20%) patient had multiple relapses. Together with the 15 previously reported cases, associated tumors occurred in seven of 12 (58%) Western patients vs. one of eight (13%) Chinese patients. Modified Rankin Scale (mRS) scores at the last follow-up (median 31 months) were available in 16 patients. Patients with bad outcomes (mRS > 2, n = 4) were more likely to have hypoventilation at onset and higher mRS scores at peak of the disease. CONCLUSIONS: In patients with different genetic background, as Chinese, the clinical phenotype of anti-mGluR5 encephalitis is similar. Fewer paraneoplastic cases were observed in Chinese patients. Most patients showed good responses to immunotherapy and cancer treatment. The clinical outcomes were favorable in most patients.
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spelling pubmed-100709492023-04-05 Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature Guo, Kundian Liu, Xu Gong, Xue Li, Aiqing Liu, Yue Li, Xingjie Zhou, Dong Hong, Zhen Front Immunol Immunology BACKGROUND: Only 15 patients of autoimmune encephalitis with metabotropic glutamate receptor 5 (mGluR5) antibodies have been reported worldwide since 2011, mostly from western countries. Patients with different genetic backgrounds are necessary to further clarify the clinical phenotype and prognosis of this rare disease. OBJECTIVE: We initially describe a case series from China to confirm the previous findings, expand the clinical phenotype, and identify the prognostic factors of autoimmune encephalitis with mGluR5 antibodies. METHODS: Observational data with follow-up were prospectively collected from autoimmune encephalitis patients with mGluR5 antibodies. Clinical information and outcomes on current and previously reported cases were combined and analyzed. RESULTS: We identified five patients (median age 35 years); two were female. The main clinical manifestations were behavioral/personality changes (five of five, 100%) and cognitive disorders (four of five, 80%), accompanied with other neurologic symptoms. Hypoventilation occurred in two (40%) patients, which was life-threatening. One patient had meningoencephalitis, suggesting a new phenotype in anti-mGluR5 encephalitis. All patients received immunotherapy. At the last follow-up (median 18 months), two (40%) patients showed complete recovery, two (40%) patients showed partial recovery, and one (20%) patient died. One (20%) patient had multiple relapses. Together with the 15 previously reported cases, associated tumors occurred in seven of 12 (58%) Western patients vs. one of eight (13%) Chinese patients. Modified Rankin Scale (mRS) scores at the last follow-up (median 31 months) were available in 16 patients. Patients with bad outcomes (mRS > 2, n = 4) were more likely to have hypoventilation at onset and higher mRS scores at peak of the disease. CONCLUSIONS: In patients with different genetic background, as Chinese, the clinical phenotype of anti-mGluR5 encephalitis is similar. Fewer paraneoplastic cases were observed in Chinese patients. Most patients showed good responses to immunotherapy and cancer treatment. The clinical outcomes were favorable in most patients. Frontiers Media S.A. 2023-03-21 /pmc/articles/PMC10070949/ /pubmed/37025999 http://dx.doi.org/10.3389/fimmu.2023.1146536 Text en Copyright © 2023 Guo, Liu, Gong, Li, Liu, Li, Zhou and Hong https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Guo, Kundian
Liu, Xu
Gong, Xue
Li, Aiqing
Liu, Yue
Li, Xingjie
Zhou, Dong
Hong, Zhen
Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature
title Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature
title_full Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature
title_fullStr Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature
title_full_unstemmed Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature
title_short Autoimmune encephalitis with mGluR5 antibodies: A case series from China and review of the literature
title_sort autoimmune encephalitis with mglur5 antibodies: a case series from china and review of the literature
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070949/
https://www.ncbi.nlm.nih.gov/pubmed/37025999
http://dx.doi.org/10.3389/fimmu.2023.1146536
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