Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology

Autoimmune gastrointestinal dysmotility (AGID), an idiopathic or paraneoplastic phenomenon, is a clinical form of limited autoimmune dysautonomia. The symptoms of AGID and gastrointestinal manifestations in patients with autoimmune rheumatic diseases are overlapping. Antineuronal autoantibodies are...

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Main Authors: Shunya Nakane, Akihiro Mukaino, Eikichi Ihara, Yoshihiro Ogawa
Format: Article
Language:English
Published: Taylor & Francis Group 2021-04-01
Series:Immunological Medicine
Subjects:
Online Access:http://dx.doi.org/10.1080/25785826.2020.1797319
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author Shunya Nakane
Akihiro Mukaino
Eikichi Ihara
Yoshihiro Ogawa
author_facet Shunya Nakane
Akihiro Mukaino
Eikichi Ihara
Yoshihiro Ogawa
author_sort Shunya Nakane
collection DOAJ
description Autoimmune gastrointestinal dysmotility (AGID), an idiopathic or paraneoplastic phenomenon, is a clinical form of limited autoimmune dysautonomia. The symptoms of AGID and gastrointestinal manifestations in patients with autoimmune rheumatic diseases are overlapping. Antineuronal autoantibodies are often detected in patients with AGID. Autoantibodies play a key role in GI dysmotility; however, whether they cause neuronal destruction is unknown. Hence, the connection between the presence of these autoantibodies and the specific interference in synaptic transmission in the plexus ganglia of the enteric nervous system has to be determined. The treatment options for AGID are not well-defined. However, theoretically, immunomodulatory therapies have been shown to be effective and are therefore used as the first line of treatment. Nonetheless, diverse combined immunomodulatory therapies should be considered for intractable cases of AGID. We recommend comprehensive autoimmune evaluation and cancer screening for clinical diagnosis of AGID. Univocal diagnostic criteria, treatment protocols, and outcome definitions for AGID are required for prompt diagnosis and treatment and appropriate management of immunotherapy, which will circumvent the need for surgeries and improve patient outcome. In conclusion, AGID, a disease at the interface of clinical immunology and neurogastroenterology, requires further investigations and warrants cooperation among specialists, especially clinical immunologists, gastroenterologists, and neurologists.
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spelling doaj.art-498075200f74463f86480a0ac48552722022-12-21T18:56:22ZengTaylor & Francis GroupImmunological Medicine2578-58262021-04-01442748510.1080/25785826.2020.17973191797319Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterologyShunya Nakane0Akihiro Mukaino1Eikichi Ihara2Yoshihiro Ogawa3Department of Molecular Neurology and Therapeutics, Kumamoto University HospitalDepartment of Molecular Neurology and Therapeutics, Kumamoto University HospitalDepartment of Gastroenterology and Metabolism, Graduate School of Medical Sciences, Kyushu UniversityDepartment of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu UniversityAutoimmune gastrointestinal dysmotility (AGID), an idiopathic or paraneoplastic phenomenon, is a clinical form of limited autoimmune dysautonomia. The symptoms of AGID and gastrointestinal manifestations in patients with autoimmune rheumatic diseases are overlapping. Antineuronal autoantibodies are often detected in patients with AGID. Autoantibodies play a key role in GI dysmotility; however, whether they cause neuronal destruction is unknown. Hence, the connection between the presence of these autoantibodies and the specific interference in synaptic transmission in the plexus ganglia of the enteric nervous system has to be determined. The treatment options for AGID are not well-defined. However, theoretically, immunomodulatory therapies have been shown to be effective and are therefore used as the first line of treatment. Nonetheless, diverse combined immunomodulatory therapies should be considered for intractable cases of AGID. We recommend comprehensive autoimmune evaluation and cancer screening for clinical diagnosis of AGID. Univocal diagnostic criteria, treatment protocols, and outcome definitions for AGID are required for prompt diagnosis and treatment and appropriate management of immunotherapy, which will circumvent the need for surgeries and improve patient outcome. In conclusion, AGID, a disease at the interface of clinical immunology and neurogastroenterology, requires further investigations and warrants cooperation among specialists, especially clinical immunologists, gastroenterologists, and neurologists.http://dx.doi.org/10.1080/25785826.2020.1797319autoimmune gastrointestinal dysmotilityautoantibodyganglionic acetylcholine receptorautoimmune autonomic ganglionopathyautoimmune rheumatic diseases
spellingShingle Shunya Nakane
Akihiro Mukaino
Eikichi Ihara
Yoshihiro Ogawa
Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology
Immunological Medicine
autoimmune gastrointestinal dysmotility
autoantibody
ganglionic acetylcholine receptor
autoimmune autonomic ganglionopathy
autoimmune rheumatic diseases
title Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology
title_full Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology
title_fullStr Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology
title_full_unstemmed Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology
title_short Autoimmune gastrointestinal dysmotility: the interface between clinical immunology and neurogastroenterology
title_sort autoimmune gastrointestinal dysmotility the interface between clinical immunology and neurogastroenterology
topic autoimmune gastrointestinal dysmotility
autoantibody
ganglionic acetylcholine receptor
autoimmune autonomic ganglionopathy
autoimmune rheumatic diseases
url http://dx.doi.org/10.1080/25785826.2020.1797319
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