Expanding our understanding of Guillain–Barré syndrome: Recent advances and clinical implications
Guillain–Barré syndrome (GBS) is a rare yet potentially life‐threatening disorder of the peripheral nervous system (PNS), characterized by substantial clinical heterogeneity. Although classified as an autoimmune disease, the immune mechanisms underpinning distinct GBS subtypes remain largely elusive...
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| Published in: | European journal of immunology Vol. 54; no. 11; pp. e2250336 - n/a |
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| Main Authors: | , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Germany
Wiley Subscription Services, Inc
01.11.2024
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| Subjects: | |
| ISSN: | 0014-2980, 1521-4141, 1521-4141 |
| Online Access: | Get full text |
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| Summary: | Guillain–Barré syndrome (GBS) is a rare yet potentially life‐threatening disorder of the peripheral nervous system (PNS), characterized by substantial clinical heterogeneity. Although classified as an autoimmune disease, the immune mechanisms underpinning distinct GBS subtypes remain largely elusive. Traditionally considered primarily antibody‐mediated, the pathophysiology of GBS lacks clarity, posing challenges in the development of targeted and effective treatments. Nevertheless, recent investigations have substantially expanded our understanding of the disease, revealing an involvement of autoreactive T cell immunity in a major subtype of GBS patients and opening new biomedical perspectives. This review highlights these discoveries and offers a comprehensive overview of current knowledge about GBS, including ongoing challenges in disease management.
Guillain–Barré syndrome (GBS) is a rare and heterogeneous disorder of the peripheral nervous system. Traditionally considered antibody‐mediated, recent research highlights the involvement of autoreactive T cells in its immunopathology. This review examines recent discoveries and provides a comprehensive overview of current knowledge, challenges in disease management, and new biomedical perspectives. |
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| Bibliography: | Paolo Ripellino and Bettina Schreiner are contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
| ISSN: | 0014-2980 1521-4141 1521-4141 |
| DOI: | 10.1002/eji.202250336 |