Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system

Patients with advanced malignancies treated with immune checkpoint inhibitors are at increased risk for developing immune-related neurological complications. It is a phenomenon of immunological twist when immunotherapy against co-stimulatory molecules activates previously normal T cells to kill tumo...

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Main Author: Marinos C. Dalakas
Format: Article
Language:English
Published: SAGE Publishing 2018-09-01
Series:Therapeutic Advances in Neurological Disorders
Online Access:https://doi.org/10.1177/1756286418799864
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spelling doaj-18e04ebdae464b6985410bad60e3e5262020-11-25T03:33:53ZengSAGE PublishingTherapeutic Advances in Neurological Disorders1756-28642018-09-011110.1177/1756286418799864Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune systemMarinos C. DalakasPatients with advanced malignancies treated with immune checkpoint inhibitors are at increased risk for developing immune-related neurological complications. It is a phenomenon of immunological twist when immunotherapy against co-stimulatory molecules activates previously normal T cells to kill tumor cells but, in so doing, the T cells become unrestrained, triggering other autoimmune diseases for which conventional immunotherapy is needed. The most common autoimmune neurological diseases, usually occurring within 2–12 weeks after immune checkpoint inhibitor initiation, include: inflammatory myopathies, myasthenia gravis, acute and chronic demyelinating polyradiculoneuropathies, vasculitic neuropathies, isolated cranial neuropathies, aseptic meningitis, autoimmune encephalitis, multiple sclerosis and hypophysitis. The neurological events can evolve rapidly, necessitating the need for vigilance at all stages of treatment, even after completion, because early immunotherapeutic interventions are effective. The review addresses these complications and the applied therapies, discusses immune pathomechanisms including triggering preexisting autoimmunity, highlights the distinction between paraneoplastic and autoimmune etiologies, and identifies uncertainties regarding risk factors, use of immune checkpoint inhibitors in patients with known immune diseases or restarting therapy after a neurological event. Although the autoimmune neurological complications are not very common, their incidence will likely increase as the use of immune checkpoint inhibitors in metastatic cancer is growing rapidly.https://doi.org/10.1177/1756286418799864
collection DOAJ
language English
format Article
sources DOAJ
author Marinos C. Dalakas
spellingShingle Marinos C. Dalakas
Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
Therapeutic Advances in Neurological Disorders
author_facet Marinos C. Dalakas
author_sort Marinos C. Dalakas
title Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
title_short Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
title_full Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
title_fullStr Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
title_full_unstemmed Neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
title_sort neurological complications of immune checkpoint inhibitors: what happens when you ‘take the brakes off’ the immune system
publisher SAGE Publishing
series Therapeutic Advances in Neurological Disorders
issn 1756-2864
publishDate 2018-09-01
description Patients with advanced malignancies treated with immune checkpoint inhibitors are at increased risk for developing immune-related neurological complications. It is a phenomenon of immunological twist when immunotherapy against co-stimulatory molecules activates previously normal T cells to kill tumor cells but, in so doing, the T cells become unrestrained, triggering other autoimmune diseases for which conventional immunotherapy is needed. The most common autoimmune neurological diseases, usually occurring within 2–12 weeks after immune checkpoint inhibitor initiation, include: inflammatory myopathies, myasthenia gravis, acute and chronic demyelinating polyradiculoneuropathies, vasculitic neuropathies, isolated cranial neuropathies, aseptic meningitis, autoimmune encephalitis, multiple sclerosis and hypophysitis. The neurological events can evolve rapidly, necessitating the need for vigilance at all stages of treatment, even after completion, because early immunotherapeutic interventions are effective. The review addresses these complications and the applied therapies, discusses immune pathomechanisms including triggering preexisting autoimmunity, highlights the distinction between paraneoplastic and autoimmune etiologies, and identifies uncertainties regarding risk factors, use of immune checkpoint inhibitors in patients with known immune diseases or restarting therapy after a neurological event. Although the autoimmune neurological complications are not very common, their incidence will likely increase as the use of immune checkpoint inhibitors in metastatic cancer is growing rapidly.
url https://doi.org/10.1177/1756286418799864
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