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Updated: May 24, 2025
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Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
Therapeutic advances in multiple sclerosis: Novel therapies (immune checkpoint inhibitors, CAR-T, Anti-CD40L)
Sarah E Conway1, Kristin Galetta2
1Brigham and Women's Hospital, Boston, MA, USA.
Abstract:
As patients with multiple sclerosis (MS) age, the risk of cancer also increases. Immune checkpoint inhibitors (ICIs) are novel monoclonal antibodies that have revolutionized cancer treatment. However, their use is limited by immune related adverse events. In patients with MS and pre-existing autoimmune disease there is concern that use of ICIs could worsen disease outcome. In the first part of this review we discuss the current data on ICIs and MS which overall suggest that they are well tolerated from the standpoint of MS disease activity. We recommend that MS not be a strict contraindication to ICI use which should depend on an individualized risk benefit discussion. In the second part, we focus on novel therapies for MS including CAR-T cell and anti-CD40L treatments. These newer therapies have the potential to address an unmet need in MS as they can cross the blood-brain and have the potential to target compartmentalized central nervous inflammation that may underly the pathophysiology of progressive MS.
Insights
Immune checkpoint inhibitors (ICIs) show promise for cancer patients with multiple sclerosis (MS), with current data suggesting good tolerability for MS disease activity. Novel MS therapies like CAR-T cells offer new hope for targeting central nervous system inflammation.
Area of Science:
- Neuroimmunology
- Oncology
- Immunotherapy
Background:
- Aging patients with multiple sclerosis (MS) face increased cancer risk.
- Immune checkpoint inhibitors (ICIs) are effective cancer treatments but carry risks of immune-related adverse events.
- Concerns exist regarding ICI use in MS patients due to potential exacerbation of autoimmune disease.
Purpose of the Study:
- To review the safety and efficacy of ICIs in patients with MS.
- To explore novel therapeutic strategies for MS, including CAR-T cell and anti-CD40L treatments.
- To assess the potential of new therapies to target central nervous system inflammation in progressive MS.
Main Methods:
- Review of current clinical data on ICI use in MS patients.
- Discussion of immune-related adverse events associated with ICIs.
- Exploration of emerging MS therapies and their mechanisms of action.
Main Results:
- Current data suggest ICIs are generally well-tolerated in MS patients regarding MS disease activity.
- MS should not be an absolute contraindication for ICI use; individualized risk-benefit assessment is recommended.
- Novel therapies like CAR-T cells and anti-CD40L can cross the blood-brain barrier.
Conclusions:
- ICI use in MS patients appears safe from an MS disease activity perspective, warranting personalized risk-benefit evaluations.
- Emerging therapies hold significant potential for treating progressive MS by targeting localized neuroinflammation.
- New treatments may address unmet needs in managing the pathophysiology of progressive MS.
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