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Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
Published on: September 9, 2022
Infections, Vaccines and Autoimmunity: A Multiple Sclerosis Perspective
Dejan Jakimovski1, Bianca Weinstock-Guttman2, Murali Ramanathan3
1Buffalo Neuroimaging Analysis Center, Department of Neurology, University at Buffalo, State University of New York, Buffalo, NY 14203, USA.
Abstract:
Background: Multiple sclerosis (MS) is a chronic neuroinflammatory and neurodegenerative disease that is associated with multiple environmental factors. Among suspected susceptibility events, studies have questioned the potential role of overt viral and bacterial infections, including the Epstein Bar virus (EBV) and human endogenous retroviruses (HERV). Furthermore, the fast development of immunomodulatory therapies further questions the efficacy of the standard immunization policies in MS patients. Topics reviewed: This narrative review will discuss the potential interplay between viral and bacterial infections and their treatment on MS susceptibility and disease progression. In addition, the review specifically discusses the interactions between MS pathophysiology and vaccination for hepatitis B, influenza, human papillomavirus, diphtheria, pertussis, and tetanus (DTP), and Bacillus Calmette-Guerin (BCG). Data regarding potential interaction between MS disease modifying treatment (DMT) and vaccine effectiveness is also reviewed. Moreover, HERV-targeted therapies such as GNbAC1 (temelimab), EBV-based vaccines for treatment of MS, and the current state regarding the development of T-cell and DNA vaccination are discussed. Lastly, a reviewing commentary on the recent 2019 American Academy of Neurology (AAN) practice recommendations regarding immunization and vaccine-preventable infections in the settings of MS is provided. Conclusion: There is currently no sufficient evidence to support associations between standard vaccination policies and increased risk of MS. MS patients treated with immunomodulatory therapies may have a lower benefit from viral and bacterial vaccination. Despite their historical underperformance, new efforts in creating MS-based vaccines are currently ongoing. MS vaccination programs follow the set back and slow recovery which is widely seen in other fields of medicine.
Insights
Standard vaccinations do not increase multiple sclerosis (MS) risk. However, immunomodulatory therapies may reduce vaccine effectiveness in MS patients, prompting research into new MS-specific vaccines.
Area of Science:
- Neuroimmunology
- Infectious Disease Immunology
- Vaccinology
Background:
- Multiple sclerosis (MS) is a chronic neuroinflammatory and neurodegenerative disease influenced by environmental factors.
- Potential roles of Epstein-Barr virus (EBV) and human endogenous retroviruses (HERV) in MS susceptibility are investigated.
- The rise of immunomodulatory therapies raises questions about standard immunization efficacy in MS patients.
Purpose of the Study:
- To review the interplay between infections, treatments, and MS susceptibility/progression.
- To examine vaccine interactions (hepatitis B, influenza, HPV, DTP, BCG) with MS pathophysiology and disease-modifying treatments (DMTs).
- To discuss HERV-targeted therapies, EBV-based vaccines, and novel vaccination strategies for MS.
Main Methods:
- Narrative review of existing literature.
- Analysis of data on vaccine interactions with MS and DMTs.
- Review of current research on HERV-targeted therapies and novel vaccine development for MS.
Main Results:
- No sufficient evidence links standard vaccination policies to increased MS risk.
- Immunomodulatory therapies may diminish vaccine benefits in MS patients.
- New MS-specific vaccine development is ongoing, despite historical challenges.
Conclusions:
- Current vaccination policies are not associated with increased MS risk.
- MS patients on immunomodulatory treatments may experience reduced vaccine efficacy.
- Ongoing research aims to develop effective MS-specific vaccines, reflecting broader medical recovery trends.
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