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Updated: May 25, 2026

High-throughput Quantitative Real-time RT-PCR Assay for Determining Expression Profiles of Types I and III Interferon Subtypes
Published on: March 24, 2015
Interferon beta for secondary progressive multiple sclerosis
Loredana La Mantia1, Laura Vacchi, Carlo Di Pietrantonj
1Unit of Neurology - Multiple Sclerosis Center, I.R.C.C.S. Santa Maria Nascente FondazioneDon Gnocchi, Via Capecelatro 66, Milano, 20148, Italy. lamantialore@gmail.com.
Interferon (IFN) beta treatments do not prevent disability progression in Secondary Progressive Multiple Sclerosis (SPMS). However, IFNs significantly reduce relapses and short-term disability, showing an anti-inflammatory effect without halting established disease progression.
Area of Science:
- Neurology
- Immunology
- Clinical Trials
Background:
- Recombinant interferons (IFNs) beta-1a and beta-1b are approved for Relapsing Remitting Multiple Sclerosis (RRMS).
- A key question is whether IFNs can slow or reverse the progressive phase of MS.
- This review focuses on the efficacy of IFNs in Secondary Progressive Multiple Sclerosis (SPMS).
Purpose of the Study:
- To determine if interferon (IFN) beta treatment is more effective than placebo in reducing disability progression in SPMS patients.
- To analyze the impact of IFNs on relapse rates and MRI-defined disease activity in SPMS.
Main Methods:
- Systematic review of randomized, placebo-controlled trials (RCTs) of IFNs versus placebo in SPMS.
- Searches included Cochrane MS Trials Register, reference lists, and regulatory agencies.
- Data extraction and risk of bias assessment were performed independently by two reviewers.
Main Results:
- Five RCTs involving 3122 patients (1829 IFN, 1293 placebo) were analyzed.
- IFN beta did not reduce the risk of sustained disability progression at 6 months over three years.
- A significant reduction in 3-month sustained progression and new relapses at three years was observed.
- MRI data suggested a decrease in active brain lesions, despite no effect on clinical progression.
- The safety profile of IFNs was consistent with known side effects in MS patients.
Conclusions:
- Recombinant IFN beta does not prevent the development of permanent physical disability in SPMS.
- IFN treatment significantly reduces the risk of relapses and short-term disability.
- The anti-inflammatory effects of IFNs do not halt established disease progression in SPMS.
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