2022 Fiscal Year Final Research Report
Basic research for the development of a treatment for subacute sclerosing panencephalitis
Project/Area Number |
18K15721
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Research Category |
Grant-in-Aid for Early-Career Scientists
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Allocation Type | Multi-year Fund |
Review Section |
Basic Section 52050:Embryonic medicine and pediatrics-related
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Research Institution | Fukushima Medical University |
Principal Investigator |
Maeda Hajime 福島県立医科大学, 公私立大学の部局等, 助教 (90746059)
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Project Period (FY) |
2021-11-01 – 2023-03-31
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Keywords | 亜急性硬化性全脳炎 / 麻疹ウイルス / ファビピラビル |
Outline of Final Research Achievements |
Subacute sclerosing panencephalitis (SSPE) is a late-onset and intractable disease. Ribavirin is administered intracerebroventricularly to patients with SSPE. However, its therapeutic efficacy is insufficient. Favipiravir demonstrates anti-viral effects against RNA viruses. In this study, the antiviral effect of favipiravir against measles virus (Edmonston strain) and SSPE virus (Yamagata-1 strain) was examined in vitro. The 50% effective concentration (EC50) of favipiravir against Edmonston and Yamagata-1 strains were 108.7 uM and 38.6 uM, respectively, which were similar to those of ribavirin. The 50% cytotoxic concentration (CC50) of favipiravir against Edmonston and Yamagata-1 strains were >1,000 uM and >1,000 uM, respectively.
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Free Research Field |
Neonatology
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Academic Significance and Societal Importance of the Research Achievements |
亜急性硬化性全脳炎(SSPE)は、麻疹ウイルス変異株(SSPEウイルス)の持続感染による遅発性ウイルス感染症である。発展途上国では麻疹の流行が続いており、日本を含む先進国では散発的な麻疹の症例が報告されている。本研究は、in vitroにおいて、ファビピラビルは、麻疹ウイルスとSSPEウイルスにリバビリンと同等のウイルス増殖阻害効果を認め、高濃度においても細胞毒性がないことを確認した。本研究は、ファビピラビルが血液脳関門を通過し、脳脊髄液で十分な血中濃度を維持できるかという課題はあるが、ファビピラビルがSSPEの新規の治療薬になる可能性があり大変意義のある研究と考える。
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