Early dexamethasone treatment exacerbates enterovirus 71 infection in mice

Fang-Hsiu Shen, Ting-Jing Shen, Tung-Miao Chang, Ih-Jen Su, Shun-Hua Chen

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

Enterovirus 71 (EV71) infection can induce encephalitis. Overt immune responses is suspected to cause severe symptoms, so anti-inflammatory agents, corticosteroids have been recommended for treatment. However, one clinical study reported that treatment with glucocorticoids, dexamethasone (Dex) exacerbates disease severity. Here we investigated Dex treatment on EV71 infection using the murine model and found that both long-term (14-day) and short-term (4-day) Dex treatment starting from 1 or 3 days postinfection increased the mortality and disease severity of infected mice. Dex treatment starting from 4 or 8 days postinfection did not affect mouse mortality and disease severity. Early Dex treatment starting from 1 day postinfection caused atrophy and enhanced apoptosis in lymphoid organs to decrease the numbers of lymphocytes (CD4(+) T cells, CD8(+) T cells, and CD19(+) B cells) and to increase viral loads in infected tissues of mice. Our results demonstrate that Dex treatment has no beneficial effect on EV71 infection.

Original languageEnglish
Pages (from-to)218-227
Number of pages10
JournalVirology
Volume464-465
DOIs
Publication statusPublished - Sept 2014
Externally publishedYes

Keywords

  • Animals
  • Anti-Inflammatory Agents/administration & dosage
  • Apoptosis/drug effects
  • B-Lymphocytes/immunology
  • CD4-Positive T-Lymphocytes/immunology
  • Dexamethasone/administration & dosage
  • Enterovirus A, Human/drug effects
  • Enterovirus Infections/drug therapy
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Viral Load

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