Herpesvirus infection leads to the rapid induction of an innate immune response. A central aspect of this host response is the production and secretion of type I interferon. The current model of virus-mediated interferon production includes three stages: sensitization, induction, and amplification. A key mediator of all three stages is the cellular transcription factor interferon regulatory factor 3 (IRF3). Although the precise details of IRF3 activation and interferon production in response to herpesvirus infection are still being elucidated, viral proteins that block components of the interferon pathway, particularly IRF3, have been identified and characterized. In vivo studies have shown that in addition to type I interferon, interleukin-15 (IL-15) and natural killer (NK) cells also play an important role in mediating resistance to herpesvirus infection. Recent investigations have demonstrated a strong association between IRF3, interferon, IL-15, and NK cells. This review will focus on herpesvirus-mediated induction of innate immunity, the central role of the type I interferon response and mechanisms used by herpesviruses to block host antiviral immunity.
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Soochow Univ, Dept Emergency & Crit Care, Affiliated Hosp 2, Suzhou, Jiangsu, Peoples R China
Univ Oklahoma, Hlth Sci Ctr, Dept Med, Pulm & Crit Care Div, Oklahoma City, OK USASoochow Univ, Dept Emergency & Crit Care, Affiliated Hosp 2, Suzhou, Jiangsu, Peoples R China
Wu, Shuhua
Metcalf, Jordan P.
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Univ Oklahoma, Hlth Sci Ctr, Dept Med, Pulm & Crit Care Div, Oklahoma City, OK USA
Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73190 USASoochow Univ, Dept Emergency & Crit Care, Affiliated Hosp 2, Suzhou, Jiangsu, Peoples R China
Metcalf, Jordan P.
Wu, Wenxin
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Univ Oklahoma, Hlth Sci Ctr, Dept Med, Pulm & Crit Care Div, Oklahoma City, OK USASoochow Univ, Dept Emergency & Crit Care, Affiliated Hosp 2, Suzhou, Jiangsu, Peoples R China
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US Army Med Res Inst Infect Dis, Dept Immunol, Div Mol & Translat Sci, Frederick, MD USAUS Army Med Res Inst Infect Dis, Dept Immunol, Div Mol & Translat Sci, Frederick, MD USA
Saikh, Kamal U.
Mott, Tiffany M.
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US Army Med Res Inst Infect Dis, Dept Immunol, Div Mol & Translat Sci, Frederick, MD USAUS Army Med Res Inst Infect Dis, Dept Immunol, Div Mol & Translat Sci, Frederick, MD USA
机构:Univ Sao Paulo, Fac Pharmaceut Sci, Dept Clin & Toxicol Anal, Lab Immunoendocrinol, BR-05508900 Sao Paulo, Brazil
Sunahara, Karen K. S.
Sannomiya, Paulina
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Univ Sao Paulo, Sch Med, Inst Heart InCor, LIM 11, BR-05508900 Sao Paulo, BrazilUniv Sao Paulo, Fac Pharmaceut Sci, Dept Clin & Toxicol Anal, Lab Immunoendocrinol, BR-05508900 Sao Paulo, Brazil
Sannomiya, Paulina
Martins, Joilson O.
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Univ Sao Paulo, Fac Pharmaceut Sci, Dept Clin & Toxicol Anal, Lab Immunoendocrinol, BR-05508900 Sao Paulo, BrazilUniv Sao Paulo, Fac Pharmaceut Sci, Dept Clin & Toxicol Anal, Lab Immunoendocrinol, BR-05508900 Sao Paulo, Brazil