The cysteine-rich region of respiratory syncytial virus attachment protein inhibits innate immunity elicited by the virus and endotoxin

被引:80
作者
Polack, FP [1 ]
Irusta, PM
Hoffman, SJ
Schiatti, MP
Melendi, GA
Delgado, MF
Laham, FR
Thumar, B
Hendry, RM
Melero, JA
Karron, RA
Collins, PL
Kleeberger, SR
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[4] INFANT Fdn, RA-1406 Buenos Aires, DF, Argentina
[5] Georgetown Univ, Dept Human Sci, Washington, DC 20057 USA
[6] Wyeth Lederle, Rochester, NY 14623 USA
[7] Inst Salud Carlos III, Madrid 28029, Spain
[8] NIAID, NIH, Bethesda, MD 20892 USA
[9] NIEHS, NIH, Res Triangle Pk, NC 27709 USA
关键词
glycoprotein; innate immunity; toll-like receptor 4;
D O I
10.1073/pnas.0409478102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The attachment protein (glycoprotein) of respiratory syncytial virus (RSV) has long been associated with disease potentiation and respiratory symptoms. The glycoprotein has a conserved cysteine-rich region (GCRR) whose function is unknown and which is not necessary for efficient viral replication. In this report, we show that the GCRR is a powerful inhibitor of the innate immune response against RSV, and that early secretion of glycoprotein is critical to modulate inflammation after RSV infection. Importantly, the GCRR is also a potent inhibitor of cytokine production mediated by several TLR agonists, indicating that this peptide sequence displays broad antiinflammatory properties. These findings have important implications for RSV pathogenesis and describe an inhibitor of TLR-mediated inflammatory responses that could have clinical applications.
引用
收藏
页码:8996 / 9001
页数:6
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