The LMP2a signalosome - A therapeutic target for Epstein-Barr virus latency and associated disease

被引:22
作者
Portis, T [1 ]
Cooper, L [1 ]
Dennis, P [1 ]
Longnecker, R [1 ]
机构
[1] Northwestern Univ, Sch Med, Dept Microbiol & Immunol, Chicago, IL 60611 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2002年 / 7卷
关键词
Epstein-Barr virus; latent membrane protein 2A; LMP2A; antiviral therapuetics; latency; viral oncogenesis; review;
D O I
10.2741/portis
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most adults are infected with Epstein-Barr virus (EBV), a virus that establishes a lifelong latent infection in B lymphocytes and is associated with a variety of cancers. In normal individuals, latent infection with EBV typically poses no health risk, but upon immunosuppression, either following organ transplantation or HIV infection, malignancies and lymphoproliferative diseases can result. We have utilized both transgenic mice and EBV transformed lymphoblastoid cell lines (LCLs) as models of EBV latent infection to explore the function of latent membrane protein 2A (LMP2A) of EBV. This has allowed us to identify important functional domains of LMP2A, essential host proteins necessary for LMP2A function, and the effect of LMP2A on normal B cell function. These studies have provided a more complete understanding of the role of LMP2A in EBV latency and tumorigenesis and may allow for the identification of novel therapeutics for the treatment or eradication of EBV latent infections and associated proliferative disorders.
引用
收藏
页码:D414 / D426
页数:13
相关论文
共 109 条
[1]   Epstein-Barr virus associated lymphoproliferations in the AIDS setting [J].
Ambinder, RF .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (10) :1209-1216
[2]   Tonsillar memory B cells, latently infected with Epstein-Barr virus, express the restricted pattern of latent genes previously found only in Epstein-Barr virus-associated tumors [J].
Babcock, GJ ;
Thorley-Lawson, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :12250-12255
[3]   The expression pattern of Epstein-Barr virus latent genes in vivo is dependent upon the differentiation stage of the infected B cell [J].
Babcock, GJ ;
Hochberg, D ;
Thorley-Lawson, DA .
IMMUNITY, 2000, 13 (04) :497-506
[4]   EBV persistence in memory B cells in vivo [J].
Babcock, GJ ;
Decker, LL ;
Volk, M ;
Thorley-Lawson, DA .
IMMUNITY, 1998, 9 (03) :395-404
[5]  
Berger C, 1999, INT J CANCER, V81, P371, DOI 10.1002/(SICI)1097-0215(19990505)81:3<371::AID-IJC10>3.0.CO
[6]  
2-D
[7]   Hodgkin and Reed-Sternberg cells in lymphocyte predominant Hodgkin disease, represent clonal populations of germinal center-derived tumor B cells [J].
Braeuninger, A ;
Kuppers, R ;
Strickler, JG ;
Wacker, HH ;
Rajewsky, K ;
Hansmann, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9337-9342
[8]   AN EPSTEIN-BARR-VIRUS TRANSFORMATION-ASSOCIATED MEMBRANE-PROTEIN INTERACTS WITH SRC FAMILY TYROSINE KINASES [J].
BURKHARDT, AL ;
BOLEN, JB ;
KIEFF, E ;
LONGNECKER, R .
JOURNAL OF VIROLOGY, 1992, 66 (08) :5161-5167
[9]   CHILDRENS CANCER DEPENDENT ON CLIMATIC FACTORS [J].
BURKITT, D .
NATURE, 1962, 194 (4825) :232-&
[10]  
BURKITT DP, 1983, CANCER, V51, P1777, DOI 10.1002/1097-0142(19830515)51:10<1777::AID-CNCR2820511003>3.0.CO