Benign and malignant Epstein-Barr virus-associated B-cell lymphoproliferative diseases

被引:35
作者
Cohen, JI [1 ]
机构
[1] NIAID, Med Virol Sect, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0037-1963(03)70003-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most Epstein-Barr virus (EBV) infections in infants and children are asymptomatic, while infection of adolescents or adults often results in infectious mononucleosis. The symptoms of infectious mononucleosis are primarily due to the T-cell proliferative response to EBV-infected B cells; thus, antiviral therapy does not affect the clinical course of disease. Failure of the cellular immune response to control EBV-induced B-cell proliferation can result in severe disease. Patients with the X-linked lymphoproliferative disease (XLPD) have a mutation in the SAP gene and EBV infection often leads to fatal infectious mononucleosis. Transplant recipients may develop lymphoproliferative disease, which often responds to treatment that enhances the immune response against EBV-infected B cells. About 50% of Hodgkin's and 20% of Burkitt's lymphomas in the United States contain EBV DNA. While chemotherapy and/or radiation therapy are mainstays of treatment, clinical trials are being developed using cytotoxic T cells directed against EBV proteins in these tumors.
引用
收藏
页码:116 / 123
页数:8
相关论文
共 74 条
[1]  
Andersson J, 1996, SCAND J INFECT DIS, P72
[2]   EPSTEIN-BARR VIRUS IN THE BONE-MARROW OF PATIENTS WITH APLASTIC-ANEMIA [J].
BARANSKI, B ;
ARMSTRONG, G ;
TRUMAN, JT ;
QUINNAN, GV ;
STRAUS, SE ;
YOUNG, NS .
ANNALS OF INTERNAL MEDICINE, 1988, 109 (09) :695-704
[3]   GNTB-A, a novel SH2D1A-associated surface molecule contributing to the inability of natural killer cells to kill Epstein-Barr-virus-infected B cells in X-linked lymphoproliferative disease [J].
Bottino, C ;
Falco, M ;
Parolini, S ;
Marcenaro, E ;
Augugliaro, R ;
Sivori, S ;
Landi, E ;
Biassoni, R ;
Notarangelo, LD ;
Moretta, L ;
Moretta, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (03) :235-246
[4]   Direct visualization of antigen-specific CD8+ T cells during the primary immune response to Epstein-Barr virus in vivo [J].
Callan, MFC ;
Tan, L ;
Annels, N ;
Ogg, GS ;
Wilson, JDK ;
O'Callaghan, CA ;
Steven, N ;
McMichael, AJ ;
Rickinson, AB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (09) :1395-1402
[5]   Large clonal expansions of CD8(+) T cells in acute infectious mononucleosis [J].
Callan, MFC ;
Steven, J ;
Krausa, P ;
Wilson, JDK ;
Moss, PAH ;
Gillespie, GM ;
Bell, JI ;
Rickinson, AB ;
McMichael, AJ .
NATURE MEDICINE, 1996, 2 (08) :906-911
[6]   Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene [J].
Coffey, AJ ;
Brooksbank, RA ;
Brandau, O ;
Oohashi, T ;
Howell, GR ;
Bye, JM ;
Cahn, AP ;
Durham, J ;
Heath, P ;
Wray, P ;
Pavitt, R ;
Wilkinson, J ;
Leversha, M ;
Huckle, E ;
Shaw-Smith, CJ ;
Dunham, A ;
Rhodes, S ;
Schuster, V ;
Porta, G ;
Yin, L ;
Serafini, P ;
Sylla, B ;
Zollo, M ;
Franco, B ;
Bolino, A ;
Seri, M ;
Lanyi, A ;
Davis, JR ;
Webster, D ;
Harris, A ;
Lenoir, G ;
St Basile, GD ;
Jones, A ;
Behloradsky, BH ;
Achatz, H ;
Murken, J ;
Fassler, R ;
Sumegi, J ;
Romeo, G ;
Vaudin, M ;
Ross, MT ;
Meindl, A ;
Bentley, DR .
NATURE GENETICS, 1998, 20 (02) :129-135
[7]   Epstein-Barr virus infection. [J].
Cohen, JI .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (07) :481-492
[8]   EPSTEIN-BARR-VIRUS LYMPHOPROLIFERATIVE DISEASE ASSOCIATED WITH ACQUIRED IMMUNODEFICIENCY [J].
COHEN, JI .
MEDICINE, 1991, 70 (02) :137-160
[9]  
COHEN JI, 2001, HARRISONS PRINCIPLES, P1109
[10]   Infusion of autologous Epstein-Barr virus (EBV) -: specific cytotoxic T cells for prevention of EBV-related lymphoproliferative disorder in solid organ transplant recipients with evidence of active virus replication [J].
Comoli, P ;
Labirio, M ;
Basso, S ;
Baldanti, F ;
Grossi, P ;
Furione, M ;
Viganò, M ;
Fiocchi, R ;
Rossi, G ;
Ginevri, F ;
Gridelli, B ;
Moretta, A ;
Montagna, D ;
Locatelli, F ;
Gerna, G ;
Comoli, P .
BLOOD, 2002, 99 (07) :2592-2598