Determining virological, serological and immunological parameters of EBV infection in the development of PTLD

被引:29
作者
Davis, JE [1 ]
Sherritt, MA
Bharadwaj, M
Morrison, LE
Elliott, SL
Kear, LM
Maddicks-Law, J
Kotsimbos, T
Gill, D
Malouf, M
Falk, MC
Khanna, R
Moss, DJ
机构
[1] Queensland Inst Med Res, Div Infect Dis & Immunol, EBV Biol Lab, Brisbane, Qld 4029, Australia
[2] Queensland Inst Med Res, Cooperat Res Ctr Vaccine Technol, Brisbane, Qld 4029, Australia
[3] Univ Queensland, Joint Oncol Program, Brisbane, Qld 4029, Australia
[4] Alfred Hosp, Melbourne, Vic, Australia
[5] Princess Alexandra Hosp, Brisbane, Qld 4102, Australia
[6] St Vincents Hosp, Sydney, NSW 2010, Australia
[7] Canberra Hosp, Canberra, ACT, Australia
基金
美国国家卫生研究院;
关键词
CTL response; Epstein-Barr virus; post-transplant lymphoproliferative disease; serology;
D O I
10.1093/intimm/dxh099
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Post-transplant lymphoproliferative disease (PTLD) in Epstein-Barr virus (EBV) seronegative solid organ transplant recipients remains a significant problem, particularly in the first year post-transplant. Immune monitoring of a cohort of high-risk patients indicated that four EBV seronegative transplant recipients developed early-onset PTLD prior to evidence of an EBV humoral response. EBV status has been classically defined serologically, however these patients demonstrated multiple parameters of EBV infection, including the generation of EBV-specific CTL, outgrowth of spontaneous lymphoblastoid cell lines, and elevated EBV DNA levels, despite the absence of a classic EBV antibody response. As EBV serology is influenced by both immunosuppression and cytomegalovirus immunoglobulin treatment, both the EBV-specific CTL response and elevated EBV levels are more reliable indicators of EBV infection post-transplant.
引用
收藏
页码:983 / 989
页数:7
相关论文
共 19 条
[11]   Infusion of cytotoxic T cells for the prevention and treatment of Epstein-Barr virus-induced lymphoma in allogeneic transplant recipients [J].
Rooney, CM ;
Smith, CA ;
Ng, CYC ;
Loftin, SK ;
Sixbey, JW ;
Gan, YJ ;
Srivastava, DK ;
Bowman, LC ;
Krance, RA ;
Brenner, MK ;
Heslop, HE .
BLOOD, 1998, 92 (05) :1549-1555
[12]  
SALVOLDO B, 2002, J IMMUNOL, V168, P909
[13]  
SAVOIE A, 1994, BLOOD, V83, P2715
[14]   Reconstitution of the latent T-lymphocyte response to Epstein-Barr virus is coincident with long-term recovery from posttransplant lymphoma after adoptive immunotherapy [J].
Sherritt, MA ;
Bharadwaj, M ;
Burrows, JM ;
Morrison, LE ;
Elliott, SL ;
Davis, JE ;
Kear, LM ;
Slaughter, RE ;
Bell, SC ;
Galbraith, AJ ;
Khanna, R ;
Moss, DJ .
TRANSPLANTATION, 2003, 75 (09) :1556-1560
[15]   Characteristics of Epstein-Barr virus primary infection in pediatric liver transplant recipients [J].
Smets, F ;
Bodeus, M ;
Goubau, P ;
Reding, R ;
Otte, JB ;
Buts, JP ;
Sokal, EM .
JOURNAL OF HEPATOLOGY, 2000, 32 (01) :100-104
[16]   Ratio between Epstein-Barr viral load and anti-Epstein-Barr virus specific T-cell response as a predictive marker of posttransplant lymphoproliferative disease [J].
Smets, F ;
Latinne, D ;
Bazin, H ;
Reding, R ;
Otte, JB ;
Buts, JP ;
Sokal, EM .
TRANSPLANTATION, 2002, 73 (10) :1603-1610
[17]   Suppression of the humoral immune response by mycophenolate mofetil [J].
Smith, KGC ;
Isbel, NM ;
Catton, MG ;
Leydon, JA ;
Becker, GJ ;
Walker, RG .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1998, 13 (01) :160-164
[18]   Frequent monitoring of Epstein-Barr virus DNA load in unfractionated whole blood is essential for early detection of posttransplant lymphoproliferative disease in high-risk patients [J].
Stevens, SJC ;
Verschuuren, EAM ;
Pronk, I ;
van der Bij, W ;
Harmsen, MC ;
The, TH ;
Meijer, CJLM ;
van den Brule, AJC ;
Middeldorp, JM .
BLOOD, 2001, 97 (05) :1165-1171
[19]   Quantitative Epstein-Barr virus (EBV) serology in lung transplant recipients with primary EBV infection and/or post-transplant lymphoproliferative disease [J].
Verschuuren, E ;
van der Bij, W ;
de Boer, W ;
Timens, W ;
Middeldorp, J ;
The, TH .
JOURNAL OF MEDICAL VIROLOGY, 2003, 69 (02) :258-266