CMV-specific T cell therapy

被引:56
作者
Einsele, Hennann [1 ]
Kapp, Markus [1 ]
Grigoleit, Goetz Ulrich [1 ]
机构
[1] Univ Wurzburg, Med Klin & Poliklin 2, D-97080 Wurzburg, Germany
关键词
D O I
10.1016/j.bcmd.2007.07.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human cytomegalovirus (CMV) infection continues to be one of the most important and life threatening complications after allogencic stem cell transplantation (SCT). The reconstitution of CMV-specific T cell responses after SCT has been demonstrated to be protective against the development of CMV disease. To improve T cell immunity against CMV in bone marrow transplant patients, different strategies were explored. On one hand, CMV-specific T cells can be selected from the donor, and can be transferred to the patient without any further in vitro expansion. On the other hand, CMV-specific T cells can be activated and expanded in vitro by stimulation with antigen presenting cells (APCs) loaded with specific proteins or peptides. Here, we review the therapeutic application of CMV-specific T cells to fight CMV infection. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:71 / 75
页数:5
相关论文
共 26 条
[1]   Phenotypic analysis of antigen-specific T lymphocytes [J].
Altman, JD ;
Moss, PAH ;
Goulder, PJR ;
Barouch, DH ;
McHeyzerWilliams, MG ;
Bell, JI ;
McMichael, AJ ;
Davis, MM .
SCIENCE, 1996, 274 (5284) :94-96
[2]   Successful modification of a pp65 antigenemia-based early treatment strategy for prevention of cytomegalovirus disease in allogeneic marrow transplant recipients [J].
Boeckh, M ;
Bowden, RA ;
Gooley, T ;
Myerson, D ;
Corey, L .
BLOOD, 1999, 93 (05) :1781-1782
[3]   Adoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA-peptide tetramers [J].
Cobbold, M ;
Khan, N ;
Pourgheysari, B ;
Tauro, S ;
McDonald, D ;
Osman, H ;
Assenmacher, M ;
Billingham, L ;
Steward, C ;
Crawley, C ;
Olavarria, E ;
Goldman, J ;
Chakraverty, R ;
Mahendra, P ;
Craddock, C ;
Moss, PAH .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (03) :379-386
[4]  
EINSELE H, 1995, BLOOD, V86, P2815
[5]   Infusion of cytomegalovirus (CMV)-specific T cells for the treatment of CMV infection not responding to antiviral chemotherapy [J].
Einsele, H ;
Roosnek, E ;
Rufer, N ;
Sinzger, C ;
Riegler, S ;
Löffler, J ;
Grigoleit, U ;
Moris, A ;
Rammensee, HG ;
Kanz, L ;
Kleihauer, A ;
Frank, F ;
Jahn, G ;
Hebart, H .
BLOOD, 2002, 99 (11) :3916-3922
[6]   Risk factors for treatment failures in patients receiving PCR-based preemptive therapy for CMV infection [J].
Einsele, H ;
Hebart, H ;
Kauffman-Schneider, C ;
Sinzger, C ;
Jahn, G ;
Bader, P ;
Klingebiel, T ;
Dietz, K ;
Löffler, J ;
Bokemeyer, C ;
Müller, CA ;
Kanz, L .
BONE MARROW TRANSPLANTATION, 2000, 25 (07) :757-763
[7]   Purification of cytomegalovirus-specific CD8 T cells from peripheral blood using HLA-peptide tetramers [J].
Keenan, RD ;
Ainsworth, J ;
Khan, N ;
Bruton, R ;
Cobbold, M ;
Assenmacher, M ;
Milligan, DW ;
Moss, PAH .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 115 (02) :428-434
[8]   Cytomegalovirus (CMV) phosphoprotein 65 makes a large contribution to shaping the T cell repertoire in CMV-exposed individuals [J].
Kern, F ;
Bunde, T ;
Faulhaber, N ;
Kiecker, F ;
Khatamzas, E ;
Rudawski, IM ;
Pruss, A ;
Gratama, JW ;
Volkmer-Engert, R ;
Ewert, R ;
Reinke, P ;
Volk, HD ;
Picker, LJ .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (12) :1709-1716
[9]   Ex vivo generation of human cytomegalovirus-specific cytotoxic T cells by peptide-pulsed dendritic cells [J].
Kleihauer, A ;
Grigoleit, U ;
Hebart, H ;
Moris, A ;
Brossart, P ;
Muhm, A ;
Stevanovic, S ;
Rammensee, HG ;
Sinzger, C ;
Riegler, S ;
Jahn, G ;
Kanz, L ;
Einsele, H .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (01) :231-239
[10]   Reversible MHC multimer staining for functional isolation of T-cell populations and effective adoptive transfer [J].
Knabel, M ;
Franz, TJ ;
Schiemann, M ;
Wulf, A ;
Villmow, B ;
Schmidt, B ;
Bernhard, H ;
Wagner, H ;
Busch, DH .
NATURE MEDICINE, 2002, 8 (06) :631-636