Adoptive cellular therapy for early cytomegalovirus infection after allogeneic stem-cell transplantation with virus-specific T-cell lines

被引:388
作者
Peggs, KS [1 ]
Verfuerth, S
Pizzey, A
Khan, N
Guiver, M
Moss, PA
Mackinnon, S
机构
[1] UCL Royal Free & UCL Med Sch, Dept Haematol, London WC1E 6HX, England
[2] Univ Birmingham, CR UK Inst Canc Studies, Birmingham, W Midlands, England
[3] Publ Hlth Lab Serv, Dept Virol, Manchester, Lancs, England
关键词
D O I
10.1016/S0140-6736(03)14634-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adoptive transfer of CMV-specific T cells offers the potential for reconstitution of viral immunity after allogeneic transplantation. However, the logistics of producing virus-specific T-cell clones has limited the application of cellular therapies. We treated 16 patients for CMV infection with polyclonal CMV-specific T-cell lines generated by short-term culture. Massive in-vivo expansions of CMV-specific cytotoxic T lymphocytes were observed, resulting in reconstitution of viral immunity. In eight cases antiviral drugs were not required, and subsequent episodes of reactivation occurred in only two patients. Our findings indicate that application of CMV-specific cell lines is both feasible and effective in a clinical environment.
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收藏
页码:1375 / 1377
页数:3
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