Multimer technologies for detection and adoptive transfer of antigen-specific T cells

被引:0
作者
Rosaely Casalegno-Garduño
Anita Schmitt
Junxia Yao
Xinchao Wang
Xun Xu
Mathias Freund
Michael Schmitt
机构
[1] University Clinic Rostock,Department of Internal Medicine III, Clinical Stem Cell Transplantation and Immunotherapy
[2] Huazhong University of Science and Technology,Center for Stem Cell Research and Application, Institute of Hematology, Union Hospital
[3] Zhongda Hospital,Department of Oncology and Hematology
[4] Southeast University,Department of Immunology
[5] Jiangsu University,undefined
来源
Cancer Immunology, Immunotherapy | 2010年 / 59卷
关键词
Tetramers; Streptamers; Flow cytometry; Adoptive T-cell transfer;
D O I
暂无
中图分类号
学科分类号
摘要
Identification and purification of antigen-specific T cells without altering their functional status are of high scientific and clinical interest. Staining with major histocompatibility complex (MHC)-peptide multimers constitutes a very powerful method to study antigen-specific T-cell subpopulations, allowing their direct visualization and quantification. MHC-peptide multimers, such as dimers, tetramers, pentamers, streptamers, dextramers and octamers have been used to evaluate the frequency of CD8+ T cells, specific for tumor/leukemia-associated antigens as well as for viral antigens, e.g., CMVpp65 and EBV-EBNA. Moreover, MHC-peptide multimers have been used for rapid and efficient ex vivo isolation and expansion of T cells. A recent development in the field of MHC-peptide multimers led to the purification of CD8+ T cells specific for leukemia antigens. This might help to select leukemia-specific donor lymphocyte infusions (DLIs), thus allowing dissection of the noxious graft-versus-host disease (GvHD) from beneficial anti-viral and even anti-leukemic effects. This review covers different types of MHC-peptide multimers and their applications, as well as the impact that multimers might have on further development of DLIs.
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页码:195 / 202
页数:7
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共 188 条
[1]  
Hebart H(2003)A CTL epitope from human cytomegalovirus IE1 defined by combining prediction of HLA binding and proteasomal immune responses in patients after allogeneic stem cell transplantation Exp Hematol 31 966-973
[2]  
Rauser G(2004)Immune evasion proteins of human cytomegalovirus do not prevent a diverse CD8 Blood 104 1075-1082
[3]  
Stevanovic S(2007) cytotoxic T-cell response in natural infection J Infect Dis 196 699-704
[4]  
Manley TJ(2008)Dendritic cell vaccination in allogeneic stem cell recipients: induction of human cytomegalovirus (HCMV)-specific cytotoxic T-lymphocyte responses even in patients receiving a transplant from an HCMV-seronegative donor Immunology 125 441-449
[5]  
Luy L(2007)A chromatic explosion: the development and future of multiparameter flow cytometry J Immunol Methods 320 30-39
[6]  
Jones T(2005)Tracking antigen-specific CD8 J Immunol 174 6266-6273
[7]  
Grigoleit GU(2005) T cells in the rat using MHC class I multimers Nat Immunol 6 593-599
[8]  
Kapp M(2002)Protective immunity to genital herpes simplex [correction of simpex] virus type 2 infection is mediated by T-bet Nat Med 8 631-637
[9]  
Hebart H(2006)Peptides chaperoned by heat-shock proteins are a necessary and sufficient source of antigen in the cross-priming of CD8 J Immunol Methods 310 136-148
[10]  
Chattopadhyay PK(2003) T cells J Biol Chem 278 4500-4509