Purification of cytomegalovirus-specific CD8 T cells from peripheral blood using HLA-peptide tetramers

被引:52
作者
Keenan, RD
Ainsworth, J
Khan, N
Bruton, R
Cobbold, M
Assenmacher, M
Milligan, DW
Moss, PAH
机构
[1] Univ Birmingham, Sch Med, CRC, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
[2] Birmingham Heartlands & Solihull NHS Trust, Birmingham, W Midlands, England
[3] Miltenyi Biotec, Bergisch Gladbach, Germany
关键词
tetramer; cytomegalovirus; magnetic selection; CD8 T cell; marrow transplant;
D O I
10.1046/j.1365-2141.2001.03106.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytomegalovirus (CMV) reactivation and disease remains an important clinical problem for patients after allogeneic stem cell transplantation. Impaired cellular immune control of viral replication is responsible for viral reactivation, and transfer of CMV-specific T cells from transplant donors can be effective in providing protection. Recent reports have indicated that the frequency of CMV-specific CD8(+) T cells in the peripheral blood of healthy donors is surprisingly high. Here we demonstrate that by using a combination of human leucocyte antigen (HLA) Class I-peptide tetramers and magnetic selection it is possible to select CMV-specific T cells from CMV antibody-positive individuals to high purity. Reliable purification of CMV-specific T cells up to 99.8% of CD8(+) cells was possible within hours. even when starting with a precursor frequency of <0.1% of peripheral blood CD8(+) T cells. CMV-specific T cells remained functional after the selection process. This novel form of antigen-specific T-cell selection should facilitate the selection of T cells for cellular immunotherapy to treat or prevent CMV disease after transplantation. In addition, this technique could potentially be applied to many antigens including against other infective agents and tumour-specific antigens.
引用
收藏
页码:428 / 434
页数:7
相关论文
共 14 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]   Initiation of signal transduction through the T cell receptor requires the peptide multivalent engagement of MHC ligands [J].
Boniface, JJ ;
Rabinowitz, JD ;
Wülfing, C ;
Hampl, J ;
Reich, Z ;
Altman, JD ;
Kantor, RM ;
Beeson, C ;
McConnell, HM ;
Davis, MM .
IMMUNITY, 1998, 9 (04) :459-466
[3]   Increased transplant-related morbidity and mortality in CMV-seropositive patients despite highly effective prevention of CMV disease after allogeneic T-cell-depleted stem cell transplantation [J].
Broers, AEC ;
van der Holt, R ;
van Esser, JWJ ;
Gratama, JW ;
Henzen-Logmans, S ;
Kuenen-Boumeester, V ;
Löwenberg, B ;
Cornelissen, JJ .
BLOOD, 2000, 95 (07) :2240-2245
[4]  
Couriel D, 1996, BONE MARROW TRANSPL, V18, P347
[5]   Cytomegalovirus seropositivity adversely influences outcome after T-depleted unrelated donor transplant in patients with chronic myeloid leukaemia: the case for tailored graft-versus-host disease prophylaxis [J].
Craddock, C ;
Szydlo, RM ;
Dazzi, F ;
Olavarria, E ;
Cwynarski, K ;
Yong, A ;
Brookes, P ;
de la Fuente, J ;
Kanfer, E ;
Apperley, JF ;
Goldman, JM .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 112 (01) :228-236
[6]   REVERSE ELISPOT ASSAY FOR CLONAL ANALYSIS OF CYTOKINE PRODUCTION .1. ENUMERATION OF GAMMA-INTERFERON-SECRETING CELLS [J].
CZERKINSKY, C ;
ANDERSSON, G ;
EKRE, HP ;
NILSSON, LA ;
KLARESKOG, L ;
OUCHTERLONY, O .
JOURNAL OF IMMUNOLOGICAL METHODS, 1988, 110 (01) :29-36
[7]   Functional heterogeneity and high frequencies of cytomegalovirus-specific CD8+ T lymphocytes in healthy seropositive donors [J].
Gillespie, GMA ;
Wills, MR ;
Appay, V ;
O'Callaghan, C ;
Murphy, M ;
Smith, N ;
Sissons, P ;
Rowland-Jones, S ;
Bell, JI ;
Moss, PAH .
JOURNAL OF VIROLOGY, 2000, 74 (17) :8140-8150
[8]   Cytomegalovirus disease in adult marrow transplant recipients receiving ganciclovir prophylaxis: a retrospective study [J].
Maltazou, H ;
Whimbey, E ;
Abi-Said, D ;
Przepiorka, D ;
Champlain, R ;
Goodrich, JM .
BONE MARROW TRANSPLANTATION, 1999, 24 (06) :665-669
[9]   CMV antigenemia following bone marrow transplantation: Risk factors and outcomes [J].
Osarogiagbon, RU ;
Defor, TE ;
Weisdorf, MA ;
Erice, A ;
Weisdorf, DJ .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2000, 6 (03) :280-288
[10]   Reconstitution of CD8 T cells is essential for the prevention of multiple-organ cytomegalovirus histopathology after bone marrow transplantation [J].
Podlech, J ;
Holtappels, R ;
Wirtz, N ;
Steffens, HP ;
Reddehase, MJ .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :2099-2104