Protection from cytomegalovirus after transplantation is correlated with immediate early 1-specific CD8 T cells

被引:308
作者
Bunde, T
Kirchner, A
Hoffmeister, B
Habedank, D
Hetzer, R
Cherepnev, G
Proesch, S
Reinke, P
Volk, HD
Lehmkuhl, H
Kern, F
机构
[1] Univ Med Berlin, Charite, Inst Med Immunol, D-10098 Berlin, Germany
[2] Univ Med Berlin, Charite, Inst Virol, D-10098 Berlin, Germany
[3] Deutsches Herzzentrum, D-13353 Berlin, Germany
[4] Charite, Med Klin Schwerpunkt Nephrol & Internist Intensiv, D-13353 Berlin, Germany
关键词
D O I
10.1084/jem.20042384
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cells are crucial for the control of cytomegalovirus (CMV) in infected individuals. Although CMV-specific T cells can be quantified by various methods, clear correlates of protection from CMV disease have not been defined. However, responses to the pp65 protein are believed to play an important role. Here, the proportions of interferon gamma-producing T cells following ex vivo activation with pools of overlapping peptides representing the pp65 and immediate early (IE)-1 proteins were determined at multiple time points and related to the development of CMV disease in 27 heart and lung transplant recipients. Frequencies of IE-1-specific CD8 T cells above 0.2 and 0.4% at day 0 and 2 wk, respectively, or 0.4% at any time during the first months discriminated patients who did not develop CMV disease from patients at risk, 50-60% of whom developed CMV disease. No similar distinction between risk groups was possible based on pp65-specific CD8 or CD4 T cell responses. Remarkably, CMV disease developed exclusively in patients with a dominant pp65-specific CD8 T cell response. In conclusion, high frequencies of IE-1 but not pp65-specific CD8 T cells correlate with protection from CMV disease. These results have important implications for monitoring T cell responses, adoptive cell therapy, and vaccine design.
引用
收藏
页码:1031 / 1036
页数:6
相关论文
共 28 条
[1]   HUMAN CYTOMEGALOVIRUS-SPECIFIC CYTO-TOXIC T-CELLS - RELATIVE FREQUENCY OF STAGE-SPECIFIC CTL RECOGNIZING THE 72-KD IMMEDIATE EARLY PROTEIN AND GLYCOPROTEIN-B EXPRESSED BY RECOMBINANT VACCINIA VIRUSES [J].
BORYSIEWICZ, LK ;
HICKLING, JK ;
GRAHAM, S ;
SINCLAIR, J ;
CRANAGE, MP ;
SMITH, GL ;
SISSONS, JGP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :919-931
[2]  
Brunner E, 2002, Nonparametric Analysis of Longitudinal Data in Factorial Experiments
[3]   Infection in organ-transplant recipients [J].
Fishman, JA ;
Rubin, RH .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (24) :1741-1751
[4]   Cytomegalovirus selectively blocks antigen processing and presentation of its immediate-early gene product [J].
Gilbert, MJ ;
Riddell, SR ;
Plachter, B ;
Greenberg, PD .
NATURE, 1996, 383 (6602) :720-722
[5]   SELECTIVE INTERFERENCE WITH CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX PRESENTATION OF THE MAJOR IMMEDIATE-EARLY PROTEIN FOLLOWING INFECTION WITH HUMAN CYTOMEGALOVIRUS [J].
GILBERT, MJ ;
RIDDELL, SR ;
LI, CR ;
GREENBERG, PD .
JOURNAL OF VIROLOGY, 1993, 67 (06) :3461-3469
[6]   Tetramer-based quantification of cytomegalovirus (CMV)-specific CD8+ T lymphocytes in T-cell-depleted stem cell grafts and after transplantation may identify patients at risk for progressive CMV infection [J].
Gratama, JW ;
van Esser, JWJ ;
Lamers, CHJ ;
Toumay, C ;
Löwenberg, B ;
Bolhuis, RLH ;
Cornelissen, JJ .
BLOOD, 2001, 98 (05) :1358-1364
[7]   Flow cytometric enumeration of antigen-specific T lymphocytes [J].
Gratama, JW ;
Kern, F .
CYTOMETRY PART A, 2004, 58A (01) :79-86
[8]   Principles and practical application of the receiver-operating characteristic analysis for diagnostic tests [J].
Greiner, M ;
Pfeiffer, D ;
Smith, RD .
PREVENTIVE VETERINARY MEDICINE, 2000, 45 (1-2) :23-41
[9]   Evaluation of CMV viral load using Taqman™ CMV quantitative PCR and comparison with CMV antigenemia in heart and lung transplant recipients [J].
Guiver, M ;
Fox, AJ ;
Mutton, K ;
Mogulkoc, N ;
Egan, J .
TRANSPLANTATION, 2001, 71 (11) :1609-1615
[10]   Sensitive detection of human cytomegalovirus peptide-specific cytotoxic T-lymphocyte responses by interferon-γ-enzyme-linked immunospot assay and flow cytometry in healthy individuals and in patients after allogeneic stem cell transplantation [J].
Hebart, H ;
Daginik, S ;
Stevanovic, S ;
Grigoleit, U ;
Dobler, A ;
Baur, M ;
Rauser, G ;
Sinzger, C ;
Jahn, G ;
Loeffler, J ;
Kanz, L ;
Rammensee, HG ;
Einsele, H .
BLOOD, 2002, 99 (10) :3830-3837