Viral antigen-specific CD8+ T-cell responses are impaired in multiple myeloma

被引:38
作者
Maecker, B
Anderson, KS
von Bergwelt-Baildon, MS
Weller, E
Vonderheide, RH
Richardson, PG
Schlossman, RL
Menezes, IA
Xia, ZN
Munshi, NC
Anderson, KC
Nadler, LM
Schultze, JL
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Biostat Sci, Boston, MA 02115 USA
关键词
T cells; multiple myeloma; tetramer;
D O I
10.1046/j.1365-2141.2003.04375.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is associated with defects of humoral and cellular immunity, however, little is known about the frequency and function of antigen-specific CD8(+) T cells. Such information might be critical for the development of immunotherapy for MM patients. As a model, we assessed the frequency and proliferation of CD8(+) T cells specific for HLA-A*0201-restricted immunodominant epitopes from influenza A (Inf A) and Epstein-Barr virus (EBV). Experiments in identical twins demonstrated reduced numbers of antigen-specific T cells after ex-vivo antigenic challenge in the MM twin when compared with the healthy twin. Similarly, the proliferation and frequency of EBV- and Inf A-specific T cells was also significantly reduced in a cohort of 24 previously untreated or conventionally treated MM patients when compared with 19 healthy individuals. In contrast, MM patients studied after receiving an autologous stem cell transplantation showed strikingly higher frequencies of EBV-specific T cells with potential to proliferate ex vivo , suggesting that EBV-specific T cells are readily expandable under these circumstances. These data identify an impaired response of CD8(+) T cells in MM patients, which might in part explain the relatively limited success of anti-MM immunisations. Prospective studies will determine whether such immune assessment strategies may identify patients more likely to benefit from cancer immunotherapy.
引用
收藏
页码:842 / 848
页数:7
相关论文
共 25 条
[1]  
Ancín I, 2000, HAEMATOLOGICA, V85, P773
[2]  
Anderson Kenneth C., 2000, Hematology Am Soc Hematol Educ Program, P147
[3]   Increased expression of non-functional killer inhibitory receptor CD94 in CD8+ cells of myeloma patients [J].
Besostri, B ;
Beggiato, E ;
Bianchi, A ;
Mariani, S ;
Coscia, M ;
Peola, S ;
Foglietta, M ;
Boccadoro, M ;
Pileri, A ;
Moretta, L ;
Massaia, M .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 109 (01) :46-53
[4]  
Bianchi A, 1997, BRIT J HAEMATOL, V97, P815
[5]   Presenting features and prognosis in 72 patients with multiple myeloma who were younger than 40 years [J].
Blade, J ;
Kyle, RA ;
Greipp, PR .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 (02) :345-351
[6]   Dendritic cells from patients with myeloma are numerically normal but functionally defective as they fail to up-regulate CD80 (B7-1) expression after huCD40LT stimulation because of inhibition by transforming growth factor-β1 and interleukin-10 [J].
Brown, RD ;
Pope, B ;
Murray, A ;
Esdale, W ;
Sze, DM ;
Gibson, J ;
Ho, PJ ;
Hart, D ;
Joshua, D .
BLOOD, 2001, 98 (10) :2992-2998
[7]   Transforming growth factor β from multiple myeloma cells inhibits proliferation and IL-2 responsiveness in T lymphocytes [J].
Cook, G ;
Campbell, JDM ;
Carr, CE ;
Boyd, KS ;
Franklin, IM .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (06) :981-988
[8]   Deregulated cytokine network and defective Th1 immune response in multiple myeloma [J].
Frassanito, MA ;
Cusmai, A ;
Dammacco, F .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 125 (02) :190-197
[9]   CYTOTOXIC LYMPHOCYTES-T RECOGNIZE A FRAGMENT OF INFLUENZA-VIRUS MATRIX PROTEIN IN ASSOCIATION WITH HLA-A2 [J].
GOTCH, F ;
ROTHBARD, J ;
HOWLAND, K ;
TOWNSEND, A ;
MCMICHAEL, A .
NATURE, 1987, 326 (6116) :881-881
[10]   Monitoring CD8 T cell responses to NY-ESO-1:: Correlation of humoral and cellular immune responses [J].
Jäger, E ;
Nagata, Y ;
Gnjatic, S ;
Wada, H ;
Stockert, E ;
Karbach, J ;
Dunbar, PR ;
Lee, SY ;
Jungbluth, A ;
Jäger, D ;
Arand, M ;
Ritter, C ;
Cerundolo, V ;
Dupont, B ;
Chen, YT ;
Old, LJ ;
Knuth, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (09) :4760-4765