Induced sensitization of tumor stroma leads to eradication of established cancer by T cells

被引:310
作者
Zhang, Bin
Bowerman, Natalie A.
Salama, Joseph K.
Schmidt, Hank
Spiotto, Michael T.
Schietinger, Andrea
Yu, Ping
Fu, Yang-Xin
Weichselbaum, Ralph R.
Rowley, Donald A.
Kranz, David M.
Schreiber, Hans
机构
[1] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
[4] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
关键词
D O I
10.1084/jem.20062056
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Targeting cancer cells, as well as the nonmalignant stromal cells cross-presenting the tumor antigen (Ag), can lead to the complete destruction of well-established solid tumors by adoptively transferred Ag-specific cytotoxic T lymphocytes (CTLs). If, however, cancer cells express only low levels of the Ag, then stromal cells are not destroyed, and the tumor escapes as Ag loss variants. We show that treating well-established tumors expressing low levels of Ag with local irradiation or a chemotherapeutic drug causes sufficient release of Ag to sensitize stromal cells for destruction by CTLs. This was shown directly using high affinity T cell receptor tetramers for visualizing the transient appearance of tumor-specific peptide-MHC complexes on stromal cells. Maximum loading of tumor stroma with cancer Ag occurred 2 d after treatment and coincided with the optimal time for T cell transfer. Under these conditions, tumor rejection was complete. These findings may set the stage for developing rational clinical protocols for combining irradiation or chemotherapy with CTL therapy.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 29 条
[1]   The role of tumor stroma in the interaction between tumor and immune system [J].
Blankenstein, T .
CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (02) :180-186
[2]   Caspase-dependent immunogenicity of doxorubicin-induced tumor cell death [J].
Casares, N ;
Pequignot, MO ;
Tesniere, A ;
Ghiringhelli, F ;
Roux, S ;
Chaput, N ;
Schmitt, E ;
Hamai, A ;
Hervas-Stubbs, S ;
Obeid, M ;
Coutant, F ;
Métivier, D ;
Pichard, E ;
Aucouturier, P ;
Pierron, G ;
Garrido, C ;
Zitvogel, L ;
Kroemer, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (12) :1691-1701
[3]   Ionizing radiation enhances immunogenicity of cells expressing a tumor-specific T-cell epitope [J].
Ciernik, IF ;
Romero, P ;
Berzofsky, JA ;
Carbone, DP .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1999, 45 (03) :735-741
[4]   Combining radiotherapy and immunotherapy: A revived partnership [J].
Demaria, S ;
Bhardwaj, N ;
McBride, WH ;
Formenti, SC .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 63 (03) :655-666
[5]  
DVORAK HF, 1986, NEW ENGL J MED, V315, P1650
[6]  
Ganss R, 2002, CANCER RES, V62, P1462
[7]   Kinetics and thermodynamics of T cell receptor-autoantigen interactions in murine experimental autoimmune encephalomyelitis [J].
Garcia, KC ;
Radu, CG ;
Ho, J ;
Ober, RJ ;
Ward, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6818-6823
[8]   Adoptive immunotherapy for cancer: building on success [J].
Gattinoni, L ;
Powell, DJ ;
Rosenberg, SA ;
Restifo, NP .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (05) :383-393
[9]   Coupling and cross-presentation [J].
Heath, WR ;
Carbone, FR .
NATURE, 2005, 434 (7029) :27-28
[10]   Quantitative analysis of the contribution of TCR/pepMHC affinity and CD8 to T cell activation [J].
Holler, PD ;
Kranz, DM .
IMMUNITY, 2003, 18 (02) :255-264