Complementary role of CD4+T cells and secondary lymphoid tissues for cross-presentation of tumor antigen to CD8+T cells

被引:62
作者
Yu, P [1 ]
Spiotto, MT [1 ]
Lee, YJ [1 ]
Schreiber, H [1 ]
Fu, YX [1 ]
机构
[1] Univ Chicago, Dept Pathol, Comm Immunol, Chicago, IL 60637 USA
关键词
CTL; antigen presentation; cellular proliferation; lymphotoxin a; cell trafficking;
D O I
10.1084/jem.20021804
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MHC class I-restricted tumor antigens can be presented to CD8(+) T cells by two distinct pathways: via direct and indirect presentation. The relative contribution of these two pathways toward the initial activation of tumor antigen-specific CD8(+) T cells and their subsequent tumor rejection is still vigorously debated. Using a tumor model able to dissect the relative contributions of direct and indirect presentation, we show unequivocally the inefficiency of direct presentation and the essential requirement of indirect presentation for the priming of naive tumor antigen-specific T cells leading to tumor rejection. Moreover, we characterize the essential environment under which indirect presentation occurs, and find efficient cross-priming of tumor-specific CD8(+) T cells in the complete absence of secondary lymphoid tissues. The independence of this process from local lymph nodes is compromised, however, in the absence of CD4(+) T cell help. Therefore, our paper demonstrates that effective immune protection against tumors requires the cross-priming of CD8(+) T cells under conditions that require either CD4(+) T cell help, or draining lymph nodes.
引用
收藏
页码:985 / 995
页数:11
相关论文
共 34 条
[21]   Essential role of lymph nodes in contact hypersensitivity revealed in lymphotoxin-α-deficient mice [J].
Rennert, PD ;
Hochman, PS ;
Flavell, RA ;
Chaplin, DD ;
Jayaraman, S ;
Browning, JL ;
Fu, YX .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (11) :1227-1238
[22]   A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell [J].
Ridge, JP ;
Di Rosa, F ;
Matzinger, P .
NATURE, 1998, 393 (6684) :474-478
[23]   A metrical result on the discrepancy of (nα) [J].
Schoissengeier, J .
GLASGOW MATHEMATICAL JOURNAL, 1998, 40 :393-425
[24]   A TUMOR ESCAPE VARIANT THAT HAS LOST ONE MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I RESTRICTION ELEMENT INDUCES SPECIFIC CD8+ T-CELLS TO AN ANTIGEN THAT NO LONGER SERVES AS A TARGET [J].
SEUNG, S ;
URBAN, JL ;
SCHREIBER, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (03) :933-940
[25]   POSITIVE AND NEGATIVE SELECTION OF AN ANTIGEN RECEPTOR ON T-CELLS IN TRANSGENIC MICE [J].
SHA, WC ;
NELSON, CA ;
NEWBERRY, RD ;
KRANZ, DM ;
RUSSELL, JH ;
LOH, DY .
NATURE, 1988, 336 (6194) :73-76
[26]   RESPONSIVENESS TO HY ANTIGEN IR GENE COMPLEMENTATION AND TARGET-CELL SPECIFICITY [J].
SIMPSON, E ;
GORDON, RD .
IMMUNOLOGICAL REVIEWS, 1977, 35 :59-75
[27]   Increasing tumor antigen expression overcomes "ignorance" to solid tumors via crosspresentation by bone marrow-derived stromal cells [J].
Spiotto, MT ;
Yu, P ;
Rowley, DA ;
Nishimura, MI ;
Meredith, SC ;
Gajewski, TF ;
Fu, YX ;
Schreiber, H .
IMMUNITY, 2002, 17 (06) :737-747
[28]   The sequence alteration associated with a mutational hotspot in p53 protects cells from lysis by cytotoxic T lymphocytes specific for a flanking peptide epitope [J].
Theobald, M ;
Ruppert, T ;
Kuckelkorn, U ;
Hernandez, J ;
Häussler, A ;
Ferreira, EA ;
Liewer, U ;
Biggs, J ;
Levine, AJ ;
Huber, C ;
Koszinowski, UH ;
Kloetzel, PM ;
Sherman, LA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (06) :1017-1028
[29]   CD40-CD40Ligand interactions and their role in cytotoxic T lymphocyte priming and anti-tumor immunity [J].
Toes, REM ;
Schoenberger, SP ;
van der Voort, EIH ;
Offringa, R ;
Melief, CJM .
SEMINARS IN IMMUNOLOGY, 1998, 10 (06) :443-448
[30]   Induction of bystander T cell proliferation by viruses and type I interferon in vivo [J].
Tough, DF ;
Borrow, P ;
Sprent, J .
SCIENCE, 1996, 272 (5270) :1947-1950