Functional cooperation between T helper cell determinants

被引:81
作者
Gerloni, M
Xiong, SD
Mukerjee, S
Schoenberger, SP
Croft, M
Zanetti, M [1 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Ctr Canc, La Jolla, CA 92093 USA
[3] La Jolla Allergy & Immunol, Div Immuneregulat, San Diego, CA 92121 USA
[4] La Jolla Allergy & Immunol, Div Immunochem, San Diego, CA 92121 USA
关键词
D O I
10.1073/pnas.230429197
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The immune response to T helper (Th) cell determinants of a variety of antigens is often poor and limits severely the potential efficacy of current therapeutic measures through vaccination. Here, we report: that an immunologically silent tumor determinant can be rendered immunogenic if linked with a dominant determinant of a parasite antigen, suggesting the existence of functional Th-Th cooperation in vivo. This phenomenon could be mimicked in part by signaling either through CD40 to the antigen-presenting cells or through OX40 to the tumor-determinant reactive T cells, with maximal effects obtained by combined anti-CD40 and anti-OX40 treatment in vivo. The data suggest that CD4 T cells reactive with a dominant determinant provide help to other CD4 T cells through up-regulating the costimulatory ability of antigen-presenting cells, in much the same way as help for CD8 cells. CD4 help for CD4 T cells represents a new immunological principle and offers new practical solutions for vaccine therapy against cancer and other diseases in which antigenic help is limiting.
引用
收藏
页码:13269 / 13274
页数:6
相关论文
共 39 条
[1]   OX40 is differentially expressed on activated rat and mouse T cells and is the sole receptor for the OX40 ligand [J].
AlShamkhani, A ;
Birkeland, ML ;
Puklavec, M ;
Brown, MH ;
James, W ;
Barclay, AN .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (08) :1695-1699
[2]   LINKED RECOGNITION OF HELPER AND CYTO-TOXIC ANTIGENIC DETERMINANTS FOR THE GENERATION OF CYTO-TOXIC LYMPHOCYTES-T [J].
CASSELL, D ;
FORMAN, J .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 532 :51-60
[3]   Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation [J].
Cella, M ;
Scheidegger, D ;
PalmerLehmann, K ;
Lane, P ;
Lanzavecchia, A ;
Alber, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :747-752
[4]   Accessory molecule and costimulation requirements for CD4 T cell response [J].
Croft, M ;
Dubey, C .
CRITICAL REVIEWS IN IMMUNOLOGY, 1997, 17 (01) :89-118
[5]   MUC-1 EPITHELIAL TUMOR MUCIN-BASED IMMUNITY AND CANCER VACCINES [J].
FINN, OJ ;
JEROME, KR ;
HENDERSON, RA ;
PECHER, G ;
DOMENECH, N ;
MAGARIANBLANDER, J ;
BARRATTBOYES, SM .
IMMUNOLOGICAL REVIEWS, 1995, 145 :61-89
[6]   EPITHELIAL MUCIN GENES [J].
GENDLER, SJ ;
SPICER, AP .
ANNUAL REVIEW OF PHYSIOLOGY, 1995, 57 :607-634
[7]  
Gerloni M, 1999, J IMMUNOL, V162, P3782
[8]   Somatic transgene immunization with DNA encoding an immunoglobulin heavy chain [J].
Gerloni, M ;
Billetta, R ;
Xiong, SD ;
Zanetti, M .
DNA AND CELL BIOLOGY, 1997, 16 (05) :611-625
[9]   Immunity to Plasmodium falciparum malaria sporozoites by somatic transgene immunization [J].
Gerloni, M ;
Ballou, WR ;
Billetta, R ;
Zanetti, M .
NATURE BIOTECHNOLOGY, 1997, 15 (09) :876-881
[10]  
GRAHAM RA, 1996, TUMOR IMMUNOLOGY IMM, P269