It is the antigen(s), stupid and other lessons from over a decade of vaccitherapy of human cancer

被引:20
作者
Buckwalter, Matthew R. [1 ]
Srivastava, Pramod K. [1 ]
机构
[1] Univ Connecticut, Sch Med, Dept Immunol, Ctr Immunotherapy Canc & Infect Dis, Farmington, CT 06030 USA
关键词
Cancer vaccines; Personalized treatment; Heat shock proteins; Melanoma; Renal cell carcinoma; Unique antigens; Shared antigens;
D O I
10.1016/j.smim.2008.07.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The lessons are: (a) human cancers certainly respond to immunological manipulations. Efforts at human cancer immunotherapy are therefore worthwhile. (b) Prophylaxis is very different from therapy of preexisting disease, and hence much enthusiasm should not be derived from successful prophylaxis studies. Even in case of infectious agents against which robust prophylaxis is routinely achieved, therapy is nearly impossible once the disease has established. (c) Studies with appropriate cancer models of mice and rats are useful. The notion that it is easy to cure cancers in mice is generally advanced the most confidently by those who have never cured a mouse of cancer by immunotherapy. (d) With a nod to James Carville, it is the antigen(s), stupid! We still do not know the identity of protective tumor antigens. If any lesson can be drawn at all, it may well be that cancer immunotherapy must move away from the one-shoe-fits-all therapeutic models of chemotherapy and must move to individualized approaches. (e) All targets are equal, but some are more equal than others. The key is specificity for cancer. That does not necessarily mean specificity for cancer cells. (f) Vaccitherapy must be attempted preferably in the minimal residual disease setting, even though this is certain to be time-taking and expensive. In the setting of bulky disease, vaccitherapy must be combined with blockade of inhibitory signals, or depletion of down-regulatory T cells. Inhibition of effector level suppression of immune response is a key. Vaccitherapy alone or immunomodulation alone is unlikely to succeed in therapy of bulky metastatic disease. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:296 / 300
页数:5
相关论文
共 59 条
[1]   High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993 [J].
Atkins, MB ;
Lotze, MT ;
Dutcher, JP ;
Fisher, RI ;
Weiss, G ;
Margolin, K ;
Abrams, J ;
Sznol, M ;
Parkinson, D ;
Hawkins, M ;
Paradise, C ;
Kunkel, L ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (07) :2105-2116
[2]   High frequency of autologous anti-melanoma CTL directed against an antigen generated by a point mutation in a new helicase gene [J].
Baurain, JF ;
Colau, D ;
van Baren, N ;
Landry, C ;
Martelange, V ;
Vikkula, M ;
Boon, T ;
Coulie, PG .
JOURNAL OF IMMUNOLOGY, 2000, 164 (11) :6057-6066
[3]   Heat shock protein-chaperoned peptides but not free peptides introduced into the cytosol are presented efficiently by major histocompatibility complex I molecules [J].
Binder, RJ ;
Blachere, NE ;
Srivastava, PK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :17163-17171
[4]   Heat-shock protein 90 associates with N-terminal extended peptides and is required for direct and indirect antigen presentation [J].
Callahan, Margaret K. ;
Garg, Manish ;
Srivastava, Pramod K. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (05) :1662-1667
[5]   Genetically engineered mouse models of mammary intraepithelial neoplasia [J].
Cardiff, RD ;
Moghanaki, D ;
Jensen, RA .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2000, 5 (04) :421-437
[6]  
Chiari R, 1999, CANCER RES, V59, P5785
[7]   A MUTATED INTRON SEQUENCE CODES FOR AN ANTIGENIC PEPTIDE RECOGNIZED BY CYTOLYTIC T-LYMPHOCYTES ON A HUMAN-MELANOMA [J].
COULIE, PG ;
LEHMANN, F ;
LETHE, B ;
HERMAN, J ;
LURQUIN, C ;
ANDRAWISS, M ;
BOON, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7976-7980
[8]   The immunodominant antigen of an ultraviolet-induced regressor tumor is generated by a somatic point mutation in the DEAD box helicase p68 [J].
Dubey, P ;
Hendrickson, RC ;
Meredith, SC ;
Siegel, CT ;
Shabanowitz, J ;
Skipper, JCA ;
Engelhard, VH ;
Hunt, DF ;
Schreiber, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (04) :695-705
[9]  
Echchakir H, 2001, CANCER RES, V61, P4078
[10]   Bedside to bench and back again: how animal models are guiding the development of new immunotherapies for cancer [J].
Finkelstein, SE ;
Heimann, DM ;
Klebanoff, CA ;
Antony, PA ;
Gattinoni, L ;
Hinrichs, CS ;
Hwang, LN ;
Palmer, DC ;
Spiess, PJ ;
Surman, DR ;
Wrzesiniski, C ;
Yu, ZY ;
Rosenberg, SA ;
Restifo, NP .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 76 (02) :333-337