The use of combination vaccinia vaccines and dual-gene vaccinia vaccines to enhance antigen-specific T-cell immunity via T-cell costimulation

被引:36
作者
Kalus, RM
Kantor, JA
Gritz, L
Yafal, AG
Mazzara, GP
Schlom, J [1 ]
Hodge, JW
机构
[1] NCI, Tumor Immunol & Biol Lab, NIH, Bethesda, MD 20892 USA
[2] NIH, Howard Hughes Med Inst, Res Scholars Program, Bethesda, MD 20892 USA
[3] Therion Biol Corp, Cambridge, MA 02142 USA
关键词
CEA; B7.1; vaccinia; combination vaccine; dual-gene vaccine; antitumor;
D O I
10.1016/S0264-410X(98)00275-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Several recombinant vaccinia viruses are currently being evaluated to induce antigen-specific immunity to a variety of infectious disease agents and tumor associated antigens. T-cell costimulation is extremely important in enhancing T-cell responses, and recombinant vaccines have now been shown to be effective vectors to express a range of these molecules. Both combination vaccines (an admixture of a recombinant vaccinia virus expressing a specific target antigen and a recombinant vaccinia virus expressing a costimulatory molecule) and dual-gene vaccines expressing both transgenes on the same vector have been shown capable of effectively enhancing antigen-specific responses via T-cell costimulation. In this report, we compare for the first time the use of both types of approaches to enhance antigen-specific T-cell responses, and we demonstrate the importance of route of vaccine administration and vaccine dose in attaining optimal T-cell responses. These studies should have direct bearing on the design of vaccine clinical trials for infectious agents and/or tumor associated antigens, in which T-cell costimulatory molecules will be employed to enhance antigen-specific T-cell responses via the use of either combination or dual-gene vaccinia vaccines. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:893 / 903
页数:11
相关论文
共 41 条
[11]  
FENNER F, 1988, SMALLPOX ITS ERRADIC, P1263
[12]   GENERATION OF HYBRID GENES AND PROTEINS BY VACCINIA VIRUS-MEDIATED RECOMBINATION - APPLICATION TO HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ENV [J].
GRITZ, L ;
DESTREE, A ;
CORMIER, N ;
DAY, E ;
STALLARD, V ;
CAIAZZO, T ;
MAZZARA, G ;
PANICALI, D .
JOURNAL OF VIROLOGY, 1990, 64 (12) :5948-5957
[13]  
HAMILTON JM, 1994, ASCO P, V961
[14]   CD28-B7 INTERACTIONS ALLOW THE INDUCTION OF CD8+ CYTOTOXIC T-LYMPHOCYTES IN THE ABSENCE OF EXOGENOUS HELP [J].
HARDING, FA ;
ALLISON, JP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (06) :1791-1796
[15]   Retrovirus-mediated gene transfer of B7-1 and MHC class II converts a poorly immunogenic neuroblastoma into a highly immunogenic one [J].
Heuer, JG ;
TuckerMcClung, C ;
Gonin, R ;
Hock, RA .
HUMAN GENE THERAPY, 1996, 7 (17) :2059-2068
[16]   Carcinoembryonic antigen as a target for cancer vaccines [J].
Hodge, JW .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1996, 43 (03) :127-134
[17]   Diversified prime and boost protocols using recombinant vaccinia virus and recombinant non-replicating avian pox virus to enhance T-cell immunity and antitumor responses [J].
Hodge, JW ;
McLaughlin, JP ;
Kantor, JA ;
Schlom, J .
VACCINE, 1997, 15 (6-7) :759-768
[18]  
HODGE JW, 1994, CANCER RES, V54, P5552
[19]   A RECOMBINANT VACCINIA VIRUS EXPRESSING HUMAN PROSTATE-SPECIFIC ANTIGEN (PSA) - SAFETY AND IMMUNOGENICITY IN A NONHUMAN PRIMATE [J].
HODGE, JW ;
SCHLOM, J ;
DONOHUE, SJ ;
TOMASZEWSKI, JE ;
WHEELER, CW ;
LEVINE, BS ;
GRITZ, L ;
PANICALI, D ;
KANTOR, JA .
INTERNATIONAL JOURNAL OF CANCER, 1995, 63 (02) :231-237
[20]  
HODGE JW, 1995, CANCER RES, V55, P3598