Recombinant Mycobacterium bovis BCG producing the N-terminal half of SIVmac251 Env antigen induces neutralizing antibodies and cytotoxic T lymphocyte responses in mice and guinea pigs

被引:34
作者
Lim, EM
Lagranderie, M
Le Grand, R
Rauzier, J
Gheorghiu, M
Gicquel, B
Winter, N
机构
[1] Inst Pasteur, Lab BCG, F-75015 Paris, France
[2] Inst Pasteur, Unite Genet Mycobacterienne, F-75015 Paris, France
[3] CEA, DSV, DPTE,Ctr Rech, Serv Sante Armees,Lab Neurovirol, F-92265 Fontenay Aux Roses, France
关键词
D O I
10.1089/aid.1997.13.1573
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recombinant Mycobacterium bovis bacillus Calmette-Guerin (rBCG) represents a good candidate for the development of vaccines against AIDS, Several HIV or SIV genes including nef, gag, and env have already been expressed by rBCG strains and shown to induce strong humoral and cellular immune responses in experimental animals, Because a broad immune response directed to multiple HIV/SIV antigens is highly desirable in order to develop effective vaccines, me have also investigated the immune response induced by an rBCG strain expressing a large N-terminal portion of the SIVmac251 Env gp110-encoding gene, The rBCG(SIVmac251Env) strain obtained was able to induce strong CTL responses in mice as well as humoral immune responses in mice and guinea pigs immunized by parenteral routes, The anti-gp110 IgGs produced mere able to neutralize in vitro growth of virulent SIVmac251 field isolates, Moreover, guinea pigs immunized by the oral route produced significant levels of anti-gp110 IgAs in the feces, demonstrating that rBCG is able to induce local humoral immunity in the intestinal mucosa. These data provide further evidence of the utility of BCG as a candidate vaccine vector against AIDS.
引用
收藏
页码:1573 / 1581
页数:9
相关论文
共 39 条
[1]   RECOMBINANT BCG EXPRESSING THE LEISHMANIA SURFACE-ANTIGEN GP63 INDUCES PROTECTIVE IMMUNITY AGAINST LEISHMANIA-MAJOR INFECTION IN BALB/C MICE [J].
ABDELHAK, S ;
LOUZIR, H ;
TIMM, J ;
BLEL, L ;
BENLASFAR, Z ;
LAGRANDERIE, M ;
GHEORGHIU, M ;
DELLAGI, K ;
GICQUEL, B .
MICROBIOLOGY-SGM, 1995, 141 :1585-1592
[2]   CHARACTERIZATION OF B-CELL EPITOPES IN THE ENVELOPE GLYCOPROTEINS OF SIMIAN IMMUNODEFICIENCY VIRUS [J].
BENICHOU, S ;
VENET, A ;
BEYER, C ;
TIOLLAIS, P ;
MADAULE, P .
VIROLOGY, 1993, 194 (02) :870-874
[3]  
BULLOCK WO, 1987, BIOTECHNIQUES, V5, P376
[4]   EFFECTIVE IMMUNIZATION AGAINST CUTANEOUS LEISHMANIASIS WITH RECOMBINANT BACILLE CALMETTE-GUERIN EXPRESSING THE LEISHMANIA SURFACE PROTEINASE GP63 [J].
CONNELL, ND ;
MEDINAACOSTA, E ;
MCMASTER, WR ;
BLOOM, BR ;
RUSSELL, DG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11473-11477
[5]   PROTECTIVE EFFECTS OF A LIVE ATTENUATED SIV VACCINE WITH A DELETION IN THE NEF GENE [J].
DANIEL, MD ;
KIRCHHOFF, F ;
CZAJAK, SC ;
SEHGAL, PK ;
DESROSIERS, RC .
SCIENCE, 1992, 258 (5090) :1938-1941
[6]  
Desrosiers R C, 1995, AIDS, V9 Suppl A, pS137
[7]   AN EPITOPE IN THE V1 DOMAIN OF THE SIMIAN IMMUNODEFICIENCY VIRUS (SIV) GP120 PROTEIN IS RECOGNIZED BY CD8+ CYTOTOXIC T-LYMPHOCYTES FROM AN SIV-INFECTED RHESUS MACAQUE [J].
ERICKSON, AL ;
WALKER, CM .
JOURNAL OF VIROLOGY, 1994, 68 (04) :2756-2759
[8]   GENETIC-CONTROL OF ANTIBODY-RESPONSES INDUCED AGAINST AN ANTIGEN DELIVERED BY RECOMBINANT ATTENUATED SALMONELLA-TYPHIMURIUM [J].
FAYOLLE, C ;
OCALLAGHAN, D ;
MARTINEAU, P ;
CHARBIT, A ;
CLEMENT, JM ;
HOFNUNG, M ;
LECLERC, C .
INFECTION AND IMMUNITY, 1994, 62 (10) :4310-4319
[9]   MYCOBACTERIAL DISEASES [J].
FINE, PEM ;
RODRIGUES, LC .
LANCET, 1990, 335 (8696) :1016-1020
[10]   EARLY SUPPRESSION OF SIV REPLICATION BY CD8+ NEF-SPECIFIC CYTOTOXIC T-CELLS IN VACCINATED MACAQUES [J].
GALLIMORE, A ;
CRANAGE, M ;
COOK, N ;
ALMOND, N ;
BOOTMAN, J ;
RUD, E ;
SILVERA, P ;
DENNIS, M ;
CORCORAN, T ;
STOTT, J ;
MCMICHAEL, A ;
GOTCH, F .
NATURE MEDICINE, 1995, 1 (11) :1167-1173