Update on the issues of HIV vaccine development

被引:7
作者
Haynes, BF
Putman, SB
Weinberg, JB
机构
关键词
AIDS; immunization; animal models; pathogenesis;
D O I
10.3109/07853899608999072
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Major scientific obstacles blocking the development of a successful preventive HIV vaccine are the extraordinary variability of HIV, the lack of an exact animal model of HIV-induced AIDS, and the lack of understanding of the correlates of positive immunity to HIV. Current HIV vaccines containing the HIV gp120 envelope have been tested in phase I and II trials but they have had a major limitation of neutralizing only T-cell tropic laboratory-adapted HIV strains grown in T-cell lines, but not neutralizing HIV primary isolates. Phase III trials of monovalent HIV gp120 envelope vaccines are being planned in the US and Thailand, but concern has been raised that recombinant monovalent gp120 may not be an appropriate immunogen for an efficious HIV vaccine. Because the immune response is probably responsible for controlling the viral load in some long-term suvivors of HIV infection, studies are now being carried out to induce similar immunity against a broad spectrum of strains of HIV primary isolates with targeted HIV experimental immunogens.
引用
收藏
页码:39 / 41
页数:3
相关论文
共 23 条
[1]  
[Anonymous], 1992, WHO TECH REP SER, P1
[2]   CELLULAR PROTEINS BOUND TO IMMUNODEFICIENCY VIRUSES - IMPLICATIONS FOR PATHOGENESIS AND VACCINES [J].
ARTHUR, LO ;
BESS, JW ;
SOWDER, RC ;
BENVENISTE, RE ;
MANN, DL ;
CHERMANN, JC ;
HENDERSON, LE .
SCIENCE, 1992, 258 (5090) :1935-1938
[3]   DEVELOPMENT OF ARTIFICIAL VACCINES AGAINST HIV USING DEFINED EPITOPES [J].
BERZOFSKY, JA .
FASEB JOURNAL, 1991, 5 (10) :2412-2418
[4]   HIV AND T-CELL EXPANSION IN SPLENIC WHITE PULPS IS ACCOMPANIED BY INFILTRATION OF HIV-SPECIFIC CYTOTOXIC T-LYMPHOCYTES [J].
CHEYNIER, R ;
HENRICHWARK, S ;
HADIDA, F ;
PELLETIER, E ;
OKSENHENDLER, E ;
AUTRAN, B ;
WAINHOBSON, S .
CELL, 1994, 78 (03) :373-387
[5]  
CIANCIOLO GJ, 1980, J IMMUNOL, V124, P2900
[6]   GENOMIC STRUCTURE OF AN ATTENUATED QUASI-SPECIES OF HIV-1 FROM A BLOOD-TRANSFUSION DONOR AND RECIPIENTS [J].
DEACON, NJ ;
TSYKIN, A ;
SOLOMON, A ;
SMITH, K ;
LUDFORDMENTING, M ;
HOOKER, DJ ;
MCPHEE, DA ;
GREENWAY, AL ;
ELLETT, A ;
CHATFIELD, C ;
LAWSON, VA ;
CROWE, S ;
MAERZ, A ;
SONZA, S ;
LEARMONT, J ;
SULLIVAN, JS ;
CUNNINGHAM, A ;
DWYER, D ;
DOWTON, D ;
MILLS, J .
SCIENCE, 1995, 270 (5238) :988-991
[7]   CD8+ T-LYMPHOCYTES OF AFRICAN-GREEN MONKEYS SECRETE AN IMMUNODEFICIENCY VIRUS-SUPPRESSING LYMPHOKINE [J].
ENNEN, J ;
FINDEKLEE, H ;
DITTMAR, MT ;
NORLEY, S ;
ERNST, M ;
KURTH, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7207-7211
[8]   CONVERSION OF AN IMMUNOGENIC HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) ENVELOPE SYNTHETIC PEPTIDE TO A TOLEROGEN IN CHIMPANZEES BY THE FUSOGENIC DOMAIN OF HIV GP41 ENVELOPE PROTEIN [J].
HAYNES, BF ;
ARTHUR, LO ;
FROST, P ;
MATTHEWS, TJ ;
LANGLOIS, AJ ;
PALKER, TJ ;
HART, MK ;
SCEARCE, RM ;
JONES, DM ;
MCDANAL, C ;
OTTINGER, J ;
BOLOGNESI, DP ;
WEINHOLD, KJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :717-727
[9]   SCIENTIFIC AND SOCIAL-ISSUES OF HUMAN-IMMUNODEFICIENCY-VIRUS VACCINE DEVELOPMENT [J].
HAYNES, BF .
SCIENCE, 1993, 260 (5112) :1279-1286
[10]  
HAYNES BF, IN PRESS SCIENCE