ENHANCEMENT OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV)-SPECIFIC CD4+ AND CD8+ CYTOTOXIC LYMPHOCYTE-T ACTIVITIES IN HIV-INFECTED ASYMPTOMATIC PATIENTS GIVEN RECOMBINANT GP160 VACCINE

被引:53
作者
KUNDU, SK
KATZENSTEIN, D
MOSES, LE
MERIGAN, TC
机构
[1] STANFORD UNIV,CTR AIDS RES,AIDS CLIN TRIALS UNIT,STANFORD,CA 94305
[2] STANFORD UNIV,DIV BIOSTAT,STANFORD,CA 94305
关键词
AIDS; VACCINATION;
D O I
10.1073/pnas.89.23.11204
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
Twenty-six human immunodeficiency virus (HIV)-infected asymptomatic patients with CD4+ lymphocytes >400 per mm3 were randomly allocated to a range of doses of recombinant gp160 or a control (recombinant hepatitis B vaccine) on a double-blind basis. Each patient received an injection at 0, 4, 12, 24, 36, and 48 weeks. Treatment assignments were decoded when all patients reached 28 weeks of the study period. HIV-1-specific CD4+ and CD8+ cytotoxic T lymphocyte (CTL) activities were assessed in vitro before vaccination and 2 weeks after each injection. There were significant increases in major histocompatibility complex-restricted HIV-1 Env-specific CD4+ and CD8+ CTL activities in 18 of 21 gp160 vaccinees. No control-injected patients showed a significant change. Neither gp160 nor control recipients showed significant changes in HIV-1 Gag- and Pol-specific CTL activities. HIV-1 Env-specific CD4+ and CD8+ CTL precursor frequencies were also measured in three vaccinees before and at 24 weeks after vaccine was started. CTL precursor frequencies also increased in both CD4+ and CD8+ populations. This study shows that this gp160 vaccine is immunogenic in enhancing HIV-1 Env-specific cytotoxic T-cell-mediated immunity in HIV-seropositive individuals.
引用
收藏
页码:11204 / 11208
页数:5
相关论文
共 30 条
[1]  
ARVIN AM, 1991, J IMMUNOL, V146, P257
[2]   ANTIGENIC PEPTIDES RECOGNIZED BY LYMPHOCYTES-T FROM AIDS VIRAL ENVELOPE-IMMUNE HUMANS [J].
BERZOFSKY, JA ;
BENSUSSAN, A ;
CEASE, KB ;
BOURGE, JF ;
CHEYNIER, R ;
LURHUMA, Z ;
SALAUN, JJ ;
GALLO, RC ;
SHEARER, GM ;
ZAGURY, D .
NATURE, 1988, 334 (6184) :706-708
[3]   PROGRESS IN VACCINES AGAINST AIDS [J].
BOLOGNESI, DP .
SCIENCE, 1989, 246 (4935) :1233-1234
[4]   HIV IMMUNIZATION - FRESH PATHWAYS TO FOLLOW [J].
BOLOGNESI, DP .
NATURE, 1990, 344 (6269) :818-819
[5]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[6]   DETECTION OF 3 DISTINCT PATTERNS OF T-HELPER CELL DYSFUNCTION IN ASYMPTOMATIC, HUMAN IMMUNODEFICIENCY VIRUS-SEROPOSITIVE PATIENTS - INDEPENDENCE OF CD4+ CELL NUMBERS AND CLINICAL STAGING [J].
CLERICI, M ;
STOCKS, NI ;
ZAJAC, RA ;
BOSWELL, RN ;
LUCEY, DR ;
VIA, CS ;
SHEARER, GM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) :1892-1899
[7]  
CLERICI M, 1991, J IMMUNOL, V146, P2214
[8]  
CLERICI M, 1991, J ACQ IMMUN DEF SYND, V7, P154
[9]   THE SAFETY AND IMMUNOGENICITY OF A HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) RECOMBINANT GP160 CANDIDATE VACCINE IN HUMANS [J].
DOLIN, R ;
GRAHAM, BS ;
GREENBERG, SB ;
TACKET, CO ;
BELSHE, RB ;
MIDTHUN, K ;
CLEMENTS, ML ;
GORSE, GJ ;
HORGAN, BW ;
ATMAR, RL ;
KARZON, DT ;
BONNEZ, W ;
FERNIE, BF ;
MONTEFIORI, DC ;
STABLEIN, DM ;
SMITH, GE ;
KOFF, WC .
ANNALS OF INTERNAL MEDICINE, 1991, 114 (02) :119-127
[10]   ALTERED REACTIVITY TO MEASLES VIRUS - ATYPICAL MEASLES IN CHILDREN PREVIOUSLY IMMUNIZED WITH INACTIVATED MEASLES VIRUS VACCINES [J].
FULGINITI, VA ;
ELLER, JJ ;
DOWNIE, AW ;
KEMPE, CH .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1967, 202 (12) :1075-+