Lymphoproliferative responses to recombinant HIV-1 envelope antigens in neonates and infants receiving gp120 vaccines

被引:41
作者
Borkowsky, W
Wara, D
Fenton, T
McNamara, J
Kang, MH
Mofenson, L
McFarland, E
Cunningham, C
Duliege, AM
Francis, D
Bryson, Y
Burchett, S
Spector, SA
Frenkel, LM
Starr, S
Van Dyke, R
Jimenez, E
机构
[1] NYU, Saul Krugman Div Infect Dis & Immun, Sch Med, Dept Pediat, New York, NY 10016 USA
[2] SUNY, Dept Pediat, Syracuse, NY USA
[3] Univ Calif San Francisco, Sch Med, Dept Pediat, San Francisco, CA 94143 USA
[4] Chiron Corp, San Francisco, CA USA
[5] VaxGen Corp, San Francisco, CA USA
[6] Univ Calif San Diego, Sch Med, Dept Pediat, San Diego, CA 92103 USA
[7] Univ Calif Los Angeles, Sch Med, Dept Pediat, Los Angeles, CA 90024 USA
[8] Harvard Univ, Sch Publ Hlth, Cambridge, MA 02138 USA
[9] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[10] NIAID, NIH, Bethesda, MD 20892 USA
[11] NICHHD, NIH, Bethesda, MD 20892 USA
[12] Univ Colorado, Hlth Sci Ctr, Dept Pediat, Denver, CO 80262 USA
[13] Childrens Hosp & Med Ctr, Seattle, WA 98105 USA
[14] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[15] Tulane Univ, Sch Med, Dept Pediat, New Orleans, LA 70112 USA
[16] San Juan City Hosp, Dept Pediat, San Juan, PR USA
关键词
D O I
10.1086/315298
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Children of mothers infected with human immunodeficiency virus type 1 (HIV-1) were immunized at birth and at 1, 3, and 5 months with 1 of 3 doses of recombinant gp 120 vaccines prepared from SF-2 or MN strains of HIV-1. A total of 126 children were not infected; 21 received adjuvant only. Vaccine recipients developed lymphoproliferative responses on greater than or equal to 2 occasions, responding more often to homologous HIV-1 antigens than did adjuvant recipients (56% vs. 14%; P < .001). Responses were appreciated after 2 immunizations and were maintained for >84 weeks after the last immunization, hn accelerated immunization schedule(birth, 2 weeks, 2 months, and 5 months) with the lowest dose of the SF-2 vaccine produced responses in all 11 vaccinees by 4 weeks. Responses to heterologous envelope antigens were also detected. Immune responses to vaccination are achievable at an age when some infection (perinatal or breast milk exposure related) may be prevented.
引用
收藏
页码:890 / 896
页数:7
相关论文
共 17 条
[1]  
ASANO Y, 1977, PEDIATRICS, V59, P3
[2]  
BEASLEY RP, 1983, LANCET, V2, P1099
[3]  
BOMFORD R, 1980, CLIN EXP IMMUNOL, V39, P435
[4]  
BOMFORD R, 1980, CLIN EXP IMMUNOL, V39, P426
[5]   EARLY DIAGNOSIS OF HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION IN CHILDREN LESS-THAN MONTHS OF AGE - COMPARISON OF POLYMERASE CHAIN-REACTION, CULTURE, AND PLASMA ANTIGEN CAPTURE TECHNIQUES [J].
BORKOWSKY, W ;
KRASINSKI, K ;
POLLACK, H ;
HOOVER, W ;
KAUL, A ;
ILMETMOORE, T .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (03) :616-619
[6]   CELL-MEDIATED AND HUMORAL IMMUNE-RESPONSES IN CHILDREN INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS DURING THE 1ST 4 YEARS OF LIFE [J].
BORKOWSKY, W ;
RIGAUD, M ;
KRASINSKI, K ;
MOORE, T ;
LAWRENCE, R ;
POLLACK, H .
JOURNAL OF PEDIATRICS, 1992, 120 (03) :371-375
[7]   EVOLUTION OF PHENOTYPIC MEMORY T-CELLS IN HIV-1 INFECTED INFANTS AND CHILDREN [J].
BORKOWSKY, W ;
MOORE, T ;
KRASINSKI, K ;
AJUANGSIMBIRI, KO ;
HOLZMAN, R .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1992, 63 (03) :280-284
[8]   CLINICAL AND IMMUNOLOGICAL RESPONSES TO HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) TYPE 1(SF2) GP120 SUBUNIT VACCINE COMBINED WITH MF59 ADJUVANT WITH OR WITHOUT MURAMYL TRIPEPTIDE DIPALMITOYL PHOSPHATIDYLETHANOLAMINE IN NON-HIV-INFECTED HUMAN VOLUNTEERS [J].
KAHN, JO ;
SINANGIL, F ;
BAENZIGER, J ;
MURCAR, N ;
WYNNE, D ;
COLEMAN, RL ;
STEIMER, KS ;
DEKKER, CL ;
CHERNOFF, D .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) :1288-1291
[9]   HIV REPLICATION DURING THE 1ST WEEKS OF LIFE [J].
KRIVINE, A ;
FIRTION, G ;
CAO, L ;
FRANCOUAL, C ;
HENRION, R ;
LEBON, P .
LANCET, 1992, 339 (8803) :1187-1189
[10]   Safety and immunogenicity of HIV recombinant envelope vaccines in HIV-infected infants and children [J].
Lambert, JS ;
McNamara, J ;
Katz, SL ;
Fenton, T ;
Kang, MH ;
VanCott, TC ;
Livingston, R ;
Hawkins, E ;
Moye, J ;
Borkowsky, W ;
Johnson, D ;
Yogev, S ;
Duliege, AM ;
Francis, L ;
Gershon, A ;
Wara, D ;
Martin, N ;
Levin, F ;
McSherry, F ;
Smith, G .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 1998, 19 (05) :451-461