Literature DB >> 9144368

Antibody to human immunodeficiency virus type 1 (HIV-1) gp160 in mucosal specimens of asymptomatic HIV-1-infected volunteers parenterally immunized with an experimental recombinant HIV-1 IIIB gp160 vaccine. The National Institute of Allergy and Infectious Diseases-sponsored AIDS Vaccine Evaluation Group.

J S Lambert1, R Viscidi, M C Walker, B Clayman, M Winget, M Wolff, D H Schwartz.   

Abstract

Twenty-two human immunodeficiency virus type 1 (HIV-1)-infected, asymptomatic volunteers with CD4 cell counts of >600 cells/mm3 who were enrolled in a phase I immunotherapy trial comparing two schedules of immunization of an HIV-1 IIIB-based recombinant gp160 (rgp160) experimental vaccine were evaluated for rgp160-specific antibodies in parotid saliva, genital secretions, and serum. When the study was unblinded, it was determined that five volunteers had received rgp160 on a month 0, 1, 2, 3, 4, and 5 immunization schedule, seven volunteers had received rgp160 on a month 0, 1, 2, and 5 schedule, five had received alum/deoxycholate placebo, and seven had received a licensed hepatitis B virus vaccine. Five volunteers consented to the donation of parotid saliva but not genital secretions. Prior to immunization, parotid saliva specimens were available for 11 of 22 volunteers, seminal plasma (SP) specimens were available for 7 of 22 volunteers, cervicovaginal lavage (CVL) specimens were available for 5 of 22 volunteers, and serum was available for 22 of 22 volunteers. These baseline specimens and specimens collected at 1 and 7 months after the final immunizations were assessed by enzyme-linked immunosorbent assay for immunoglobulin G (IgG) and IgA antibodies specific for HIV-1 LAI rgp160 or HIV-1 MN rgp160. No augmentation in HIV rgp160-specific IgG or IgA antibody production in either parotid saliva or serum specimens of vaccinees compared to that in controls was observed after immunization. There were insufficient numbers of SP or CVL specimens available for statistical comparisons between vaccinees and controls. Overall, anti-LAI rgp160 IgG antibodies were detected in the parotid saliva specimens of 20 of 22 volunteers, the seminal plasma specimens of 11 of 11 volunteers, and the CVL specimens of 6 of 6 volunteers and in 21 of 22 serum specimens. Fewer volunteers expressed anti-LAI rgp160 IgA antibodies in mucosal or serum specimens: 11 of 22 parotid saliva specimens, 3 of 11 SP specimens, 3 of 5 CVL samples, and 12 of 22 sera.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9144368      PMCID: PMC170523          DOI: 10.1128/cdli.4.3.302-308.1997

Source DB:  PubMed          Journal:  Clin Diagn Lab Immunol        ISSN: 1071-412X


  19 in total

1.  Envelope-specific antibodies in the saliva of individuals vaccinated with recombinant HIV-1 gp160.

Authors:  M B Vasudevachari; K W Uffelman; J Kovacs; C K Yeh; H C Lane; N P Salzman
Journal:  J Acquir Immune Defic Syndr (1988)       Date:  1992

2.  Secretory IgA antibodies to human immunodeficiency virus in the parotid saliva of patients with AIDS and AIDS-related complex.

Authors:  D W Archibald; C E Barr; J P Torosian; M F McLane; M Essex
Journal:  J Infect Dis       Date:  1987-04       Impact factor: 5.226

3.  HIV-1 recombinant gp160 vaccine induced antibodies in serum and saliva. The NIAID AIDS Vaccine Clinical Trials Network.

Authors:  G J Gorse; J H Rogers; J E Perry; F K Newman; S E Frey; G B Patel; R B Belshe
Journal:  Vaccine       Date:  1995-02       Impact factor: 3.641

Review 4.  Mucosal immunity in the female genital tract: relevance to vaccination efforts against the human immunodeficiency virus.

Authors:  J Mestecky; W H Kutteh; S Jackson
Journal:  AIDS Res Hum Retroviruses       Date:  1994       Impact factor: 2.205

5.  HIV-1 recombinant gp160 vaccine given in accelerated dose schedules. NIAID AIDS Vaccine Clinical Trials Network.

Authors:  G J Gorse; D H Schwartz; B S Graham; T J Matthews; D M Stablein; S E Frey; R B Belshe; M L Clements; P F Wright; M Eibl
Journal:  Clin Exp Immunol       Date:  1994-11       Impact factor: 4.330

6.  A randomized, placebo-controlled study of the immunogenicity of human immunodeficiency virus (HIV) rgp160 vaccine in HIV-infected subjects with > or = 400/mm3 CD4 T lymphocytes (AIDS Clinical Trials Group Protocol 137).

Authors:  F T Valentine; S Kundu; P A Haslett; D Katzenstein; L Beckett; C Spino; M Borucki; M Vasquez; G Smith; J Korvick; J Kagan; T C Merigan
Journal:  J Infect Dis       Date:  1996-06       Impact factor: 5.226

7.  Immunization of HIV-infected patients with rgp160: modulation of anti-rgp120 antibody spectrotype.

Authors:  R Biselli; L D Loomis; V Del Bono; D S Burke; R R Redfield; D L Birx
Journal:  J Acquir Immune Defic Syndr (1988)       Date:  1994-10

8.  Antibodies to recombinant gp160 in mucosal secretions and sera of persons infected with HIV-1 and seronegative vaccine recipients.

Authors:  A Funkhouser; M L Clements; S Slome; B Clayman; R Viscidi
Journal:  AIDS Res Hum Retroviruses       Date:  1993-07       Impact factor: 2.205

9.  Placebo-controlled trial of vaccination with recombinant glycoprotein D of herpes simplex virus type 2 for immunotherapy of genital herpes.

Authors:  S E Straus; L Corey; R L Burke; B Savarese; G Barnum; P R Krause; R G Kost; J L Meier; R Sekulovich; S F Adair
Journal:  Lancet       Date:  1994-06-11       Impact factor: 79.321

10.  Presence of human immunodeficiency virus (HIV) type 1 and HIV-1-specific antibodies in cervicovaginal secretions of infected mothers and in the gastric aspirates of their infants.

Authors:  K Nielsen; P Boyer; M Dillon; D Wafer; L S Wei; E Garratty; R E Dickover; Y J Bryson
Journal:  J Infect Dis       Date:  1996-04       Impact factor: 5.226

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.