首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >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.
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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.

机译:用实验性重组HIV-1 IIIB gp160疫苗进行肠胃外免疫的无症状HIV-1感染志愿者粘膜标本中的人类1型免疫缺陷病毒(HIV-1)gp160抗体。美国过敏和传染病研究所赞助的艾滋病疫苗评估小组。

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摘要

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.
机译:我进行了一项I期免疫疗法试验的22名感染了1型人类免疫缺陷病毒(HIV-1)的无症状志愿者,其CD4细胞计数> 600细胞/ mm3,比较了两种基于HIV-1 IIIB的免疫方案评估了重组gp160(rgp160)实验疫苗在腮腺唾液,生殖器分泌物和血清中的rgp160特异性抗体。当进行无盲研究时,确定有5名志愿者在0、1、2、3、4和5个月的免疫接种计划接受了rgp160,七名志愿者在0、1、2、5个月的免疫接种计划接受了rgp160 ,其中五名接受了明矾/脱氧胆酸盐安慰剂,七名接受了许可的乙肝病毒疫苗。五名志愿者同意捐赠腮腺唾液,但不接受生殖器分泌物。免疫前,22名志愿者中有11名腮腺唾液标本,22名志愿者中有7名精浆(SP)标本,22名志愿者中有5名宫颈阴道灌洗(CVL)标本,22名志愿者中有血清标本。 22名志愿者。通过酶联免疫吸附法对这些免疫球蛋白G(IgG)和对HIV-1 LAI rgp160或HIV-1 MN rgp160特异的IgA抗体进行评估,评估了这些基线标本以及在最终免疫后1和7个月收集的标本。免疫后,在腮腺唾液或疫苗的血清标本中,与对照组相比,HIV rgp160特异性IgG或IgA抗体产量均未增加。没有足够数量的SP或CVL标本可用于疫苗接种者和对照之间的统计比较。总体而言,在22名志愿者的20例腮腺唾液样本,11名志愿者的11例精浆血浆样本和6名志愿者的6例CVL样本以及22份血清样本中的21例中检测到了抗LAI rgp160 IgG抗体。较少的志愿者在粘膜或血清样本中表达抗LAI rgp160 IgA抗体:22腮腺唾液样本中有11,11 SP样本中有3,5 CVL样本中有3和22血清中有12。

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