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在未感染过牛痘的成年人中,先用重组牛痘病毒gp160进行初免,再用rgp160进行加强免疫,以增强1型人类免疫缺陷病毒中和抗体。美国国立过敏与传染病研究所艾滋病疫苗临床试验网络。

Augmentation of human immunodeficiency virus type 1 neutralizing antibody by priming with gp160 recombinant vaccinia and boosting with rgp160 in vaccinia-naive adults. The NIAID AIDS Vaccine Clinical Trials Network.

作者信息

Graham B S, Matthews T J, Belshe R B, Clements M L, Dolin R, Wright P F, Gorse G J, Schwartz D H, Keefer M C, Bolognesi D P

机构信息

Dept. of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232.

出版信息

J Infect Dis. 1993 Mar;167(3):533-7. doi: 10.1093/infdis/167.3.533.

Abstract

Twelve vaccinia-naive volunteers were inoculated with recombinant vaccinia virus expressing the human immunodeficiency virus type 1 (HIV-1) strain IIIB (HIV-1IIIB) envelope glycoprotein gp160 and subsequently immunized with 640 micrograms of recombinant (r) gp160 protein produced in baculovirus. After booster immunization with rgp160, the sera of all vaccinees showed strong antibody responses detected by Western blot and ELISA; 8 had neutralizing activity and 5 had fusion inhibition activity against the homologous strain; 5 blocked binding of CD4 cells to gp120. Cross-reactive neutralization of HIV-1MN was detected in 3 of 8 sera that neutralized HIV-1IIIB. The combination of live recombinant vaccinia followed by subunit booster immunization was more immunogenic than either product alone and represents a promising approach for HIV-1 immunoprophylaxis. Further definition of recombinant vaccinia safety and augmentation of immune responses to geographically prevalent HIV-1 strains will be necessary before expanding clinical trials to high-risk groups.

摘要

12名未曾接种过痘苗的志愿者接种了表达1型人类免疫缺陷病毒(HIV-1)IIIB株包膜糖蛋白gp160的重组痘苗病毒,随后用杆状病毒生产的640微克重组(r)gp160蛋白进行免疫。用rgp160加强免疫后,所有疫苗接种者的血清通过蛋白质印迹法和酶联免疫吸附测定显示出强烈的抗体反应;8人具有中和活性,5人对同源毒株具有融合抑制活性;5人阻断了CD4细胞与gp120的结合。在8份中和HIV-1IIIB的血清中有3份检测到对HIV-1MN的交叉反应中和作用。活重组痘苗随后进行亚单位加强免疫的联合方案比单独使用任何一种产品更具免疫原性,是一种有前景的HIV-1免疫预防方法。在将临床试验扩大到高危人群之前,有必要进一步明确重组痘苗的安全性并增强对地理上流行的HIV-1毒株的免疫反应。

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