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甲型肝炎减毒活疫苗研发的新发现。

New findings in live, attenuated hepatitis A vaccine development.

作者信息

Provost P J, Bishop R P, Gerety R J, Hilleman M R, McAleer W J, Scolnick E M, Stevens C E

出版信息

J Med Virol. 1986 Oct;20(2):165-75. doi: 10.1002/jmv.1890200208.

Abstract

Strain CR326F of hepatitis A virus, derived from a fecal specimen of Costa Rican patient 033-03, was passed 15 times in fetal rhesus monkey kidney (FRhK6) cell cultures plus eight times in human diploid lung (MRC5) cell cultures to yield variant F and 16 times in MRC5 cell cultures to yield variant F'. Both variants were purified by limit dilution passages. Virulence for marmosets was assessed at six different passage levels, including variants F and F'. There was a gradual loss of virulence with in vitro passage. Variant F retained slight virulence for marmosets; variant F' showed no evidence of virulence. Both variants induced hepatitis A antibody in most marmosets that received them, and the animals were immune to infection when challenged. Variants F and F' were also assessed in chimpanzees. As in marmosets, F retained slight virulence but F' did not. Experimental vaccines made from variants F and F' were then inoculated parenterally into adult human volunteers. A portion of recipients of variant F showed brief, low-order enzyme elevations; none was seen in recipients of F', although their occurrence could not be totally ruled out. As in the animal models, F' appeared more attenuated than F. Most persons developed hepatitis A antibody, indicating the feasibility of developing a live, attenuated hepatitis A vaccine for human beings.

摘要

甲型肝炎病毒CR326F毒株源自哥斯达黎加患者033 - 03的粪便样本,在恒河猴胎儿肾(FRhK6)细胞培养物中传代15次,再在人二倍体肺(MRC5)细胞培养物中传代8次,得到变体F;在MRC5细胞培养物中传代16次,得到变体F'。两种变体均通过有限稀释传代进行纯化。在六个不同传代水平评估了对狨猴的毒力,包括变体F和F'。随着体外传代,毒力逐渐丧失。变体F对狨猴仍保留轻微毒力;变体F'未显示出毒力迹象。两种变体在大多数接受它们的狨猴中都诱导产生了甲型肝炎抗体,并且这些动物在受到攻击时对感染具有免疫力。变体F和F'也在黑猩猩中进行了评估。与在狨猴中一样,F保留了轻微毒力,但F'没有。然后将由变体F和F'制成的实验性疫苗经肠胃外接种给成年人类志愿者。一部分接受变体F的受试者出现了短暂的、低水平的酶升高;接受F'的受试者中未观察到这种情况,尽管不能完全排除其发生的可能性。与动物模型一样,F'似乎比F更减毒。大多数人产生了甲型肝炎抗体,这表明开发一种用于人类的减毒活甲型肝炎疫苗是可行的。

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