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一种佐剂化合物,可增强 fractional doses(分数剂量)的 Sabin 灭活脊髓灰质炎病毒疫苗(sIPV)的免疫原性,并在大鼠模型中提供长期保护。

An adjuvant compound that enhances immunogenicity at fractional doses of the Sabin-inactivated poliovirus vaccine (sIPV) with a long duration of protection in a rat model.

机构信息

The Fifth Department of Biological Products, Institute of Medical Biology, Chinese Academy of Medical Science and Peking Union Medical College, Kunming, China.

The Outreach Department of Certification with World Health Organization, Institute of Medical Biology, Chinese Academy of Medical Science and Peking Union Medical College, Kunming, China.

出版信息

J Med Virol. 2019 Jan;91(1):14-21. doi: 10.1002/jmv.25298. Epub 2018 Oct 9.

Abstract

BACKGROUND

At the same dosage, the new generation of Sabin-inactivated poliovirus vaccine (sIPV) is less immunogenic than the traditional oral polio vaccine (OPV) dosage in China. The useful adjuvant might be a necessary strategy to strengthen the immune protective effects.

METHODS

In this study, we produced an adjuvant compound (named KML05) that could promote immunogenicity and fractional doses of sIPV with a long duration of protection in a rat model. The compound adjuvant had both advantages and a function of MF59 and carbopol971P.

RESULTS

The effect seroconversion of experimental animals immunized with KML05 could be extended to one-eighth of the dose. According to the result of the geometric mean titers (GMTs), KML05 adjuvant could save eight times the amount of sIPV D-antigen usage, but aluminum hydroxide adjuvant could save twice at the same titers. Additionally, it was found that there was a significant difference in the GMT titer of poliovirus type 2 between animals immunized by KML05 and alum adjuvant (P < 0.05). At 12th-month postvaccination, the neutralization titers stimulated by IPV-KML05 were maintained over a longer time period in immunized animals.

CONCLUSION

Our research team developed KML05 adjuvant, which combined carbopol971P with MF59, increased antibody responses to sIPV for a longer duration of protection in a rat model.

摘要

背景

在相同剂量下,新一代萨宾灭活脊髓灰质炎疫苗(sIPV)在中国的免疫原性不如传统的口服脊髓灰质炎疫苗(OPV)。有用的佐剂可能是增强免疫保护效果的必要策略。

方法

在这项研究中,我们生产了一种佐剂化合物(命名为 KML05),它可以在大鼠模型中提高 sIPV 的免疫原性和亚单位剂量,延长保护时间。该佐剂化合物具有 MF59 和卡波姆 971P 的优点和功能。

结果

实验动物用 KML05 免疫后的血清转化率可以延长到八分之一剂量。根据几何平均滴度(GMT)的结果,KML05 佐剂可以节省 8 倍 sIPV D 抗原的用量,而氢氧化铝佐剂在相同滴度下可以节省两倍。此外,还发现 KML05 佐剂免疫的动物的脊髓灰质炎病毒 2 型 GMT 滴度与铝佐剂有显著差异(P<0.05)。在接种后 12 个月,KML05-IPV 刺激的中和滴度在免疫动物中维持更长时间。

结论

我们的研究团队开发了 KML05 佐剂,它结合了卡波姆 971P 和 MF59,提高了 sIPV 的抗体反应,延长了大鼠模型的保护时间。

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