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b型多聚核糖醇磷酸酯与解毒脂寡糖联合使用在兔模型中的免疫效果

Immunological efficiency of type b polyribosyl ribitol phosphate combined with detoxified lipooligosaccharide in a rabbit model.

作者信息

Arsang Amin, Siadat Seyed Davar, Saberpour Masoumeh, Nojoomi Farshad

机构信息

Department of Mycobacteriology & Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran.

Department of Influenza and Other Respiratory Viruses, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Iran J Microbiol. 2025 Feb;17(1):106-112. doi: 10.18502/ijm.v17i1.17807.

Abstract

BACKGROUND AND OBJECTIVES

type b could cause severe life-threatening infections in children. Combine vaccines have reduced invasive diseases, but disease management is still necessary. The aim of this research was to evaluate the immunological efficiency of polyribosyl-ribitol-phosphate combined with detoxified lipooligosaccharide (PRP-dLOS) in a rabbit model.

MATERIALS AND METHODS

PRP purification, LOS extraction, and endotoxin evaluation were performed using modified CY medium, hot phenol, and limulus amebocyte lysate methods, respectively. Rabbit groups were immunized with PRP (10 μg), dLOS (20 μg), and PRP-dLOS combine (10 μg+20 μg) three times on days 0, 14, and 28. Serum samples were acquired on days 0, 14, and 28 post-immunization, then IgM and IgG levels were assayed by enzyme-linked immunosorbent assay.

RESULTS

The concentrations of PRP, dLOS, and endotoxin were 1160 mg/L, 440 μg/mL, and 1450 EU/mL, respectively. PRP-dLOS combine led to a significant increase in IgG and IgM levels on days 14 and 28 post-immunization. After immunization with PRP-dLOS combine, serum levels of IgM and IgG increased from 16.8 to 29.3 μg/mL and 29.8 to 61.4 μg/mL, respectively from day 14 to day 28.

CONCLUSION

PRP-dLOS combine is a promising approach for Hib management without the fear of delay in immune responses and interference with other vaccines.

摘要

背景与目的

b型(病菌)可在儿童中引发严重的危及生命的感染。联合疫苗已减少侵袭性疾病,但疾病管理仍然必要。本研究的目的是在兔模型中评估多聚核糖基核糖醇磷酸与解毒脂寡糖(PRP-dLOS)联合使用的免疫效率。

材料与方法

分别使用改良CY培养基、热酚法和鲎试剂法进行PRP纯化、LOS提取和内毒素评估。在第0、14和28天,用PRP(10μg)、dLOS(20μg)和PRP-dLOS联合制剂(10μg + 20μg)对兔组进行三次免疫。在免疫后第0、14和28天采集血清样本,然后通过酶联免疫吸附测定法检测IgM和IgG水平。

结果

PRP、dLOS和内毒素的浓度分别为1160mg/L、440μg/mL和1450EU/mL。PRP-dLOS联合制剂在免疫后第14天和第28天导致IgG和IgM水平显著升高。用PRP-dLOS联合制剂免疫后,从第14天到第28天,血清IgM和IgG水平分别从16.8μg/mL增加到29.3μg/mL和从29.8μg/mL增加到61.4μg/mL。

结论

PRP-dLOS联合制剂是一种有前景的b型流感嗜血杆菌管理方法,无需担心免疫反应延迟和对其他疫苗的干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abc3/12049763/624d28591e0e/IJM-17-106-g001.jpg

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