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用嵌合VP4或VP6蛋白经鼻内免疫刺激小鼠产生的针对轮状病毒感染的非抗体依赖性保护作用。

Antibody-independent protection against rotavirus infection of mice stimulated by intranasal immunization with chimeric VP4 or VP6 protein.

作者信息

Choi A H, Basu M, McNeal M M, Clements J D, Ward R L

机构信息

Division of Infectious Diseases, Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

出版信息

J Virol. 1999 Sep;73(9):7574-81. doi: 10.1128/JVI.73.9.7574-7581.1999.

Abstract

This study was to determine whether individual rotavirus capsid proteins could stimulate protection against rotavirus shedding in an adult mouse model. BALB/c mice were intranasally or intramuscularly administered purified Escherichia coli-expressed murine rotavirus strain EDIM VP4, VP6, or truncated VP7 (TrVP7) protein fused to the 42.7-kDa maltose-binding protein (MBP). One month after the last immunization, mice were challenged with EDIM and shedding of rotavirus antigen was measured. When three 9-microg doses of one of the three rotavirus proteins fused to MBP were administered intramuscularly with the saponin adjuvant QS-21, serum rotavirus immunoglobulin G (IgG) was induced by each protein. Following EDIM challenge, shedding was significantly (P = 0.02) reduced (i.e., 38%) in MBP::VP6-immunized mice only. Three 9-micrograms doses of chimeric MBP::VP6 or MBP::TrVP7 administered intranasally with attenuated E. coli heat-labile toxin LT(R192G) also induced serum rotavirus IgG, but MBP::VP4 immunization stimulated no detectable rotavirus antibody. No protection against EDIM shedding was observed in the MBP::TrVP7-immunized mice. However, shedding was reduced 93 to 100% following MBP::VP6 inoculation and 56% following MBP::VP4 immunization relative to that of controls (P = <0.001). Substitution of cholera toxin for LT(R192G) as the adjuvant, reduction of the number of doses to 1, and challenge of the mice 3 months after the last immunization did not reduce the level of protection stimulated by intranasal administration of MBP::VP6. When MBP::VP6 was administered intranasally to B-cell-deficient microMt mice that made no rotavirus antibody, shedding was still reduced to <1% of that of controls. These results show that mice can be protected against rotavirus shedding by intranasal administration of individual rotavirus proteins and that this protection can occur independently of rotavirus antibody.

摘要

本研究旨在确定单个轮状病毒衣壳蛋白是否能在成年小鼠模型中刺激产生针对轮状病毒排泄的保护作用。将纯化的大肠杆菌表达的鼠轮状病毒株EDIM的VP4、VP6或与42.7 kDa麦芽糖结合蛋白(MBP)融合的截短型VP7(TrVP7)蛋白经鼻内或肌肉内给予BALB/c小鼠。最后一次免疫后1个月,用EDIM攻击小鼠,并检测轮状病毒抗原的排泄情况。当将三种与MBP融合的轮状病毒蛋白之一的三个9微克剂量与皂苷佐剂QS-21一起肌肉内给药时,每种蛋白均诱导产生血清轮状病毒免疫球蛋白G(IgG)。用EDIM攻击后,仅在MBP::VP-6免疫的小鼠中,排泄量显著(P = 0.02)降低(即38%)。将三个9微克剂量的嵌合MBP::VP6或MBP::TrVP7与减毒大肠杆菌不耐热毒素LT(R192G)一起经鼻内给药也诱导产生血清轮状病毒IgG,但MBP::VP4免疫未刺激产生可检测到的轮状病毒抗体。在MBP::TrVP7免疫的小鼠中未观察到针对EDIM排泄的保护作用。然而,相对于对照组,MBP::VP6接种后排泄量降低了93%至100%,MBP::VP4免疫后降低了56%(P = <0.001)。用霍乱毒素替代LT(R192G)作为佐剂,将剂量减少至1剂,并在最后一次免疫后3个月攻击小鼠,并未降低经鼻内给予MBP::VP6所刺激的保护水平。当将MBP::VP6经鼻内给予不产生轮状病毒抗体的B细胞缺陷型microMt小鼠时,排泄量仍降低至对照组的<1%。这些结果表明,经鼻内给予单个轮状病毒蛋白可保护小鼠免受轮状病毒排泄,且这种保护作用可独立于轮状病毒抗体而发生。

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