中华实验和临床病毒学杂志
中華實驗和臨床病毒學雜誌
중화실험화림상병독학잡지
CHINESE JOURNAL OF EXPERIMENTAL AND CLINICAL VIROLOGY
2014年
3期
178-180
,共3页
张福顺%郝春生%宋敬东%张硕%李阿茜%刘林%李川%张全福%梁米芳
張福順%郝春生%宋敬東%張碩%李阿茜%劉林%李川%張全福%樑米芳
장복순%학춘생%송경동%장석%리아천%류림%리천%장전복%량미방
杆状病毒科%柯萨奇病毒感染%病毒样颗粒%免疫遗传学
桿狀病毒科%柯薩奇病毒感染%病毒樣顆粒%免疫遺傳學
간상병독과%가살기병독감염%병독양과립%면역유전학
Baculoviride%Coxsackievirus infeclions%Virus-like particles%Iimmunogenetics
目的 研究柯萨奇病毒A组16型(Coxsackievirus A16,CA16)病毒样颗粒(Virus-like particles,VLPs)的免疫原性.方法 利用杆状病毒-昆虫细胞表达系统共表达3CD及P1蛋白,制备CA16病毒样颗粒,通过SDS-PAGE及透射电镜等方法对VLPs进行鉴定,以氢氧化铝佐剂免疫ICR小鼠,并对乳鼠经颅腔攻毒.对病毒样颗粒疫苗的免疫原性及保护效果进行评价.结果 将重组CA163CD及P1蛋白的杆状病毒转染SF9细胞,可以产生类似CA16病毒颗粒的大小为27 ~ 30 nm的VLPs.小鼠免疫试验结果显示CA16 VLPs可以刺激产生较高水平的抗CA16病毒的特异性IgG抗体及中和抗体,乳鼠攻毒试验结果显示,母传抗体保护率高达90%.结论 CA16 VLPs可以刺激小鼠产生较高水平的体液免疫反应,并且母传抗体可以保护乳鼠抵御经颅腔的病毒攻击.
目的 研究柯薩奇病毒A組16型(Coxsackievirus A16,CA16)病毒樣顆粒(Virus-like particles,VLPs)的免疫原性.方法 利用桿狀病毒-昆蟲細胞錶達繫統共錶達3CD及P1蛋白,製備CA16病毒樣顆粒,通過SDS-PAGE及透射電鏡等方法對VLPs進行鑒定,以氫氧化鋁佐劑免疫ICR小鼠,併對乳鼠經顱腔攻毒.對病毒樣顆粒疫苗的免疫原性及保護效果進行評價.結果 將重組CA163CD及P1蛋白的桿狀病毒轉染SF9細胞,可以產生類似CA16病毒顆粒的大小為27 ~ 30 nm的VLPs.小鼠免疫試驗結果顯示CA16 VLPs可以刺激產生較高水平的抗CA16病毒的特異性IgG抗體及中和抗體,乳鼠攻毒試驗結果顯示,母傳抗體保護率高達90%.結論 CA16 VLPs可以刺激小鼠產生較高水平的體液免疫反應,併且母傳抗體可以保護乳鼠牴禦經顱腔的病毒攻擊.
목적 연구가살기병독A조16형(Coxsackievirus A16,CA16)병독양과립(Virus-like particles,VLPs)적면역원성.방법 이용간상병독-곤충세포표체계통공표체3CD급P1단백,제비CA16병독양과립,통과SDS-PAGE급투사전경등방법대VLPs진행감정,이경양화려좌제면역ICR소서,병대유서경로강공독.대병독양과립역묘적면역원성급보호효과진행평개.결과 장중조CA163CD급P1단백적간상병독전염SF9세포,가이산생유사CA16병독과립적대소위27 ~ 30 nm적VLPs.소서면역시험결과현시CA16 VLPs가이자격산생교고수평적항CA16병독적특이성IgG항체급중화항체,유서공독시험결과현시,모전항체보호솔고체90%.결론 CA16 VLPs가이자격소서산생교고수평적체액면역반응,병차모전항체가이보호유서저어경로강적병독공격.
Objective To study the immunogenicity of virus-like particles (VLPs) of Coxsackievirus A16.Methods Recombinant CA16 VLPs were prepared by co-expressing 3CD and P1 proteins using baculovirus expression system.Purified VLPs were identified by SDS-PAGE and transmission electronmicroscope(TEM).The immunogenicity of CA16 VLPs was evaluated in ICR mice.Humoral immune response was identified by ELISA and neutralization assay and the protection effects the neonatal mouse against CA16 virus were also evaluated.Results Recombinant CA16 VLPs exhibited as electrondense spherical particles of 27-30 nm size,which were similar to the morphology and size of authentic virions under TEM observation.The VLPs induced high levels of CA16 virus-specific serum IgG antibodies and neutralization antibodies.Furthermore,VLPs-immunized mother mice conferred protection (survival rate up to 90%) on neonatal mice against a lethal CA16 challenge of 104 plaque-forming units CA16.Conclusion CA16 VLPs produced by baculovirus expression system were capable to induce specific humoralimmune responses in mice and the neutralization antibodies could protect the neonatal mouse from lethal CA16 virus challenge.