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L1 Recombinant Proteins of HPV Tested for Antibody Forming Using Sera of HPV Quadrivalent Vaccine
被引:6
作者:
Akuzum, Begum
[1
]
Kim, Sinae
[2
,3
]
Tam Thanh Nguyen
[2
,3
]
Hong, Jeawoo
[1
]
Lee, Siyoung
[3
]
Kim, Eunhye
[2
,3
]
Kim, Joohee
[1
]
Choi, Yeook
[1
]
Jhun, Hyunjhung
[3
,4
]
Lee, Youngmin
[5
]
Kim, Hyunwoo
[6
]
Sohn, Dong Hyun
[7
]
Kim, Soohyun
[1
,2
]
机构:
[1] Konkuk Univ, Dept Biomed Sci & Technol, Lab Cytokine Immunol, 120 Neungdong Ro, Seoul 05029, South Korea
[2] Konkuk Univ, Coll Vet Med, Seoul 05029, South Korea
[3] YbdYbiotech Res Ctr, Seoul 08589, South Korea
[4] Korea Food Res Inst, Res Grp Nutraceut Metab Syndrome, Wonju 55365, South Korea
[5] Inje Univ, Pusan Paik Hosp, Dept Med, Coll Med, Busan 47392, South Korea
[6] Jeju Natl Univ, Dept Internal Med, Div Nephrol, Sch Med, Jeju 63243, South Korea
[7] Pusan Natl Univ, Dept Microbiol & Immunol, Sch Med, Yangsan 50612, South Korea
关键词:
Papillomaviridae;
L1 capsid proteins;
Recombinant proteins;
Enzyme-linked immunosorbent assay;
Western blot;
VIRUS-LIKE PARTICLES;
HUMAN-PAPILLOMAVIRUS TYPE-16;
GRADE CERVICAL LESIONS;
MAJOR CAPSID PROTEIN;
NEUTRALIZING EPITOPES;
ESCHERICHIA-COLI;
EXPRESSION;
CYTOKINE;
CANCER;
WOMEN;
D O I:
10.4110/in.2018.18.e19
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Virus-like particles (VLPs) derived from human papillomavirus (HPV) L1 capsid proteins were used for HPV quadrivalent recombinant vaccine. The HPV quadrivalent vaccine is administrated in a 3-dose regimen of initial injection followed by subsequent doses at 2 and 6 months to prevent cervical cancer, vulvar, and vaginal cancers. The type 6,11,16, or 18 of HPV infection is associated with precancerous lesions and genital warts in adolescents and young women. The HPV vaccine is composed ofviral LI capsid proteins are produced in eukaryotic expression systems and purified in the form of VLPs. Four different the L1 protein of3 different subtypes of HPV: HPV11, HPV16, and HPV18 were expressed in Escherichia coli divided into 2 fragments as N- and C-terminal of each protein in order to examine the efficacy of HPV vaccine. Vaccinated sera failed to recognize N-terminal L1 HPV type 16 and type 18 by western blot while they detected N-terminal L1 protein ofHPV type 11. Moreover, the recombinant C-terminal L1 proteins of type 16 was non-specifically recognized by the secondary antibody conjugated with horseradish peroxidase. This expression and purification system may provide simple method to obtain robust recombinant L1 protein of HPV subtypes to improve biochemical analysis of antigens with immunized sera.
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页数:13
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