Development of Yersinia pestis F1 antigen-loaded liposome vaccine against plague using microneedles as a delivery system

被引:17
|
作者
Chen, Yuan-Chuan [1 ,2 ]
Chen, Shiu-Jau [3 ,4 ]
Cheng, Hwei-Fang [2 ]
Yeh, Ming-Kung [5 ]
机构
[1] Univ Calif Berkeley, Program Comparat Biochem, Berkeley, CA 94720 USA
[2] Minist Hlth & Welf, Food & Drug Adm, Taipei 11561, Taiwan
[3] Mackay Mem Hosp, Dept Neurosurg, Taipei 10449, Taiwan
[4] Mackay Med Coll, Dept Med, New Taipei 25245, Taiwan
[5] Natl Def Med Ctr, Sch Pharm, Taipei 11490, Taiwan
关键词
Plague vaccine; Microneedle; Skin vaccination; F1-liposome; Cytokine response test; TRANSDERMAL DRUG-DELIVERY; CELL-MEDIATED DEFENSE; PROTECTS;
D O I
10.1016/j.jddst.2019.101443
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The F1 protein of Yersinia pestis is a major antigen for triggering immunity against plague in animals. It was currently used as a model antigen to establish a technology platform for highly efficient antibody induction. F1 antigen-loaded liposomes (F1-liposomes) were prepared using the patent formulation of the platform. The F1-liposome was further tested in vitro using phosphate-buffered saline (PBS) as solvent and its F1 protein content was determined by bicinchoninic acid (BCA) assay. The prepared F1-liposomes were administered into immunocompetent Balb/c mice using microneedles to have them immunized. The blood of these immunized mice was periodically taken out every 7 days for 45 days for the evaluation of the anti-F1 IgG titer using enzymelinked immunosorbent assay (ELISA). Furthermore, to confirm the immune responses, the contents of interleukin-4 (IL-4), interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) were determined 35 days post immunization using the BIO-Plex pro assay. The mice administered with F1-liposome demonstrated the strongest immunity by the anti-F1 IgG antibody titer assay, the cytokine response test and the animal challenge test, compare with the controls (PBS and F1-Alugel). These results show that it is possible to develop an effective F1-liposomes plague vaccine using microneedles as a delivery tool.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Fraction 1 capsular antigen (F1) purification from Yersinia pestis CO92 and from an Escherichia coli recombinant strain and efficacy against lethal plague challenge
    Andrews, GP
    Heath, DG
    Anderson, GW
    Welkos, SL
    Friedlander, AM
    INFECTION AND IMMUNITY, 1996, 64 (06) : 2180 - 2187
  • [32] Lack of IL-1 receptor antagonistic activity of the capsular F1 antigen of Yersinia pestis.
    Krakauer, T
    Heath, D
    FASEB JOURNAL, 1998, 12 (04): : A262 - A262
  • [33] Comparison of the immunological and protective responses elicited by microencapsulated formulations of the F1 antigen from Yersinia pestis
    Reddin, KM
    Easterbrook, TJ
    Eley, SM
    Russell, P
    Mobsby, VA
    Jones, DH
    Farrar, GH
    Williamson, ED
    Robinson, A
    VACCINE, 1998, 16 (08) : 761 - 767
  • [34] Screening and identification of DNA nucleic acid aptamers against F1 protein of Yersinia pestis using SELEX method
    Shafiei, Nafiseh
    Mahmoodzadeh Hosseini, Hamideh
    Amani, Jafar
    Mirhosseini, Seyed Ali
    Jafary, Hanieh
    MOLECULAR BIOLOGY REPORTS, 2024, 51 (01)
  • [35] Purification and characterization of a recombinant Yersinia pestis V-F1 "Reversed" fusion protein for use as a new subunit vaccine against plague
    Goodin, Jeremy L.
    Powell, Bradford S.
    Enama, Jeff T.
    Raab, Ronald W.
    McKown, Robert L.
    Coffman, George L.
    Andrews, Gerard P.
    PROTEIN EXPRESSION AND PURIFICATION, 2011, 76 (01) : 136 - 144
  • [36] Purification and protective efficacy of monomeric and modified Yersinia pestis capsular F1-V antigen fusion proteins for vaccination against plague
    Goodin, Jeremy L.
    Nellis, David F.
    Powell, Bradford S.
    Vyas, Vinay V.
    Enama, Jeffrey T.
    Wang, Lena C.
    Clark, Patrick K.
    Giardina, Steven L.
    Adamovicz, Jeffery J.
    Michiel, Dennis F.
    PROTEIN EXPRESSION AND PURIFICATION, 2007, 53 (01) : 63 - 79
  • [37] A comparison of immunogenicity and protective immunity against experimental plague by intranasal and/or combined with oral immunization of mice with attenuated Salmonella serovar Typhimurium expressing secreted Yersinia pestis F1 and V antigen
    Liu, Wen-Tssann
    Hsu, Hui-Ling
    Liang, Chung-Chih
    Chuang, Chuan-Chang
    Lin, Huang-Chi
    Liu, Yu-Tien
    FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2007, 51 (01): : 58 - 69
  • [38] A recombinant prototrophic Yersinia pestis strain over-produces F1 antigen with enhanced serological activity
    Dentovskaya, SV
    Shaikhutdinova, RZ
    Anisimov, AP
    GENUS YERSINIA: ENTERING THE FUNCTIONAL GENOMIC ERA, 2003, 529 : 419 - 421
  • [39] ANTIGEN F1 FROM YERSINIA-PESTIS FORMS AQUEOUS CHANNELS IN LIPID BILAYER-MEMBRANES
    RODRIGUES, CG
    CARNEIRO, CMM
    BARBOSA, CTF
    NOGUEIRA, RA
    BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1992, 25 (01) : 75 - 79
  • [40] Co-delivery of Vi polysaccharide in enhancing stability and immunity of LcrV protein—a potential vaccine candidate of Yersinia pestis against plague
    Krubha Athirathinam
    Selvasudha Nandakumar
    Shanmugarathinam Alagarsamy
    Ruckmani Kandasamy
    Macromolecular Research, 2023, 31 : 961 - 969