Chitosan and Sodium Alginate Combinations Are Alternative, Efficient, and Safe Natural Adjuvant Systems for Hepatitis B Vaccine in Mouse Model

被引:26
作者
AbdelAllah, Nourhan H. [1 ]
Abdeltawab, Nourtan F. [2 ]
Boseila, Abeer A. [3 ]
Amin, Magdy A. [2 ]
机构
[1] NORCB, Viral Control Unit, Cairo 12654, Egypt
[2] Cairo Univ, Dept Microbiol & Immunol, Fac Pharm, Cairo 11562, Egypt
[3] Natl Org Drug Control & Res NODCAR, Cairo 11562, Egypt
关键词
VIRUS; ANTIGEN; NONRESPONDERS; NANOPARTICLES; EFFICACY; SUBSETS; TH1;
D O I
10.1155/2016/7659684
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Hepatitis B viral (HBV) infections represent major public health problem and are an occupational hazard for healthcare workers. Current alum-adjuvanted HBV vaccine is the most effective measure to prevent HBV infection. However, the vaccine has some limitations including poor response in some vaccinee and being a frost-sensitive suspension. The goal of our study was to use an alternative natural adjuvant system strongly immunogenic allowing for a reduction in dose and cost. We tested HBV surface antigen (HBsAg) adjuvanted with chitosan (Ch) and sodium alginate (S), both natural adjuvants, either alone or combined with alum in mouse model. Mice groups were immunized subcutaneously with HBsAg adjuvanted with Ch or S, or triple adjuvant formula with alum (Al), Ch, and S, or double formulations with AlCh or AlS. These were compared to control groups immunized with current vaccine formula or unadjuvanted HBsAg. We evaluated the rate of seroconversion, serum HBsAg antibody, IL-4, and IFN-gamma. levels. The results showed that the solution formula with Ch or S exhibited comparable immunogenic responses to Al-adjuvanted suspension. The AlChS gave significantly higher immunogenic response compared to controls. Collectively, our results indicated that Ch and S are effective HBV adjuvants offering natural alternatives, potentially reducing dose.
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页数:8
相关论文
共 34 条
[1]  
[Anonymous], 2007, American Veterinary Medical Association Panel on Euthanasia, P1
[2]  
[Anonymous], 2011, Epidemiology and Prevention of Vaccine-Preventable Diseases
[3]  
Arai K., 1968, B TOKAI REG FISH RES, V56, P89, DOI [10.3390/md12126236, DOI 10.3390/MD12126236]
[4]   Biopolymer encapsulated live influenza virus as a universal CD8+T cell vaccine against influenza virus [J].
Boesteanu, Alina C. ;
Babu, Nadarajan S. ;
Wheatley, Margaret ;
Papazoglou, Elisabeth S. ;
Katsikis, Peter D. .
VACCINE, 2010, 29 (02) :314-322
[5]   Alginate coated chitosan nanoparticles are an effective subcutaneous adjuvant for hepatitis B surface antigen [J].
Borges, Olga ;
Silva, Marta ;
de Sousa, Adriano ;
Borchard, Gerrit ;
Junginger, Hans E. ;
Cordeiro-da-Silva, Anabela .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2008, 8 (13-14) :1773-1780
[6]   Excellent response rate to a double dose of the combined hepatitis A and B vaccine in previous nonresponders to hepatitis B vaccine [J].
Cardell, Kristina ;
Akerlind, Britt ;
Sallberg, Matti ;
Fryden, Aril .
JOURNAL OF INFECTIOUS DISEASES, 2008, 198 (03) :299-304
[7]  
Chosewood LC., 2007, BIOSAFETY MICROBIOLO, V5th
[8]   Vaccines with Aluminum-containing Adjuvants: Optimizing Vaccine Efficacy and Thermal Stability [J].
Clapp, Tanya ;
Siebert, Paul ;
Chen, Dexiang ;
Braun, LaToya Jones .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 100 (02) :388-401
[9]   Booster immunization of low- and non-responders after a standard three dose hepatitis B vaccine schedule - Results of a post-marketing surveillance [J].
Clemens, R ;
Sanger, R ;
Kruppenbacher, J ;
Hobel, W ;
Stanbury, W ;
Bock, HL ;
Jilg, W .
VACCINE, 1997, 15 (04) :349-352
[10]   Adjuvanticity effect of sodium alginate on subcutaneously injected BCG in BALB/c mice [J].
Dobakhti, Faramarz ;
Naghibi, Taraneh ;
Taghikhani, Mohammad ;
Ajdary, Soheila ;
Rafinejad, Ali ;
Bayati, Khosrow ;
Rafiei, Shahnaz ;
Rafiee-Tehrani, Morteza .
MICROBES AND INFECTION, 2009, 11 (02) :296-301