Microemulsion can improve the immune-enhancing activity of propolis flavonoid on immunosuppression and immune response

International Journal of Biological Macromolecules

Volumn 63, Issue , 2014, Pages 126-132

  Fan, Yunpeng ^a   Ma, Lin ^a   Zhang, Weimin ^a   Xu, Yingying ^a   Suolangzhaxi, ^a   Zhi, Xiaoyan ^a   Cui, Enhui ^a   Song, Xiaoping ^a  

^a NORTHWEST A F UNIVERSITY   (China)

Author keywords

Immune response; Immune enhancing activity; Propolis flavonoid microemulsion

Indexed keywords

AVIAN INFLUENZA RECOMBINANT NEWCASTLE DISEASE VIRUS BIVALENT VACCINE; CYCLOPHOSPHAMIDE; FLAVONOID; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; INTERLEUKIN 2; INTERLEUKIN 6; PROPOLIS FLAVONOID; UNCLASSIFIED DRUG; VIRUS VACCINE;

ADJUVANT THERAPY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIBODY TITER; ARTICLE; CONTROLLED STUDY; DOSE RESPONSE; DRUG DOSAGE FORM COMPARISON; DRUG EFFICACY; DRUG FORMULATION; DRUG MEGADOSE; IMMUNE DEFICIENCY; IMMUNE RESPONSE; IMMUNITY; LOW DRUG DOSE; LYMPHOCYTE PROLIFERATION; MALE; MICROEMULSION; NONHUMAN; PROTEIN BLOOD LEVEL;

AVES; GALLUS GALLUS; NEWCASTLE DISEASE VIRUS;

3-(4,5-DIMETHYLTHIAZOL-2-YL)-2,5-DIPHENYLTETRAZOLIUM BROMIDE; AI; AVIAN INFLUENZA; BC; BLANK CONTROL; CTX; CYTOXAN; IGG; IGM; IL-2; IL-6; IMMUNE RESPONSE; IMMUNE-ENHANCING ACTIVITY; IMMUNOGLOBULINS G; IMMUNOGLOBULINS M; INTERLEUKIN-2; INTERLEUKIN-6; MTT; NC; ND; NEWCASTLE DISEASE; NORMAL CONTROL; PBS; PF; PFM; PHA; PHOSPHATE BUFFERED SALINE; PHYTOHEMAGGLUTININ; POLYOXYETHYLENE (40) HYDROGENATED CASTOR OIL; PROPOLIS FLAVONOID; PROPOLIS FLAVONOID MICROEMULSION; RH-40; VACCINE CONTROL; VC;

ANIMALS; CELL PROLIFERATION; CHICKENS; EMULSIONS; FLAVONOIDS; IMMUNITY, INNATE; IMMUNOSUPPRESSION; INFLUENZA IN BIRDS; INFLUENZA VACCINES; LYMPHOCYTE ACTIVATION; NEWCASTLE DISEASE; NEWCASTLE DISEASE VIRUS; PROPOLIS;

EID: 84888094231     PISSN: 01418130     EISSN: 18790003     Source Type: Journal    
DOI: 10.1016/j.ijbiomac.2013.09.039     Document Type: Article

References (41)

1. Harandi A.M., Medaglini D., Shattock R.J. Working group convened by EUROPRISE, vaccine adjuvants: a priority for vaccine research. Vaccine 2010, 28:2363-2366.
2. Jiang L.J. The immunopotentiators and delivery systems for use in vaccines. Prog. Microbiol. Immunol. 2012, 40:1-8.
3. Steinman R.M. Dendritic cells in vivo: a key target for a new vaccine science. Immunity 2008, 29:319-324.
4. Aguilar J.C., Rodríguez E.G. Vaccine adjuvants revisited. Vaccine 2007, 25:3752-3762.
5. Tritto E., Mosca F., De G.E. Mechanism of action of licensed vaccine adjuvants. Vaccine 2009, 27:3331-3334.
6. Steven G.R., Sylvie B., Rhea N.C., Martin F. New horizons in adjuvants for vaccine development. Trends Immunol. 2009, 1:23-32.
7. Rey-Ladino J., Ross A.G., Cripps A.W., McManus D.P., Quinn R. Natural products and the search for novel vaccine adjuvants. Vaccine 2011, 29:6464-6471.
8. Chen X.M., Nie W.J., Fan S.R., Zhang J.F., Wang Y.X., Lu J.X., Jin L.Q. A polysaccharide from Sargassum fusiforme protects against immunosuppression in cyclophosphamide-treated mice. Carbohydr. Polym. 2012, 90:1114-1119.
9. El Ashry E.S.H., Ahmad T.A. The use of propolis as vaccine's adjuvant. Vaccine 2012, 31:31-39.
10. Wang H., Wang M.Y., Chen J., Tang Y., Dou J., Yu J., Xi T., Zhou C.L. A polysaccharide from Strongylocentrotus nudus eggs protects against myelosuppression and immunosuppression in cyclophosphamide-treated mice. Int. Immunopharmacol. 2011, 11:1946-1953.
11. Burdock G.A. Review of the biological properties and toxicity of bee propolis (propolis). Food. Chem. Toxicol. 1998, 36:347-363.
12. Castaldo S., Capasso F. Propolis, an old remedy used in modern medicine. Fitoterapia 2002, 73:S1-S6.
13. Popova M., Silici S., Kaftanoglu O., Bankova V. Antibacterial activity of Turkish propolis and its qualitative and quantitative chemical composition. Phytomedicine 2005, 12:221-228.
14. Cristina M.M., Liviu A.M., Daniel S.D., Flore C., Robin F.A.M., Helge S. Interactions among flavonoids of propolis affect antibacterial activity against the honeybee pathogen Paenibacillus larvae. J. Invertebr. Pathol. 2012, 110:68-72.
15. Sirivan A., Suresh A., Nijsiri R., Somsak R., Shigetoshi K. Chemical constituents of Thai propolis. Fitoterapia 2013, 88:96-100.
16. Banskota A.H., Tezuka Y., Kadota S. Recent progress in pharmacological research of propolis. Phytother. Res. 2001, 15:561-571.
17. Trusheva B., Popova M., Koendhori E.B., Tsvetkova I., Naydenski C., Bankova V. Indonesian propolis: chemical composition, biological activity and botanical origin. Nat. Prod. Res. 2011, 6:606-613.
18. Sarciaux J.M., Acar L., Sado P.A. Using microemulsion formulations for drug delivery of therapeutic peptides. Int. J. Pharm. 1995, 120:127-136.
19. Constantinides P.P. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects. Pharm. Res. 1995, 12:1561-1572.
20. Lawrence M.J., Rees G.D. Microemulsion-based media as novel drug delivery systems. Adv. Drug. Deliver. Rev. 2012, 64:175-193.
21. Reinhard H.H.N. Potentials of new nanocarriers for dermal and transdermal drug delivery. Eur. J. Pharm. Biopharm. 2011, 77:1-2.
22. Fanun M. Microemulsions Properties and Applications 2009, 5-10. Taylor and Francis, New York.
23. Fanun M. Colloids in drug delivery 2010, 125-130. Taylor and Francis, New York.
24. Monzer F. Microemulsions as delivery systems. Curr. Opin. Colloid Interface 2012, 17:306-313.
25. Zhang B.K., Wang D.Y., Kong X.F., Hu Y.L. Studies on immunoenhancement of propolis flavone. J. Yangzhou Univ. 2006, 27:20-22.
26. Kong X.F., Hu Y.L., Rui R., Wang D.Y., Li X.R. Effects of Chinese herbal medicinal ingredients on peripheral lymphocyte proliferation and serum antibody serum antibody titer after vaccination in chicken. Int. Immunopharmacol. 2004, 4:975-982.
27. Yuan J., Liu J.G., Hu Y.L., Fan Y.P., Wang D.Y., Guo L.W., Nguyen T.L., Zhao X.J., Liu X., Liu C., Wu Y. The immunological activity of propolis flavonoids liposome on the immune response against ND vaccine. Int. J. Biol. Macromol. 2012, 51:400-405.
28. Zhao X.J., Fan Y.P., Wang D.Y., Hu Y.L., Guo L.W., Ruan S.L., Zhang J., Yuan J. Immunological adjuvant efficacy of glycyrrhetinic acid liposome against Newcastle disease vaccine. Vaccine 2011, 29:9611-9617.
29. Cruz-Chamorro L., Puertollano M.A., Puertollano E., Cienfuegos G., Pablo M.A. Examination of host immune resistance against Listeria monocytogenes infection in cyclophosphamide-treated mice after dietary lipid administration. Clin. Nutr. 2007, 26:631-639.
30. Moshira E., Maki M., Kikuyasu N., Kenji K., Takashi O., Olli V., Paavo T., Yoshikazu H. Preventive and therapeutic effects of sugar cane extract on cyclophosphamide-induced immunosuppression in chickens. Int. Immunopharmacol. 2004, 4:983-990.
31. Cao F.H., Ouyang W.Q., Wang Y.P. Preparation of O/W ginseng saponins-based nanoemulsion and its amplified immune response. J. Chin. Mat. Med. 2010, 35:439-443.
32. Li S.P., Hao Y.S., Ouyang W.Q. Preparation of W/O Astragalus polysaccharide and Echinacea extract-based nano-emulsion and its amplified immune response. J. Northwest. Agric. Forest. Univ. 2011, 39:10-16.
33. Yang H.C. Animal Immunology 2003, 129-130. China Agricultural University Press, Beijing.
34. Marciani D.J., Press J.B., Reynolds R.C., Pathak A.K., Pathak V., Gundy L.E., Farmer J.T., Koratich M.S., May R.D. Development of semisynthetic triterpenoid saponin derivatives with immune stimulating activity. Vaccine 2000, 18:3141-3151.
35. Li C.H., Santoso S., Lo D.D. Quantitative analysis of T cell homeostatic proliferation. Cell. Immunol. 2007, 250:45-54.
36. Huang X.Y., Hu Y.L., Zhao X.N., Yu L., Wang J.M., Zhang F., Sun J.L. Sulfated modification can enhance the adjuvant activity of Astragalus polysaccharide for ND vaccine. Carbohydr. Polym. 2008, 73:303-308.
37. Letsch A., Scheibenbogen C. Quantification and characterization of specific T-cells by antigen-specific cytokine production using ELISPOT assay or intracellular cytokine staining. Methods 2003, 31:143-149.
38. Nhiem N.X., Kiem P.V., Minh C.V., Tai B.H., Tung N.H., Ha D.T., Soung K.S., Kim J.H., Ahn J.Y., Lee Y.M., Kim Y.H. Structure-activity relationship of lupane-triterpene glycosides from Acanthopanax koreanum on spleen lymphocyte IL-2 and IFN-gamma. Bioorg. Med. Chem. Lett. 2010, 20:4927-4931.
39. Irie T., Watarai S., Kodama H. Humoral immune response of carp (Cyprinus carpio) induced by oral immunization with liposome-entrapped antigen. Dev. Comp. Immunol. 2003, 27:413-421.
40. Lu C.P. Veterinary Microbiology 2001, 101-103. China Agriculture Press, Beijing.
41. Herr M., Bostedt H., Failing K. IgG and IgM levels in dairy cows during the periparturient period. Theriogenology 2011, 75:377-385.