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脂质体瘤苗抗小鼠H_(22)腹水型肝癌作用研究 被引量:5

The antitumor effect of liposomal tumor vaccine on H_(22) hepatoma
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摘要 目的观察脂质体瘤苗的抗癌作用,寻找有效的抗肿瘤疫苗。方法制备H22肝癌细胞的脂质体瘤苗,将该瘤苗通过腹腔接种,免疫荷瘤的BalB/c小鼠(LAg组),同时设单用抗原免疫组(Ag组)和DHanks组作为对照,比较各组小鼠的生存期,并用MTT法检测外周血和脾淋巴细胞对H22肝癌细胞的体外杀伤作用。结果LAg免疫的BalB/c鼠的平均生存期及脾和外周血淋巴细胞毒活性均高于Ag组及DHanks组(P<0.05),Ag组及DHanks组两者之间差异无显著性(P>0.05)。结论单用H22抗原不能诱导有效的抗肝癌免疫反应,用脂质体包裹后,其抗肝癌作用可明显增强,脂质体瘤苗有潜在的临床应用前景。 Objective To observe the antitumor effect of liposomal tumor vaccine and explore the effectice tumor vaccine formulation. Methods The soluble antigen of H22 hepatoma (Ags) was extracted using 3M KC1 and purified by centrifugation and dialysis. This antigen was entrapped into the MLVs (muhilamellar vesicles) liposomes by mechanical dispersion to constitute the liposomal tumor vaccine. Sixty BalB/c mice inoculated with H22 Hepatoma cell beforehand were divided into three groups at random and were inoculated intraperitoneally with liposomal tumor vaccine (LAg group), the soluble antigen of H22 hepatoma(Ag group)and D-Hanks(D-Hanks group), respectively, eight days later reinoculated. Their survival time was observed and the lymphocyte cytotoxicity was valued by MTF assay. Results LAg group had a longer survival periods and stronger lymphocyte cytotoxicity compared with those treated with Ag and D-Hanks ( P 〈 0.05), but the difference between Ag group and D-Hanks group were not significant ( P 〉 0.05). Conclusion The antitumor immune response of mice with tumor elicited by H22 Ags entrapped in liposomes was enhanced significantly, although no effective response was induced by H22 Ags only,
出处 《胃肠病学和肝病学杂志》 CAS 2005年第4期366-368,共3页 Chinese Journal of Gastroenterology and Hepatology
关键词 脂质体 瘤苗 H22肝癌细胞 liposomes Tumor vaccine H22 hepatoma
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  • 1Nakanishi T, Kunisawa, J, Hayashi A, et al. Positively charged liposome functions as an efficient immunoadjuvant in immune responses to soluble proteins. Biochem Biophysic Res Commun, 1997,240(3):793-793.
  • 2SCHROIT A J. KEY. M. E. Induction of syngeneic tumor specific immunity by liposomes reconstituted with L2C tumor-cell antigens. Immunology, 1983,498(3) :431-438.
  • 3张玲芝.脂质体的制备[A]..见:A脂质体的制备及其在生物医学中的应用[C].北京:北京医大、中国协和医大联合出版社,1998.18-25.
  • 4Babai I, Samira S, Barenholz Y, et al. A novel influnenza subunit vaccine composed of liposome encapsulated haemagglutinin/neuranimidase and IL-2or GM-CSF. 1. Vaccine characterization and efficacy studies in mice. Vaccine, 1999,17(9-10): 1223-1238.
  • 5Sleele G Jr, Raikumar, Ross D MD, et al. Specific active immunotherapy with butanol-extracted, tumor-associated antigens incorporated into liposomes.Surgery, 1984,96(2) :352-359.
  • 6Khemka V,See D,See J,et al. The capacity of a combined liposomal hepatitis B and C vaccine to stimulate humoral and cellular responses in mice. Virallmmunol, 1998,11 (2): 73-78.
  • 7Fukuda T, Kimiya T, Takahashi M, et al. Induction of protection against oral infection with cytotoxin-producing Escherichia coli O 157:H7 in mice by shige-like toxin-liposome conjugate. Int-Arch-Allergy-lmmunol, 1998, 116(4) :313-317.
  • 8Meny, Audran R, Thomasin C, et al. MHC class l-and class Ⅱ-restricted processing and presentation of microencapsulated antigens. Vaccine, 1999;17(9-10), 1047-1056.
  • 9Ousoren C,Storm G. Role of, acrophages in the localisation of liposimes in lympy nodes after subcutaneous administration. Int J Pharm, 1999,183( 1 ):37-41.
  • 10Kenneth LR, Liso R, Sandra G, et al. Characteriza-tion of antigen-presenting cells and present exogenous in association with class 1 MHC molecules. The Journal of Lmmunology, 1993, (150) :549-552.

同被引文献39

  • 1张国庆,刘诚明,孙伟,庞作良,欧江华,王宏江,阿迪力.自体肿瘤细胞疫苗在食管及贲门癌术后的主动免疫研究[J].中国肿瘤临床,2004,31(23):1334-1336. 被引量:3
  • 2高天慧,段芳龄,周云,尚佳,刘明月.β-榄香烯对脂质体瘤苗抗小鼠H_(22)肝癌的免疫增强作用[J].中国误诊学杂志,2005,5(18):3409-3411. 被引量:3
  • 3蒋晓山,程广泽,胡波.NDV/β-榄香烯瘤苗的临床应用研究[J].中国肿瘤临床与康复,1996,3(2):5-7. 被引量:7
  • 4南方,何太平.BLP25脂质体疫苗治疗肺癌和前列腺癌的研究[J].国际生物制品学杂志,2006,29(5):219-221. 被引量:2
  • 5LeGrue S J,Kahan B D,Pellis N R.Extraction of a Murine Tumor-specific Transplantation Antigen with 1-butanol.I.partial Purification by Isoelectric Focusing[J]. J Natl Cancer Inst, 1980,65(1):191-196.
  • 6Samuel J, Budzynski W A,Reddish M A, et al. lmmunog, enicity and Antitumor Activity of a Liposomal MUC1 Peptide based Vaccine[J]. Int J Cancer, 1998,75(2) : 295 -302.
  • 7Ravindra P V, Tiwari A K, Sharma B, et aI. Newcastle disease virus as an oncolytic agent[J]. Indian J Med Res, 2009,130(5) :507-513.
  • 8Wong J, Schulman A, Kelly K,et al. Detection of free peritoneal cancer cells in gastric cancer using cancer specific Newcastle disease virus[J]. J Gastrointest Surg, 2010,14 (1) : 7-14.
  • 9Altomonte J, Marozin S, Schmid R M, et al. Engineered new-castle disease virus as an improved oncolytic agent against hepa toeellular carcinoma[J]. Mol Ther, 2010,18(2) : 275-284.
  • 10Sarfati-Mizrahi D, Lozano-Dubernard B, Soto-Priante E, et al. Protective dose of a recombinant Newcastle disease Lasota-avian influenza virus H5 vaccine against H5N2 highly pathogenic avian influenza virus and velogenic viscerotropic Newcastle disease virus in broilers with high maternal antibody levels[J]. Avian Dis, 2010, 54(1 Suppl) : S239-S241.

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