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A study on the inhibitory effect on transplanted tumor growth expressing HCV NS3 protein by HCV minigene vaccine based on invariant chain substitution in mice / 中华肝脏病杂志
Chinese Journal of Hepatology ; (12): 801-804, 2005.
Artigo em Chinês | WPRIM | ID: wpr-276347
ABSTRACT
<p><b>OBJECTIVES</b>To establish a transplanted tumor producing HCV NS3 protein in mice and study the therapeutic effect of minigene vaccine based on invariant chain substitution.</p><p><b>METHODS</b>SP2/0-NS3 cells expressing HCV NS3 antigen were injected subcutaneously into BALB/ c mice. After three days of inoculation, different therapeutical reagents were injected intramuscularly into different groups of mice. The boost immunization was carried out two weeks after the first immunization. The efficiency of HCV NS3 Th1 minigene vaccine was estimated after 60 days observation.</p><p><b>RESULTS</b>For saline, pCI-neo, pHCV-NS3 and pHCV-NS3-Th1 treated groups, the induction period needed for tumor growth was 16.17+/-2.55, 14.40+/-1.82, 16.75+/-2.36, and 24.00+/-5.57 days (t =2.623, P =0.034 vs saline, t =3.713, P =0.010 vs pCI-neo and t =2.425, P =0.045 vs pHCV-NS3) respectively. The tumorigenesis rates were 100%, 100%, 57.1% (8/14, chi2 = 6.190, P = 0.013 vs saline and chi2 = 6.608, P = 0.010 vs pCI-neo) and 46.7% (7/15, chi2 = 9.707, P = 0.002 vs saline and chi2 = 10.311, P = 0.001 vs pCI-neo ) respectively. The survival rates were 0, 0, 50.0% (7/14, chi2 = 5.787, P = 0.016 vs saline and chi2 = 9.333, P = 0.002 vs pCI-neo) and 53.3% (8/15, chi2 = 6.651, P = 0.010 vs saline and chi2 = 10.311, P = 0.001 vs pCI-neo) respectively. The average tumor diameter of the pHCV-NS3-Th1 treated group was significantly smaller compared with the control groups and the pHCV-NS3 treated group (P =0.001). Moreover, the average survival time of tumor-bearing mice immunized with pHCV-NS3-Th1 was 6 days longer compared with the saline treated group, 12 days longer compared with the pCI-neo treated group (P =0.001), and 6 days compared with the pHCV-NS3 treated group.</p><p><b>CONCLUSION</b>HCV NS3 Th1 epitope vaccine might be a potential biotherapy candidate against HCV infection.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Células Tumorais Cultivadas / Vacinas contra Hepatite Viral / Vacinas Sintéticas / Distribuição Aleatória / Proteínas não Estruturais Virais / Usos Terapêuticos / Genética / Metabolismo / Camundongos Endogâmicos BALB C Limite: Animais Idioma: Chinês Revista: Chinese Journal of Hepatology Ano de publicação: 2005 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Células Tumorais Cultivadas / Vacinas contra Hepatite Viral / Vacinas Sintéticas / Distribuição Aleatória / Proteínas não Estruturais Virais / Usos Terapêuticos / Genética / Metabolismo / Camundongos Endogâmicos BALB C Limite: Animais Idioma: Chinês Revista: Chinese Journal of Hepatology Ano de publicação: 2005 Tipo de documento: Artigo