Treatment of Chronic Hepatitis B with Vaccine or Vaccine-Antibody Complex Loaded pDC and mDC
Author(s) -
İbrahim Hatipoğlu,
Duygu Ercan,
Soner Aksu,
İbrahim Söğüt,
S. Sekmen,
Gazi Turgut,
Deniz Duralı,
Aynur Başalp
Publication year - 2013
Publication title -
viral hepatitis journal
Language(s) - English
Resource type - Journals
eISSN - 2147-2939
pISSN - 1307-9441
DOI - 10.4274/vhd.55265
Subject(s) - medicine , chronic hepatitis , antibody , hepatitis b vaccine , virology , immunology , hepatitis b virus , virus , hbsag
© Viral Hepatit Dergisi, Ga le nos Ya y› ne vi ta ra f›n dan ba s›l m›fl t›r. / Viral Hepatitis Journal, pub lis hed by Ga le nos Pub lis hing. ABS TRACT Objective: In this study, we aimed to develop new alternative dendritic cell (DC) vaccine by using synergic effect of between vaccine or vaccine-antibody loaded plasmacytoid dendritic cell (pDC) and conventional DC/myeloid DC (cDC/mDC) to treat chronic hepatitis B. Materials and Methods: pDCs and mDCs derived from bone marrow of chronic hepatitis B model (HBV-tg) mice in the presence of flt-3L in in vitro and loaded with vaccine or vaccine-antibody complex and then HBV-tg mice were immunized intraperitoneally two times at two weeks intervals. Anti-HBsAg response was detected by ELISA, decrease of HBV DNA was investigated by RT-qPCR. Results: At day 8, flow cytometry analyses have shown that the frequency of mDCs was about 65% and pDC was about 35%. Anti-HBsAg response was induced in HBV-tg mice but it was not significant statistically and we did not detected decrease of HBV DNA in plasma. Conclusion: Even though pDC and mDC were derived from bone marrows, vaccine or vaccine-antibody complex may protect synergic effect between DCs. (Viral Hepatitis Journal 2013; 19(1): 27-31)
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom