Induction of anti-HBs in HB vaccine nonresponders in vivo by hepatitis B surface antigen-pulsed blood dendritic cells

被引:29
作者
Akbar, Fazle [1 ]
Furukawa, Shinya [1 ]
Yoshida, Osamu [1 ]
Hiasa, Yoichi [1 ]
Horiike, Norio [1 ]
Onji, Morikazu [1 ]
机构
[1] Ehime Univ, Grad Sch Med, Dept Gastroenterol & Metabol, Toon City, Ehime 7910295, Japan
关键词
Anti-HBs; dendritic cells; HB vaccine; HBsAg; HBsAg-pulsed dendritic cells; vaccine nonresponders; VIRUS; NONRESPONSIVENESS; REVACCINATION; RESPONDERS; PREVENTION; FAILURE; DNA;
D O I
10.1016/j.jhep.2007.02.021
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background/Aims: Antigen-pulsed dendritic cells (DCs) are now used for treatment of patients with cancers, however, the efficacy of these DCs has never been evaluated for prophylactic purposes. The aim of this study was (1) to prepare hepatitis B surface antigen (HBsAg)-pulsed human blood DCs, (2) to assess immunogenicity of HBsAg-pulsed DCs in vitro and (3) to evaluate the efficacy of HBsAg-pulsed DCs in hepatitis B (HB) vaccine nonresponders. Methods: Human peripheral blood DCs were cultured with HBsAg to prepare HBsAg-pulsed DCs. The expression of immunogenic epitopes of HBsAg on HBsAg-pulsed DCs was assessed in vitro. Finally, HBsAg-pulsed DCs were administered, intradermally to six HB vaccine nonresponders and the levels of antibody to HBsAg (anti-HBs) in the sera were assessed. Results: HB vaccine nonresponders did not exhibit features of immediate, early or delayed adverse reactions due to administration of HBsAg-pulsed DCs. Anti-HBs were detected in the sera of all HB vaccine nonresponders within 28 days after administration of HBsAg-pulsed DCs. Conclusions: This study opens a new field of application of antigen-pulsed DCs for prophylactic purposes when adequate levels of protective antibody cannot be induced by traditional vaccination approaches. (c) 2007 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 66
页数:7
相关论文
共 29 条
[1]
Akbar Sk. Md. Fazle, 2004, Current Drug Targets - Inflammation and Allergy, V3, P305, DOI 10.2174/1568010043343787
[2]
Akbar Sk. Md. Fazle, 2004, Current Drug Targets - Infectious Disorders, V4, P93, DOI 10.2174/1568005043340885
[3]
Akbar SMF, 2004, INT J MOL MED, V14, P295
[4]
Epidemiology and prevention of hepatitis B [J].
Alter, MJ .
SEMINARS IN LIVER DISEASE, 2003, 23 (01) :39-46
[5]
Failure of a reinforced triple course of hepatitis B vaccination in patients transplanted for HBV-related cirrhosis [J].
Angelico, M ;
Di Paolo, D ;
Trinito, MO ;
Petrolati, A ;
Araco, A ;
Zazza, S ;
Lionetti, R ;
Casciani, CU ;
Tisone, G .
HEPATOLOGY, 2002, 35 (01) :176-181
[6]
Arima S, 2003, INT J MOL MED, V11, P169
[7]
Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[8]
Revaccination against hepatitis B virus of non-responding and low-responding infants immunised at birth. A parallel evaluation of rubella and tetanus vaccine [J].
Belloni, C ;
Tinelli, C ;
Orsolini, P ;
Pistorio, A ;
Avanzini, A ;
Moretta, A ;
Gulminetti, R ;
Bogliolo, O ;
Chirico, G ;
Rondini, G .
VACCINE, 1998, 16 (04) :399-402
[9]
Vaccination against hepatitis B in health care workers [J].
Bonanni, P ;
Bonaccorsi, G .
VACCINE, 2001, 19 (17-19) :2389-2394
[10]
THE CELLULAR BASIS FOR LACK OF ANTIBODY-RESPONSE TO HEPATITIS-B VACCINE IN HUMANS [J].
EGEA, E ;
IGLESIAS, A ;
SALAZAR, M ;
MORIMOTO, C ;
KRUSKALL, MS ;
AWDEH, Z ;
SCHLOSSMAN, SF ;
ALPER, CA ;
YUNIS, EJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :531-538