Rendi-Wagner Pamela, Wiedermann Gerhard, Stemberger Heinrich, Kollaritsch Herwig
Department of Specific Prophylaxis and Tropical Medicine, Institute of Pathophysiology, University of Vienna, Vienna, Austria.
Wien Klin Wochenschr. 2002 Mar 28;114(5-6):175-80.
The currently available recombinant hepatitis B vaccines are safe, efficacious and immunogenic. Nevertheless, a high rate of low- and nonresponsiveness to the current vaccine poses a problem since this group remains susceptible to infection with hepatitis B virus. Efforts are underway to develop new vaccines and strategies to enhance seroprotection rates. One possibility under investigation is the low-dose intradermal administration of vaccine since the immune system is well represented in both the epidermis and the dermis. Despite encouraging results concerning the immunogenicity in previous non-responders, the main difficulty is the technique of administration and unacceptable local adverse effects. Promising data have emerged from clinical trials evaluating the immunogenicity of new recombinant vaccines containing the complete pre-S1 and pre-S2 regions of HbsAg and, more recently, of novel adjuvanted hepatitis B vaccines. Future approaches include DNA vaccination and expression of HbsAg determinants in live recombinant vectors.
目前可用的重组乙型肝炎疫苗安全、有效且具有免疫原性。然而,当前疫苗的低应答率和无应答率较高,这构成了一个问题,因为这部分人群仍易感染乙型肝炎病毒。目前正在努力研发新疫苗和策略以提高血清保护率。正在研究的一种可能性是低剂量皮内接种疫苗,因为免疫系统在表皮和真皮中都有充分体现。尽管先前对无应答者的免疫原性研究结果令人鼓舞,但主要困难在于接种技术和难以接受的局部不良反应。评估含有完整前S1和前S2区域的新型重组疫苗以及最近新型佐剂乙型肝炎疫苗免疫原性的临床试验已出现了有前景的数据。未来的方法包括DNA疫苗接种和在活重组载体中表达乙肝表面抗原决定簇。