Choi Sangho, Jeong Hang Jin, Ju Young Ran, Gill Byoungchul, Hwang Kyu-Jam, Lee Jeongmin
Division of Zoonoses, Center for Immunology and Pathology, Korea National Institute of Health, Korea Centers for Diseases Control and Prevention, Cheongju 363-700, Republic of Korea.
J Microbiol Biotechnol. 2014 Dec 28;24(12):1728-35. doi: 10.4014/jmb.1407.07048.
Scrub typhus, caused by infection with Orientia tsutsugamushi, is a mite-borne zoonotic disease endemic to the Asian-Pacific region. In Korea, the incidence of this disease has increased with climate changes, and over 10,000 cases of infection were reported in 2013. Although this infection is treatable with antibiotics such as doxycycline and azithromycin, an effective prophylactic vaccine against O. tsutsugamushi would be more desirable for preventing scrub typhus in endemic areas. In this study, we investigated the 56-kDa type-specific antigen (TSA56), which is a major outer membrane protein of O. tsutsugamushi, as a vaccine candidate. Intranasal immunization of recombinant TSA56 (rec56) induced a higher level of TSA56- specific IgG than that induced by intramuscular immunization of tsa56-expressing DNA (p56). Both types of immunization induced a cell-mediated immune response to TSA56, as demonstrated by the splenic cell proliferation assay. Mice immunized with p56, followed by rec56 plus heat-labile enterotoxin B subunit from E. coli, had a stronger protection from a homologous challenge with the O. tsutsugamushi Boryong strain than with other combinations. Our preliminary results suggest that an effective human vaccine for scrub typhus can include either recombinant TSA56 protein or tsa56-expressing DNA, and provide the basis for further studies to optimize vaccine performance using additional antigens or different adjuvants.
恙虫病由恙虫东方体感染引起,是一种由螨传播的人畜共患病,流行于亚太地区。在韩国,这种疾病的发病率随气候变化而上升,2013年报告的感染病例超过10000例。尽管这种感染可用强力霉素和阿奇霉素等抗生素治疗,但一种有效的抗恙虫东方体预防性疫苗对于在流行地区预防恙虫病更为理想。在本研究中,我们研究了恙虫东方体的主要外膜蛋白56 kDa型特异性抗原(TSA56)作为候选疫苗。重组TSA56(rec56)鼻内免疫诱导的TSA56特异性IgG水平高于表达tsa56的DNA(p56)肌肉内免疫诱导的水平。如脾细胞增殖试验所示,两种免疫方式均诱导了对TSA56的细胞介导免疫反应。用p56免疫小鼠,随后用rec56加来自大肠杆菌的不耐热肠毒素B亚单位免疫,与其他组合相比,对恙虫东方体保宁菌株的同源攻击具有更强的保护作用。我们的初步结果表明,一种有效的恙虫病人类疫苗可以包括重组TSA56蛋白或表达tsa56的DNA,并为进一步研究使用其他抗原或不同佐剂优化疫苗性能提供了基础。