Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
Emerg Microbes Infect. 2017 Dec 20;6(12):e116. doi: 10.1038/emi.2017.106.
Scrub typhus, caused by Orientia tsutsugamushi infection, has been a serious public health issue in the Asia-Pacific region, with rising incidence and sporadic outbreaks. However, human protective immunity against specific antigens has been poorly characterized for this bacterium. In addition, immunity produced in early vaccine trials or even after natural infections, did not last long and had poor cross-reactivity among various genotypes. Here, we systematically investigated the kinetics and magnitude of specific adaptive immunity against two membrane antigens, 56 kDa type-specific antigen (TSA56) and surface cell antigen A (ScaA), that are involved in bacterial adhesion and invasion of the host in 64 recovered scrub typhus patients. Antibody responses to the bacterial antigens in patients were generally short-lived and waned to baseline levels 2 years after recovery. The anti-TSA56 IgG responses were predominantly composed of the IgG1 and IgG3 subclasses and persisted for up to 1 year after recovery, whereas IgG specific to ScaA primarily consisted of more transient IgG1, with limited responses by other subclasses. Cellular immunity, including CD4 and CD8 T-cells specific to membrane antigens, also rapidly declined from 1 year after infection, as measured by enzyme-linked immunospot (ELISPOT) assays and flow cytometry. The short longevity of antigen-specific adaptive immunity might be attributable to limited memory responses, as observed in earlier vaccine studies using whole bacterial antigens. Finally, we identified HLA-A*0201-restricted and highly conserved CD8 T-cell epitopes in the TSA56 antigen, which may be valuable tools for assessing cellular immunity against O. tsutsugamushi and developing an effective scrub typhus vaccine.
恙虫病由恙虫东方体感染引起,一直是亚太地区严重的公共卫生问题,发病率和散发疫情不断上升。然而,针对这种细菌,人类针对特定抗原的保护性免疫仍未得到很好的描述。此外,早期疫苗试验甚至自然感染后产生的免疫作用持续时间短,且不同基因型之间的交叉反应性差。在这里,我们系统地研究了两种膜抗原(56 kDa 型特异性抗原(TSA56)和表面细胞抗原 A(ScaA))的特异性适应性免疫的动力学和幅度,这两种抗原参与细菌的黏附和宿主的入侵,共调查了 64 名痊愈的恙虫病患者。患者对细菌抗原的抗体反应通常持续时间短,在恢复后 2 年内降至基线水平。抗 TSA56 IgG 反应主要由 IgG1 和 IgG3 亚类组成,并在恢复后持续长达 1 年,而针对 ScaA 的 IgG 主要由更短暂的 IgG1 组成,其他亚类的反应有限。细胞免疫,包括针对膜抗原的 CD4 和 CD8 T 细胞,也从感染后 1 年开始迅速下降,如酶联免疫斑点(ELISPOT)和流式细胞术检测所示。抗原特异性适应性免疫的短暂寿命可能归因于记忆反应有限,如早期使用全细菌抗原的疫苗研究中观察到的那样。最后,我们在 TSA56 抗原中鉴定了 HLA-A*0201 限制性和高度保守的 CD8 T 细胞表位,这可能是评估针对恙虫东方体的细胞免疫和开发有效恙虫病疫苗的有价值工具。