Suzaki Yuriko, Ami Yasushi, Nagata Noriyo, Naito Seishiro, Kato Hiroshi, Taneichi Maiko, Takahashi Motohide, Komiya Takako, Satoh Sachihiro, Gondaira Fumio, Sugiyama Junichi, Nakano Yoshio, Mori Masahito, Komuro Katsutoshi, Uchida Tetsuya
Division of Experimental Animals Research, Department of Safety Research on Biologics, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama, Tokyo 208-0011, Japan.
Int Arch Allergy Immunol. 2002 Apr;127(4):294-8. doi: 10.1159/000057746.
We previously reported that the purified Shiga toxins (Stx) Stx1 and Stx2, when coupled with liposomes, induced substantial production of anti-Stx1 and anti-Stx2 IgG antibody, respectively, in mice. The levels of anti-Stx antibody in the sera of mice immune to Stx-liposome correlated well with the protection against subsequent challenge with Stx. Furthermore, mice immunized with a mixture of Stx1-liposome and Stx2-liposome were successfully protected against oral infection with cytotoxin-producing Escherichia coli O157:H7.
In this study, the induction of protection against Stx2 by Stx2-liposomes was evaluated in monkeys.
Stx2-liposomes induced a substantial amount of anti-Stx2 IgG antibodies as well as Stx2 neutralizing antibodies in monkeys. Test monkeys were successfully protected against challenge with lethal doses of Stx2. Moreover, these monkeys showed no apparent symptoms, while nonimmunized control monkeys died within 4 days with hemorrhagic gastroenteritis and renal disorder. In addition, as shown by other cases involving antigen-liposome conjugates, Stx2-liposome did not induce anti-Stx2 IgE antibody production, though it stimulated the production of a substantial amount of anti-Stx2 IgG antibodies.
These results suggest that Stx-liposome conjugates may serve as candidate vaccines to induce protection against death caused by cytotoxin-producing E. coli infection.
我们之前报道过,纯化的志贺毒素(Stx)Stx1和Stx2与脂质体偶联后,分别在小鼠体内诱导产生大量的抗Stx1和抗Stx2 IgG抗体。对Stx-脂质体免疫的小鼠血清中抗Stx抗体水平与抵抗随后Stx攻击的保护作用密切相关。此外,用Stx1-脂质体和Stx2-脂质体混合物免疫的小鼠成功抵抗了产细胞毒素的大肠杆菌O157:H7的口服感染。
在本研究中,评估了Stx2-脂质体对猴子抗Stx2保护作用的诱导情况。
Stx2-脂质体在猴子体内诱导产生了大量的抗Stx2 IgG抗体以及Stx2中和抗体。受试猴子成功抵抗了致死剂量Stx2的攻击。此外,这些猴子没有出现明显症状,而未免疫的对照猴子在4天内死于出血性肠胃炎和肾脏疾病。另外,正如其他涉及抗原-脂质体偶联物的案例所示,Stx2-脂质体虽然刺激产生了大量的抗Stx2 IgG抗体,但并未诱导抗Stx2 IgE抗体的产生。
这些结果表明,Stx-脂质体偶联物可能作为候选疫苗,诱导抵抗产细胞毒素的大肠杆菌感染所致死亡的保护作用。