Naito Seishiro, Taneichi Maiko, Kato Hiroshi, Tanaka Yuriko, Ami Yasushi, Suzaki Yuriko, Mori Masahito, Nakano Yoshio, Yamamura Hiroyuki, Morokuma Kazunori, Ohkuma Kunio, Miyake Hidekazu, Kiniwa Mamoru, Komuro Katsutoshi, Uchida Tetsuya
Department of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Int Arch Allergy Immunol. 2002 Dec;129(4):314-9. doi: 10.1159/000067588.
We have previously reported that intraperitoneal injection with OVA-liposome conjugates induces OVA-specific and IgE-selective unresponsiveness in mice.
In the present study, the effects of oral pre-treatment with OVA-liposome conjugates or with plain OVA solution on anti-OVA IgG antibody production were investigated in mice after subsequent immunization with alum-adsorbed OVA. Control mice received only the immunization.
The levels of serum anti-OVA IgG antibody in mice receiving oral administration of OVA-liposome were comparable to those in the control mice. However, in mice receiving oral administration of the same dose of plain OVA, levels of serum anti-OVA IgG antibody were significantly lower than those in control mice. Surprisingly, anti-OVA IgE antibody production was completely inhibited in mice receiving oral administration of OVA-liposome conjugates. Splenic CD4(+) T cells of mice receiving oral administration of OVA-liposome and those of control mice produced comparable levels of cytokines, while those of mice receiving oral administration of plain OVA solution produced significantly lower levels of cytokines than those in the other two groups.
Orally administered OVA-liposome did not affect anti-OVA IgG production but did inhibit anti-OVA IgE antibody production, while orally administered OVA solution inhibited production of both IgG and IgE antibodies. These results suggest that antigen-liposome conjugates can possibly be orally administered in order to control antigen-specific IgE antibody production, without affecting IgG antibody production.
我们之前报道过,腹腔注射卵清蛋白-脂质体偶联物可诱导小鼠产生卵清蛋白特异性和IgE选择性无反应性。
在本研究中,在用明矾吸附的卵清蛋白对小鼠进行后续免疫后,研究了口服卵清蛋白-脂质体偶联物或普通卵清蛋白溶液预处理对抗卵清蛋白IgG抗体产生的影响。对照小鼠仅接受免疫。
口服卵清蛋白-脂质体的小鼠血清抗卵清蛋白IgG抗体水平与对照小鼠相当。然而,口服相同剂量普通卵清蛋白的小鼠血清抗卵清蛋白IgG抗体水平明显低于对照小鼠。令人惊讶的是,口服卵清蛋白-脂质体偶联物的小鼠中抗卵清蛋白IgE抗体的产生被完全抑制。口服卵清蛋白-脂质体的小鼠和对照小鼠的脾脏CD4(+) T细胞产生的细胞因子水平相当,而口服普通卵清蛋白溶液的小鼠产生的细胞因子水平明显低于其他两组。
口服卵清蛋白-脂质体不影响抗卵清蛋白IgG的产生,但抑制抗卵清蛋白IgE抗体的产生,而口服卵清蛋白溶液则抑制IgG和IgE抗体的产生。这些结果表明,抗原-脂质体偶联物可能可以口服,以控制抗原特异性IgE抗体的产生,而不影响IgG抗体的产生。