Jimenez J C, Fontaine J, Grzych J M, Capron M, Dei-Cas E
Institut Pasteur de Lille, France.
Ann Trop Med Parasitol. 2009 Dec;103(8):693-703. doi: 10.1179/000349809X12502035776351.
The mechanisms involved in the induction of the immune response in humans or experimental hosts infected with Giardia intestinalis are not well understood. The results of previous studies indicate that the parasite induces a mixed Th1/Th2 response and that, in experimentally infected mice, the parasite's excreted/secreted (E/S) proteins contain cysteine proteases that are recognised by the murine immune system. In the present study, the possible effects of the E/S proteases of G. intestinalis on the host's humoral and cellular immune responses were investigated in BALB/c mice immunized with the parasite's E/S proteins. High titres of specific IgG(1), IgG(2a) and IgE antibodies were detected after immunization with native E/S proteins. Spleen cells stimulated with such proteins in vitro showed a significant antigen-specific proliferative response accompanied by the production of high concentrations of interleukin-4 (IL-4), interleukin-5 (IL-5) and interleukin-10 (IL-10) but little secretion of interferon-gamma (IFN-gamma). When, before use, the proteases in the E/S proteins were inhibited, by heat treatment or the addition of E-64, they elicited much lower titres of specific IgG(1) and IgE in mice while, in splenocytes in vitro, they triggered much lower production of IL-4, IL-5 and IL-10 and reduced antigen-specific proliferation. Since E-64 only inhibits cysteine proteases, these results indicate that the excreted/secreted cysteine proteases of G. intestinalis may be involved in the induction and regulation of a specific immune response in the infected host.
对于感染了肠道贾第虫的人类或实验宿主中诱导免疫反应的机制,目前尚未完全了解。先前的研究结果表明,该寄生虫可诱导混合的Th1/Th2反应,并且在实验感染的小鼠中,寄生虫分泌/排泄(E/S)蛋白中含有的半胱氨酸蛋白酶可被小鼠免疫系统识别。在本研究中,在用寄生虫的E/S蛋白免疫的BALB/c小鼠中,研究了肠道贾第虫E/S蛋白酶对宿主体液免疫和细胞免疫反应的可能影响。用天然E/S蛋白免疫后,检测到高滴度的特异性IgG(1)、IgG(2a)和IgE抗体。体外经此类蛋白刺激的脾细胞显示出显著的抗原特异性增殖反应,并伴有高浓度白细胞介素-4(IL-4)、白细胞介素-5(IL-5)和白细胞介素-10(IL-10)的产生,但干扰素-γ(IFN-γ)分泌很少。当在使用前通过热处理或添加E-64抑制E/S蛋白中的蛋白酶时,它们在小鼠中引发的特异性IgG(1)和IgE滴度要低得多,而在体外脾细胞中,它们引发的IL-4、IL-5和IL-10产生量要低得多,并且抗原特异性增殖降低。由于E-64仅抑制半胱氨酸蛋白酶,这些结果表明肠道贾第虫分泌/排泄的半胱氨酸蛋白酶可能参与了感染宿主中特异性免疫反应的诱导和调节。