Villareall B B, Melendro E I, Ramos F, Ximénez C
Faculty of Chemical Sciences, University of Sinaloa, Culiacán Sinaloa, México.
Arch Med Res. 1992 Spring;23(1):69-72.
Several immunization schedules with E. histolytica trophozoites were tested on Balb/c mice in order to induce antibody responses, both in intestinal secretions and in serum. Mice were immunized either orally, systemically, or using one of two combined schedules: the oral route followed by the systemic route (footpad), or vice versa. Each of the immunization schedules used in this project induced an anti-E. histolytica antibody response and there appears to be a correlation between the immunization route employed and the immunoglobulin isotype induced in the gut. Secretory IgA production is favored by the oral administration of trophozoites, whereas mucosal IgG appears to be enhanced by the systemic immunization route. Both schedules are effective in the induction of secretory IgA in the gut, yet higher and earlier levels of IgA appear in orally immunized mice. When systemic immunization is employed, the increase in antibody levels in the intestinal fluid is slower, and IgG is the predominant class. The combined oral/systemic routes of immunization appear to be comparably effective for the induction of local and systemic IgA and IgM antibody production. However, mice immunized first systemically and then locally produce more IgG in both compartments. Combined schedules modify the isotype pattern of antibody responses in serum and in intestinal secretions when compared with single (i.e., oral or systemic) schedules, but they do not appear to favor a secretory IgA immune response.
为了在肠道分泌物和血清中诱导抗体反应,在Balb/c小鼠上测试了几种用溶组织内阿米巴滋养体进行免疫的方案。小鼠通过口服、全身免疫或使用两种联合方案之一进行免疫:口服途径后接全身途径(足垫),或反之。本项目中使用的每种免疫方案都诱导了抗溶组织内阿米巴抗体反应,并且所采用的免疫途径与肠道中诱导的免疫球蛋白同种型之间似乎存在相关性。口服滋养体有利于分泌型IgA的产生,而全身免疫途径似乎会增强黏膜IgG。两种方案在诱导肠道分泌型IgA方面均有效,但口服免疫的小鼠中IgA水平更高且出现更早。当采用全身免疫时,肠液中抗体水平的增加较慢,且IgG是主要类别。口服/全身联合免疫途径在诱导局部和全身IgA及IgM抗体产生方面似乎同样有效。然而,先进行全身免疫然后进行局部免疫的小鼠在两个部位产生的IgG更多。与单一(即口服或全身)方案相比,联合方案改变了血清和肠道分泌物中抗体反应的同种型模式,但它们似乎并不有利于分泌型IgA免疫反应。