Fló J, Roux M E, Massouh E
Department of Biological Chemistry, Faculty of Exact and Natural Sciences, University of Buenos Aires, Argentina.
Infect Immun. 1994 Nov;62(11):4948-54. doi: 10.1128/iai.62.11.4948-4954.1994.
Malnourished rats during suckling were orally immunized with cholera toxin (CT) after different periods of refeeding. Intestinal fluids, sera, and supernatant fluids from cultured mesenteric lymph node (MLN) cells were obtained after rats were given three doses of CT and analyzed by enzyme-linked immunosorbent assay (ELISA) to evaluate the specific antibody response. Serum-specific immunoglobulin G (IgG), IgA, and IgM were severely diminished in malnourished rats immunized with three doses of CT after 1 week of refeeding when compared with those of controls. Also, a decreased IgA ELISA titer of the intestinal fluids and abrogation of the capacity to neutralize the CT in the intestinal ligated loop test were found. When a booster was given at 113 days of age, the immune response continued to be affected in the serum and the intestinal fluid. The results from the analysis of the supernatant fluids from cultured MLN cells were coincident with those mentioned above. When one dose of CT was administered into Peyer's patches (PP) after 1 week of refeeding, an impaired immune response was found in the intestinal fluid of malnourished rats during suckling compared with that of controls. This result together with the analysis of supernatant from MLN and PP cell cultures suggests that antigen triggering in the PP was affected. When the refeeding period was extended to 30 days and then the first dose of CT was administered, the antibody immune responses in intestinal fluid serum and supernatant fluid approached control values. These observations reinforce the fact that the gut-associated lymphoid tissue immaturity of the rats when they received the first CT dose (at 28 days old) was the main reason for the decreased immune response observed in the experimental group.
哺乳期营养不良的大鼠在不同的再喂养期后口服霍乱毒素(CT)进行免疫。在给大鼠注射三剂CT后,收集肠液、血清以及培养的肠系膜淋巴结(MLN)细胞的上清液,并通过酶联免疫吸附测定(ELISA)进行分析,以评估特异性抗体反应。与对照组相比,再喂养1周后接受三剂CT免疫的营养不良大鼠的血清特异性免疫球蛋白G(IgG)、IgA和IgM显著减少。此外,还发现肠液的IgA ELISA滴度降低,并且在肠结扎环试验中中和CT的能力丧失。当在113日龄时给予加强免疫时,血清和肠液中的免疫反应仍然受到影响。培养的MLN细胞上清液的分析结果与上述结果一致。再喂养1周后,向派尔集合淋巴结(PP)注射一剂CT,发现哺乳期营养不良大鼠的肠液免疫反应与对照组相比受损。该结果与MLN和PP细胞培养上清液的分析结果表明,PP中的抗原触发受到影响。当再喂养期延长至30天,然后给予第一剂CT时,肠液、血清和上清液中的抗体免疫反应接近对照值。这些观察结果进一步证实,大鼠在接受第一剂CT(28日龄)时肠道相关淋巴组织不成熟是实验组免疫反应降低的主要原因。