Svennerholm A M, Holmgren J
Infect Immun. 1977 Feb;15(2):360-9. doi: 10.1128/iai.15.2.360-369.1977.
An in vitro culture technique with synthesis of 14C-labeled protein has been used to study immunoglobulin and specific-antibody formation by spleen, mesenteric lymph nodes, Peyer's patches, and small intestine of rabbits, which were immunized twice subcutaneously with Vibrio cholerae lipopolysaccharide (LPS) and enterotoxin; saline-injected rabbits served as controls. Newly synthesized immunoglobulin G (IgG), IgA, and IgM were quantitated by liquid scintillation after their isolation by means of affinity chromatography from columns with immunoglobulin class-specific antibodies coupled to Sepharose. Specific antibodies were similarly measured after purification from gels derivatized with LPS or cholera toxin. The isolated antibodies had full biological activity as studied in protection tests. The immunization increased the overall IgM synthesis in the spleen. It also enhanced the production of IgA and IgG in Peyer's patches and of IgA in intestine. Significant synthesis of radiolabeled antibodies against both V. cholerae LPS and enterotoxin was found in spleen as well as in Peyer's patches of immunized animals. Titration with an enzyme-linked immunosorbent assay (ELISA) showed significant levels of IgG as well as IgA antibodies in incubation medium from all the studied tissues, whereas specific IgM was only found for spleen and mesenteric lymph nodes. Simultaneous tissue incubations at 37 degrees C and in an ice bath indicated that the major part of the antibodies registered with the ELISA represented de novo synthesis.
一种采用合成14C标记蛋白的体外培养技术,已用于研究经霍乱弧菌脂多糖(LPS)和肠毒素两次皮下免疫的兔脾脏、肠系膜淋巴结、派尔集合淋巴结及小肠中免疫球蛋白和特异性抗体的形成;注射生理盐水的兔作为对照。通过亲和层析从与免疫球蛋白类别特异性抗体偶联至琼脂糖的柱中分离后,利用液体闪烁法对新合成的免疫球蛋白G(IgG)、IgA和IgM进行定量。从用LPS或霍乱毒素衍生化的凝胶中纯化后,以类似方式测量特异性抗体。如在保护试验中所研究的,分离出的抗体具有完全的生物学活性。免疫增加了脾脏中总的IgM合成。它还增强了派尔集合淋巴结中IgA和IgG以及肠道中IgA的产生。在免疫动物的脾脏以及派尔集合淋巴结中发现了针对霍乱弧菌LPS和肠毒素的放射性标记抗体的显著合成。用酶联免疫吸附测定(ELISA)滴定显示,所有研究组织的孵育培养基中IgG以及IgA抗体水平显著,而特异性IgM仅在脾脏和肠系膜淋巴结中发现。在37℃和冰浴中同时进行组织孵育表明,ELISA检测到的大部分抗体代表从头合成。