Ishizaka K, Okudaira H, King T P
J Immunol. 1975 Jan;114(1 Pt 1):110-5.
Ragweed antigen E loses its major antigenic determinant after denaturation in 8 M urea. The urea-denatured (UD) antigen and alpha-polypeptide chain isolated from the denatured molecule possess their own antigenic determinant(s) but lack the major determinant of the native molecule. The UD antigen and alpha-chain, however, are capable of priming mouse T cells specific for antigen E. Priming of A/J mice with the modified antigen enhanced both IgG and IgE antibody responses to antigen E. Both UD antigen-primed spleen cells and alpha-chain-primed spleen cells collaborate with DNP-primed cells to give an adoptive secondary anti-DNP antibody response to DNP-ragweed antigen in syngeneic irradiated mice. Pretreatment of A/J mice with an i.v. injection of alpha-chain partially suppressed both IgE and IgG antibody responses to antigen E. Weekly injections of alpha-chain or UD antigen to antigen E-primed animals depressed on-going IgE antibody response, and suppressed secondary IgE antibody response to antigen E. Transfer of spleen cells from animals treated with the modified antigen to irradiated recipients followed by challenge with native antigen showed that the adoptive secondary response was suppressed by injections of modified antigen to the donors. The results indicate that the immunocompetent cell population was changed by the treatment and provide an experimental model to analyze the immunologic effect of hyposensitization treatment.
豚草抗原E在8M尿素中变性后失去其主要抗原决定簇。从变性分子中分离出的尿素变性(UD)抗原和α-多肽链具有自身的抗原决定簇,但缺乏天然分子的主要决定簇。然而,UD抗原和α链能够引发针对抗原E的小鼠T细胞。用修饰抗原对A/J小鼠进行致敏增强了对抗原E的IgG和IgE抗体反应。用UD抗原致敏的脾细胞和用α链致敏的脾细胞都能与用二硝基苯(DNP)致敏的细胞协同作用,在同基因照射小鼠中产生对DNP-豚草抗原的过继性二次抗DNP抗体反应。给A/J小鼠静脉注射α链预处理部分抑制了对抗原E的IgE和IgG抗体反应。每周给抗原E致敏的动物注射α链或UD抗原可抑制正在进行的IgE抗体反应,并抑制对抗原E的二次IgE抗体反应。将经修饰抗原处理的动物的脾细胞转移到经照射的受体,然后用天然抗原进行攻击,结果表明,给供体注射修饰抗原可抑制过继性二次反应。结果表明,处理改变了免疫活性细胞群体,并提供了一个实验模型来分析脱敏治疗的免疫学效果。