Parish C R
J Exp Med. 1971 Jul 1;134(1):21-47. doi: 10.1084/jem.134.1.21.
Flagellin (mol.wt. 40,000) from S. adelaide organisms and a series of acetoacetyl derivatives of flagellin were tested for their ability to induce humoral and cell-mediated immunity in adult rats. It was found that unmodified flagellin was an excellent inducer of antibody formation but a poor inducer of delayed-type hypersensitivity. In contrast, increasing acetoacetylation steadily destroyed the ability of flagellin to initiate antibody formation but enhanced the capacity of the molecule to induce flagellin-specific cell-mediated immunity and antibody tolerance. In fact, it appeared that in adult rats antibody formation and cell-mediated immunity may well be opposing immunological processes. Furthermore, the affinity of the acetoacetyl flagellins for anti-flagellin antibodies appeared to determine the type of immune response which predominated. High affinity antigen produced antibody formation whereas low affinity antigen induced cell-mediated immunity and antibody tolerance. The importance of affinity was further evidenced by the fact that a CNBr digest of flagellin induced humoral and cellular immune responses identical to an acetoacetylated flagellin of comparable antigenic activity. From these studies it was proposed that both humoral and cell-mediated immunity can be directed against the same antigenic determinants but that the specificity requirements for delayed hypersensitivity (and antibody tolerance) are less than those required for antibody formation. Some remarkable immunological features of the flagellin system were revealed. Flagellin induced comparable delayed-type hypersensitivity when injected in either saline or FCA. Furthermore, FCA only slightly enhanced the delayed responses induced by the acetoacetyl flagellins and in fact these preparations produced antibody tolerance whether injected in saline or adjuvant. Finally, in contrast to the adult tolerance induced by the acetoacetylated flagellins, which existed only at the antibody level, tolerance in neonatal rats existed at the level of both humoral and cell-mediated immunity. This finding is the first indication of a fundamental difference between neonatal and adult tolerance. The significance of these findings is discussed in the light of current immunological concepts and a hypothesis proposed to explain these phenomena.
对来自阿德莱德沙门氏菌的鞭毛蛋白(分子量40,000)及其一系列乙酰乙酰化衍生物在成年大鼠中诱导体液免疫和细胞介导免疫的能力进行了测试。结果发现,未修饰的鞭毛蛋白是抗体形成的优秀诱导剂,但却是迟发型超敏反应的不良诱导剂。相反,乙酰乙酰化程度的增加稳步破坏了鞭毛蛋白引发抗体形成的能力,但增强了该分子诱导鞭毛蛋白特异性细胞介导免疫和抗体耐受的能力。事实上,在成年大鼠中,抗体形成和细胞介导免疫似乎很可能是相互对立的免疫过程。此外,乙酰乙酰化鞭毛蛋白与抗鞭毛蛋白抗体的亲和力似乎决定了占主导地位的免疫反应类型。高亲和力抗原产生抗体形成,而低亲和力抗原诱导细胞介导免疫和抗体耐受。鞭毛蛋白的溴化氰消化产物诱导的体液免疫和细胞免疫反应与具有相当抗原活性的乙酰乙酰化鞭毛蛋白相同,这一事实进一步证明了亲和力的重要性。从这些研究中提出,体液免疫和细胞介导免疫都可以针对相同的抗原决定簇,但迟发型超敏反应(和抗体耐受)的特异性要求低于抗体形成所需的要求。揭示了鞭毛蛋白系统一些显著的免疫学特征。鞭毛蛋白无论是注射到盐水中还是弗氏完全佐剂(FCA)中,都能诱导相当的迟发型超敏反应。此外,FCA仅略微增强了乙酰乙酰化鞭毛蛋白诱导的迟发型反应,实际上这些制剂无论注射到盐水中还是佐剂中都会产生抗体耐受。最后,与仅在抗体水平存在的乙酰乙酰化鞭毛蛋白诱导的成年耐受相反,新生大鼠的耐受存在于体液免疫和细胞介导免疫水平。这一发现首次表明新生耐受与成年耐受之间存在根本差异。根据当前的免疫学概念讨论了这些发现的意义,并提出了一个假说来解释这些现象。