Louis J A, Chiller J M, Weigle W O
J Exp Med. 1973 Dec 1;138(6):1481-95. doi: 10.1084/jem.138.6.1481.
Studies were performed to define the cellular parameters involved in the interference with the induction of immunologic unresponsiveness to human gamma globulin (HGG) by bacterial lipopolysaccharide (LPS). Mice which were injected with deaggregated HGG (tolerogen) and with LPS did not become tolerant to that antigen, but rather became primed to a subsequent challenge with immunogen. The ability to prime with tolerogen and LPS was also demonstrated in an adoptive transfer system. The temporal relationship between the injection of tolerogen and that of LPS was critical for priming to occur. The injection of tolerogen and LPS not only primed mice to HGG, but also resulted in a primary antibody response to HGG. The capacity of LPS to interfere with the induction of tolerance was restricted to B cells and did not affect the ability to induce unresponsiveness in T cells. The secondary response to HGG in mice primed by tolerogen and LPS was found to be T-cell independent. These observations are interpreted and discussed from the standpoint of the ability of LPS to circumvent required T-cell cooperation and to modulate to tolerogenic stimulus into an immunogenic signal.
开展了多项研究以确定参与干扰细菌脂多糖(LPS)诱导对人丙种球蛋白(HGG)免疫无反应性的细胞参数。注射了去聚合HGG(耐受原)和LPS的小鼠并未对该抗原产生耐受,而是对随后的免疫原攻击产生了致敏。在过继转移系统中也证明了用耐受原和LPS进行致敏的能力。注射耐受原和LPS的时间关系对于致敏的发生至关重要。注射耐受原和LPS不仅使小鼠对HGG致敏,还导致了对HGG的初次抗体反应。LPS干扰耐受诱导的能力仅限于B细胞,并不影响诱导T细胞无反应性的能力。发现由耐受原和LPS致敏的小鼠对HGG的二次反应是T细胞非依赖性的。从LPS规避所需T细胞合作以及将致耐受刺激调节为免疫原性信号的能力的角度对这些观察结果进行了解释和讨论。