Ben-Sasson S Z, Lipscomb M F, Tucker T F, Uhr J W
J Immunol. 1978 Jun;120(6):1902-6.
Peritoneal exudate lymphocytes (PEL) from immune guinea pigs that adhere to antigen-pulsed macrophages (MO) were cultured for 1 week to yield a population enriched in antigen-specific (selected) T cells. These cells bind specifically within hours to fresh autologous antigen-pulsed MO. Thd dissociation of these selected PEL from antigen-pulsed MO was studied. No evidence was obtained that factors in the culture medium play a role in dissociation. Lymphocytes that have dissociated from antigen-pulsed MO are usually fully capable of rebinding to MO freshly pulsed with antigen, suggesting that there is no deficiency in the lymphocytes ability to bind. In contrast, readding antigen to cultures during incubation prevents the predicted dissociation. Moreover, repulsing MO cultured without selected PEL restores their capacity to bind fresh selected PEL. These findings indicate that decay of antigen associated with with MO is the major mechanism underlying the observed dissociation.
来自免疫豚鼠的腹腔渗出淋巴细胞(PEL),这些淋巴细胞能黏附于抗原刺激的巨噬细胞(MO),将其培养1周以获得富含抗原特异性(经筛选的)T细胞的细胞群体。这些细胞在数小时内就能特异性结合新鲜的自体抗原刺激的MO。对这些经筛选的PEL与抗原刺激的MO的解离进行了研究。没有证据表明培养基中的因素在解离过程中起作用。从抗原刺激的MO解离的淋巴细胞通常完全有能力重新结合新鲜的抗原刺激的MO,这表明淋巴细胞的结合能力没有缺陷。相比之下,在培养期间向培养物中重新添加抗原可防止预期的解离。此外,用未经筛选的PEL培养后再重新刺激MO可恢复其结合新鲜筛选的PEL的能力。这些发现表明,与MO相关的抗原衰减是观察到的解离的主要机制。