Ptak W, Asherson G L
Immunology. 1969 Nov;17(5):769-75.
Mice sensitized to oxazolone show contact sensitivity which can be assessed by painting oxazolone on the ear and measuring the increase in ear thickness at 24 hours. Contact sensitivity can be transferred passively by peritoneal exudate, lymph node and bone marrow cells. When CBA mice are challenged immediately after transfer, at a 3:1 donor recipient ratio, the peritoneal exudate cells give bigger transferred reactions than lymph node cells. The converse is true on challenge at 6 days after transfer, at which time the lymph node cells give bigger transferred reactions than the peritoneal exudate cells. These results suggest that different types or functional states of cells are involved in these two types of transfer. The possibility that the successful transfer with delayed challenge by lymph node cells was due to active sensitization by antigen transferred with the cells, was made unlikely by passive transfer into `tolerant' recipients. Mice first show contact sensitivity when challenged at 3 days (about 72 hours) after sensitization. The lymph nodes develop the ability to transfer contact sensitivity with delayed challenge at the same time but the bone marrow only acquires this activity at 5 days.
对恶唑酮致敏的小鼠表现出接触敏感性,可通过在耳部涂抹恶唑酮并测量24小时后耳部厚度的增加来评估。接触敏感性可通过腹腔渗出液、淋巴结和骨髓细胞进行被动转移。当CBA小鼠在转移后立即以3:1的供体受体比例受到攻击时,腹腔渗出液细胞产生的转移反应比淋巴结细胞更大。在转移后6天受到攻击时则相反,此时淋巴结细胞产生的转移反应比腹腔渗出液细胞更大。这些结果表明,这两种转移涉及不同类型或功能状态的细胞。淋巴结细胞延迟攻击成功转移是由于细胞转移的抗原主动致敏的可能性,通过被动转移到“耐受”受体中而变得不太可能。小鼠在致敏后3天(约72小时)受到攻击时首次表现出接触敏感性。淋巴结在同一时间发展出延迟攻击转移接触敏感性的能力,但骨髓仅在5天时获得这种活性。