Paul W E, Siskind G W, Benacerraf B
J Exp Med. 1968 Jan 1;127(1):25-42. doi: 10.1084/jem.127.1.25.
In vitro antigen stimulation of DNA synthesis in lymph node cultures from immunized guinea pigs can be obtained with very low (10(-4) microg/ml) antigen concentrations in the culture fluid. Immunization with low doses of DNP-GPA leads to a cell population capable of being stimulated, on the average, by low concentration of antigen whereas immunization with large antigen doses results in a sensitive cell population requiring, on the average, high antigen concentrations for stimulation. These findings correlate well with the affinity for hapten of the serum antibodies produced by these guinea pigs. Both delayed reactions in vivo and DNA synthesis in vitro can be stimulated by hapten conjugated to proteins different from that used in primary immunization. However the immunizing conjugate is much more effective in terms of antigen concentration required for a given response. These results can be understood in terms of a thermodynamically driven interaction of antigen (or "processed" antigen) with cell-associated antibody.
在免疫豚鼠的淋巴结培养物中,体外抗原刺激DNA合成可在培养液中极低(10⁻⁴微克/毫升)的抗原浓度下实现。用低剂量的二硝基苯 - 豚鼠白蛋白(DNP - GPA)免疫会产生一群细胞,平均而言,该细胞群能够被低浓度抗原刺激;而用大剂量抗原免疫则会产生一群敏感细胞,平均而言,需要高浓度抗原才能刺激。这些发现与这些豚鼠产生的血清抗体对半抗原的亲和力密切相关。体内迟发型反应和体外DNA合成均可由与初次免疫所用蛋白质不同的蛋白质偶联的半抗原刺激。然而,就给定反应所需的抗原浓度而言,免疫偶联物的效果要显著得多。这些结果可以从抗原(或“加工过的”抗原)与细胞相关抗体的热力学驱动相互作用来理解。