Berthon P, Gohin I, Lantier I, Olivier M
Institut National de la Recherche Agronomique, Centre de Tours, Nouzilly, France.
Vet Immunol Immunopathol. 1994 Jun;41(3-4):275-94. doi: 10.1016/0165-2427(94)90102-3.
In vitro culture conditions were determined to induce an anti-Salmonella abortusovis antibody synthesis from lymph node leucocytes of three immunized sheep and two unprimed lambs maintained in culture in the presence of heat-inactivated bacteria for 2 weeks. Humoral immune responses were assessed by enumerating specific antibody-secreting cells using ELISASPOT and by titrating immunoglobulins secreted into culture supernatants using ELISA techniques. Optimal secondary antibody response was observed from cultures performed with fetal calf serum (compared with horse serum) and with an antigen concentration of one to ten bacteria per cell. This kind of antigenic stimulation allowed induction of numerous antibody-secreting cells without adsorption of the secreted antibodies. Maximal numbers of antibody-secreting cells could reach a rate of 1% of the sheep leucocytes initially put into culture. Kinetic profiles of antibody production from boosted lymph node cells were characterized by an ascending phase from the sixth to the twelfth day of culture and then showed a plateau phase until Day 14. Most of the responses were composed of IgM and IgG1 antibodies, traces of IgG2 being detected at the end of experiments. From the twelfth day of antigenic stimulation, the IgM isotype was preferentially expressed with high antigen concentration (100 bacteria per cell), whereas the highest amounts of IgG1 were detected at lower concentration (one to ten bacteria per cell). While anti-Salmonella IgM appeared to be mainly specific for the lipopolysaccharide (LPS) cell wall fraction, some IgG1 recognized other bacterial antigens. Kinetic profiles and magnitudes of primary antibody responses induced in vitro from lamb lymph node cells did not differ from those defined in cultures of sheep boosted leucocytes. But these immune reactions were mainly made up of anti-LPS IgM. Few anti-Salmonella IgG1 were detected from the tenth day of culture. So these in vitro assays allowed induction of antibody synthesis from either in vivo sensitized or unprimed sheep lymph node leucocytes. This methodology would permit achievement of more detailed studies on interactions between Salmonella and lymph node leucocytes, leading to a better understanding of the mechanisms controlling bacterial dissemination through the lymphoid tissue.
确定体外培养条件,以诱导三只免疫绵羊和两只未免疫羔羊的淋巴结白细胞合成抗绵羊流产沙门氏菌抗体。这些细胞在热灭活细菌存在的情况下在培养物中维持2周。通过使用酶联免疫斑点法(ELISASPOT)计数特异性抗体分泌细胞,并使用酶联免疫吸附测定(ELISA)技术滴定分泌到培养上清液中的免疫球蛋白,来评估体液免疫反应。在用胎牛血清(与马血清相比)和抗原浓度为每细胞一到十个细菌的条件下进行的培养中,观察到了最佳的二次抗体反应。这种抗原刺激能够诱导大量抗体分泌细胞,而不会吸附分泌的抗体。抗体分泌细胞的最大数量可达到最初接种到培养物中的绵羊白细胞的1%。加强免疫的淋巴结细胞产生抗体的动力学特征是在培养的第六天到第十二天为上升期,然后在第14天之前呈现平台期。大多数反应由IgM和IgG1抗体组成,在实验结束时检测到微量的IgG2。从抗原刺激的第十二天开始,在高抗原浓度(每细胞100个细菌)下优先表达IgM同种型,而在较低浓度(每细胞一到十个细菌)下检测到最高量的IgG1。虽然抗绵羊流产沙门氏菌IgM似乎主要针对脂多糖(LPS)细胞壁部分,但一些IgG1识别其他细菌抗原。从羔羊淋巴结细胞体外诱导的初次抗体反应的动力学特征和幅度与加强免疫的绵羊白细胞培养中确定的特征没有差异。但这些免疫反应主要由抗LPS IgM组成。从培养的第十天开始检测到少量抗绵羊流产沙门氏菌IgG1。因此,这些体外试验能够诱导体内致敏或未免疫的绵羊淋巴结白细胞合成抗体。这种方法将有助于对沙门氏菌与淋巴结白细胞之间的相互作用进行更详细的研究,从而更好地理解控制细菌通过淋巴组织传播的机制。