Koszinowski U, Bandlow G
Clin Exp Immunol. 1975 Apr;20(1):143-54.
Guinea-pigs were immunized with different cells infected with vaccinia virus, herpes simplex virus type 1, herpesvirus saimiri, and the virus of vesicular stomatitis. Development of cellular immunity against these viruses was observed with transformation of blood and spleen lymphocytes and with the migration inhibition test using peritoneal exudate cells. Cellular immunity against vaccinia virus was first seen 6 days after the inoculation of cell-bound vaccinia virus by lymphocyte transformation. The avtivation of the vaccinia virus specific cellular immune response could be induced with tissue culturrus. Since infectious virus particles are not synthesized within this time period, it is likely that virus-induced antigens in the cell surface are active in production of cellular immunity. Vaccines from heterologous host cells were more effective inducers of an immune response than syngeneic cell cultures. For in vitro testing of cellular immunity to viruses, viral antigens could be used in both infective and inactivated form. Delayed hypersensitivity to viral antigens was always accompanied by immune reactions to the host cells used for virus propagation.
用感染痘苗病毒、1型单纯疱疹病毒、赛米利疱疹病毒和水疱性口炎病毒的不同细胞对豚鼠进行免疫。通过血液和脾淋巴细胞的转化以及使用腹腔渗出细胞的迁移抑制试验,观察到针对这些病毒的细胞免疫的发展。通过淋巴细胞转化,在接种结合细胞的痘苗病毒6天后首次观察到针对痘苗病毒的细胞免疫。痘苗病毒特异性细胞免疫反应的激活可以用组织培养物诱导。由于在这段时间内不会合成感染性病毒颗粒,因此细胞表面的病毒诱导抗原可能在细胞免疫的产生中起作用。来自异源宿主细胞的疫苗比同基因细胞培养物更有效地诱导免疫反应。对于病毒细胞免疫的体外检测,病毒抗原可以以感染性和灭活形式使用。对病毒抗原的迟发型超敏反应总是伴随着对用于病毒繁殖的宿主细胞的免疫反应。