Armerding D, Rossiter H
Infect Immun. 1980 Jun;28(3):799-811. doi: 10.1128/iai.28.3.799-811.1980.
Inoculation of mice with live influenza virus results in the induction of cytotoxic thymus-derived (T) lymphocytes and of bone marrow-derived (B) cells producing antiviral antibodies. An assay system was developed to evaluate both types of immune responses on a cellular basis within the same lymphocyte pool with no need to separate out the different effector cell classes. The test system represented a modification of the 51Cr-release assay. T-cell activity was measured exclusively in the absence of active complement using targets that were compatible for determinants encoded by the mouse major histocompatibility gene complex, H-2. H-2-different and even xenogeneic target cells were lysed in the presence of either non-inactivated fetal calf serum or normal rabbit serum as a complement source. Cytotoxicity was mediated in the latter case by direct interaction of B-cell-produced immunoglobulin directed to viral antigens expressed by the target cell and complement. Antibody-dependent cell-mediated cytotoxicity mechanisms did not contribute to cytotoxicity in the test system described. It was demontrated that the cytolytic B-cell responses of one particular strain of mice (BALB/c) against different influenza A viruses were restricted to the immunizing virus on the effector cell level. In another strain of mice (C3H), B cells revealed a broad cross-reactive response resembling that of killer T cells.
用活流感病毒接种小鼠可诱导细胞毒性胸腺来源(T)淋巴细胞和产生抗病毒抗体的骨髓来源(B)细胞。开发了一种检测系统,可在同一淋巴细胞库中基于细胞水平评估这两种免疫反应,无需分离不同的效应细胞类别。该测试系统是对51Cr释放试验的一种改进。T细胞活性仅在无活性补体存在的情况下进行测量,使用与小鼠主要组织相容性基因复合体H-2编码的决定簇相容的靶细胞。在非灭活胎牛血清或正常兔血清作为补体来源的情况下,H-2不同甚至异种靶细胞会被裂解。在后一种情况下,细胞毒性是由B细胞产生的针对靶细胞表达的病毒抗原的免疫球蛋白与补体的直接相互作用介导的。在所描述的测试系统中,抗体依赖性细胞介导的细胞毒性机制对细胞毒性没有贡献。已证明,一种特定品系小鼠(BALB/c)针对不同甲型流感病毒的溶细胞性B细胞反应在效应细胞水平上仅限于免疫病毒。在另一品系小鼠(C3H)中,B细胞表现出广泛的交叉反应,类似于杀伤性T细胞的反应。