流感病毒抗原和植物血凝素刺激豚鼠脾淋巴细胞后蛋白质和DNA合成的比较

J. Süss, A. Stelzner, K.-H. Vogt, J. Schmidt
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引用次数: 1

摘要

两种体外方法证明细胞介导的免疫反应进行比较:蛋白质和DNA合成检测体外流感病毒抗原和丝裂原诱导的淋巴细胞刺激。用14C-或3h -亮氨酸和3h -胸腺嘧啶对流感病毒抗原致敏的豚鼠脾淋巴细胞进行了微适应淋巴细胞转化试验。作为t细胞刺激的阳性对照,测定了pha诱导的淋巴细胞刺激。得到了以下结果:1。14c -亮氨酸和3h -胸苷在最佳和次优pha剂量下培养淋巴细胞的掺入动力学在数量上相似,但在时间上不同。蛋白质和dna合成刺激试验的结果与流感病毒抗原相关,这不能通过细胞和单一体液参数的比较来描述。在CFA中注射流感病毒抗原比在水悬液中注射抗原诱导更强烈的细胞介导反应,但两种CMI方法的结果是相关的。在实验条件下,每只动物注射30 ~ 50 μg病毒蛋白,并通过肌肉-腹腔联合免疫程序诱导最佳CMI。在pss测试中测量蛋白质合成的早期刺激比经典的LTT要快得多。
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Comparison of protein and DNA synthesis assays of guinea pig spleen lymphocytes after stimulation with influenza virus antigen and phytohemagglutinin

Two in vitro-methods for demonstration of cell-mediated immune response are compared: Protein and DNA synthesis for detection of in vitro influenza virus antigen- and mitogen-induced lymphocyte stimulation. Guinea pig spleen lymphocytes sensitized with influenza virus antigen were tested in a microadaptation of the lymphocyte transformation test using 14C- or 3H-leucine and 3H-thymidme. As a positive control for T-cell stimulation PHA-induced lymphocyte stimulation was measured.

The following results were obtained:

  • 1.

    Kinetics of the incorporation of 14C-leucine and 3H-thymidine in lymphocytes incubated with optimal and suboptimal PHA-doses respectively are quantitatively similar but different in time.

  • 2.

    The results of the protein- and DNA-synthesis stimulation assays were correlated against influenza virus antigens, this could not be described by the comparison of cellular and single humoral parameters.

  • 3.

    The administration of influenza virus antigens in CFA induced a more intensive cell-mediated reaction than injections of antigens in aqueous suspensions, but the results of both methods of CMI were correlated.

  • 4.

    The optimal CMI under the exeprimental conditions described is induced by an administration of 30 to 50 μg virus protein per animal and by a combined intramuscular — intraperitoneal immunization procedure.

  • 5.

    The measurement of the early stimulation of protein synthesis in the PSS-test is substantially more rapid than for the classical LTT.

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