首页> 美国卫生研究院文献>Journal of Virology >Influenza virus nucleoprotein-specific immunoglobulin G subclass and cytokine responses elicited by DNA vaccination are dependent on the route of vector DNA delivery.
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Influenza virus nucleoprotein-specific immunoglobulin G subclass and cytokine responses elicited by DNA vaccination are dependent on the route of vector DNA delivery.

机译:DNA疫苗接种引起的流感病毒核蛋白特异性免疫球蛋白G亚类和细胞因子应答取决于载体DNA递送的途径。

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摘要

Endpoint immunoglobulin G (IgG) titers and cytotoxic T-lymphocyte (CTL) activities were identical between mice immunized via the intramuscular and epidermal (gene gun) routes with 100 and 1 micrograms, respectively, of an influenza virus nucleoprotein (NP) expression vector. However, examination of the relative levels of two IgG subclasses demonstrated that muscle inoculation resulted in predominantly IgG2a responses, whereas gene gun immunization yielded a preponderance of IgG1 antibodies. Inasmuch as these data suggested that muscle inoculation and gene gun delivery elicited Th1-like and Th2-like responses, respectively, gamma interferon release profiles from antigen-stimulated splenocytes were remarkably similar between these groups. Interleukin-4 (IL-4) production assays, on the other hand, revealed qualitative differences that could be correlated with the divergent IgG subclass data. Waning gamma interferon production in gene gun-immunized animals was countered by a marked increase in IL-4 production following the third immunization, as was the case in control animals immunized with inactivated influenza virus formulated with Freund's adjuvant. In contrast, significant levels of IL-4 production were not observed in the intramuscular DNA inoculation group, despite similar decreases in gamma interferon production with increasing immunizations. These data show that intramuscular inoculation leads to Th1-like responses due to elevated IgG2a levels, production of gamma interferon, CTL activity, and lack of IL-4. However, gene gun responses are more difficult to categorize because of the presence of significant gamma interferon and CTL activity on the one hand and elevated IgG1 antibodies and increasing IL-4 production with successive immunizations on the other. In addition, there was a lack of correlation between IgG isotype ratios and cytokine production in all of the NP DNA-immunized animals, in that IgG subclass ratios remained fixed while cytokine production patterns fluctuated with successive immunizations. These data are consistent with the idea that the types of responses elicited following DNA immunization. are dependent on both the identity of the antigen and the route of DNA administration.
机译:分别通过分别以100和1微克的流感病毒核蛋白(NP)表达载体通过肌内和表皮(基因枪)途径免疫的小鼠之间的终点免疫球蛋白G(IgG)滴度和细胞毒性T淋巴细胞(CTL)活性相同。但是,对两种IgG亚类的相对水平的检查表明,肌肉接种主要导致IgG2a反应,而基因枪免疫产生了大量IgG1抗体。由于这些数据表明肌肉接种和基因枪传递分别引发了Th1类和Th2类反应,因此,抗原刺激的脾细胞中的γ干扰素释放曲线在这些组之间非常相似。另一方面,白介素4(IL-4)的生产测定揭示了定性差异,其可能与发散的IgG亚类数据相关。在第三次免疫后,基因枪免疫动物的γ-干扰素产量下降被IL-4产量的显着增加所抵消,就像用弗氏佐剂配制的灭活流感病毒免疫的对照动物的情况一样。相比之下,尽管随着免疫接种的增加,γ-干扰素的产生量也有​​类似的下降,但在肌内DNA接种组中并未观察到明显的IL-4产生量。这些数据表明,由于IgG2a水平升高,γ干扰素产生,CTL活性和缺乏IL-4,肌肉内接种会导致类似Th1的反应。然而,由于一方面存在明显的γ干扰素和CTL活性,另一方面存在不断升高的免疫力,IgG1抗体升高和IL-4产量增加,因此基因枪反应更难以归类。此外,在所有NP DNA免疫的动物中,IgG同种型比率与细胞因子产生之间均缺乏相关性,因为IgG亚类比率保持固定,而细胞因子产生模式随连续免疫而波动。这些数据与DNA免疫后引起的反应类型一致。取决于抗原的身份和DNA施用途径。

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