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Induction of antigen-specific cytotoxic T lymphocytes by immunization with negatively charged soluble antigen through scavenger receptor-mediated delivery

机译:通过清除剂受体介导的带负电荷的可溶性抗原免疫来诱导抗原特异性细胞毒性T淋巴细胞

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摘要

Antigen-specific cytotoxic T lymphocytes (CTL) are essential for the immunotherapy against cancer or infection diseases although, conventionally, immunization with antigens in soluble form cannot induce CTL. In the present study, we have demonstrated for the first time that ovalbumin (OVA)-specific CTL can be induced without any adjuvants by immunization with soluble OVA with negative charges through scavenger-mediated delivery of antigens to antigen presenting cells (APC). Succinylated, maleylated and aconitylated derivatives were synthesized to allow the introduction of negative charges. All these derivatives can induce OVA-specific CTL and, especially, the CTL activity of mice immunized with maleylated derivatives was comparable with that with OVA emulsified with CFA, known to be the strongest adjuvant. Efficient antigen-specific T cell proliferation and IFN-gamma production were also observed for the OVA derivatives. The OVA derivatives also showed significant protective effects on the growth of OVA-expressing E.G7 tumor cells. In conclusion, the present study demonstrates that the introduction of negative charges to soluble antigens will be a useful strategy for the development of vaccines.
机译:抗原特异性细胞毒性T淋巴细胞(CTL)对于针对癌症或感染性疾病的免疫疗法至关重要,尽管通常情况下,以可溶形式的抗原免疫无法诱导CTL。在本研究中,我们首次证明卵清蛋白(OVA)特异的CTL可以在无任何佐剂的情况下通过清除剂介导的抗原向抗原呈递细胞(APC)介导的可溶性负电荷OVA免疫而诱导。合成琥珀酰化,马来酰化和乌头酰化的衍生物以引入负电荷。所有这些衍生物都可以诱导OVA特异性CTL,尤其是,用马来酰化衍生物免疫的小鼠的CTL活性与已知用CFA乳化的OVA是最强的佐剂相当。对于OVA衍生物,还观察到有效的抗原特异性T细胞增殖和IFN-γ产生。 OVA衍生物还对表达OVA的E.G7肿瘤细胞的生长显示出显着的保护作用。总之,本研究表明向可溶性抗原中引入负电荷将是开发疫苗的有用策略。

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