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通过清道夫受体介导的递送,用带负电荷的可溶性抗原免疫诱导抗原特异性细胞毒性T淋巴细胞。

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

作者信息

Yamasaki Yasuomi, Ikenaga Tomoko, Otsuki Takayuki, Nishikawa Makiya, Takakura Yoshinobu

机构信息

Department of Biopharmaceutics and Drug Metabolism, Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-Ku, Kyoto 606-8501, Japan.

出版信息

Vaccine. 2007 Jan 2;25(1):85-91. doi: 10.1016/j.vaccine.2006.07.017. Epub 2006 Jul 31.

Abstract

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.

摘要

抗原特异性细胞毒性T淋巴细胞(CTL)对于癌症或感染性疾病的免疫治疗至关重要,然而,传统上,以可溶性形式的抗原进行免疫接种并不能诱导CTL。在本研究中,我们首次证明,通过清道夫介导的抗原递送至抗原呈递细胞(APC),用带负电荷的可溶性卵清蛋白(OVA)进行免疫接种,无需任何佐剂即可诱导OVA特异性CTL。合成了琥珀酰化、马来酰化和乌头酰化衍生物以引入负电荷。所有这些衍生物均可诱导OVA特异性CTL,特别是用马来酰化衍生物免疫的小鼠的CTL活性与用已知最强佐剂弗氏完全佐剂(CFA)乳化的OVA免疫的小鼠相当。对于OVA衍生物,还观察到有效的抗原特异性T细胞增殖和γ干扰素产生。OVA衍生物对表达OVA的E.G7肿瘤细胞的生长也显示出显著的保护作用。总之,本研究表明,向可溶性抗原引入负电荷将是疫苗开发的一种有用策略。

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