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用辐照后的子孢子免疫小鼠鉴定具有 CD8 表位的非 CSP 抗原。

Identification of non-CSP antigens bearing CD8 epitopes in mice immunized with irradiated sporozoites.

机构信息

Michael Heidelberger Division, Department of Pathology, New York University School of Medicine, NY 10016, United States.

出版信息

Vaccine. 2011 Oct 6;29(43):7335-42. doi: 10.1016/j.vaccine.2011.07.081. Epub 2011 Jul 30.

Abstract

Immunization of BALB/c mice with irradiated sporozoites (IrSp) of Plasmodium yoelii can lead to sterile immunity. The circumsporozoite protein (CSP) plays a dominant role in protection. Nevertheless after hyper-immunization with IrSp, complete protection is obtained in CSP-transgenic BALB/c mice that are T-cell tolerant to the CSP and cannot produce antibodies [CSP-Tg/JhT(-/-)]. This protection is mediated exclusively by CD8(+) T cells [1]. To identify the non-CSP protective T cell antigens, we studied the properties of 34 P. yoelii sporozoite antigens that are predicted to be secreted and to contain strong Kd-restricted CD8(+) T cell epitopes. The synthetic peptides corresponding to the epitopes were used to screen for the presence of peptide-specific CD8(+) T cells secreting interferon-γ (IFN-γ) in splenocytes from CSP-Tg/JhT(-/-) BALB/c mice hyper immunized with IrSp. However, the numbers of IFN-γ-secreting splenocytes specific for the non-CSP antigen-derived peptides were 20-100 times lower than those specific for the CSP-specific peptide. When mice were immunized with recombinant adenoviruses expressing selected non-CSP antigens, the animals were not protected against challenge with P. yoelii sporozoites although large numbers of CD8(+) specific T cells were generated.

摘要

用辐射后的约氏疟原虫(Plasmodium yoelii)孢子(IrSp)免疫 BALB/c 小鼠可以导致无菌免疫。环子孢子蛋白(CSP)在保护中起主要作用。尽管 IrSp 超免疫后,对 CSP 耐受且不能产生抗体的 CSP 转基因 BALB/c 小鼠(CSP-Tg/JhT(-/-))中获得完全保护。这种保护仅由 CD8(+) T 细胞介导[1]。为了鉴定非 CSP 保护性 T 细胞抗原,我们研究了 34 种预测分泌并含有强 Kd 限制的 CD8(+) T 细胞表位的约氏疟原虫孢子抗原的特性。相应的合成肽用于筛选来自 IrSp 超免疫的 CSP-Tg/JhT(-/-) BALB/c 小鼠脾细胞中分泌干扰素-γ(IFN-γ)的肽特异性 CD8(+) T 细胞的存在。然而,针对非 CSP 抗原衍生肽的 IFN-γ 分泌脾细胞的数量比针对 CSP 特异性肽的数量低 20-100 倍。当用表达选定的非 CSP 抗原的重组腺病毒免疫小鼠时,尽管产生了大量的 CD8(+)特异性 T 细胞,但动物未受到约氏疟原虫孢子的挑战。

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