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在缺乏特异性抗原呈递细胞的情况下,用与I类主要组织相容性复合体结合的免疫原性肽和白细胞介素-2体外激活初始CD8⁺T细胞所产生的保护性免疫。

Protective immunity from naive CD8+ T cells activated in vitro with MHC class I binding immunogenic peptides and IL-2 in the absence of specialized APCs.

作者信息

Hauser C, Zipprich F, Leblond I, Wirth S, Hügin A W

机构信息

Allergy Unit, Division of Immunology and Allergy, Department of Dermatology, Hôpital Cantonal Universitaire, Geneva, Switzerland.

出版信息

J Immunol. 1999 Jul 1;163(1):330-6.

Abstract

Ag-specific CTL can protect against tumors and some viral infections and may be useful for adoptive immunotherapy. Here, we show that purified CD8+ T cells from naive C57BL/6 mice can be primed in vitro with different immunogenic peptides, which bind to MHC class I gene products, and IL-2 to exhibit specific and MHC-restricted effector function in vitro and in vivo protection against lymphocytic choriomeningitis virus infection and B16.F10 melanoma lung metastases. Limiting dilution assays in the absence of feeder cells with highly purified CD8+ T cells from two transgenic mice strains, each expressing a different MHC class I-restricted TCR, indicated that only peptide and IL-2, but not TCR- cells, were required for the growth of naive CD8+ T cells. These alternative minimal requirements for the activation and expansion of specific CD8+ T lymphocytes, without the need for professional APC, may be exploited for adoptive immunotherapy.

摘要

抗原特异性细胞毒性T淋巴细胞(CTL)可预防肿瘤和某些病毒感染,可能对过继性免疫治疗有用。在此,我们表明,从新生C57BL/6小鼠中纯化的CD8+ T细胞可在体外与不同的免疫原性肽一起致敏,这些肽与MHC I类基因产物结合,以及与白细胞介素-2一起,以在体外表现出特异性和MHC限制性效应功能,并在体内预防淋巴细胞性脉络丛脑膜炎病毒感染和B16.F10黑色素瘤肺转移。在没有饲养细胞的情况下,对来自两个转基因小鼠品系的高度纯化的CD8+ T细胞进行有限稀释分析,每个品系表达不同的MHC I类限制性TCR,结果表明,幼稚CD8+ T细胞的生长仅需要肽和白细胞介素-2,而不需要TCR-细胞。这些激活和扩增特异性CD8+ T淋巴细胞的替代性最低要求,无需专业抗原呈递细胞(APC),可用于过继性免疫治疗。

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