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T-cell receptor repertoires of tumor-infiltrating lymphocytes after hyperthermia using functionalized magnetite nanoparticles

机译:使用功能化的磁铁矿纳米粒子进行热疗后肿瘤浸润淋巴细胞的T细胞受体库

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摘要

Aim: Accumulating evidence has indicated that hyperthermia using magnetite nanoparticles induces antitumor immunity. This study investigated the diversity of T-cell receptors (TCRs) in tumor-infiltrating lymphocytes after hyperthermia using magnetite nanoparticles.Materials & methods: Functionalized magnetite nanoparticles, N-propionyl-4-S-cysteaminylphenol (NPrCAP)/magnetite, were synthesized by conjugating the melanogenesis substrate NPrCAP with magnetite nanoparticles. NPrCAP/magnetite nanoparticles were injected into B16 melanomas in C57BL/6 mice, which were subjected to an alternating magnetic field for hyperthermia treatment. Results: Enlargement of the tumor-draining lymph nodes was observed after hyperthermia. The TCR repertoire was restricted in tumor-infiltrating lymphocytes, and expansion of Vβ11+ T cells was preferentially found. DNA sequences of the third complementaritydetermining regions revealed the presence of clonally expanded T cells. Conclusion: These results indicate that the T-cell response in B16 melanomas after hyperthermia is dominated by T cells directed toward a limited number of epitopes and that epitope-specific T cells frequently use a restricted TCR repertoire.
机译:目的:越来越多的证据表明,使用磁铁矿纳米粒子的高温会诱导抗肿瘤免疫力。本研究利用磁铁矿纳米颗粒研究了热疗后肿瘤浸润淋巴细胞中T细胞受体(TCRs)的多样性。材料与方法:合成了功能化的磁铁矿纳米颗粒N-丙酰基-4-S-半胱氨酰酚(NPrCAP)/磁铁矿将黑色素生成底物NPrCAP与磁铁矿纳米粒子结合。将NPrCAP /磁铁矿纳米颗粒注射到C57BL / 6小鼠的B16黑色素瘤中,将其置于交变磁场中进行高温治疗。结果:热疗后观察到引流淋巴结肿大。 TCR谱系局限于肿瘤浸润淋巴细胞中,并优先发现Vβ11+ T细胞的扩增。第三互补决定区的DNA序列揭示了克隆扩增的T细胞的存在。结论:这些结果表明,热疗后B16黑色素瘤中的T细胞反应主要由定向到有限表位的T细胞控制,并且表位特异性T细胞经常使用受限的TCR谱库。

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