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巨噬细胞暴露于多壁碳纳米管所释放的炎症细胞因子可上调 T 淋巴细胞和抗体的产生。

Up-regulation of T lymphocyte and antibody production by inflammatory cytokines released by macrophage exposure to multi-walled carbon nanotubes.

机构信息

Faculdade de Engenharia Elétrica e Computação, Universidade de Campinas, Campinas, SP, Brazil.

出版信息

Nanotechnology. 2011 Jul 1;22(26):265103. doi: 10.1088/0957-4484/22/26/265103. Epub 2011 May 17.

DOI:10.1088/0957-4484/22/26/265103
PMID:21576788
Abstract

Our data demonstrate that multi-walled carbon nanotubes (MWCNTs) are internalized by macrophages, subsequently activating them to produce interleukin (IL)-12 (IL-12). This cytokine induced the proliferative response of T lymphocytes to a nonspecific mitogen and to ovalbumin (OVA). This increase in the proliferative response was accompanied by an increase in the expression of pro-inflammatory cytokines, such as interferon-gamma (IFNγ), tumor necrosis factor-alpha (TNFα) and IL-6, in mice inoculated with MWCNTs, whether or not they had been immunized with OVA. A decrease in the expression of transforming growth factor-beta (TGFβ) was observed in the mice treated with MWCNTs, whereas the suppression of the expression of both TGFβ and IL-10 was observed in mice that had been both treated and immunized. The activation of the T lymphocyte response by the pro-inflammatory cytokines leads to an increase in antibody production to OVA, suggesting the important immunostimulatory effect of carbon nanotubes.

摘要

我们的数据表明,多壁碳纳米管(MWCNTs)被巨噬细胞内化,随后激活它们产生白细胞介素(IL)-12(IL-12)。这种细胞因子诱导 T 淋巴细胞对非特异性有丝分裂原和卵清蛋白(OVA)的增殖反应。这种增殖反应的增加伴随着促炎细胞因子的表达增加,如干扰素-γ(IFNγ)、肿瘤坏死因子-α(TNFα)和 IL-6,在接种 MWCNTs 的小鼠中观察到,无论它们是否用 OVA 免疫。在接受 MWCNTs 治疗的小鼠中观察到转化生长因子-β(TGFβ)的表达下降,而在既接受治疗又接受免疫的小鼠中观察到 TGFβ 和 IL-10 的表达均受到抑制。促炎细胞因子激活 T 淋巴细胞反应导致对 OVA 的抗体产生增加,这表明碳纳米管具有重要的免疫刺激作用。

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