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多分散酸功能化单壁碳纳米管靶向激活 T 和 B 细胞,以抑制小鼠模型中的急性和慢性移植物抗宿主病。

Poly dispersed acid-functionalized single walled carbon nanotubes target activated T and B cells to suppress acute and chronic GVHD in mouse model.

机构信息

Faculty of Life Sciences and Biotechnology, South Asian University, Akbar Bhawan, Chanakyapuri, New Delhi, 110021, India.

Faculty of Life Sciences and Biotechnology, South Asian University, Akbar Bhawan, Chanakyapuri, New Delhi, 110021, India.

出版信息

Immunol Lett. 2020 Aug;224:30-37. doi: 10.1016/j.imlet.2020.05.006. Epub 2020 Jun 3.

Abstract

Graft versus host disease (GVHD) results from hyper-activation of transplanted lymphocytes against the host antigens. Bone marrow transplantation in humans as well as some cases of blood transfusion and organ transplantation are associated with a strong GVH reaction resulting in GVHD that in many cases may be fatal. We had previously shown that poly-dispersed acid-functionalized single-walled carbon nanotubes (AF-SWCNTs) specifically target activated T and B lymphocytes and kill them. In the present study, efficacy of AF-SWCNTs to suppress the GVH reaction was tested in the mouse model. Acute GVHD was induced in mice by administering intravenously 30 or 60 million spleen cells from a parental strain (C57bl/6 mouse, MHC haplotype H-2) to host (C57bl/6 x Balb/c) F1 mice (MHC haplotype H-2)and waiting for 8-10 days. Chronic GVHD was similarly induced by administration of 30 million parent spleen cells to F1 mice and waiting for a period of 60 days. Our results demonstrate a marked decline in splenomegaly and recovery of spleen T (both CD4 and CD8) and B cells in GVHD mice treated with AF-SWCNTs. AF-SWCNTs treatment also limited T and B cell proliferation by restricting S-phage of cell cycle. Generation of anti-host cytotoxic T cells (CTLs) was also markedly suppressed by AF-SWCNT treatment of acute GVHD mice, and a significant reduction in the generation of anti-host antibodies could also be demonstrated. Taken together, our results suggest that the AF-SWCNTs can be considered as a potential therapeutic agent for treating GVHD.

摘要

移植物抗宿主病(GVHD)是由于移植淋巴细胞对宿主抗原的过度激活而引起的。人类骨髓移植以及某些输血和器官移植的情况与强烈的 GVH 反应相关,导致 GVHD,在许多情况下可能是致命的。我们之前已经表明,多分散酸官能化单壁碳纳米管(AF-SWCNTs)特异性靶向激活的 T 和 B 淋巴细胞并杀死它们。在本研究中,在小鼠模型中测试了 AF-SWCNTs 抑制 GVH 反应的功效。通过静脉内给予来自亲本品系(C57bl/6 小鼠,MHC 单倍型 H-2)的 30 或 6000 万个脾细胞来诱导急性 GVHD 至宿主(C57bl/6 x Balb/c)F1 小鼠(MHC 单倍型 H-2),并等待 8-10 天。通过给予 3000 万个亲本脾细胞至 F1 小鼠并等待 60 天同样诱导慢性 GVHD。我们的结果表明,在用 AF-SWCNTs 处理的 GVHD 小鼠中,脾肿大和脾 T(CD4 和 CD8 两者)和 B 细胞的恢复明显下降。AF-SWCNTs 处理还通过限制细胞周期的 S 期来限制 T 和 B 细胞增殖。急性 GVHD 小鼠的 AF-SWCNT 处理也明显抑制了抗宿主细胞毒性 T 细胞(CTL)的产生,并且可以证明抗宿主抗体的产生也显著减少。总之,我们的结果表明,AF-SWCNTs 可被视为治疗 GVHD 的潜在治疗剂。

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