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环孢素A和他克莫司(FK506)在体内对T细胞受体表达有不同影响。

Cyclosporin a and tacrolimus (FK506) differentially alter T-cell receptor expression in vivo.

作者信息

Miller Jamie Leigh, Ericson Solveig Gronning

机构信息

Department of Microbiology/Immunology/Cell Biology, and Blood and Marrow Transplant and Hematologic Malignancy Program of Mary Babb Randolph Cancer Center, West Virginia University, Morgantown, West Virginia, USA.

出版信息

Immunopharmacol Immunotoxicol. 2007;29(1):105-18. doi: 10.1080/08923970701282890.

DOI:10.1080/08923970701282890
PMID:17464771
Abstract

Cyclosporin A (CSA) and tacrolimus (FK506) are two common immunosuppressive agents used post blood and marrow transplantation. Despite similarity in their accepted modes of action, we observed polarized effects of CSA and FK506 on the in vivo human T cell repertoire. To determine the possible mechanism for this difference, the effects of CSA and FK506 on cell viability, cell proliferation, interleukin-2 production, and calcineurin inhibition were determined in vitro. Our data suggest that a secondary mechanism of action exists for the different T-cell repertoire induced by exposure to CSA and FK506.

摘要

环孢素A(CSA)和他克莫司(FK506)是血液和骨髓移植后常用的两种免疫抑制剂。尽管它们公认的作用方式相似,但我们观察到CSA和FK506对体内人类T细胞库有极化效应。为了确定这种差异的可能机制,我们在体外测定了CSA和FK506对细胞活力、细胞增殖、白细胞介素-2产生和钙调神经磷酸酶抑制的影响。我们的数据表明,暴露于CSA和FK506所诱导的不同T细胞库存在第二种作用机制。

相似文献

1
Cyclosporin a and tacrolimus (FK506) differentially alter T-cell receptor expression in vivo.环孢素A和他克莫司(FK506)在体内对T细胞受体表达有不同影响。
Immunopharmacol Immunotoxicol. 2007;29(1):105-18. doi: 10.1080/08923970701282890.
2
Concentrations of cyclosporin A and FK506 that inhibit IL-2 induction in human T cells do not affect TGF-beta1 biosynthesis, whereas higher doses of cyclosporin A trigger apoptosis and release of preformed TGF-beta1.抑制人T细胞中白细胞介素-2诱导的环孢素A和FK506浓度不影响转化生长因子-β1的生物合成,而更高剂量的环孢素A会引发细胞凋亡并释放预先形成的转化生长因子-β1。
J Leukoc Biol. 2005 May;77(5):748-58. doi: 10.1189/jlb.0904503. Epub 2005 Feb 16.
3
Modulation of the electrophoretic mobility of the linker for activation of T cells (LAT) by the calcineurin inhibitors CsA and FK506: LAT is a potential substrate for PKC and calcineurin signaling pathways.钙调神经磷酸酶抑制剂环孢素A(CsA)和他克莫司(FK506)对T细胞活化连接蛋白(LAT)电泳迁移率的调节:LAT是蛋白激酶C(PKC)和钙调神经磷酸酶信号通路的潜在底物。
Cell Signal. 2003 Jan;15(1):85-93. doi: 10.1016/s0898-6568(02)00046-3.
4
Human T cell responses to human and porcine endothelial cells are highly sensitive to cyclosporin A and FK506 in vitro.在体外,人类T细胞对人类和猪内皮细胞的反应对环孢菌素A和FK506高度敏感。
Transplantation. 1999 Nov 27;68(10):1552-60. doi: 10.1097/00007890-199911270-00020.
5
The mechanism of action of cyclosporin A and FK506.环孢素A和FK506的作用机制。
Clin Immunol Immunopathol. 1996 Sep;80(3 Pt 2):S40-5. doi: 10.1006/clin.1996.0140.
6
The hydroxylamine of sulfamethoxazole synergizes with FK506 and cyclosporin A, inhibiting T-cell proliferation.磺胺甲恶唑的羟胺与FK506和环孢素A协同作用,抑制T细胞增殖。
J Pharmacol Exp Ther. 1997 Apr;281(1):540-8.
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Molecular and biological actions of cyclosporin A and FK506 on T cell development and function.环孢素A和FK506对T细胞发育和功能的分子及生物学作用。
Transfus Sci. 1994 Sep;15(3):207-20. doi: 10.1016/0955-3886(94)90133-3.
8
Identification of calcineurin as a key signalling enzyme in T-lymphocyte activation.鉴定钙调神经磷酸酶为T淋巴细胞激活中的关键信号酶。
Nature. 1992 Jun 25;357(6380):695-7. doi: 10.1038/357695a0.
9
Superior T-cell suppression by rapamycin and FK506 over rapamycin and cyclosporine A because of abrogated cytotoxic T-lymphocyte induction, impaired memory responses, and persistent apoptosis.与雷帕霉素和环孢素A相比,雷帕霉素和FK506对T细胞的抑制作用更强,原因在于其可消除细胞毒性T淋巴细胞诱导、损害记忆反应并导致持续凋亡。
Transplantation. 2003 May 15;75(9):1581-90. doi: 10.1097/01.TP.0000053752.87383.67.
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Calcineurin mutants render T lymphocytes resistant to cyclosporin A.钙调神经磷酸酶突变体使T淋巴细胞对环孢素A产生抗性。
Mol Pharmacol. 1996 Sep;50(3):506-11.

引用本文的文献

1
Selective clinical and immune response of the oligoclonal autoreactive T cells in Omenn patients after cyclosporin A treatment.环孢素 A 治疗后 Omenn 患者寡克隆自身反应性 T 细胞的选择性临床和免疫反应。
Clin Exp Immunol. 2012 Feb;167(2):338-45. doi: 10.1111/j.1365-2249.2011.04508.x.
2
Tacrolimus once-daily formulation: in the prophylaxis of transplant rejection in renal or liver allograft recipients.他克莫司每日一次剂型:用于预防肾或肝移植受者的移植排斥反应。
Drugs. 2007;67(13):1931-43. doi: 10.2165/00003495-200767130-00012.