Antithymocyte globulin combined with cyclosporine A down-regulates T helper 1 cells by modulating T cell immune response cDNA 7 in aplastic anemia
Antithymocyte globulin combined with cyclosporine A down-regulates T helper 1 cells by modulating T cell immune response cDNA 7 in aplastic anemia
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抗胸腺细胞球蛋白联合环孢菌素 A 通过调节 T 细胞免疫反应 cDNA 7 下调再生障碍性贫血中 T 辅助细胞 1
DOI:
10.1007/s12032-015-0647-2
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发表时间:
2015-06
期刊:
影响因子:
3.4
通讯作者:
Xu Kailin
中科院分区:
文献类型:
--
作者:
Fu Chunling;Zeng Lingyu;Li Zhenyu;Xu Kailin
Antithymocyte globulin (ATG) combined with cyclosporine A (CsA) has been widely used as a standard regimen in the treatment of aplastic anemia (AA), especially in severe aplastic anemia (SAA). Abnormally activated T cells might be the immune pathogenesis of AA. T cell immune response cDNA 7 (TIRC7) has been demonstrated its essential role in T cell activation; however, little is known about the role of TIRC7 in AA. In this study, we documented that TIRC7 levels in CsA group were higher than that in ATG + CsA (AC) group only in the follow-up phase (P< 0.05;P< 0.05); nevertheless, TIRC7 levels in SAA group were elevated than non severe aplastic anemia group not only in the treatment phase (P< 0.05;P< 0.05) but also in the follow-up phase (P< 0.05;P< 0.01). The trend of changes of T helper (Th) 1, Th17 and Th22 levels before and after treatment was similar to the changes of TIRC7 levels in either AC group or CsA group. Thus, TIRC7 might be involved in the pathogenesis of AA and AC might down-regulate Th1 cells by modulating the expression of TIRC7 in AA.
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DOI:
10.1155/2013/513542
发表时间:
2013
期刊:
Evidence-based complementary and alternative medicine : eCAM
影响因子:
--
作者:
Hsu HY;Kuan YC;Lin TY;Tsao SM;Hsu J;Ma LJ;Sheu F
通讯作者:
Sheu F
影响因子:
4.6
作者:
Utku, N;Heinemann, T;Blumberg, RS
通讯作者:
Blumberg, RS
影响因子:
--
作者:
通讯作者:
--
DOI:
10.1007/978-3-642-67483-9
发表时间:
1979
期刊:
[Rinsho ketsueki] The Japanese journal of clinical hematology
影响因子:
--
作者:
Kensuke Usuki
通讯作者:
Kensuke Usuki
影响因子:
20.3
作者:
de Latour, Regis Peffault;Visconte, Valeria;Young, Neal S.
通讯作者:
Young, Neal S.