期刊文献+

IL-2,IL-7,IL-15和IL-21在艾滋病免疫疗法中的应用前景(英文) 被引量:2

Prospect of IL-2,IL-7,IL-15 and IL-21 for HIV immune-based therapy
下载PDF
导出
摘要 高效抗反转录病毒疗法可以有效地减少HIV的复制,但却不能完全恢复CD4+T细胞的数量。即使病毒血清学指标得到良好控制的病人,CD4+T细胞数也很难达到正常水平。目前研究表明:γ链细胞因子在始动、维持及调节免疫稳态和炎症反应中发挥重要作用。γ链细胞因子具有多重功能,如在健康及疾病中作为调节和效应分子发挥作用,因此,该家族因子、受体及其信号转导通路可成为治疗性干预的潜在靶点。γ链细胞因子IL-2,IL-7,IL-15和IL-21是T细胞稳态的重要调节者,因此成为升高T细胞水平和功能及增强AIDS免疫受累患者疫苗诱发病毒特异性T细胞应答等免疫治疗中的主要可选靶点之一。 Although highly active antiretroviral therapy(HAART) can effectively reduce the HIV replication,complete recovery of CD4+ T cells does not always occur,even among patients with high virological control.Current researches on γ-chain cytokines have understood the biology and their crucial roles in initiating,maintaining,and regulating the immunologic homeostasis and the inflammatory processes.Due to the multiple functions such as the regulatory and effector cellular function in healthy and disease state,these molecules,their receptors,and their signal transduction pathways are promising candidates for therapeutic interference.The common γ-chain cytokines IL-2,IL-7,IL-15,and IL-21 are primary regulators of T cell homeostasis and thus have been considered prime immunotherapeutic candidates,both for increasing T cell levels/function and augmenting vaccine-elicited viral-specific T cell responses in immunocompromised AIDS patients.The objective of this review is to update the role of the common γ-chain cytokines IL-2,IL-7,IL-15,and IL-21 in HIV AIDS pathogenesis.
出处 《中南大学学报(医学版)》 CAS CSCD 北大核心 2011年第11期1037-1045,1020,共9页 Journal of Central South University :Medical Science
基金 suported by National Science and Technolgy lmportant Item of China(2008ZX10001-008,2008ZX10005-003,2009ZX10005-015)
关键词 γ链细胞因子 人类免疫缺陷病毒 发病机制 CD4 γ-chain cytokines human immunodeficiency virus pathogenesis CD4
  • 相关文献

参考文献47

  • 1K Shen, E J Delp. Wavelet base rate scalable video compression[J]. IEEE Trans on Circuits and Systems, 1999,9(1):301-318.
  • 2Sodagar, H J Lee, Y Q Zhang. Scalable wavelet coding for synthetic/natural hybrid images[J]. IEEE Trans on Circuits and Systems,1999,9(2):332-344.
  • 3ISO.IEC IS 14496-2, Information technology-coding of audio-visual objects[S].
  • 4W Li. Overview of fine granularity scalability in MPEG-4 video standard[J]. IEEE Trans on Circuits and Systems,2001,11(3):301-317.
  • 5F Wu,S Li, Y Q Zhang.DCT-prediction based progressive fine granularity scalable coding[OB/OL]. http://research. microsoft.com/china/papers,2000-9-10.
  • 6F WU, Y Q Zhang. A framework for efficient progressive fine scalability video coding[J]. IEEE Trans on Circuits and Systems,2001,11(3):332-344.
  • 7Letoumeau S, Krieg C, Pantaleo G, et al. IL-2- and CD25-dependent immunoregulatory mechanisms in the homeostasis of T- cell subsets [J]. J Allergy Clin Immunol, 2009,123 (4):758- 762.
  • 8Brandenburg S, Takahashi T, de la Rosa M, et al. IL-2 induces in vivo suppression by CD4 ( + ), CD25 ( + ), FoxP3 ( + ) regulatory T cells [J]. Eur J Immunol, 2008,38 ( 6 ) : 1643 - 1653.
  • 9Anaya J P, Sias J J. The use of interleukin-2 in human immunodeficiency vi brus infection [ J ]. Pharmacotherapy, 2005,25( 1 ) :86-95.
  • 10Temcsgen Z. lnterleukin-2 for the treatment of human immunod- eficiency virus infection [ J ]. Drugs Today ( Barr ) , 2006,42 (12) :791-801.

二级参考文献15

  • 1Rooney CM, Smith CA, Ng CY, et al. hffusion of cytotoxic T cells for the prevention and treatment of Epstein-Barr virus-induced lym- phoma in allogeneic transplant recipients. Blood, 1998; 92 (5): 1549 - 1555.
  • 2Waiter EA, Greenberg PD, Gilbert M J, et al. Reconstitution of cel- lular immunity against cytomegalovirus in recipients of allogeneic bone marrow by transfer of T cell clones from the donor. N Engl J Med, 1995; 333(16): 1038-1044.
  • 3Feuchtinger T, Matthes-Martin S, Richard C, et al. Safe adoptive transfer of virus-specific T-cell immunity for the treatment of systemic adenovirus infection after allogeneic stem cell transplantation. Br J Haematol, 2006 ; 134 ( 1 ) :64 - 76.
  • 4Rosenberg SA, Dudley ME, Restifo NP. Cancer immunotherapy. N Engl J Med, 2008;359(10) :1072.
  • 5Gattinoni L, Klebanoff CA, Palmer DC, et al. Acquisition of full ef- fector function in vitro paradoxically impairs the in vivo antitumor effi- cacy of adoptively transferred CD8^+ T cells. J Clin Invest, 2005; 115(6) :1616 - 1626.
  • 6Ramadan G. Epstein-Barr virus-transformed B-cells as efficient anti- gen presenting ceils to propagate Aspergillus-specific cytotoxic T-lym- phocytes. Egypt J Immunol, 2008 ; 15 ( 1 ) : 145 - 157.
  • 7Tanchot C, Lemonnier FA, P6ramau B, et al. Differential require- ments for survival and proliferation of CD8 naive or memory T cells. Science, 1997 ;276(5321 ) :2057 -2062.
  • 8Chen HW, Liao CH, Ying C, et al. Ex vivo expansion of dendritic- cell-activated antigen-specific CD4^+ T ceils with anti-CD3/CD28, interleukin-7, and interleukin-15: potential for adoptive T cell im- munotherapy. Clin Immunol, 2006 ; 119 ( 1 ) :21 - 31.
  • 9Jaleco S, Kinet S, Hassan J, et al. IL-7 and CD4^+ T-cell prolifera- tion. Blood, 2002; 100 ( 13 ) :4676 - 4677; author reply 4677 - 4678.
  • 10Beadling C, Johnson KW, Smith KA. Isolation of interleukin 2-in- duced immediate-early genes. Proc Nat Acad Sci USA, 1993; 90 (7) : 2719 -2723.

共引文献5

同被引文献14

引证文献2

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部