Acute Thymic Involution and Mechanisms for Recovery

被引:28
作者
Ansari, Abdur Rahman [1 ,2 ,3 ]
Liu, Huazhen [1 ]
机构
[1] Huazhong Agr Univ, Dept Basic Vet Med, Coll Anim Sci & Vet Med, Wuhan 430070, Hubei, Peoples R China
[2] CVAS, Sect Anat & Histol, Dept Basic Sci, Jhang, Pakistan
[3] UVAS, Lahore, Pakistan
基金
中国国家自然科学基金;
关键词
Acute; Thymus; Atrophy; Thymic involution; Mechanistic recovery; PROGRAMMED CELL-DEATH; TOLL-LIKE RECEPTORS; EPITHELIAL-CELLS; BETULINIC ACID; GROWTH-FACTOR; THYMOCYTE APOPTOSIS; PLASMODIUM-BERGHEI; MYASTHENIA-GRAVIS; PARACOCCIDIOIDES-BRASILIENSIS; FRANCISELLA-TULARENSIS;
D O I
10.1007/s00005-017-0462-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute thymic involution (ATI) is usually regarded as a virulence trait. It is caused by several infectious agents (bacteria, viruses, parasites, fungi) and other factors, including stress, pregnancy, malnutrition and chemotherapy. However, the complex mechanisms that operate during ATI differ substantially from each other depending on the causative agent. For instance, a transient reduction in the size and weight of the thymus and depletion of populations of T cell subsets are hallmarks of ATI in many cases, whereas severe disruption of the anatomical structure of the organ is also associated with some factors, including fungal, parasitic and viral infections. However, growing evidence shows that ATI may be therapeutically halted or reversed. In this review, we highlight the current progress in this field with respect to numerous pathological factors and discuss the possible mechanisms. Moreover, these new observations also show that ATI can be mechanistically reversed.
引用
收藏
页码:401 / 420
页数:20
相关论文
共 198 条
[1]   Interleukins 1β and 6 but not transforming growth factor-β are essential for the differentiation of interleukin 17-producing human T helper cells [J].
Acosta-Rodriguez, Eva V. ;
Napolitani, Giorgio ;
Lanzavecchia, Antonio ;
Sallusto, Federica .
NATURE IMMUNOLOGY, 2007, 8 (09) :942-949
[2]   Mammalian Toll-like receptors [J].
Akira, S .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (01) :5-11
[3]   FACTORS AFFECTING OUTCOME IN MYASTHENIA GRAVIS [J].
Andersen, Jintana B. ;
Gilhus, Nils Erik ;
Sanders, Donald B. .
MUSCLE & NERVE, 2016, 54 (06) :1041-1049
[4]   Thymic alterations in Plasmodium berghei-infected mice [J].
Andrade, C. F. ;
Gameiro, J. ;
Nagib, P. R. A. ;
Carvalho, B. O. ;
Talaisys, R. L. ;
Costa, F. T. M. ;
Verinaud, L. .
CELLULAR IMMUNOLOGY, 2008, 253 (1-2) :1-4
[5]   Activation of Melanoma Differentiation-Associated Gene 5 Causes Rapid Involution of the Thymus [J].
Anz, David ;
Thaler, Raffael ;
Stephan, Nicolas ;
Waibler, Zoe ;
Trauscheid, Michael J. ;
Scholz, Christoph ;
Kalinke, Ulrich ;
Barchet, Winfried ;
Endres, Stefan ;
Bourquin, Carole .
JOURNAL OF IMMUNOLOGY, 2009, 182 (10) :6044-6050
[6]   Thymic atrophy in the mouse is a soluble problem of the thymic environment [J].
Aspinall, R ;
Andrew, D .
VACCINE, 2000, 18 (16) :1629-1637
[7]  
Aspinall R, 1997, J IMMUNOL, V158, P3037
[8]  
이건호, 2014, [Anatomy & Biological Anthropology, 해부·생물인류학], V27, P197
[9]   A thymus candidate in lampreys [J].
Bajoghli, Baubak ;
Guo, Peng ;
Aghaallaei, Narges ;
Hirano, Masayuki ;
Strohmeier, Christine ;
McCurley, Nathanael ;
Bockman, Dale E. ;
Schorpp, Michael ;
Cooper, Max D. ;
Boehm, Thomas .
NATURE, 2011, 470 (7332) :90-U101
[10]   MicroRNAs: new regulators of immune cell development and function [J].
Baltimore, David ;
Boldin, Mark P. ;
O'Connell, Ryan M. ;
Rao, Dinesh S. ;
Taganov, Konstantin D. .
NATURE IMMUNOLOGY, 2008, 9 (08) :839-845