Literature DB >> 20483662

Getting back at nature: understanding thymic development and overcoming its atrophy.

Tracy S P Heng1, Ann P Chidgey, Richard L Boyd.   

Abstract

T cell development is a complex and tightly regulated process involving reciprocal interactions between the thymic stroma and differentiating thymocytes. Normal thymic function is critical for immunity and microenvironmental defects predispose to dysregulation in the T cell compartment. Thymic structure and function are also severely damaged by chemotherapy and pre-transplant conditioning. Furthermore, poor immune competence with ageing is closely linked to thymic atrophy. Overcoming such thymic defects would have immediate application in many diseases, especially the recovery of cancer patients from cytotoxic treatment. Reversing the thymus ageing process via inhibition of atrophic factors such as sex steroids or administration of thymopoietic growth factors is one possible approach. Moreover, it is becoming clear a common thymic epithelial progenitor exists, raising the possibility for de novo thymus generation using emerging stem cell and tissue engineering technologies. Achievement of this goal will open up many avenues for the application of thymus-based immune rejuvenation and manipulation. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20483662     DOI: 10.1016/j.coph.2010.04.006

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  15 in total

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10.  Regulation of in vitro human T cell development through interleukin-7 deprivation and anti-CD3 stimulation.

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