Literature DB >> 28960415

Thymic Atrophy: Experimental Studies and Therapeutic Interventions.

S Majumdar1, D Nandi1.   

Abstract

The thymus is essential for T cell development and maturation. It is extremely sensitive to atrophy, wherein loss in cellularity of the thymus and/or disruption of the thymic architecture occur. This may lead to lower naïve T cell output and limited TCR diversity. Thymic atrophy is often associated with ageing. What is less appreciated is that proper functioning of the thymus is critical for reduction in morbidity and mortality associated with various clinical conditions including infections and transplantation. Therefore, therapeutic interventions which possess thymopoietic potential and lower thymic atrophy are required. These treatments enhance thymic output, which is a vital factor in generating favourable outcomes in clinical conditions. In this review, experimental studies on thymic atrophy in rodents and clinical cases where the thymus atrophies are discussed. In addition, mechanisms leading to thymic atrophy during ageing as well as during various stress conditions are reviewed. Therapies such as zinc supplementation, IL7 administration, leptin treatment, keratinocyte growth factor administration and sex steroid ablation during thymic atrophy involving experiments in animals and various clinical scenarios are reviewed. Interventions that have been used across different scenarios to reduce the extent of thymic atrophy and enhance its output are discussed. This review aims to speculate on the roles of combination therapies, which by acting additively or synergistically may further alleviate thymic atrophy and boost its function, thereby strengthening cellular T cell responses.
© 2017 The Foundation for the Scandinavian Journal of Immunology.

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Year:  2017        PMID: 28960415     DOI: 10.1111/sji.12618

Source DB:  PubMed          Journal:  Scand J Immunol        ISSN: 0300-9475            Impact factor:   3.487


  23 in total

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4.  Comparative analysis of thymic subpopulations during different modes of atrophy identifies the reactive oxygen species scavenger, N-acetyl cysteine, to increase the survival of thymocytes during infection-induced and lipopolysaccharide-induced thymic atrophy.

Authors:  Shamik Majumdar; Vasista Adiga; Abinaya Raghavan; Supriya Rajendra Rananaware; Dipankar Nandi
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6.  Breast milk interleukin-7 and thymic gland development in infancy.

Authors:  Elham M Hossny; Dalia H El-Ghoneimy; Rasha H El-Owaidy; Mohamed G Mansour; Mohammad T Hamza; Amira F El-Said
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7.  Infant cortisol stress-response is associated with thymic function and vaccine response.

Authors:  M Nazmul Huda; Shaikh M Ahmad; Md Jahangir Alam; Afsana Khanam; Md Nure Alam Afsar; Yukiko Wagatsuma; Rubhana Raqib; Charles B Stephensen; Kevin D Laugero
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8.  Blood autophagy defect causes accelerated non-hematopoietic organ aging.

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9.  The antipsychotic medication, risperidone, causes global immunosuppression in healthy mice.

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Review 10.  How does spaceflight affect the acquired immune system?

Authors:  Taishin Akiyama; Kenta Horie; Eiichi Hinoi; Manami Hiraiwa; Akihisa Kato; Yoichi Maekawa; Akihisa Takahashi; Satoshi Furukawa
Journal:  NPJ Microgravity       Date:  2020-05-07       Impact factor: 4.415

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