Rejuvenation of the aging thymus: growth hormone-mediated and ghrelin-mediated signaling pathways
Open accessAbstract
One of the major fundamental causes for the aging of the immune system is the structural and functional involution of the thymus, and the associated decline in de novo naïve T-lymphocyte output. This loss of naïve T-cell production weakens the ability of the adaptive immune system to respond to new antigenic stimuli and eventually leads to a peripheral T-cell bias to the memory phenotype. While the precise mechanisms responsible for age-associated thymic involution remain unknown, a variety of theories have been forwarded including the loss of expression of various growth factors and hormones that influence the lymphoid compartment and promote thymic function. Extensive studies examining two hormones, namely growth hormone (GH) and ghrelin (GRL), have demonstrated their contributions to thymus biology. In the current review, we discuss the literature supporting a role for these hormones in thymic physiology and age-associated thymic involution and their potential use in the restoration of thymic function in aged and immunocompromised individuals.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The causes of age-related decline in lymphocyte development are multifactorial, involving changes in hematopoietic stem cells and progenitors as well as local tissue and systemic environments.
“The causes of this age-related reduction in lymphocyte development are multifactorial and include changes in HSCs and progenitor cells (11,12) as well as the local tissue and systemic environments (13,14).”
From Causes, consequences, and reversal of immune system aging (2013) · cites this paper as [13]
Growth hormone and IGF-1 can stimulate thymopoiesis.
“For example, numerous reports have demonstrated that growth hormone (GH) and IGF-1 can stimulate thymopoiesis (13,42).”
From Causes, consequences, and reversal of immune system aging (2013) · cites this paper as [13]
Age-related changes in the endocrine system contribute to declines in lymphopoiesis.
“this has led to the conclusion that age-related changes in the endocrine system contribute to declines in lymphopoiesis.”
From Causes, consequences, and reversal of immune system aging (2013) · cites this paper as [13]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 129 · Cited by 119
Research works printed but not linked: 4
- [18]Aspinall R Mitchell W Reversal of age-associated thymic atrophy: treatments, delivery, and side effects Exp Gerontol 2008 43 7 700 705 18562142
- [19]Lynch HE Goldberg GL Chidgey A Van den Brink MR Boyd R Sempowski GD Thymic involution and immune reconstitution Trends Immunol 2009 30 7 366 373 19540807 PMC2750859
- [32]Welniak LA Sun R Murphy WJ The role of growth hormone in T-cell development and reconstitution J Leukoc Biol 2002 71 3 381 387 11867675
- [64]Dardenne M Smaniotto S de Mello-Coelho V Villa-Verde DM Savino W Growth hormone modulates migration of developing T cells Ann N Y Acad Sci 2009 Feb 1153 1 5 19236321
- Authors
- Taub, D. D., Murphy, W. J., & Longo, D. L.
- Affiliations
- National Institutes of Health (US)
- University of California Davis Medical Center (US)
- Corresponding author
- Taub, Dennis D
- ORCID
- Murphy, William J
- Venue
- Current Opinion in Pharmacology
- Publisher
- Elsevier BV
- Published
- 2010-08
- Volume
- 10
- Issue
- 4
- Pages
- 408-424
- ISSN
- 1471-4892 (ISSN-L)
- PMC
- PMC2914845
- OpenAlex
- W2038363738
- Cited by
- 119
- References
- 129
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 5 · 2023: 7 · 2022: 8 · 2021: 7 · 2020: 4 · 2019: 2 · 2018: 5 · 2017: 8 · 2016: 9 · 2015: 11 · 2014: 7 · 2013: 15 · 2012: 13
- FWCI
- 5.21
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Pharmacology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (Z01AG000758)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Health Sciences › Medicine › Neurology › Myasthenia Gravis and Thymoma
- Keywords
- thymic involution, growth hormone, ghrelin, immunosenescence, immunocompromised patients, hormone signaling pathways
- MeSH terms
- Aging, Animals, Humans, Receptors, Somatotropin, Growth Hormone, T-Lymphocytes, Thymus Gland, Signal Transduction, Cytokines, Immunocompromised Host, Ghrelin, Receptors, Ghrelin, Immune System Phenomena
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review