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Telomere Length, Telomerase Activity, and Replicative Potential in HIV Infection: Analysis of CD4+ and CD8+T Cells from HIV-discordant Monozygotic Twins
Open accessAbstract
To address the possible role of replicative senescence in human immunodeficiency virus (HIV) infection, telomere length, telomerase activity, and in vitro replicative capacity were assessed in peripheral blood T cells from HIV+ and HIV− donors. Genetic and age-specific effects on these parameters were controlled by studying HIV-discordant pairs of monozygotic twins. Telomere terminal restriction fragment (TRF) lengths from CD4+ T cells of HIV+ donors were significantly greater than those from HIV− twins. In contrast, telomere lengths in CD8+ T cells from HIV+ donors were shorter than in HIV− donors. The in vitro replicative capacity of CD4+ cells from HIV+ donors was equivalent to that of HIV− donors in response to stimulation through T cell receptor CD3 and CD28. Little or no telomerase activity was detected in freshly isolated CD4+ or CD8+ lymphocytes from HIV+ or HIV− donors, but was induced by in vitro stimulation of both HIV+ and HIV− donor cells. These results suggest that HIV infection is associated with alterations in the population dynamics of both CD4+ and CD8+ T cells, but fail to provide evidence for clonal exhaustion or replicative senescence as a mechanism underlying the decline in CD4+ T cells of HIV-infected donors.
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“Telomere lengths of CD8+ T cells are shorter in HIV patients compared to healthy individuals, but this observation was not found in CD4+ T cells.”
From The struggle of a good friend getting old: cellular senescence in viral responses and therapy (2021) · cites this paper as Palmer et al, 1997
In the citing paper
“Interestingly, certain hallmarks of cellular senescence are also found in T cells from patients with HIV (Effros et al, 1996; Wolthers et al, 1996; Palmer et al, 1997; Nelson et al, 2012; Pereira Ribeiro et al, 2016).”
From The struggle of a good friend getting old: cellular senescence in viral responses and therapy (2021) · cites this paper as Palmer et al, 1997
In the citing paper
“These finds were also independent on whether HIV patients were on antiretroviral therapy (Effros et al, 1996; Wolthers et al, 1996; Palmer et al, 1997).”
From The struggle of a good friend getting old: cellular senescence in viral responses and therapy (2021) · cites this paper as Palmer et al, 1997
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“Telomere lengths of CD8+ T cells are shorter in HIV patients compared to healthy individuals, but this observation was not found in CD4+ T cells.”
From The struggle of a good friend getting old: cellular senescence in viral responses and therapy (2021) · cites this paper as Palmer et al, 1997
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Citations
Cites
The serial cultivation of human diploid cell strains
Hayflick, L., & Moorhead, P. S. (1961) · Experimental Cell Research · doi:10.1016/0014-4827(61)90192-6 · Cited by 8,508
Telomeres shorten during ageing of human fibroblasts
Harley, C. B., Futcher, A. B., & Greider, C. W. (1990) · Nature · doi:10.1038/345458a0 · Cited by 5,750
Rapid turnover of plasma virions and CD4 lymphocytes in HIV-1 infection
Ho, D. D., Neumann, A. U., Perelson, A. S., Chen, W., Leonard, J. M., & Markowitz, M. H. (1995) · Nature · doi:10.1038/373123a0 · Cited by 4,261
Identification of a specific telomere terminal transferase activity in tetrahymena extracts
Greider, C. W., & Blackburn, E. H. (1985) · Cell · doi:10.1016/0092-8674(85)90170-9 · Cited by 3,400
The RNA Component of Human Telomerase
Feng, J., Funk, W. D., Wang, S.-S., Weinrich, S. L., Avilion, A. A., Chiu, C.-P., Adams, R. R., Chang, E., Allsopp, R. C., Yu, J., et al. (1995) · Science · doi:10.1126/science.7544491 · Cited by 2,227
Telomere length predicts replicative capacity of human fibroblasts.
Allsopp, R. C., Vaziri, H., Patterson, C., Goldstein, S., Younglai, E. V., Futcher, A. B., Greider, C. W., & Harley, C. B. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.21.10114 · Cited by 2,200
Moskophidis, D., Lechner, F., Pircher, H., & Zinkernagel, R. M. (1993) · Nature · doi:10.1038/362758a0 · Cited by 1,240
Evidence for a mitotic clock in human hematopoietic stem cells: loss of telomeric DNA with age.
Vaziri, H., Dragowska, W., Allsopp, R. C., Thomas, T. E., Harley, C. B., & Lansdorp, P. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.21.9857 · Cited by 1,132
Telomerase activity in normal and malignant hematopoietic cells.
Broccoli, D., Young, J. W., & de Lange, T. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9082 · Cited by 754
Genetic determination of telomere size in humans: a twin study of three age groups.
Slagboom, P. E., Droog, S., & Boomsma, D. I. (1994) · PubMed Central · Cited by 734
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Effros, R. B. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9063-9_47 · Cited by 4
Downey, J. S., Attaf, M., Moyle, G. J., Gazzard, B., Gotch, F. M., & Imami, N. (2011) · AIDS · doi:10.1097/qad.0b013e32834b35a9 · Cited by 4
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Liu, Z., & Wong, J. T. (1999) · Clinical Immunology · doi:10.1006/clim.1999.4766 · Cited by 4
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Ajasin, D., & Eugenín, E. A. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-65944-7_15 · Cited by 3
Preserved CD4 T-cell telomere length during long-lasting HIV-2 infection
Rego, R. T., Albuquerque, A. S., Foxall, R. B., Cavaleiro, R., Soares, R. S., Baptista, A. P., Soares, M. V. D., Gómes, P., & Sousa, A. E. (2012) · AIDS · doi:10.1097/qad.0b013e32835ab234 · Cited by 3
Effects of Subcutaneous IL‐2 Therapy on Telomere Lengths in PBMC in HIV‐Infected Patients
Aladdin, H., Larsen, C. S., Schjerling, P., Møller, B. K., Buhl, M. R., Gerstoft, J., Pedersen, B. K., & Ullum, H. (2001) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.2001.00876.x · Cited by 3
The long and the short of telomeres in bone marrow recipient SCID patients
Sarzotti‐Kelsoe, M., Daniell, X. G., Whitesides, J. F., & Buckley, R. H. (2010) · Immunologic Research · doi:10.1007/s12026-010-8192-8 · Cited by 2
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Clark, D. R., & Wolthers, K. C. (2000) · Springer eBooks · doi:10.1007/978-94-017-0685-8_4 · Cited by 2
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(2000) · Pure Amsterdam UMC · doi:10.1002/1521-4141(200007)30:7 · Cited by 1
Aging and HIV Disease: Synergistic Immunological Effects?
Effros, R. B. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_47 · Cited by 1
Apoptosis in HIV disease pathogenesis
Nath, A. (2001) · Advances in cell aging and gerontology · doi:10.1016/s1566-3124(01)06005-9 · Cited by 1
Valcke, H. S. (2009) · Cited by 1
Telomeres and Replicative Senescence
Allsopp, R., Wang, S., Kim, N., & Harley, C. B. (1998) · CRC Press eBooks · doi:10.1201/b14256-24 · Cited by 1
Constraints on the CD8 T cell response in chronic HBV infection
Das, A. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)
li, Y. (2010) · Digital Commons-TMC (Texas Medical Center)
Anti-Aging Medicine LiteratureWatch
Pawelec, G. (1998) · Rejuvenation Research · doi:10.1089/rej.1.1998.1.275
VIH : nouvelle vision du renouvellement des lymphocytes T CD4+.
Fleury, S., Soudeyns, H., & Pantaleo, G. (1999) · médecine/sciences · doi:10.4267/10608/1465
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Rapid Telomere Shortening in Children
Zeichner, S. L., Palumbo, P. E., Feng, Y., Xiao, X., Gee, D., Sleasman, J. W., Goodenow, M. M., Biggar, R. J., & Dimitrov, D. S. (2016)
de Araújo, M. L. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.5.2017.tde-06012017-103130
Inflammation and CMV-associated lymphocyte senescence in chronic HIV infection
Heath, J. (2018) · Memorial University Research Repository (Memorial University)
Tardif, M. R. (2005) · Corpus Université Laval (Université Laval)
Fauce, S. R., & Effros, R. B. (2008) · Springer eBooks · doi:10.1007/978-0-387-76842-7_4
Aging and HIV Disease: Synergistic Immunological Effects?
Effros, R. B. (2018) · Springer eBooks · doi:10.1007/978-3-319-64597-1_47-1
Anti-Aging Medicine LiteratureWatch
(1998) · Rejuvenation Research · doi:10.1089/rej.1.1998.1.79
Telomere length dynamics in adults living with HIV: A systematic review
Massamba, M. K. Y., Madurai, L., Archary, D., & Mahomed, S. (2026) · BMC Infectious Diseases · doi:10.1186/s12879-026-13243-4
Allen (1999) · doi:10.1002/(sici)1097-4652(199907)180:1
Metadata
- Authors
- Palmer, L. D., Weng, N.-P., Levine, B. L., June, C. H., Lane, H. C., & Hodes, R. J.
- Affiliations
- National Institutes of Health (US)
- Venue
- The Journal of Experimental Medicine
- Publisher
- Rockefeller University Press
- Published
- 1997-04-07
- Volume
- 185
- Issue
- 7
- Pages
- 1381-1386
- ISSN
- 0022-1007 (ISSN-L)
- 1540-9538
- PMC
- PMC2196247
- OpenAlex
- W2114119969
- Cited by
- 129
- References
- 20
- Citations by year
- 2026: 1 · 2024: 2 · 2022: 1 · 2021: 3 · 2019: 1 · 2018: 4 · 2017: 3 · 2016: 2 · 2015: 1 · 2014: 3 · 2013: 5 · 2012: 2
- FWCI
- 5.96
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Experimental Medicine (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Infectious Diseases › HIV-related health complications and treatments
- Keywords
- HIV infection, telomere length, telomerase activity, replicative senescence, CD4+ T cells, CD8+ T cells, terminal restriction fragments, CD4+ T cell decline
- MeSH terms
- Adult, Cells, Cultured, Humans, Lymphocyte Activation, Middle Aged, Twins, Monozygotic, CD4-Positive T-Lymphocytes, HIV Infections, T-Lymphocyte Subsets, Telomere, Cellular Senescence, CD8-Positive T-Lymphocytes, Telomerase
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