Literature DB >> 24412212

Changes in naïve and memory T-cells in elite swimmers during a winter training season.

Ana Maria Teixeira1, Luís Rama2, Humberto M Carvalho2, Grasiely Borges2, Tiago Carvalheiro3, Michael Gleeson4, Francisco Alves5, Hélder Trindade3, Artur Paiva3.   

Abstract

High intensity training regimens appear to put athletes at a higher risk of illness. As these have been linked to alterations in the proportions of differentiated T cells, how training load affects these populations could have important implications for athlete susceptibility to disease. This study examined the effect of a winter training season on the proportions of circulating naïve and memory T cells subsets of high competitive level swimmers. Blood samples were taken at rest at 4 time-points during the season: before the start of the season (t0-September), after 7weeks of an initial period of gradually increasing training load (t1-November), after 6weeks of an intense training cycle (t2-February) and 48h after the main competition (t3-April) and from eleven non-athlete controls at 2 similar time-points (t2 and t3). CD4, CD8 and gamma-delta (γδ) T cells expressing the naïve (CCR7(+)CD45RA(+)), central-memory (CM-CCR7(+)CD45RA(-)), effector-memory (EM-CCR7(-)CD45RA(-)) and terminal effector (TEMRA-CCR7(-)CD45RA(+)) were quantified by flow cytometry. Statistical analyses were performed using multilevel modeling regression. Both T CD4(+) naïve and CM presented a linear increase in response to the first moment of training exposure, and had an exponential decrease until the end of the training exposure. As for TCD4(+) EM, changes were observed from t2 until the end of the training season with an exponential trend, while TCD4(+) TEMRA increased linearly throughout the season. TCD8(+) naïve increased at t1 and decreased exponentially thereafter. TCD8(+) TEMRA values decreased at t1 and increased exponentially until t3. γδT-EM had an increase at t1 and an exponential decrease afterwards. In contrast, γδT-TEMRA decreased at t1 and exponentially increased during the remaining 20weeks of training. An increase in TEMRA and EM T cells alongside a decrease in naïve T cells could leave athletes more susceptible to illness in response to variation in training stimulus during the season.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CCR7; CD45RA; Exercise; Training load; γδ T cells

Mesh:

Year:  2014        PMID: 24412212     DOI: 10.1016/j.bbi.2014.01.002

Source DB:  PubMed          Journal:  Brain Behav Immun        ISSN: 0889-1591            Impact factor:   7.217


  10 in total

1.  Lifelong training improves anti-inflammatory environment and maintains the number of regulatory T cells in masters athletes.

Authors:  Luciele G Minuzzi; Luis Rama; Nicolette C Bishop; Fátima Rosado; António Martinho; Artur Paiva; Ana M Teixeira
Journal:  Eur J Appl Physiol       Date:  2017-04-08       Impact factor: 3.078

2.  Long-term swimming training modifies acute immune cell response to a high-intensity session.

Authors:  José P Morgado; Cristina P Monteiro; Catarina N Matias; Joana F Reis; Júlia Teles; Maria José Laires; Francisco Alves
Journal:  Eur J Appl Physiol       Date:  2018-01-08       Impact factor: 3.078

3.  Dimethyl Fumarate Selectively Reduces Memory T Cells and Shifts the Balance between Th1/Th17 and Th2 in Multiple Sclerosis Patients.

Authors:  Qi Wu; Qin Wang; Guangmei Mao; Catherine A Dowling; Steven K Lundy; Yang Mao-Draayer
Journal:  J Immunol       Date:  2017-03-03       Impact factor: 5.422

4.  Long-term physical training in adolescent sprint and middle distance swimmers alters the composition of circulating T and NK cells which correlates with soluble ICAM-1 serum concentrations.

Authors:  Hannah L Notbohm; Moritz Schumann; Stefan Fuhrmann; Jan Klocke; Sebastian Theurich; Wilhelm Bloch
Journal:  Eur J Appl Physiol       Date:  2021-03-11       Impact factor: 3.078

Review 5.  Does Regular Exercise Counter T Cell Immunosenescence Reducing the Risk of Developing Cancer and Promoting Successful Treatment of Malignancies?

Authors:  James E Turner; Patricia C Brum
Journal:  Oxid Med Cell Longev       Date:  2017-07-02       Impact factor: 6.543

6.  An attempt to induce an immunomodulatory effect in rowers with spirulina extract.

Authors:  Artur Juszkiewicz; Piotr Basta; Elżbieta Petriczko; Bogusław Machaliński; Jerzy Trzeciak; Karolina Łuczkowska; Anna Skarpańska-Stejnborn
Journal:  J Int Soc Sports Nutr       Date:  2018-02-20       Impact factor: 5.150

7.  The Cellular Composition of the Innate and Adaptive Immune System Is Changed in Blood in Response to Long-Term Swimming Training.

Authors:  José P Morgado; Catarina N Matias; Joana Filipa Reis; Dalia Curto; Francisco Bessone Alves; Cristina P Monteiro
Journal:  Front Physiol       Date:  2020-05-12       Impact factor: 4.566

Review 8.  Exercise and the immune system: taking steps to improve responses to cancer immunotherapy.

Authors:  Michael P Gustafson; Courtney M Wheatley-Guy; Allison C Rosenthal; Dennis A Gastineau; Emmanuel Katsanis; Bruce D Johnson; Richard J Simpson
Journal:  J Immunother Cancer       Date:  2021-07       Impact factor: 13.751

Review 9.  Is immunosenescence influenced by our lifetime "dose" of exercise?

Authors:  James E Turner
Journal:  Biogerontology       Date:  2016-03-29       Impact factor: 4.277

Review 10.  Debunking the Myth of Exercise-Induced Immune Suppression: Redefining the Impact of Exercise on Immunological Health Across the Lifespan.

Authors:  John P Campbell; James E Turner
Journal:  Front Immunol       Date:  2018-04-16       Impact factor: 7.561

  10 in total

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