Marathon training and immune function
Abstract
Many components of the immune system exhibit adverse change after marathon-type exertion. These immune changes occur in several compartments of the immune system and body (e.g. the skin, upper respiratory tract mucosal tissue, lung, peritoneal cavity, blood and muscle). Of all immune cells, natural killer (NK) cells, neutrophils and macrophages (of the innate immune system) exhibit the greatest changes in response to marathon competition, both in terms of numbers and function. Many mechanisms appear to be involved, including exercise-induced changes in stress hormone and cytokine concentrations, body temperature changes, increases in blood flow and dehydration. During this 'open window' of immune dysfunction (which may last between 3 and 72 hours, depending on the immune measure), viruses and bacteria may gain a foothold, increasing the risk of subclinical and clinical infection. Of the various nutritional and pharmacological countermeasures to marathon-induced immune perturbations that have been evaluated thus far, ingestion of carbohydrate beverages during intense and prolonged exercise has emerged as the most effective. However, carbohydrate ingestion during a marathon attenuates increases in plasma cytokines and stress hormones, but is largely ineffective against changes in other immune components including suppression of NK and T-cell function, and salivary IgA output. Other countermeasures, such as glutamine, antioxidant supplements and ibuprofen, have had disappointing results and thus the search for companion agents to carbohydrate continues.
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Potential pitfalls to long-term training with low carbohydrate availability include perturbations to immune function, impaired training intensity, reduced ability to oxidise exogenous carbohydrate during competition and increased muscle protein oxidation.
“Despite the theoretical rationale for the training-low paradigm, potential pitfalls to longterm training with low CHO availability include perturbations to immune function [67] impaired training intensity [55], reduced ability to oxidise exogenous CHO during competition [68] and increased muscle protein oxidation [69].”
From New strategies in sport nutrition to increase exercise performance (2016) · cites this paper as [67]
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References 10 · Cited by 150
- Authors
- Nieman, D. C.
- Affiliations
- Appalachian State University (US)
- Corresponding author
- Nieman, David C
- ORCID
- Nieman, David C
- Venue
- Sports Medicine
- Published
- 2007
- Volume
- 37
- Issue
- 4
- Pages
- 412-415
- ISSN
- 0112-1642 (ISSN-L)
- OpenAlex
- W1980705794
- Cited by
- 150
- References
- 10
- Citations by year
- 2026: 3 · 2025: 9 · 2024: 3 · 2023: 3 · 2022: 9 · 2021: 7 · 2020: 8 · 2019: 6 · 2018: 9 · 2017: 8 · 2016: 12 · 2015: 12 · 2014: 9 · 2013: 13 · 2012: 7
- FWCI
- 8.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Sports Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Sports Performance and Training
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Keywords
- marathon running, exercise immunology, natural killer cells, neutrophils, macrophages, innate immunity, cytokines, stress hormones, carbohydrate intake, infection risk, salivary IgA, glutamine, antioxidant supplements, ibuprofen, T cell function
- MeSH terms
- Physical Exertion, Humans, Immune System, Running, United States
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