Systemic inflammation
Chronic systemic inflammation (SI) is the result of release of pro-inflammatory cytokines from immune-related cells and the chronic activation of the innate immune system. It can contribute to the development or progression of certain conditions such as cardiovascular disease, cancer, diabetes mellitus, chronic kidney disease, non-alcoholic fatty liver disease, autoimmune and neurodegenerative disorders,[1] and coronary heart disease.[2]
Mechanisms
[edit]Release of pro-inflammatory cytokines and activation of the innate immune system may be the result of either external (biological or chemical agents) or internal (genetic mutations/variations) factors. The cytokine Interleukin 6 and C-reactive protein are common inflammatory markers used to diagnose systemic inflammation risk.[3] Baseline C-reactive protein levels deviate due to natural genetic variation, but significant increases can result from risk factors such as smoking, obesity, lifestyle, and high blood pressure.[3] Excess advanced glycation end-products attach to RAGE receptors to produce chronic inflammation.[4]
Systemic chronic inflammation increases with age (also known as inflammaging) due to unresolved acute inflammation and an individual's exposome. Age-related systemic chronic inflammation is associated with several cytokines including CXCL9, TRAIL, interferon gamma, CCL11, and CXCL1, and a proposed measurement of chronic systemic inflammation based on these cytokines (iAge) correlates with immunosenescence and predicts risk for cardiovascular disease, frailty syndrome, and multimorbidity.[5] Damaged proteins and other cellular debris can provoke chronic inflammation in the innate immune system.[6]
Comorbidities
[edit]It is firmly established that systemic markers for inflammation predict coronary heart disease complications with or without existing heart disease.[2] Inflammation also plays a role in diabetes risk and new research continues to support this conclusion.[7] Cancer is often caused by chronic inflammation.[8]
Research suggests chronic inflammation plays a major role in COVID-19 morbidity.[9][10] In severe cases, COVID-19 causes a cytokine storm which contributes to excessive and uncontrolled inflammation of organs, particularly respiratory tissues.[11][12] If untreated, this increased inflammation can result in reduced immune response, pneumonia, lymphoid tissue damage, and death.[11] Individuals with abnormal cytokine production, such as those with obesity or systemic chronic inflammation, have poorer health outcomes from COVID-19.[9][10] Elevated cytokine production alters the innate immune response which leads to abnormal T-cell and B-Cell function that decreases control of viral replication and host defense.[9] Anti-viral therapeutic drugs which also reduce inflammation seem to be the most effective treatment, but research is still ongoing.[12] Reactive oxygen species are upregulated during inflammation as part of the immune response to defend against pathogens.[13] However, excessive inflammation causes dangerous levels of reactive oxygen species which cause oxidative stress to tissues.[13] The immune system naturally produces antioxidant compounds to regulate and detoxify reactive oxygen species.[13] Anti-oxidative therapy with supplements such as vitamin C, vitamin E, curcumin, or baicalin is speculated to reduce infection severity in COVID-19,[14][12] but previous research has not found antioxidants supplementation to be effective in the prevention of other diseases.[15] Shifting from the typical western diet to a Mediterranean diet or plant-based diet may improve COVID-19 health outcomes by reducing prevalence of comorbidities (i.e. obesity or hypertension), decreasing intake of pro-inflammatory foods, and increasing consumption of anti-inflammatory and antioxidant nutrients.[12][16][17]
Research
[edit]While SI may be induced by multiple external factors, research suggests that a lack of control by tolerogenic dendritic cells and T-regulatory cells (Treg) is possibly the primary risk factor for the development of SI. In functioning immune responses, T-helper and T-cytotoxic cells are activated by presentation of antigens by antigen-presenting cells (APCs). Chief among these are dendritic cells (DCs). When a DC presents an antigen to a Treg cell, a signal is then sent to the nucleus of the DC, resulting in the production of indoleamine 2,3-dioxygenase (IDO). IDO inhibits T cell responses by depleting tryptophan and producing kynurenine, which is toxic to the cell.[citation needed]
Individuals susceptible to developing chronic systemic inflammation appear to lack proper functioning of Treg cells and TDCs. In these individuals, a lack of control of inflammatory processes results in multiple chemical and food intolerances, and autoimmune diseases.[citation needed]
See also
[edit]References
[edit]- ^ Furman, David; Campisi, Judith; Verdin, Eric; Carrera-Bastos, Pedro; Targ, Sasha; Franceschi, Claudio; Ferrucci, Luigi; Gilroy, Derek W.; Fasano, Alessio; Miller, Gary W.; Miller, Andrew H. (December 2019). "Chronic inflammation in the etiology of disease across the life span". Nature Medicine. 25 (12): 1822–1832. doi:10.1038/s41591-019-0675-0. ISSN 1546-170X. PMC 7147972. PMID 31806905.
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- ^ a b Sproston, Nicola R.; Ashworth, Jason J. (2018-04-13). "Role of C-Reactive Protein at Sites of Inflammation and Infection". Frontiers in Immunology. 9: 754. doi:10.3389/fimmu.2018.00754. ISSN 1664-3224. PMC 5908901. PMID 29706967.
- ^ Green AS (2018). "mTOR, glycotoxins and the parallel universe". Aging. 10 (12): 3654–3656. doi:10.18632/aging.101720. PMC 6326656. PMID 30540565.
- ^ Sayed, Nazish; Huang, Yingxiang; Nguyen, Khiem; Krejciova-Rajaniemi, Zuzana; Grawe, Anissa P.; Gao, Tianxiang; Tibshirani, Robert; Hastie, Trevor; Alpert, Ayelet; Cui, Lu; Kuznetsova, Tatiana (2021-07-26). "Author Correction: An inflammatory aging clock (iAge) based on deep learning tracks multimorbidity, immunosenescence, frailty and cardiovascular aging". Nature Aging. 1 (8): 748. doi:10.1038/s43587-021-00102-x. ISSN 2662-8465. PMID 37117770.
- ^ Franceschi C, Garagnani P, Salvioli S (2017). "Inflammaging and 'Garb-aging'". Trends in Endocrinology and Metabolism. 28 (3): 199–212. doi:10.1016/j.tem.2016.09.005. hdl:11585/579512. PMID 27789101.
- ^ Tsalamandris, Sotirios; Antonopoulos, Alexios S.; Oikonomou, Evangelos; Papamikroulis, George-Aggelos; Vogiatzi, Georgia; Papaioannou, Spyridon; Deftereos, Spyros; Tousoulis, Dimitris (February 2019). "The Role of Inflammation in Diabetes: Current Concepts and Future Perspectives". European Cardiology Review. 14 (1): 50–59. doi:10.15420/ecr.2018.33.1. ISSN 1758-3756. PMC 6523054. PMID 31131037.
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- ^ a b Yang, Jing; Zheng, Ya; Gou, Xi; Pu, Ke; Chen, Zhaofeng; Guo, Qinghong; Ji, Rui; Wang, Haojia; Wang, Yuping; Zhou, Yongning (May 2020). "Prevalence of comorbidities and its effects in patients infected with SARS-CoV-2: a systematic review and meta-analysis". International Journal of Infectious Diseases. 94: 91–95. doi:10.1016/j.ijid.2020.03.017. ISSN 1201-9712. PMC 7194638. PMID 32173574.
- ^ a b Tang, Yujun; Liu, Jiajia; Zhang, Dingyi; Xu, Zhenghao; Ji, Jinjun; Wen, Chengping (2020-07-10). "Cytokine Storm in COVID-19: The Current Evidence and Treatment Strategies". Frontiers in Immunology. 11: 1708. doi:10.3389/fimmu.2020.01708. ISSN 1664-3224. PMC 7365923. PMID 32754163.
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- ^ a b c Mittal, Manish; Siddiqui, Mohammad Rizwan; Tran, Khiem; Reddy, Sekhar P.; Malik, Asrar B. (2014-03-01). "Reactive Oxygen Species in Inflammation and Tissue Injury". Antioxidants & Redox Signaling. 20 (7): 1126–1167. doi:10.1089/ars.2012.5149. ISSN 1523-0864. PMC 3929010. PMID 23991888.
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