Microbiota and Its Impact on the Immune System in COVID-19-A Narrative Review.
Marzena JabczykJustyna NowakBartosz HudzikBarbara Zubelewicz-SzkodzinskaPublished in: Journal of clinical medicine (2021)
The microbiota is of interest for the development of a therapeutic strategy against SARS-CoV-2 coronavirus disease 2019 (COVID-19) due to its impact on the host immune system. Proven communications of the gut microbiota with the pulmonary microbiota (gut-lung axis) and the pathway of neural connections between the gut and brain (gut-brain axis) may be important in the face of the pandemic. SARS-CoV-2 was shown to affect almost all organs because of the presence of a host receptor known as angiotensin converting enzyme 2 (ACE2). The ACE2 receptor is mainly present in the brush border of intestinal enterocytes, ciliary cells, and type II alveolar epithelial cells in the lungs. The transport function of ACE2 has been linked to the ecology of gut microbes in the digestive tract, suggesting that COVID-19 may be related to the gut microbiota. The severity of COVID-19 may be associated with a number of comorbidities, such as hypertension, diabetes, obesity, and/or old age; therefore, attention is also paid to multiple morbidities and the modulation of microbiota through comorbidities and medications. This paper reviews the research in the context of the state of the intestinal microbiota and its impact on the cells of the immune system during the SARS-CoV-2 pandemic.
Keyphrases
- sars cov
- angiotensin converting enzyme
- coronavirus disease
- respiratory syndrome coronavirus
- angiotensin ii
- induced apoptosis
- type diabetes
- cell cycle arrest
- blood pressure
- cardiovascular disease
- metabolic syndrome
- white matter
- insulin resistance
- pulmonary hypertension
- resting state
- signaling pathway
- body mass index
- endoplasmic reticulum stress
- systematic review
- oxidative stress
- skeletal muscle
- brain injury
- randomized controlled trial
- physical activity
- glycemic control
- high fat diet induced
- cerebral ischemia
- drug induced