Key Targets for COVID-19 Research

Key Targets for COVID-19 Research

Mar 11, 2021

The COVID-19 pandemic has taken hold of our lives for nearly an entire year, and although we now have vaccines being distributed, there is still a lot we don’t know. SARS-CoV-2 research is ongoing, and likely to continue for many years to come. Many different biomarkers have shown promise for diagnosing and predicting the prognosis or outcome of infection by SARS-CoV-2. Our featured products for March 2021 are three such biomarkers, angiotensin I converting enzyme 2 (ACE2)interleukin 6 (IL6) and C reactive protein (CRP).

 

ACE2 is an angiotensin-converting enzyme responsible for the breakdown of Angiotensins I and II, has an important role negatively regulating the renin-angiotensin system (RAS), and has been shown to facilitate viral transmission of SARS coronavirus 2 (SARS-CoV-2), the cause of COVID-19.1,2,3 Recent studies have shown that SARS-CoV-2 gains entry into cells expressing ACE2, but not cells expressing other coronavirus receptors, or cells that do not express ACE2.3 The mechanism for infection with SARS-CoV-2 involves the spike glycoprotein on the surface of the virus binding to the ACE2 receptor, allowing for viral RNA to be released into the cell, initiating infection.4 ACE2 is highly expressed in alveolar epithelial cells, indicating that the lungs are typically where the initial infection occurs in humans.5 After initial infection, the virus often spreads to other areas of the body with high levels of ACE2 through blood circulation, often resulting in multi-organ injury.6

 

IL6 is a cytokine involved in inflammation and maturation of B cells, mainly found at the site of inflammation, from where it induces an inflammatory response.7 As COVID-19 can  often result in cytokine release syndrome, or a ‘cytokine storm’, IL6 has been found at elevated levels in patients with COVID-19.8,9 IL6, along with other cytokines including TNFa, IP10, MCP1, CCL3, IL2, IL2R, and IL7, have been seen to increase in more severe cases of COVID-19.10 IL6 and IL2R in particular increase according to the severity of the case, and IL6 levels are high among non-survivors.10 Another study showed that IL6 levels in serum could help to determine the severity of COVID-19 cases and predict the outcome for patients.11

 

CRP is a cytokine involved in the activation and amplification of the complement system.12 As CRP is often elevated as a result of inflammation, it is also often found at high levels in patients with COVID-19.9,10,11 Similar to IL6, CRP is found at high levels in patients with severe cases and poor prognosis of COVID-19 infection.8,10,11 CRP especially could be useful as an early predictor of severe COVID-19, as CRP levels are not typically high during viral infections.13

 

To elevate your research on COVID-19 and associated biomarkers, check out our Human ACE2IL6, and CRP ELISA kits and related antibodies:

 

Human Angiotensin I Converting Enzyme 2 (RDR-ACE2-Hu)

Detection Range: 15.625-1000pg/mL

Sensitivity: 7.7pg/mL

Human Interleukin 6 ELISA Kit (RDR-IL6-Hu)

Detection Range: 7.812-500pg/mL

Sensitivity: 3.11pg/mL

Human C reactive protein ELISA Kit (RDR-CRP-Hu)

Detection range: 0.156-10ng/mL

Sensitivity: 0.057ng/mL

 

Related Antibody Products:

Rabbit anti-Human ACE2 Polyclonal Antibody

Rabbit anti-Human IL6 Polyclonal Antibody

Rabbit anti-Human IL6R Polyclonal Antibody

Rabbit anti-Human CRP Polyclonal Antibody

 

To see our full list of COVID-19 related ELISA kits, visit this News Post.

To search our full catalogue of ELISA kits, visit our ELISA Page.

 

Reddot Biotech is now offering antibodies! To search our full catalogue of antibody products, visit our Antibody Page.

 

 

 

References and further reading:

1. ACE2 angiotensin I converting enzyme 2 [Homo sapiens (human)] - Gene - NCBI.  Ncbi.nlm.nih.gov. https://www.ncbi.nlm.nih.gov/gene/59272. Published 2021. Accessed March 11, 2021.

2. Riordan JF. Angiotensin-I-converting enzyme and its relatives. Genome Biol. 2003;4(8):225. doi:10.1186/gb-2003-4-8-225

3. Zhou P, Yang XL, Wang XG, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020;579(7798):270-273. doi:10.1038/s41586-020-2012-7

4. Li W, Moore MJ, Vasilieva N, et al. Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426(6965):450-454. doi:10.1038/nature02145

5. Hamming, I., Timens, W., Bulthuis, M. L. C., Lely, A. T., Navis, G. V., & van Goor, H. (2004). Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis. The Journal of Pathology: A Journal of the Pathological Society of Great Britain and Ireland, 203(2), 631-637.

6. Zou X, Chen K, Zou J, Han P, Hao J, Han Z. Single-cell RNA-seq data analysis on the receptor ACE2 expression reveals the potential risk of different human organs vulnerable to 2019-nCoV infection. Front Med. 2020;14(2):185-192. doi:10.1007/s11684-020-0754-0

7. IL6 interleukin 6 [Homo sapiens (human)] - Gene - NCBI. Ncbi.nlm.nih.gov. https://www.ncbi.nlm.nih.gov/gene/3569. Published 2021. Accessed March 11, 2021.

8. Gallo Marin B, Aghagoli G, Lavine K, et al. Predictors of COVID-19 severity: A literature review. Rev Med Virol. 2021;31(1):1-10.doi:10.1002/rmv.2146

9. Ponti G, Maccaferri M, Ruini C, Tomasi A, Ozben T. Biomarkers associated with COVID-19 disease progression. Crit Rev ClinLabSci. 2020;57(6):389-399. doi:10.1080/10408363.2020.1770685

10. Velavan TP, Meyer CG. Mild versus severe COVID-19: Laboratory markers. Int J Infect Dis. 2020;95:304-307.doi:10.1016/j.ijid.2020.04.061

11. Liu F, Li L, Xu M, et al. Prognostic value of interleukin-6, C-reactive protein, and procalcitonin in patients with COVID-19. J ClinVirol. 2020;127:104370. doi:10.1016/j.jcv.2020.104370

12. CRP C-reactive protein [Homo sapiens (human)] - Gene - NCBI. Ncbi.nlm.nih.gov. https://www.ncbi.nlm.nih.gov/gene/1401. Published 2021. Accessed March 11, 2021.

13. Paces J, Strizova Z, Smrz D, Cerny J. COVID-19 and the immune system. Physiol Res. 2020 Jul 16;69(3):379-388. doi:10.33549/physiolres.934492. Epub 2020 May 29. PMID: 32469225.

 

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