Abstract Background The COVID‐19 pandemic has demanded effective therapeutic protocol from researchers and clinicians across the world. Currently, a large amount of primary data have been generated from several preclinical studies. At least 300 clinical trials are underway for drug repurposing against COVID‐19; the clinician needs objective evidence‐based medication to treat COVID‐19. Observations Single‐stranded RNA viral genome of SARS‐CoV‐2 encodes structural proteins (spike protein), non‐structural enzymatic proteins (RNA‐dependent RNA polymerase, helicase, papain‐like protease, 3‐chymotrypsin‐like protease) and other accessory proteins. These four enzymatic proteins on spike protein are rate‐limiting steps in viral replications and, therefore, an attractive target for drug development against SARS‐CoV‐2. In silico and in vitro studies have identified various potential epitomes as candidate sequences for vaccine development. These studies have also revealed potential targets for drug development and drug repurposing against COVID‐19. Clinical trials utilizing antiviral drugs and other drugs have given inconclusive results regarding their clinical efficacy and side effects. The need for angiotensin‐converting enzyme (ACE‐2) inhibitors/angiotensin receptor blockers and corticosteroids has been recommended. Western countries have adopted telemedicine as an alternative to prevent transmission of infection in the population. Currently, no proven, evidence‐based therapeutic regimen exists for COVID‐19. Conclusion The COVID‐19 pandemic has put tremendous pressure on researchers to evaluate and approve drugs effective against the disease. Well‐controlled randomized trials should assess medicines that are not marketed with substantial evidence of safety and efficacy and more emphasis on time tested approaches for drug evaluation.

2019-20 coronavirus outbreak

Pandemic

Coronavirus Infections

Betacoronavirus

10.1111/bcpt.13600

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Citations (11)

Medicinal plants: Treasure for antiviral drug discovery

Phytotherapy Research (2021)

Sofi Imtiyaz Ali Wajid Mohammad Sheikh Muzafar Ahmad Rather V. Venkatesalu Showkeen Muzamil Bashir

The pandemic of viral diseases like novel coronavirus (2019‐nCoV) prompted the scientific world to examine antiviral bioactive compounds rather than nucleic acid analogous, protease inhibitors, or other toxic synthetic molecules. The emerging viral infections significantly associated with 2019‐nCoV have challenged humanity's survival. Further, there is a constant emergence of new resistant viral strains that demand novel antiviral agents with fewer side effects and cell toxicity. Despite significant progress made in immunization and regenerative medicine, numerous viruses still lack prophylactic vaccines and specific antiviral treatments that are so often influenced by the generation of viral escape mutants. Of importance, medicinal herbs offer a wide variety of therapeutic antiviral chemotypes that can inhibit viral replication by preventing viral adsorption, adhering to cell receptors, inhibiting virus penetration in the host cell, and competing for pathways of activation of intracellular signals. The present review will comprehensively summarize the promising antiviral activities of medicinal plants and their bioactive molecules. Furthermore, it will elucidate their mechanism of action and possible implications in the treatment/prevention of viral diseases even when their mechanism of action is not fully understood, which could serve as the base for the future development of novel or complementary antiviral treatments.

Treasure

10.1002/ptr.7039

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Citations (65)

Repurposing of Mycobacterium indicus pranii for the severe form of COVID‐19 patients in India: A cohort study

Journal of Medical Virology (2021)

Naveed Nazir Shah Khurshid Ahmad Dar Syed Quibtiya Aaliya Mohi Ud Din Azad Mehvish Mushtaq

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) induces the production of proinflammatory cytokines, which results in a cytokine storm, and immune-modulators like Mycobacterium indicus pranii (MIP) might ameliorate coronavirus disease of 2019 (COVID-19) related cytokine storm. Therefore, the present study evaluates whether MIP offers an advantage in the treatment of severe COVID-19 patients infected with SARS-CoV-2. A prospective MIP cohort study was conducted in chest disease hospitals in Srinagar, Jammu and Kashmir, India. In the present prospective, randomized clinical study, critically severe COVID-19 patients were divided into two groups, the MIP group (n = 105) and the best standard treatment (BST) group (n = 210). Procalcitonin, ferritin, high-sensitive C-reactive protein, D-dimer levels, and interleukin levels on 5th-day posttreatment were significantly reduced in the MIP group compared to the BST group. Compared to the BST group, 105 consecutive patients with severe COVID-19 in the MIP group reported early weaning off ventilation, resolution of chest architecture (computed tomography [CT] scan), a significant increase in SpO2 levels, and decreased mortality with a hazard ratio: 0.234 (95% confidence interval: 0.264-2.31) (p = 0.001). MIP restored SpO2 , immune/inflammatory response, normalized lung abnormalities (chest CT scan), and reduced mortality without any serious complications. However, there is a need for placebo-controlled double-blind and controlled clinical trials to confirm the efficacy.

Procalcitonin

Cytokine Storm

Proinflammatory cytokine

10.1002/jmv.27547

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Citations (10)

Immunotoxicogenomics: A systemic approach in the study of toxicants

Elsevier eBooks (2024)

Prince Ahad Mir Md Sadique Hussain Indrani Jadhav Wajid Mohammad Sheikh Insha Qadir

10.1016/b978-0-443-18502-1.00012-2

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Citations (0)