Int J Med Sci 2021; 18(2):314-324. doi:10.7150/ijms.51935 This issue Cite


Perspective Adjunctive Therapies for COVID-19: Beyond Antiviral Therapy

Ping Ho1, Jing-Quan Zheng2,3,4, Chia-Chao Wu5, Yi-Chou Hou6, Wen-Chih Liu7, Chien-Lin Lu8, Cai-Mei Zheng9,10,11, Kuo-Cheng Lu12 Corresponding address, You-Chen Chao13,14

1. Division of General Surgery, Department of Surgery, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 231, Taiwan.
2. Division of Pulmonary Medicine, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
3. Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
4. Division of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan.
5. Division of Nephrology, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
6. Division of Nephrology, Department of Medicine, Cardinal-Tien Hospital, School of Medicine, Fu-Jen Catholic University, New Taipei City 234, Taiwan.
7. Division of Nephrology, Department of Medicine, Taipei Hospital, Ministry of Health and Welfare, New Taipei City 242, Taiwan.
8. Division of Nephrology, Department of Medicine, Fu Jen Catholic University Hospital, School of Medicine, Fu Jen Catholic University, New Taipei City 242, Taiwan.
9. Division of Nephrology, Department of Internal Medicine, Taipei Medical University Shuang Ho Hospital, 235 New Taipei City, Taiwan.
10. Division of Nephrology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, 110 Taipei, Taiwan.
11. Taipei Medical University-Research Center of Urology and Kidney (TMU-RCUK), Taipei Medical University, 110 Taipei, Taiwan.
12. Division of Nephrology, Department of Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 231, Taiwan.
13. Division of Gastroenterology, Department of Internal Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 231, Taiwan.
14. School of Medicine, Tzu Chi University, Hualien 970, Taiwan.

Ho P, Zheng JQ, Wu CC, Hou YC, Liu WC, Lu CL, Zheng CM, Lu KC, Chao YC. Perspective Adjunctive Therapies for COVID-19: Beyond Antiviral Therapy. Int J Med Sci 2021; 18(2):314-324. doi:10.7150/ijms.51935.
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The coronavirus disease 2019 (COVID-19) pandemic is the largest health crisis ever faced worldwide. It has resulted in great health and economic costs because no effective treatment is currently available. Since infected persons vary in presentation from healthy asymptomatic mild symptoms to those who need intensive care support and eventually succumb to the disease, this illness is considered to depend primarily on individual immunity. Demographic distribution and disease severity in several regions of the world vary; therefore, it is believed that natural inherent immunity provided through dietary sources and traditional medicines could play an important role in infection prevention and disease progression. People can boost their immunity to prevent them from infection after COVID-19 exposure and can reduce their inflammatory reactions to protect their organ deterioration in case suffering from the disease. Some drugs with in-situ immunomodulatory and anti-inflammatory activity are also identified as adjunctive therapy in the COVID-19 era. This review discusses the importance of COVID-19 interactions with immune cells and inflammatory cells; and further emphasizes the possible pathways related with traditional herbs, medications and nutritional products. We believe that such pathophysiological pathway approach treatment is rational and important for future development of new therapeutic agents for prevention or cure of COVID-19 infection.

Keywords: COVID-19, traditional medicines, statins, melatonin, indomethacin, vitamins and minerals


The coronavirus disease 2019 (COVID-19) outbreak is the greatest major threat experienced by the human race in living memory [1, 2]. As of October 2020, over 44 million reported cases of COVID-19 and over 1 million deaths around the world have been noted and are still rapidly increasing. As this COVID-19 pandemic continues, the understanding and active surveillance of high-risk population, along with taking appropriate preventive measures, has become critical. Compared to previous coronaviruses, severe acute respiratory syndrome (SARS)-coronavirus (CoV)-1 and Middle East respiratory syndrome (MERS)-CoV, SARS-CoV-2, which is responsible for COVID-19, has higher transmissibility, even in those with milder or no symptoms [3]. The number of secondary cases per infected individual varies among different regions and is estimated to range from 2.0 to 2.5 [4]. This has been suggested to be related to different viral epidemiologic characteristics, viral viability and infectivity in aerosols and surroundings [5].

Patients with SARS-CoV-2 experience a clinical spectrum, from mild/asymptomatic forms to acute respiratory distress syndrome (ARDS) requiring ventilator support and admission to an intensive care unit (ICU). Clinical symptoms vary and include respiratory involvement to damage to multiple organs, including the heart, liver, and kidney and organs of the gastrointestinal tract, among others. Ten to twenty percent of symptomatic patients experience disease progression and 3-5% require intensive care unit (ICU) admission [6]. Elderly patients more than 60 years of age and those who are male, obese and have underlying comorbid conditions (e.g., hypertension, diabetes mellitus, chronic respiratory disorders, etc.), tend to have poor clinical outcomes [7]. Unfortunately, SARS-CoV-2 infection is still out of control, and no effective drug or vaccine is currently available. In this review, we discuss the pathophysiology of COVID-19, possible adjunctive therapies for COVID-19 and reasonable therapies for different comorbid conditions beyond the antiviral medications.

Novel pathophysiological pathways associated with COVID-19

SARS-CoV-2 enters the human lung, heart and kidney cells through the binding of its spike (S) proteins to angiotensin-converting enzyme-2 (ACE2) receptors on host cells [13, 14]. It has been demonstrated that SARS-CoV-2 has 10- to 20-fold higher affinity for ACE2 than SARS-CoV-1, which might be related to its higher contagiousness [15]. ACE2 downregulation after the binding of SARS-CoV-2 to ACE2 impairs downstream angiotensin-II (Ang-II) metabolism. The resultant Ang-II accumulation induces pulmonary vasoconstriction, acute lung injury, lung edema and eventual lung fibrosis [16-18]. Severe COVID-19 cases are characterized by endothelial dysfunction and hypercoagulability states, resulting in thrombosis and pulmonary embolism [19]. Progressive pulmonary microvasculature damage further enhances viral invasion and destruction [20]. Possible pathological pathways after SARS-CoV-2 entry are depicted in Figure 1.

 Figure 1 

Possible pathophysiological pathways after SARS-CoV-2 entry. When SARS-CoV-2 enters cells, its surface spike (S) glycoprotein must be cleaved at two different sites by host cell proteases. ACE2-dependent entry at the cell membrane is triggered by S protein cleavage performed by host proteases furin and/or TMPRSS2. Intracellular activation of S protein is mediated by cathepsins in lysosomes and/or by furin in the trans-Golgi network (TGN) [8, 9]. SARS-CoV-2 replication is inhibited by the synthetic furin inhibitor [10]. After entry into the host cell, the virus downregulates ACE2 expression, which in turn upregulates Ang II. Upregulated Ang II interacts with its receptor, AT1R, and modulates the gene expression of several inflammatory cytokines via NF-κB signaling. This Ang II/AT1R interaction also promotes macrophage activation, which produces the inflammatory cytokines that may cause ARDS or MAS. Some metalloproteases, such as ADAM17, shed these proinflammatory cytokines and ACE2 receptors to the soluble form, which aids in the loss of the protective function of surface ACE2 and may aggravate SARS-CoV-2 pathogenesis [11]. SARS-CoV-2-infected monocytes and macrophages produce large amounts of numerous types of proinflammatory cytokines and chemokines, which contribute to local tissue inflammation and a dangerous systemic inflammatory response known as a cytokine storm. Both local tissue inflammation and the cytokine storm play fundamental roles in the development of COVID-19-related complications, such as acute respiratory distress syndrome (ARDS), which is a main cause of death in COVID-19 patients [12]. Abbreviations: AngII: angiotensin II, ARDS: adult respiratory distress syndrome, ATG: angiotensinogen, MAS: macrophage activation syndrome, MODS: multiple organ dysfunction syndrome.

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Patients with severe CoV-19 infection further experience a systemic inflammatory response and acute respiratory distress syndrome (ARDS), which results from “cytokine storm syndrome” [21], an aberrant interaction among interferons, interleukins, chemokines, etc. As a result, severe COVID-19 patients express higher amounts of proinflammatory cytokines, including interleukin (IL)-6, IL-10, IL-1β, monocyte chemoattractant protein 1 (MCP1) and tumor necrosis factor (TNF)-α [22, 23]. In addition, SARS-CoV-2-infected lung epithelial cells produce IL-6 and IL-8, potent chemo-attractors for both neutrophils and T cells [24], resulting in further destruction.

A principal defense against SARS-CoV-2 involves both cell and antibody mediated immunity. Although serum antibodies are detected for approximately 2 weeks in all patients [25], their longevity and long-term protection is still unknown. T-cell responses against the SARS-CoV-2 spike protein correlate well with serum antibody titers in COVID-19 patients and are being clinically applied for the development of novel vaccines [26, 27]. The infiltration of these cells into the lungs and other organs further destroys and exaggerates COVID-19 severity [28, 29]. Innate immunity is conferred primarily by epithelial cells, alveolar macrophages and dendritic cells (DCs), which fight against the virus as first line immunity [24] until adaptive immunity is activated. The infiltration of neutrophils potentiates innate immunity [30, 31] and induces lung injury. T regulatory lymphocyte (Treg) levels were demonstrated to be significantly reduced in severe COVID-19 patients [32]. As infection progresses, the activation and tissue infiltration of T cells with concomitant reduction in circulating T cells (CD4+ T cells, CD8+ T cells) occurs, which determines the severity of COVID-19 [33]. Interestingly, aberrant pathological cytotoxic T cells derived from CD4+ T cells are noted among severe COVID-19 patients [34]. The infiltration of these cytotoxic T cells and inflammatory monocytes exaggerates lung destruction [35]. The expression of IFN-γ by CD4+ T cells also tends to be lower in severe cases than in moderate cases [32]. Apart from known anti-inflammatory pathways, drugs and traditional medicines with immunomodulatory, antiviral, antithrombotic, anti-cytokine and antifibrotic properties are being studied for possible use in COVID-19 patients.

Heme oxygenase (HO-1) is an antioxidant enzyme that cleaves heme into carbon monoxide, ferrous iron and biliverdin, and these downstream products limit inflammation and oxidative stress [36, 37]. Patients with comorbid conditions related to metabolic syndrome (diabetes, obesity, hypertension, cardiovascular disease) generally have lower HO-1 levels and increased susceptibility to inflammation [38-41] and are more prone to the triggering of cytokine storms related to COVID-19 [42]. This might explain the increased susceptibility and higher mortality and morbidity among these patients. A Taiwanese study revealed an association between higher HO-1 expression in the HO1 (-497A/*) genotype and lower susceptibility to SARS coronavirus infection [43]. Clinically, medications and herbs that exert anti-inflammatory and cytoprotective effects by increasing HO-1 include resveratrol (RESV; tri-hydroxyl stilbene), pterostilbene [44-46], curcumin [47, 48], HMG CoA reductase inhibitors (statins) [49, 50] and melatonin [51, 52].

Generally, therapeutic options for SARS-CoV-2 infection should focus on vaccines to enhance immunity and medications to modulate the immune system, suppress inflammation, disturb virus-cell interactions, inhibit viral replication, etc. At present, no vaccine is available against COVID-19. Infected patients are currently treated with antivirals, anti-inflammatories, herbal medicines, plasma exchange, etc. (Table 1). The possible underlying mechanisms regulated by these medicines during the COVID-19 era are depicted in Figure 2.

 Table 1 

Potential Adjunctive Therapies for COVID-19

Antiviral activitiesResveratrol, curcumin, vitamin D (ACE2)
Statins (cholesterol-lowering activity in virus cell membrane)
Anti-inflammatory activitiesVitamin D
Resveratrol and stilbene-based natural compounds
Iron chelators
Antioxidant activitiesResveratrol and stilbene-based natural compounds
Vitamin C and zinc
Antithrombotic activitiesStatins
Immunomodulatory activitiesVitamin D
Vitamin C
 Figure 2 

Potential pathways regulated by medications and/or herbs in treatment/prevention of COVID-19 infection. Resveratrol (stilbene-based natural compounds), curcumin and statins inhibit the viral entry and destruction, improve the cell/tissue damage by preventing inflammatory cells infiltration and reduce cytokine storm related with COVID-19 infection. N. sativa (black seed) and Zinc (Zn) inhibit viral entry and NF-kb related inflammatory pathways. Melatonin inhibits monocyte/ macrophage activation and inflammatory cytokines release. Indomethacin and iron chelators responsible for blocking NF-kb and NLRP3 related inflammatory pathways and inhibiting inflammasome formation. Vitamin D inhibits COVID-19 viral entry, activates ACE2 and cathelicidin production, decreases inflammatory pathways, reduces inflammatory mediators release and improves cytokine storm. Ascorbic acid (Vitamin C) acts as a potent antioxidant with immunomodulatory actions especially by activation of immune cells. Zinc enhancing the Zinc (Zn) uptake by cells and enhancing human immunity. Abbreviations: HMBG1: High mobility group box 1, NF-κb: nuclear factor-κB, NLRP3: NOD-, LRR- and pyrin domain-containing protein 3.

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Possible adjunctive therapies for COVID-19

Medications and Herbs with Antiviral, Anti-inflammatory and Antioxidant activities

Resveratrol and stilbene-based natural compounds

Plant polyphenols, nonflavonoids and flavonoids are found abundantly in grapes, red wine, mulberry and peanuts and are used as health remedies for their antioxidant, antitumor and antiviral properties [53]. Resveratrol (RESV) is a stilbene based nonflavonoid polyphenol that modulates inflammation and exerts reno- and neuroprotective effects through its antioxidant and anti-inflammatory properties [54-57]. RESV is demonstrated to be neuroprotective in several ways, including stimulating the Nrf2 pathway and reducing NF-kB activity [58], activating Sirt1 signaling in neurons [59], etc. Nrf2, a member of the cap'n'collar (CNC) basic-leucine-zipper transcription factors, and its signaling are also of interest for COVID-19 patients because Nrf2 serves as an anti-inflammatory, anti-apoptotic, and antioxidant factor through different pathways [60].

In addition, RESV exerts antiviral effects in viral infections through several mechanisms, such as the activation of ERK1/2 signaling [61], the promotion of cell proliferation and the enhancement of SIR1 signaling [62], which subsequently improve cellular survival and DNA repair [63]. RESV also reduces Middle East respiratory syndrome coronavirus (MERS-CoV) viral-induced apoptosis [64, 65] and decreases inflammation by interfering with the NF-κB pathway [66, 67]. A recent study demonstrated the novel use of RESV in the treatment of COVID-19 [68], indicating that the effects of RESV may occur through the disruption of the SARS-CoV-2 spike protein and the inhibition of the human ACE2 receptor complex [68]. Although RESV in supplemental doses is considered safe, future clinical and experimental studies are still needed to evaluate the dose, efficacy, and safety of resveratrol in fighting against COVID-19.


Another natural phenol mostly studied for its antiviral effects is curcumin, a phenolic acid extracted from the rhizome of Curcuma longa Linn (family Zingiberaceae). It is a yellow pigment of turmeric and a primary component of curry and the flavanol found in green tea. Curcumin improves neurodegenerative disorders by increasing NF-E2-related factor 2 (Nrf2)/heme oxygenase 1 (HO-1) protein expression and decreasing the apoptosis of PC12 cells [69]. Similar to other plant phenols, curcumin possesses anti-inflammatory and immunomodulatory activities, as well as anticancer, anti-arthritic and anti-atherosclerosis effects [47]. Previous data have shown that curcumin exerts antiviral activities against the human immunodeficiency virus (HIV), herpes simplex virus, Chikungunya virus, Zika virus, hepatitis and adenovirus [70-72]. From molecular docking studies of SARS-CoV2 viral proteins and potential antiviral agents, curcumin inhibits the entry of SARS-CoV2 by binding to the viral S protein and the viral attachment sites of the ACE2 receptor protein [73]. Similarly, the antithrombotic, anti-cytokine and antifibrotic properties of curcumin may benefit severe COVID-19 patients [74, 75]. Further, intranasal application of curcumin may effectively prevent SARS-CoV2 infection through inhibiting the local ACE2 receptor. Despite robust preclinical data, there is still no known safety dose or availability of cucurmin among COVID-19 patients. Therefore, well-controlled studies are crucial for assessing any possible curcumin benefit in COVID-19.

N. sativa (black seed) and zinc (Zn)

N. sativa L. (black seed) has been used primarily as a traditional medicine for a variety of diseases, including skin diseases, bronchial asthma, gastrointestinal disorders, toothache, diabetes mellitus, hypertension, etc. [76-78], for more than 2000 yr (16). Recently, many studies have demonstrated that N. sativa seeds not only have antioxidant [79], anti-inflammatory, immunomodulatory and antitumor properties [80, 81] but also possess antimicrobial [82], antidermatophytic [83] and anti-cytomegalovirus [84] properties. It has been demonstrated that N. sativa L. improves lung inflammation by promoting a balance between pro- and anti-inflammatory pathways through modulatory actions on interleukin-4 (IL-4) and interferon-γ [85]. N. sativa oil exhibits antiviral effects by promoting the upregulation of both innate immunity (splenic M & phi expression) and adaptive immunity (the stimulation of the CD4+ T lymphocytes) in a murine cytomegalovirus model [84]. Black seed oil supplementation also decreases viral load and improves biochemical parameters in individuals with hepatitis C virus (HCV) infection [86]. From these findings, the possible therapeutic potential of N. sativa seed and its active compounds are being extensively studied in COVID-19 patients. A recent molecular-docking-based study [87] revealed that active ingredients of N. sativa, nigellidine and α-hederin, serve as natural inhibitors of SARS-CoV-2 [87].

Recently, N. sativa and Zn combined supplementation in COVID-19 patients was proposed on the basis of the hypothesis that the bioactive agents of N. sativa, thymoquinone and nigellimine block SARS-CoV-2 entry into pneumocytes, enhance zinc (Zn) uptake by cells and enhance human immunity. The immune-boosting activities of Zn are pleiotropic and participate in the activation of adaptive and acquired immunities, as well as intracellular antioxidant activities. On the other hand, the availability of Zn to pneumocytes is crucial in COVID-19 patients because Zn inhibits viral entry, blocks polyprotein processing [88], and inhibits recombinant SARS-CoV virus RNA-dependent RNA polymerase (RdRp) activity [89]. Thus, combined N. sativa and Zn supplementation might represent a complementary approach to antiviral treatment against COVID-19 and needs additional clinical trials.

HMG CoA reductase inhibitors (statins)

Since patients at greater risk for SARS-CoV-2 infection have common comorbidities, whether their routine medications are associated with COVID-19 severity is an interesting topic. Among these, statins, which are lipid-lowering drugs, are considered possible agents for their pleiotropic anti-inflammatory effects. The cholesterol within lipid rafts in the viral envelope is important for viral entry of coronaviruses, including SARS-CoV, and depleting cholesterol results in a significant reduction in viral mRNA [78]. Lipid rafts play an important role in developing new therapies, and statins disturb viral binding by decreasing cholesterol and disrupting lipid rafts. Moreover, statins exert an anti-inflammatory effect by inhibiting the toll-like receptor (TLR)-MYD88-NF-kB pathway [90]. This anti-inflammatory effect is independent of the cholesterol-lowering effect and is also supported by clinical studies [91]. However, the efficacy of statins as an immunomodulatory treatment for viral infections is still controversial. Earlier observational studies suggested that statin therapy reduced mortality in influenza viral infections [92]. It also demonstrated that statin therapy was related to reduced H1N1 severity in hospitalized patients [93]. However, sensitivity analysis concluded that the mortality improvement in response to statins was related to unmeasured confounding factors [94]. On the other hand, a multicenter clinical trial revealed that patients with infection-induced ARDS on statin therapy exhibited higher IL-18 levels, related deterioration due to ARDS and increased mortality [95].

Another consideration for statin therapy in COVID-19 patients is its antithrombotic activity. Markedly elevated D-dimer levels and a high risk of thrombogenicity were noted among critically ill COVID-19 patients [96-98]. In the JUPITER trial, statins have been demonstrated to significantly decrease the rate of deep vein thrombosis [99]. Statins exert antithrombotic actions through various mechanisms, such as reduced tissue factor expression, decreased platelet aggregation, and increased endothelial cell thrombomodulin expression [100]. However, reliable evidence for statin use in COVID-19 is still lacking, and more clinical trials, focusing on patient population, drug effectiveness, type, dosage, etc., are required.


Melatonin, the primary pineal gland hormone, is a regulator of circadian and seasonal rhythms that is known for its anti-inflammatory and immunomodulatory actions [101, 102]. Melatonin influences neutrophils, CD4 T cells, CD8 T cells, and B cells through membrane melatonin receptors [103] and modulates the production and release of various cytokines [101]. Geng-Chin et al. [104] revealed that melatonin protected against ventilator-related lung injury through the upregulation of IL-10 production. Similar studies on protective effects in the lung were also related to melatonin related circadian immunity and anti-inflammatory effects [105, 106].

Based on recent data, COVID-19 most severely affects those aged 60 years' and above, males, and those with comorbid conditions [7]. Since lower plasma melatonin concentration is noted in individuals at approximately age 60, in males and in different comorbid conditions [7, 107, 108], the susceptibility of these populations to severe COVID-19 might be related to their increased melatonin requirement. Melatonin is generally safe for both short- and long-term use at a pharmacological oral dose of 2 mg once a day in the early evening. A recently proposed prophylactic protocol for melatonin use in COVID-19 patients is 2 mg oral melatonin once a day immediately after contact with an infected person. Combined use with other long-term medications, such as antihypertensive agents, oral hypoglycemic agents and anti-inflammatory drugs, appears safe [109].


Indomethacin is a potent anti-inflammatory agent that non-selectively inhibits cyclooxygenase (COX)-1 and -2 enzymes and is mostly used to treat inflammatory conditions. Indomethacin exerts anti-inflammatory actions through the inhibition of TNF, IL-6 and superoxide free radicals [110]. Since indomethacin inhibits COX-2 and viral protein synthesis [111], antiviral activities against different viruses have been explored, including herpes virus 6 [112], cytomegalovirus [113], hepatitis B virus [114], etc. Thus, recent in vivo and in vitro studies consider the use of indomethacin in COVID-19 era. Amici et al revealed that in in vitro studies of monkey VERO cells (SARS-CoV) and in in vivo studies of dogs (canine coronavirus, CCoV), indomethacin significantly reduced both SARS-CoV and CCoV by inhibiting viral RNA synthesis [115]. In contrast, other authors revealed potential severe and late complications related to the use of ibuprofen in COVID-19 patients [116, 117]. Thus, novel use of indomethacin in this COVID-19 era should be balanced with its gastrointestinal, renal, and hematological side effects. Given the cost and availability of indomethacin, RCT trials on outpatients or on patients with documented SARS-CoV-2 infection without cytokine storm should be further studied.

Iron chelators

Excess intracellular iron may promote excessive oxidative and nitrosative stress, which may correlate with ARDS and pulmonary fibrosis [118, 119]. Generally, hyperferritinemia is common during systemic inflammation. A biological protein sequence study found that SARS-CoV-2 protein sequence forms a complex with porphyrin within hemoglobin and dissociates the heme iron, resulting in increased free iron levels among severe COVID-19 patients [120]. Increased serum ferritin levels may represent a marker of disease progression or a key modulator of a vicious cycle of events that contributes to a hyperinflammatory condition and further tissue damage [121]. Iron chelators, including deferoxamine (DFO), not only reduce iron overload but also possess immunomodulatory and anti-inflammatory actions [122]. In addition, DFO decreases IL-6 and endothelial inflammation [123], the most important mechanism related to multiorgan damage and failure among COVID-19 patients [123]. Therefore, iron-chelating agents are believed to improve clinical outcomes and systemic manifestations of COVID-19. However, large RCTs are needed to evaluate the dosage, efficacy, and safety of iron-chelating agents as adjunctive therapy in COVID-19.

Vitamins and minerals associated with immunomodulatory activities

Vitamin D

Vitamin D deficiency is a known pandemic and global public health problem that varies based on age, ethnicity, and latitude. Aged, obese, and dark-skinned populations have higher risk for vitamin D deficiency. Environmental factors, including a lack of or reduced r sun (UV-B) exposure, living with air pollution and smoking, are attributed to vitamin D deficiency. The presence of comorbid conditions, such as sepsis, diabetes mellitus, chronic respiratory disease, and cancer, are closely related to vitamin D deficiency [124]. Interestingly, in this COVID-19 pandemic, a similarity in prevalent areas and the nature of SARS-CoV-2 infection and vitamin D deficiency was observed [125], which might explain the importance of vitamin D supplementation in COVID-19 [7].

An analysis of community outbreaks of COVID-19 has revealed that regions with certain latitude, temperature, and humidity are more prone to the spread of infection. The virus is thermolabile, and less sunlight, lower temperatures and decreased humidity seem to be favorable for COVID-19 [126, 127]. Clinical studies found a close relationship between vitamin D deficiency and vulnerability to COVID-19 in various populations. A negative association was noted between mean vitamin D levels and COVID-19 mortality in European countries. Regional variation was also noted with the parallel increase in vitamin D deficiency and COVID-19 severity. Inhabitants of southern European countries have lower vitamin D levels than inhabitants of northern countries, where a higher number of COVID-19 cases and higher fatality have been noted. In the United States, a disproportionately higher mortality from COVID-19 has been noted among African Americans (AAs) [128, 129], and the top 3 comorbid conditions among patients who died of COVID-19 are hypertension, diabetes, and chronic kidney disease. It has been demonstrated that a higher prevalence of vitamin D insufficiency is noted among AAs than other Americans [130, 131] due to reduced vitamin D production and insufficient supplementation. This population also tends to have a higher incidence of comorbid conditions, including cardiovascular disease, diabetes, osteoporosis and certain cancers, than whites [130]. This calls attention to the relationship between vitamin D deficiency and the severity of COVID-19 and the importance of vitamin D supplementation as possible adjuvant therapy.

Our previous study demonstrated that vitamin D supplementation efficiently increased serum antimicrobial cathelicidin levels, which paralleled increased serum 25-hydroxyvitamin D (25D) levels in uremic hyperparathyroidism patients [132]. In other words, vitamin D supplementation increased circulating 25D levels, which improved innate immunity by entering circulating monocytes, increasing local 1,25 dihydroxy-vitamin D (1,25D) production and inducing the production of the antimicrobial peptides cathelicidin and β-defensin [133]. Cathelicidin inhibits viral entry and elicits an antiviral status in infected host cells in inhibiting viral replication [134]. Defensins directly inhibit viral particles and indirectly inhibit viral entry [135]. Mounting evidence suggests that defensins are also responsible for innate immunity, including the activation of T cells, the recruitment and differentiation of macrophages and dendritic cells, and the release of proinflammatory cytokines [136]. Vitamin D supplementation also modulates adaptive immunity in individuals with COVID-19 through different pathways. First, vitamin D suppresses the maturation and antigen presentation of dendritic cells. Second, vitamin D increases cytokine production by T- helper cells and promotes the efficiency of T-reg lymphocytes. Last, vitamin D suppresses the cytokine storm and related tissue destruction. This suggests that adequate vitamin D supplementation both attenuates COVID-19-induced immunosuppression and enhances anti-inflammatory actions.

Adequate vitamin D supplementation is also required for reducing RAS activity and increasing ACE2 concentrations in acute lung injury. In other words, adequate vitamin D supplementation induces the ACE2/Ang‐(1‐7) axis and suppresses the renin and ACE/Ang II/AT1R axis [137]. Similarly, the increased ACE2 was responsible for viral entrapment and inactivation. Clinically, vitamin D deficiency was found to be associated with an increased incidence of COVID-19 [138]. Linking the supplementation of vitamin D to improved COVID-19 outcomes is still impossible in this pandemic. Since vitamin D in therapeutic doses is unlikely to harm and may even prevent disease progression in these patients, it should be recommended to all COVID-19 patients. Vitamin D deficiency might be correctable, and supplementation is considered safe and is easily accessible [139]. People at risk of COVID-19 should consider supplementation with high doses of vitamin D 10,000 IU daily for a few weeks to rapidly achieve therapeutic levels of 25(OH)D, followed by 5000 IU/day, with the goal of a 25(OH)D concentration of ~40-60 ng/ml [140]. Future randomized studies are needed to examine vitamin D doses in COVID-19 patients with different underlying conditions.

Ascorbic acid (vitamin C)

Vitamin C, especially at higher doses, acts as a potent antioxidant with immunomodulatory actions and significantly accumulates within immune cells [141]. Possessing such a powerful antioxidant to clear ROS-related cellular toxicity may indicate the use of vitamin C as adjuvant therapy in symptomatic COVID-19 patients. For example, vitamin C decreases the duration and severity of cold symptoms [142]. Several studies are underway to understand the possible mechanisms of action and dose of vitamin C supplementation in individuals with COVID-19. A phase II study is evaluating whether high-dose IV vitamin C infusion (12 g infusion over 4 hours every 12 hours for 7 days) ameliorates the symptoms and progression of severe COVID-19 pneumonia [143].


As previously described, Zn supplementation is considered important for its immune-boosting activities against various viral infections. However, oral supplementation alone is not sufficient to promote Zn availability in infected pneumocytes. Chloroquine and active ingredients of N. sativa should be used in combination with Zn to enhance Zn entry into and its effects within pneumocytes. However, it is not clear how to use such a combination or the doses to use in different COVID-19 populations. Black seed oil at doses of 40-80 mg/kg/day is used safely as an adjunctive therapy; however, the Zn recommended daily allowance (RDA) varies according to age, sex, and general health conditions. Zn doses above the RDA are also dangerous because of toxicity. Therefore, future clinical studies on the effects and doses of Zn combined with chloroquine or N. sativa in different COVID-19 populations is needed.


The demographic distribution and severity of the COVID-19 outbreak vary around the world. Whether such distribution is associated with dietary habits, the use of traditional and herbal medicines, differences in geographical distribution or vitamin or mineral deficiencies is still unknown. In this brief review, we discussed traditional health remedies, drugs, vitamins, and minerals with possible use as adjunctive therapies in the COVID-19 era. This is important since we are still experiencing uncontrollable COVID-19 spread and currently have no vaccine or curative medicine. Current evidence does not support the use of such adjunctive treatments in COVID-19; however, we eagerly await results of the rigorous clinical trials on the efficacy and safety of therapies that slow viral spread and improve outcomes.

What does this article add?

  • The treatment of COVID-19 is still unclear until now. However, people can boost their immunity to prevent them from infection after COVID-19 exposure and can reduce their inflammatory reactions to protect their organ deterioration in case suffering from the disease. This review discusses the herbs, medications and nutritional compounds possibly improve their immune systems and regulate the inflammatory reactions related with COVID-19 infection. Although many topics saturated with possible COVID-19 treatments, in this review, we want to convince our readers the importance of COVID-19 interactions with immune cells and inflammatory cells; and further emphasize on the possible pathways related with traditional herbs and nutritional products. Definitely, we need randomized clinical studies to prove the effectiveness of mono or combined therapies. To conclude, we believe that such pathophysiological pathway approach treatment is rational and important for future development of new therapeutic agents for prevention or cure of COVID-19 infection.

Competing Interests

The authors have declared that no competing interest exists.


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Author contact

Corresponding address Corresponding author: Kuo-Cheng Lu, MD, kuochenglucom.

Received 2020-8-13
Accepted 2020-11-2
Published 2021-1-1

Citation styles

Ho, P., Zheng, J.Q., Wu, C.C., Hou, Y.C., Liu, W.C., Lu, C.L., Zheng, C.M., Lu, K.C., Chao, Y.C. (2021). Perspective Adjunctive Therapies for COVID-19: Beyond Antiviral Therapy. International Journal of Medical Sciences, 18(2), 314-324.

Ho, P.; Zheng, J.Q.; Wu, C.C.; Hou, Y.C.; Liu, W.C.; Lu, C.L.; Zheng, C.M.; Lu, K.C.; Chao, Y.C. Perspective Adjunctive Therapies for COVID-19: Beyond Antiviral Therapy. Int. J. Med. Sci. 2021, 18 (2), 314-324. DOI: 10.7150/ijms.51935.

Ho P, Zheng JQ, Wu CC, Hou YC, Liu WC, Lu CL, Zheng CM, Lu KC, Chao YC. Perspective Adjunctive Therapies for COVID-19: Beyond Antiviral Therapy. Int J Med Sci 2021; 18(2):314-324. doi:10.7150/ijms.51935.

Ho P, Zheng JQ, Wu CC, Hou YC, Liu WC, Lu CL, Zheng CM, Lu KC, Chao YC. 2021. Perspective Adjunctive Therapies for COVID-19: Beyond Antiviral Therapy. Int J Med Sci. 18(2):314-324.

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