Cytokine Response in SARS-CoV-2 Infection in the Elderly

Introduction

The emergence of the highly contagious Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) in the latter half of 2019, followed by its rapid spread worldwide and its ability to cause severe infections in humans, often with fatal consequences,¹ led the World Health Organization (WHO) to declare it as a global pandemic on 11 March 2020.² By 25 September, the WHO report confirmed more than 32 million cases of infections and over 979,212 confirmed deaths worldwide.³

In the past few decades, three new Coronaviruses have posed a global threat to public health. Severe acute respiratory syndrome coronavirus (SARS-CoV) identified in 2002, Middle East respiratory syndrome coronavirus (MERS-CoV) emergent in 2012, and the newly identified SARS-CoV-2 in the latter half of 2019, all share similarities of animal reservoirs, unpredictable emergence, rapid spread and serious infectious outcomes in humans, collectively leading to high rates of mortality in the human population.⁴

Out of all Covid-19 infected patients, significantly large numbers (80%) showed mild symptoms and only 20% of these infected individuals exhibited severe complications associated with comorbidities requiring hospitalization. Moreover, out of these 20%, 5% patients experienced critical symptoms associated with excess cytokine production such as hypoxia and ARDS, which lead to multiple organ failure and eventually death.⁵

Several factors such as easy mode of transmission of SARS-CoV-2, infectivity in the incubation period, differing clinical course ranging from asymptomatic forms to severe pathological manifestations of the disease in the infected population associated with comorbidities, lack of clear treatment options and delay in vaccine production, all point to an unprecedented health-care crisis.

One of the main reasons of death in SARS-CoV-2-infected patients is abnormal immune response, which include uncontrolled secretion of cytokines also referred to as CS. With the numbers of infected individuals needing hospitalization still high in most countries around the world, a greater understanding of the virus, its pathogenesis and host cytokine response is required.

Receptors for Coronaviruses

The host innate immune system detects viral infections through pattern recognition receptors (PRRs). Host PRRs detect viral components, pathogen-associated molecular patterns, which include genomic DNA, single-stranded (ss) RNA, double-stranded (ds) RNA, RNA with 5′-triphosphate ends and viral proteins. Currently, three classes of PRRs are known to be involved in the recognition of virus-specific components in innate immune cells, namely toll-like receptors (TLRs), retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs) and NOD-like receptors (NLRs). Among these receptor types, TLRs and RLRs are important for the production of type I interferons (IFNs) and various cytokines, whereas NLRs are known to regulate interleukin (IL)-1β maturation through activation of caspase-1.^6,7 A study found that the SARS-CoV-2 isolated from human airway epithelial cells was closer to bat-SL-CoVZC45 and bat-SL-CoVZXC21 at the whole-genome level.⁸ Additionally, the external subdomain of the Covid-19 receptor-binding domain (RBD) bore greater similarity to severe SARS-CoV.⁹ Angiotensin-converting enzyme 2 (ACE2), a metallopeptidase, is a recognized host cell receptor of SARS-CoV-2 and plays a crucial role in virus and cellular membrane fusion via the spike protein, facilitating infection.¹⁰ This is also the receptor for SARS-CoV and HCoV-NL63.^11,12 Zhou et al proved that the SARS-CoV-2 does not use other coronavirus receptors such as aminopeptidase N, and dipeptidyl peptidase-4.¹³ Another study found that the RBD domain of the SARS-CoV-2 and S-protein support strong interaction with human ACE2 molecules.¹⁴ High levels of ACE2 expression have been identified in type II alveolar cells of lung,^15,16 upper and stratified epithelial cells of esophagus, absorptive enterocytes from ileum and colon,¹⁶ cholangiocytes,¹⁷ myocardial cells, kidney proximal tubule cells, and bladder urothelial cells.¹⁵ Since studies suggest that ACE2 plays a pivotal role in cellular entry; hence, SARS-CoV-2 may preferentially target ACE2-expressing cells leading to infection Figure 1. These findings indicate that organs with high ACE2-expressing cells may potentially be at a higher risk for Covid-19 infection.

Figure 1 Entry of SARS-CoV-2 into the epithelial cells; firstly, the virion interacts with serine protease TMPRSS2; secondly, S-glycoprotein ligands on virus particles bind to the ACE-2 receptor; thirdly, the virus releases its genetic material (RNA) into host cells.

Additionally, a transmembrane serine protease 2 (TMPRSS2) is another key protein involved in the SARS-CoV-2 cell entry process Figure 1. It is the main host cell serine protease, which cleaves the S protein of human CoVs on the cell membrane. This enables virus to release fusion peptide for membrane fusion. Both receptors are co-expressed in lung epithelial cells, the upper epithelial and gland cells of oesophagus and absorptive enterocytes from ileum and colon; suggesting an alternate mode of infection.¹⁸ The expression of ACE2 increases in individuals who have type I and II diabetes, as treatment options include ACE inhibitors and angiotensin-receptor blockers (ARBs). Additionally, hypertension, also treated with ACE inhibitors and ARBs, results in increased expression of ACE2.¹⁹ The increase in ACE2 receptors from hypertension medications, and diabetes medications is the basis of the initial hypotheses that suggest ACE2 upregulation may explain the correlation between these conditions. However, there is certainly not a consensus on these conclusions, with other evidence contradicting these claims to show that ACE2 protects patients from severe acute lung failure.²⁰ The only known is that there is a correlation between severity of Covid-19 cases and patients with hypertension, diabetes, and obesity.

Cytokines in Viral Infections

Cytokines play an important role in establishing an antiviral state as the nonspecific first line of defense in viral infections. The network of cytokines in inflammatory diseases is a very complex system. These immune-modulatory peptides, produced by a broad range of cells such as B-lymphocytes, T lymphocytes, macrophages, mast cells, stromal cells and endothelial cells, etc., to regulate different cellular processes and interactions, such as cellular development, repair, hematopoiesis, inflammation, etc., through the transduction of signals mediated by binding to cellular receptors.²¹ In addition, cytokines have pleiotropic activity, i.e. they often have multiple functions, acting on different target cells to affect the function of other cytokines in an additive, synergistic or antagonistic manner.²² Therefore, cytokines are critical communication mediators for the immune system and are essential for host defense against pathogens. Intracellular signaling cascades are activated by the detection of viral components by immune cells with the resultant secretion of type I IFNs, proinflammatory cytokines and chemokines, as well as an increased expression of co-stimulatory molecules such as CD40, CD80 and CD86.⁶ Type I IFNs induce cell-intrinsic antimicrobial states in both virus infected and neighbouring cells to resolve viral infection, by activating intracellular signaling pathways via a type I IFN receptor.²³ They also regulate gene expression of a set of genes, such as protein kinase R and 2′-5′-oligoadenylate synthase, which are involved in eliminating viral components from infected cells, inducing apoptosis of infected cells and conferring resistance against viral infection in uninfected cells.⁶ Type I IFNs are produced by immune cells such as dendritic cells (DCs), macrophages, NK cells as well as other cells like fibroblasts.⁶ Proinflammatory cytokines such as IL-1β, IL-6, and tumor necrosis factor (TNF)-α are predominantly secreted by monocytes and activated macrophages as well as by nonimmune cells, such as fibroblasts and endothelial cells. They are critical for pathological pain as well as eliminating virus infection by up-regulation of inflammatory reactions and recruiting innate and acquired immune cells.²⁴ Aberrant induction and/or imbalance of various proinflammatory cytokines may induce severe systemic inflammatory response syndrome,²⁵ resulting in systemic inflammation, organ dysfunction and organ failure. Co-stimulatory molecules are essential for natural killer (NK) cell activation. As NK cells are involved in the recognition of altered cells, they can directly destroy infected cells as well as promote recruitment and response of the other components of the immune system by the release of cytokines and chemokines.²⁶ Similarly, co-stimulatory molecules are also involved in the activation of T cells, leading to acquired immune reactions. Failure to mount effective cytokine responses against viral agents can sometimes lead to systematic infection, while excessive cytokine production may lead to pathogenicity, severe symptoms or even fatality such as seen in SARS, MERS and SARS-CoV-2 infected patients. A fine balance of cytokine production and inhibition is required in countering viral infections, the tilting of which may result in severe pathogenesis.

Cytokines in Coronavirus

SARS-CoV infects airway and alveolar epithelial cells. Infection of hematopoietic cells such as DCs, monocyte-macrophages, and other peripheral blood mononuclear cell-derived cells by the virus is abortive. Infection of DCs by SARS-CoV induces low-level expression of antiviral cytokines IFN-αβ, moderate up-regulation of pro-inflammatory cytokines such as TNF and IL-6, and a significant up-regulation of inflammatory chemokines CCL3, CCL5, CCL2, and CXCL10.^27,28 Similarly, SARS-CoV-infected macrophages and airway epithelial cells (AECs) show delayed and increased levels of IFN and other pro-inflammatory cytokines.^28,29 The delayed but exaggerated production of these cytokines and chemokines induces a dysregulation of innate immune response. Elevated levels of pro-inflammatory cytokines (IFN-γ, IL-1, IL-6, IL-12, and TGFβ) and chemokines (CCL2, CXCL10, CXCL9, and IL-8) were found in the sera of SARS patients with severe disease compared to individuals with uncomplicated SARS.^30,31 Whereas SARS patients with severe disease had very low levels of the anti-inflammatory cytokine, IL-10,³¹ individuals with lethal SARS showed increased levels of pro-inflammatory cytokines and chemokines such as IFN (IFN-α and IFN-γ) and IFN-stimulated genes (ISGs) (CXCL10 and CCL-2) compared to healthy controls or individuals with mild-moderate disease.³² These results gave early suggestions for a possible role for IFNs and ISGs in the immunopathogenesis of SARS in humans. Thus, dysregulated and/or exaggerated cytokine and chemokine responses by SARS-CoV-infected AECs, DCs, and macrophages play an important role in SARS pathogenesis.

Similar to SARS, MERS-CoV infection of human airway epithelial cells induces significant and delayed IFN and proinflammatory cytokine (IL-1β, IL-6, and IL-8) responses.³³ MERS-CoV replicates in naïve and activated human monocyte-macrophages.³⁴ This contrasts with SARS-CoV, which abortively infects monocyte-macrophages, DCs and T cells. MERS-CoV infection of human leukemic cell line (THP-1) cells, a monocyte cell line, and human peripheral blood monocyte-derived macrophages and DCs exhibited delayed but increased levels of pro-inflammatory cytokines and chemokines (CCL-2, CCL-3, CCL-5, IL-2, and IL-8).³⁵ However, induction of IFN-α/β by monocyte, macrophages and DCs was not significant except for plasmacytoid dendritic cells, which produced large amounts of IFNs upon MERS-CoV infection.³⁶ Studies showed elevated levels of serum pro-inflammatory cytokines (IL-6 and IFN-α) and chemokines (IL-8, CXCL-10, and CCL5) in individuals with severe MERS compared to those with mild to moderate MERS infection.³⁷ Elevated serum cytokine levels in patients infected with MERS correlated with lung pathology due to high neutrophil and monocyte numbers in lungs and in the peripheral blood.^37,38 In conclusion, SARS-CoV and MERS-CoV infect human airway epithelial cells, inducing proinflammatory cytokines.

Cytokines in SARS-CoV-2

SARS-CoV-2 shares phylogenetic similarities with two other betacoronaviruses, i.e. SARS-CoV and MERS-CoV as well as some clinical features of beta-coronavirus infections.³⁹ SARS-CoV-2 and host cell interactions lead to the strong production of immune mediators. The secretion of large quantities of chemokines and cytokines such as IL-1, IL-6, IL-8, IL-21, TNF-b and MCP-1, in turn recruit lymphocytes and leukocytes to the site of infection. Infected individuals with SARS-CoV-2 can broadly be classified as asymptomatic or confirmed cases experiencing mild respiratory symptoms (cold-like symptoms to mild pneumonia), severe respiratory illness (serious pneumonia and shortness of breath) or fatal cases with multi-organ and systemic manifestations (sepsis, septic shock, and multiple organ dysfunction syndromes, hypoxia and blood clotting) often resulting in death. A study of the inflammatory cytokines and C-Reactive Protein (CRP) profiles of serum samples from a hospital in Wuhan, found higher values of cytokines such as IFN-γ, TNF-α, IL-3, IL-4, IL-6, IL-10 and CRP in patients with Covid-19 compared to healthy controls, suggesting an activation of immune response to SARS-CoV-2 infection.⁴⁰ Also, only IL-6, IL-10 and CRP showed increased expression along with disease severity. Another study from China showed that about 20% of patients developed severe disease. Out of these, individuals with serious underlying health conditions were at a higher risk of death. A fatality of 4% was reported in a minority of patients presented with respiratory failure, septic shock and multi-organ dysfunction.⁴¹ All these studies ascertained increased level or proinflammatory cytokines are linked to SARS-CoV-2 related deaths.

Cytokine Storm in Covid-19

Historically coronaviruses exhibited relatively mild, self-limiting common cold-like phenotypes in humans. Four beta coronaviruses are, i.e. HCoV 229E, NL63, OC43, and HKU1, globally endemic and account for 10–30% of upper respiratory tract infections in adults. However, recently two highly pathogenic viruses, SARS-CoV and MERS-CoV, have caused global epidemics with resultant lung pathology and high rates of morbidity and mortality linked to excessive and aberrant non-effective host immune responses associated with a cytokine storm.⁴² Cytokine storm or cytokine storm syndrome (CSS), is an acute and systemic expression of a vigorous immune system, resulting in the excessive synthesis and release of more than 150 inflammatory cytokines such as IFN-γ, IFN-α, IFN-β, TNF-α, IL-1, IL-6, IL-8, IL-12 and MCP-1 among others.²⁷ An exaggerated and often imbalanced secretion of both pro-inflammatory and anti-inflammatory cytokines, found to be elevated in the serum, leads to a positive feedback cycle between cytokines and immune cells, culminating in a fierce and often lethal interplay between them. The unifying clinical feature of CS is a massive inflammatory reaction, which progresses to cause acute respiratory distress syndrome, multiple organ dysfunction and eventually death.⁴³ The clinical symptoms, which develop due to these dysregulated pathways, are fever, redness, swelling, tachycardia, tachypnea, hypotension, extreme fatigue and nausea. Elevated cytokine production has been associated with poor clinical outcome and pathogenesis during respiratory corona viral infections in humans.^31,39 The emergence of SARS-CoV-2, the most severe beta coronavirus so far and the causative agent of an acute and highly transmissible respiratory infection, even in the asymptomatic incubation period, has led to a worldwide pandemic. Covid-19 infections are generally associated with upper respiratory tract infections, the signs and symptoms of which commonly include fever, headache, and cough with some patients exhibiting lower respiratory tract infections.⁴⁴ A significant percentage of cases present with acute respiratory distress syndrome that requires mechanical ventilation support and a subgroup of patients with severe Covid-19 can experience the “cytokine storm syndrome”, characterized by a fulminant and fatal hyper-cytokinemia associated with multi-organ failure.⁴⁵

In SARS-CoV-2 infection, antigen-presenting cells, such as macrophages and dendritic cells process and present viral antigens to T cells, leading to T cell activation and differentiation, including the production of cytokines associated with the different T cell subsets CD8, CD4 and γδ-T cells. Moreover, Th17 cells may play a role in host defense against the pulmonary virus infection by mediating the recruitment of neutrophils and macrophages to infected tissues, significantly determining the pathogenesis of associated inflammation.⁴⁶ Hence, these cells cause a massive release of cytokines for immune response amplification, promote accumulation of immune cells at inflammatory sites, and enhance tissue pathologies and pulmonary edema.

A study by Huang et al reported the level of inflammatory factors in a cluster of patients in Wuhan with Covid-19. They measured cytokine and chemokine levels in 41 in-patients (including 13 ICU patients and 28 non-ICU patients) and found that ICU patients had higher plasma levels of IL2, IL7, IL10, G-CSF, IP10, MCP1, MIP1A, and TNFα compared to non-ICU patients.⁴⁷ Notably, the difference of serum IL-6 levels between ICU and non-ICU patients was not significant. However, in another retrospective, multicentre cohort study, a significant elevation of IL-6 levels was detected in the non-survival group of patients with Covid-19, as compared with that of the survivals.⁴⁸ Another study analyzed the cytokines in 123 patients and found serum IL-6 levels in severe group were significantly higher than that in mild group.⁴⁹ Other reports also confirmed the elevation of IL-6 in critically ill patients with Covid-19.⁵⁰ et al also showed high levels of IL-6, TNFα, IL-1β, IL-8, IL2R, together with persistently elevated levels of erythrocyte sedimentation rate and CRP, associated with ARDS, hypercoagulation and disseminated intravascular coagulation, manifested as thrombosis, thrombocytopenia, gangrene of extremities.⁴¹ Cytokine storm amplifies immune cell recruitment at the site of infection causing tissue damage and in severe conditions may lead to multiple organ dysfunction and eventually death.

Cytokine Storm in the Elderly

Since the initial outbreak of infection in Wuhan, China, Covid-19 has claimed thousands of lives and steadily spread to almost every country across the world. Elderly people exhibit a higher risk for Covid-19 infection leading to serious illness and/or death. Increased cytokine production is a major contributory factor to age-related prognosis or death.

Poor Prognosis in Elder Covid-19 Patients

A study in China found the case fatality ratio to be 1·38% (1·23–1·53%). However, substantially higher ratios were recorded in older age groups (0·32% [0·27–0·38], where individuals aged <60 years had a ratio of 6·4% [5·7–7·2%] and those aged ≥60 years), up to 13·4% (11·2–15·9%).⁵¹ At the start of the pandemic, Italy was one of the countries with the highest number of fatalities. According to data from the website, “Statista. Health & Pharmaceuticals-State of Health”,⁵² by 30th June 2020, the mortality rate in Italy appeared to be higher for elderly patients, especially above 80 years. As per the statistics, the mortality rate increased significantly with increasing age, i.e. 10.1% in patients aged 60–69 years, 26.4% in 70–79 years and 58.9% in patients more than 80 years old.⁵² The median age of Italian patients who tested positive for SARS-CoV-2 and died in the first phase of the pandemic was 82 years.⁵³ Similarly, in the United States of America, poor patient prognosis can also be linked to increase in patient age with 26.4% mortality in 65–74 years, 26.1% in 75–84 years and 33.16% in patients more than 85 years old recorded till 13th July 2020.⁵⁴ The mortality rate trends compared between Italy and the US differ slightly with respect to the fact that more deaths have been reported in the US population in a relatively younger population aged 45 and above. This rate is found to increase with age and peak in individuals aged 80 years or more.^53–55 Recent studies indicate that the infection fatality ratio (IFR) is the strongest predictor of a Covid-19 patient’s risk of dying. A study in England found that the IFR for age groups 15–44 years was close to zero. For 65–74 years, the IFR was 3.1%, which then increased substantially to 11.6% for patients ≥75 years.⁵⁶ For Spain, the IFR was close to zero for patients under 50 years. This increased to 3.4% for infected individuals aged 70–79 years and then rose sharply to 7.2% for those aged ≥80 years old.⁵⁶ Elderly patients with SARS also exhibited a poor prognosis with mortality rates of 50% in patients over the age of 65 years.⁵⁷

Cytokine Secretion by Immune Cells in the Elderly

In SARS patients with ARDS progressed to late phase fibrosis, pneumonia, systemic inflammation responses and multiple organ failure.⁵⁸ The lungs of SARS patients with ARDS were also associated with inflammatory cytokine induction including IL-1, IL-6, IL-8, CXCL-10, and TNFα.⁵⁹ On recognizing infiltration by such coronaviruses, the innate immune system, initiates a rapid anti-viral signaling cascade, leading to the cytokine storm syndrome in severe patients, often progressing to the multi-organ dysfunction and eventually death. The reason behind the inequivalent cytokine secretions in different age groups although not clear, is statistically significant in elderly patients. Our immune system generates antibodies against viral infections throughout our lifetime. Depending upon prior exposures, some of these antibodies may potentially cross-react with SARS-CoV-2 and help in neutralizing the infection. Following immunization, decreased antibody production as well as shortened duration of protective immunity are characteristic features in the elderly.⁶⁰ Also, the decrease in humoral immune response with increase in age is both quantitative and qualitative, as characteristics such as affinity, specificity and class of antibody produced are affected. Studies report a progressive decline in both numbers and size of germinal centers of B cell follicles.⁶¹ However, the effects of age on antibody affinity maturation are often conflicting. Studies show intrinsic B cell defects in aged mice and humans. These defects include a decreases in Ig class switch recombination (CSR), activation-induced cytidine deaminase (AID) and E47 transcription factor. Variations in the effects on somatic hypermutation (SHM) also depends on the system studied. For example, increase in AID in mice resulted in improved CSR but not SHM. Microarray analysis of human B cell subsets are now being used to link B cell defects with aging and such studies may help to select agents for an improved immune response in the aged population.⁶²

T follicular helper (Tfh) cells, which are a subset of CD4⁺ T cells, are essential in directing B cell activities such as proliferation, isotype switching and antibody production.⁶³ Tfh cells produce specific cytokines in response to a viral infection and can be found within germinal centers (GC). Intrinsic age-related defects in Tfh function can lead to reduced B cell expansion, differentiation, IgG production and affinity maturation.⁶⁴ Also, various age-related changes in the secondary lymphoid organs microenvironment impact cell repertoire and protective capacity. For example, CCL21 expression which reduces CD4 T cell priming and antibodies generation post vaccination, is significantly impacted in intact aged mice leading to a reduction in protective capacity.⁶⁵ These factors contribute to reduced Tfh differentiation and ability to generate a robust response to vaccination in aged individuals. Hence, elderly individuals have reduced protection against subsequent infection.

Li et al provided a detailed clinical and epidemiological description of the first 425 cases reported in the epicenter of the SARS-CoV-2 outbreak, the city of Wuhan in Hubei province, China.⁶⁶ The median age of patients was 59 years. Higher morbidity and mortality rates were reported among the elderly and those suffering from coexisting conditions. The majority (56%) of infected patients were male. Notably, no cases were reported in children aged 15 years or younger, either suggesting that children were less likely to be infected or their symptoms were mild and escaped detection.⁶⁷ According to a study by Qiu et al, 36 children (median age 8·3 [SD 3·5] years) infected with Covid-19 were found to have severe acute respiratory syndrome. However, the majority of children remained asymptomatic, making the identification of infections and determination of prevalence difficult and facilitating community transmission.⁶⁸

Natural killer (NK) cells are effector cells of the innate immune system important for control of viral infections. Physiological ageing is linked to changes in the composition, phenotype and function of circulating NK cells, also known as NK cell immunesenescence.⁶⁹ Virus-infected cells encounter NK cells as the first line of defense. Immunogerontological studies suggest that NK cell immunesenescence contributes to the higher incidence of viral infection in older adults.⁷⁰ NK cell activation results in production of inflammatory cytokines, such as IFN-γ and TNF-α by cytotoxic degranulation.⁷¹ These cytokines in addition to having antiviral effects, also play a role in the activation and/or maturation of DCs,⁷² macrophages, and T cells.⁷¹ Additionally, NK cells exhibit regulatory functions such as the regulation of immune responses in viral infections.⁷³ They are also known to produce granulocyte-macrophage colony-stimulating factor,⁷⁴ IL-5, IL-13,⁷⁵ and IL-10,⁷³ thereby effecting downstream immune responses. NK cells can also affect the production of chemokines, such as CCL3, CCL4, and CCL5, which recruit other effector cells to sites of inflammation.⁷⁶

The regulatory T cells (Tregs) are a subpopulation of T cells, which facilitate tissue repair through multiple mechanisms limiting inflammatory damage to tissues. Tregs also play an important role in resolution of acute lung damage.⁷⁷ Tregs can produce IL-10, an anti-inflammatory cytokine to suppress excess immune responses⁷⁸ and thus serve a protective function in lung injury by reducing TNF-α production and neutrophil activity.⁷⁹ TGF-β is essential for the development of Tregs whereas, IL-6 and IL-2 obstruct Treg polarization.⁸⁰ Studies in humans indicated that T_regs from both young and elderly individuals similarly inhibited the proliferation of responder cells. However, the production of IL-10 drops in cells in the elderly.⁸¹ Thus, in contrast to children and young adults, elderly individuals exhibit decreased NK and Treg cell activity in addition to limited humoral activity and function. This leads to excessive release of pro-inflammatory cytokines such as IL-6 and TNF-α which further tilt the balance of proinflammatory cytokine release. Such hyperinflammatory changes induce a cytokine storm leading to loss of immune regulatory control, resulting in mass recruitment of immune cells to the site of tissue injury (Figure 2). This is also associated with comorbidities.

Figure 2 Comparison of immune responses in Covid-19 infection in individuals <40 years and >60 years old.

Cytokine Storm Targeted Therapies

The inflammatory repertoire of Covid-19 remains unclear and hence, therapeutic options for prognosis and recovery of severe cases remain limited, with most treatment options focusing on supportive therapy. However, it is almost certain that anti-inflammatory therapies would play a preventative role in severe cases preventing exacerbation. Currently, a variety of anti-inflammatory agents such as steroids, glucocorticoids, chloroquine/hydroxychloroquine, immunosuppressive agents and inflammatory cytokines antagonists are being tested and trialed in severe patients with varying results.

Tocilizumab

A promising therapeutic strategy using inhibitory agents targeting key cytokines in Covid-19 patients is the use of tocilizumab, a recombinant humanised IL-6 blocking monoclonal antibody against the IL-6 receptor. Successful outcomes in some individuals were reported in a Chinese study using IL-6 blockade with anti-IL-6 antibody.⁸² A retrospective study in 20 patients with severe Covid-19, found that using tocilizumab, led to a reduction in fever and lung lesion opacity as well as recovery of lymphocytes in peripheral blood of patients.⁸³ Another retrospective multicenter Italian cohort study of 544 adult patients with severe Covid-19 pneumonia found that administration of intravenous or subcutaneous tocilizumab prevented intubation or death in such patients.⁸⁴ However, safety risks associated with the use of tocilizumab, especially with corticosteroids and increased risk of opportunistic infections need to be investigated further before more widespread use is possible.

Anakinra

A study of the use of the immunomodulatory agent Anakinra, a recombinant IL-1 receptor antagonist that blocks the activity of cytokines IL1α and IL1β, in Covid-19 patients with severe respiratory distress, found that the drug reduced need for invasive mechanical ventilation in ICU patients and reduced mortality in cases with severe complications, without serious side effects.⁸⁵

Corticosteroids

Another therapeutic strategy used in severe cases of SARS-CoV-2, common with the treatment of other coronaviruses such as SARS and MERS, is the empirical administration of corticosteroids, which are known to inhibit and suppress inflammatory responses. A meta-analysis of the safety and efficacy of corticoid treatment in the treatment all three coronavirus infections found that corticosteroid use in subjects delayed virus clearing and did not convincingly improve survival, reduce hospitalization duration, ICU admission rate or use of mechanical ventilation.⁸⁶ Another meta-analysis of 15 studies found that corticosteroid use to be associated with increased mortality in patients with coronavirus pneumonia.⁸⁷ Currently, as per WHO guidelines, steroids are approved forms of therapy for Covid-19 treatment outside of clinical trials.

Chloroquine and Hydroxychloroquine

Traditionally known as anti-malarial drugs, chloroquine and hydroxychloroquine, are reported to have some anti-viral activity against viruses such as Ebola, dengue, H5N1 and SARS. These drugs have now been used in the treatment of Covid-19 in some countries.⁸⁸ Both drugs accumulate in acidic organelles such as lysosomes, leading to an increase in endosomal pH, which interferes with viral replication and entry/exit from the infected host cell.⁸⁹ Another, possible mechanism of action against SARS-CoV-2 is that both drugs reduce ACE2 receptor glycosylation, preventing the binding of virion particles with host cell.^89,90 The anti-inflammatory effects of antimalarials are demonstrated by the fact that they are used to treat autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. Chloroquine and hydroxychloroquine may block the events that lead to ARDS, such as blocking the production of IL-6 and other pro-inflammatory cytokines such as IL-1 and TNF-α involved in the cytokine storm.⁹⁰ An early Chinese study of over 100 Chinese Covid-19 patients showed that chloroquine phosphate had good efficacy.⁹¹ Another study of a non-randomized clinical trial in France conducted on 20 Covid-19 patients who received hydroxychloroquine treatment reported good efficacy.⁹² However, more studies focusing on Covid-19 treatment with chloroquine and hydroxychloroquine are required to prove efficacy and beneficial effects.

Conclusion

Cytokine storm is one of the main factors associated with Covid-19 death in elderly individuals. Age-related immune imbalance with comorbidities leads to excessive release of pro-inflammatory cytokines. Resultant systemic hyper-inflammatory changes induce a CS leading to further loss of immune regulation, resulting in recruitment of excessive immune cells to the site of inflammation. Thus, identification of cytokine storm immunology and early-targeted therapies are important factors in patient prognosis and recovery in Covid-19.