key: cord-0880424-w973anbb
authors: Robinson, Philip C; Morand, Eric
title: Divergent effects of acute versus chronic glucocorticoids in COVID-19
date: 2021-01-18
journal: Lancet Rheumatol
DOI: 10.1016/s2665-9913(21)00005-9
sha: be41a5007a36e17da2e119c03bfe4e19aff0da23
doc_id: 880424
cord_uid: w973anbb

nan

The COVID-19 pandemic has precipitated a search for both effective treatments and patient factors that predict poor outcome. Although agents ranging from convalescent plasma to Janus kinase (JAK) inhibitors have been trialled, to date the best evidenced acute therapy for severe COVID-19 is glucocorticoids. However, chronic glucocorticoid use has been found to increase the risk of poor outcomes in patients with COVID-19. This situation creates an interesting dichotomy.

Much of the pathology of severe acute COVID-19 is driven by the consequences of unconstrained activity of the host inflammatory response. Glucocorticoids have been found to be an effective treatment for COVID-19 in the acute setting, with 6 mg of dexamethasone (equiva lent to 40 mg daily of prednisone) daily for up to 10 days reducing mortality from 25·7% to 22·9% (rate ratio [RR] 0·83, 95% CI 0·75-0·93). 1 These results were even more striking in patients who required oxygen (RR 0·82, 95% CI 0·72-0·94 ) or invasive ventilation (RR 0·64, 95% CI 0·51-0·81); notably those receiving no respiratory support did not benefit.

In contrast to the effect of acute glucocorticoids, registry data suggests that chronic glucocorticoids increase the odds of hospitalisation for COVID-19 in patients with rheumatic disease, with an adjusted odds ratio (aOR) of 2·05 (95% CI 1·06-3·96) in those taking 10 mg or more prednisone equivalent. 2 Patients with inflammatory bowel disease on any dose of systemic glucocorticoids had increased odds of COVID-19 related death (OR 11·62, 95% CI 2·09-64·74). 3 In both these studies, logistic regression models adjusted for disease severity to address confounding by indication. This deleterious effect has even been reported for inhaled therapy, wherein patients with chronic obstructive pulmonary disease and asthma using inhaled gluco corticoids had an increased risk for COVID-19 death compared with those taking other respiratory medi cations (eg, people with chronic obstructive pulmonary disease taking any dose, adjusted hazard ratio [aHR] 1·39, 95% CI 1·10-1·76; people with asthma taking high dose, aHR 1·55, 95% CI 1·10-2·18). 4 Why might this dichotomy exist? These divergent effects of glucocorticoids exist alongside the divergent effects of the immune system itself on health-profound immunodeficiency is just as harmful as its opposite, the excessive immunity, as exemplified by autoimmune disease but also by systemic inflammatory reactions during acute COVID-19. Glucocorticoids suppress effec tor T cells but can increase regulatory T-cell numbers, 5 indicating the sophistication of the actions of supraphys io log ical concentrations of glucocorticoids on immunity. However, the role of endogenous gluco corticoids in controlling immune responses is context-dependent, with acute stress inducing activation of the hypothalamo-pituitary-adrenal (HPA) axis and suppressing glucocorticoid pro duc tion, 6 but chronic stress, which disrupts the HPA axis differently, able to trigger the onset of autoimmune disease. 7 This situation highlights the additional impact of time, or chronicity, on the net outcome of the inter action between gluco corticoids and immunity. So, are the divergent effects of acute glucocorticoids benefiting established COVID-19 versus chronic steroids increas ing the risk of poor outcomes, due to dose, timing, or something else?

The short answer is that we do not yet know. Why should acute glucocorticoids work? Many studies indicate the massive overproduction of multiple cytokines during acute COVID-19, indicative of hyperinflammation. Clinically relevant therapeutic effects in acute COVID-19 of targeted anti-cytokine therapies such as tocilizumab (antiinterleukin-6 receptor) have not been shown; 8 in con trast, glucocorticoids, via their direct actions on the promiscuous transcription factor NF-κB as well as the induction of antiinflammatory proteins such as glucocorticoid-induced leucine zipper (GILZ), have extremely broad immune effects. While we await under standing of the chief cytokine culprits of severe COVID-19, it might be that broad targeting is more fruitful; murine studies suggest the potential of greater effects of dual cytokine blockade than those of blocking individual cyto kines. 9 This is further supported by the evidence, albeit limited, that JAK kinase inhibitors such as baricitinib, which also have a mechanism encompassing blockade of multiple cytokines, can be beneficial for the treatment of COVID-19.

How does this differ from the effect of chronic glucocorticoids on risk of severe COVID-19? Known risks for poor COVID-19 outcomes include obesity and other adverse health indicators, which might be associated with glucocorticoid use. 10 Intriguingly, suppression of type I interferon (IFN) by neutralising anti-IFN autoantibodies, which in some cases even pre-date SARS-COV-2 infection, has been shown to correlate strongly with adverse outcomes in COVID-19; 11 type I IFNs are a crucial component of the innate immune response to viral infection. The effects of glucocorticoids on the IFN pathway remain incompletely understood; low pharmacological concentrations of glucocorticoids such as those achieved with oral doses of glucocorticoids do not appear to suppress IFN production, as Toll-like receptordependent activation of NF-κB during the events lead ing to IFN transcription evades glucocorticoid inhibition. 12 However, glucocorticoids do suppress events entrained by IFN receptor ligation, typically measured via readouts of IFN gene expression, including during viral respiratory infection. These effects can result in increased viral replication, another risk factor for poor COVID-19 outcomes. 13 Resting levels of the glucocorticoid medi ator GILZ constrain initiation of T-cell and B-cell activa tion, 14, 15 potentially explaining weaker adaptive immune responses during initial stages of infection in patients taking glucocorticoids that could also result in higher viral load.

In the end, countless hypotheses could explain the divergence between beneficial acute and harmful chronic effects of glucocorticoids on COVID-19; resolving this will require intensive biological profiling and potentially machine learning approaches. The data demonstrate that broad suppression of the aberrant hyperinflammatory response during acute severe COVID-19 is beneficial, however this has only been shown during a critical window of illness severity, and this finding is at odds with higher risk in patients taking chronic, lower dose glucocorticoids. There is little doubt that even with wide spread vaccination COVID-19 will remain a threat for a subset of patients, potentially including those receiv ing glucocorticoid treatment for autoimmune disease. There fore, it behoves us to continue to investigate and clarify the divergent effects of treatments such as gluco corticoids in order to educate patients and health-care providers.

PR reports personal fees from Abbvie, Eli Lilly, Gilead, and Roche; grants and personal fees from Novartis, Janssen, UCB Pharma, and Pfizer; and non-financial support from BMS, outside the submitted work. EM reports grants and personal fees from Astra Zeneca, Bristol Myers Squibb, Eli Lilly, Janssen, GlaxoSmithKline, and EMD Serono; personal fees from Biogen, AbbVie, Wolf, Neovacs, UCB, Sanofi, Novartis, and Amgen;, outside the submitted work. 

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