key: cord-0698371-8to9wquv
authors: Ladani, Amit P.; Loganathan, Muruga; Danve, Abhijeet
title: Managing rheumatic diseases during COVID-19
date: 2020-09-08
journal: Clin Rheumatol
DOI: 10.1007/s10067-020-05387-8
sha: 76aa94fa32a6d115bc039aa5110310876097320f
doc_id: 698371
cord_uid: 8to9wquv

Rheumatology practice, during Coronavirus Disease 2019 (COVID-19) pandemic, has faced multifaceted challenges. Rheumatologists routinely prescribe immunosuppressant medications to their patients with multisystem autoimmune rheumatic diseases who are concerned about the increased risk of acquiring COVID-19 infection and are anxious to know if they should continue or hold these medications. Rheumatologists are often inundated by calls from their patients and physician colleagues caring for COVID-19 patients in hospitals, about how to manage the immunosuppression. Physicians face the challenging task of keeping up with the most up-to-date information on COVID-19. There are uncertainties about the mode of spread, clinical features, management options as well as long-term complications of COVID-19. Data are rapidly evolving and different studies on treatment options are showing contradictory results. It is known that viral illnesses can trigger a flare-up of underlying rheumatic disease that was previously in remission. To further complicate the scenario, some of the immunosuppressants have shown to have antiviral properties. This has created dilemma in the light of current COVID-19 crisis, as whether to continue or stop the immunosuppressive agents which could be essential to prevent complications of the rheumatic diseases including organ failure but also there is concern about acquiring COVID-19 or developing serious infection. Until we get an effective vaccine, immunosuppressant management for rheumatic diseases as well as other autoimmune diseases and transplants will pose difficult questions. This article is an attempt to review and understand COVID-19 and its impact on the immune system with special emphasis on managing medications used for autoimmune rheumatic diseases. We have provided general guidance about decision making, in regards to the immunosuppressive agents used in rheumatology practice with an understanding that this may change in near future.

After severe acute respiratory syndrome (SARS) and Middle Eastern respiratory syndrome (MERS), severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the third major viral outbreak in 21 st century. SARS-CoV-2 originated in Wuhan Province in China in December 2019 and its state media reported the first known mortality on January 11, 2020. World Health Organization (WHO) declared COVID-19 as Public Health Emergency of International Concern on January 30, 2020 [1] and as global pandemic on March 11, 2020 [2] . So far almost 11 million positive cases and more than half a million deaths have been reported worldwide with approximately 129 thousand deaths noted in the USA alone [3] .

SARS-CoV-2, a single-stranded ribonucleic acid (RNA) beta-coronavirus of the Ortho Coronaviridae subfamily is thought to have originated from bats, as it has almost 96% genetic similarity to bat coronavirus genetic structure [4, 5] . Two forms of the virus have been identified-S type (~30%) and L type (70%), with the latter being more infectious and aggressive than the former, original strain [6] . COVID-19 mainly affects upper and lower respiratory tract, but also can also cause several other symptoms such as thromboembolism, neurological, and gastrointestinal disturbances. Most common reason for death is respiratory failure followed by sepsis and secondary infection [7] .

There is no satisfactory antiviral against COVID-19; however, remdesivir, lopinavir/ritonavir (with and without interferon beta-1b and ribavirin) [8] , and hydroxychloroquine (HCQ) are being used and various clinical trials are underway. Remdesivir has shown some promise in vitro [9] . There are also anecdotal reports showing the ability of lopinavirritonavir to decrease viral load and improve outcomes [10] . There was tremendous interest about HCQ initially due to existing scientific evidence of in vitro activity against SARS-CoV-2 [11, 12] , but enthusiasm is fading away after results from more recent studies [13] . Also, agents like vitamin C [14] and histamine-2 (H2) receptor antagonistfamotidine are being studied [15] . To treat the cytokine storm caused by infection, anti-cytokine therapies including tocilizumab, anakinra, and JAK inhibitors like baricitinib are being tried. In an ongoing landmark trial [RECOVERY] from the UK, dexamethasone was reported to be lifesaving. (ClinicalTrials.gov Identifier: NCT04381936).

Approximately 4.5% to 5.3% (14.7 to 23.5 million) of the United States (US) population have one or more autoimmune diseases of which 40% (2% of population) have autoimmune rheumatic disease [16] . Various trials are underway to determine whether rheumatic medications can potentially be used as preventative therapy, post-exposure prophylaxis and to counteract cytokine storm seen in critically ill COVID-19 patients.

The scientific and research community is interested in the potential role of interleukin (IL)-6 inhibitor like tocilizumab, IL-1 inhibitor-like anakinra, and janus kinase (JAK) inhibitor-like baricitinib in preventing cytokine storm besides investigating preventative and/or post-exposure use of antimalarials like HCQ and chloroquine (CQ).

To better understand the existing conundrum, we extensively reviewed recently published articles and guidelines issued by various societies. We also streamlined the data and attempted to come up with provisional recommendations for managing of rheumatic medications in COVID-19 infected patients.

The SARS-CoV-2 virus enters respiratory tract, infecting cells via angiotensin-converting enzyme (ACE)-2 receptors [17] . These receptors are expressed by the cells in the heart, lungs, blood vessels, kidneys, liver, and gastrointestinal tract [18] . It replicates in either ribosomes or the endoplasmic reticulum. During this replication process, RNA proteolysis leads to production of polypeptides, nonstructural proteins, and RNAdependent RNA polymerase (RdRp). The RNA translation process is followed by reassembly of its outer structural products. Finally, viral multiplication occurs and viral particles get out of infected cells via exocytosis to re-infect other cells (see Fig. 1 ).

Subsequently, the host mounts an immune response using both the innate and adaptive defense mechanisms. Macrophages, dendritic cells, and natural killer cells play an important role. Memory and regulatory T cells produced during the process preserve their memory in case of future attacks and regulate overactive immune response respectively. Cytokines that are released during the process of trying to eliminate virus cause inflammation (see Fig. 2 ). In COVID-19, initial inflammatory response is seen as increased levels of tumor necrosis factor (TNF)-alpha, IL-1 beta (both short lasting for 1-2 days), and IL-6 (longer lasting) [19] . Lymphocytes are the main target cells in COVID-19. Age-dependent T-and B-cell function defect along with excess production of type 2 cytokines ( IL-4, IL-5, IL-6, IL-10, IL-13) causes uncontrolled viral replication and increased inflammatory response [20] . Low peripheral CD4 and CD8 T-cell count is observed along with hyperactive CD8 T cells. These hyperactive CD8 T cells contain more cytotoxic granules that stain positive for perforins and/or granulysin [21] . IL-6 has been implicated in the consolidation phase of organizing pneumonia and also in prolonging QT interval, leading to torsade de pointes [22, 23] .

Coagulopathy in COVID-19 infection manifest as either low grade DIC (thrombocytopenia, increased d-dimer, prolonged PT), or localized pulmonary thrombotic microangiopathy (increased LDH and ferritin) [24] . Some patients with rheumatic diseases like adult-onset Still's disease (AOSD) and systemic lupus erythematosus (SLE) [25, 26] also show unregulated systemic hyperinflammation, presenting as macrophage activation syndrome (MAS). MAS is a subset of hemophagocytic lymphohistiocytosis (HLH) leading to rapid evolution of multiple organ failure and this is similar to the hyperinflammation seen in the setting of COVID-19 infection [20] .

An exaggerated host immune response leads to cytokine storm which then leads to multiple organ dysfunction. It is not clear why only some patients develop cytokine storm; however, host genetic risk is suspected as a causation or propagation of these complications [27] .

Mild COVID-19 is characterized by fever, dry or mildly productive cough, and fatigue. Features of critical illness include respiratory failure, acute respiratory distress syndrome (ARDS), sepsis, septic shock, and heart failure [7] . COVID-19 pneumonia can range from mild to severe [28] . An early study reported fever, dyspnea, and dry cough as common presenting symptoms, similar to SARS-CoV-1 and MERS-CoV; however, very few with SARS-CoV-2 had upper respiratory symptoms (rhinorrhea and sore throat) and intestinal symptoms (diarrhea) which is common with other coronavirus infections [20] . Data from > 70,000 patients released by Chinese CDC reported that 81% had mild, 14% had severe, and 5% had critical illness disease [29] . In a small prospective cohort study of 12 patients in Hamburg, Germany, autopsy showed deep vein thrombosis (DVT) in 58% (7 out of 12) patients even though it was not suspected antemortem, while pulmonary embolism (PE) was directly related to death in 33% (4 out of 12) patients [30] .

The severity of disease has not shown to be associated to viral load [31] . COVID-19 diagnosis can be confirmed by doing real-time reverse-transcription polymerase chain reaction (RT-PCR) assay or high-throughput sequencing from nasal and pharyngeal swab specimen [28] . Though chestcomputed tomography (CT) manifestations vary among different patients, with COVID-19, bilateral consolidation with ground glass opacities are typical CT manifestations [22] .

American College of Rheumatology (ACR) formed COVID-19 clinical task force on March 26, 2020 with aim to provide clinical guidance to rheumatologists. This task force did not identify rheumatic diseases as a risk factor that predicted poor outcome in patients with COVID-19 [32] . Risk factors that predict poor outcomes in those with COVID-19 include older age (> 65 years), obesity, hypertension, diabetes mellitus, chronic lung disease, chronic kidney disease (CKD), and cardiovascular disease (CVD) [33] . Biomarkers that predict poor outcomes include lymphopenia, elevated levels of creactive protein (CRP), D-dimer, IL-6, and LDH [34] .

The mortality rate with COVID-19 is thought to be around 3.7% [35] , compared to < 1% from influenza. Case fatality rate of this virus, from data available so far, is estimated to be around 1% which puts it between the range of 0.6% (seen with the 1957 influenza pandemic) and 2% (seen with the 1918 influenza pandemic) [36] . Chinese CDC data from a large study showed average case fatality being 2.3% but as high as 49% in those with critical illness [37] .

With the exception of few case reports and some preliminary data from ongoing studies, there is no definitive evidence of effectiveness of any of the current agents that are being used (mostly on compassionate basis) to treat any coronavirus including SARS-CoV-2 [38, 39] . The United States Food and Drug Administration (USFDA) has approved three medications (HCQ sulfate, CQ phosphate, and remdesivir) for Emergency Use Authorization (EUA) for COVID-19 [40] . HCQ and CQ are already FDA-approved drugs and were available to be prescribed outside EUA indications [40] . Adenosine analogue remdesivir had shown promise in vitro effect in a SARS-CoV-2 control group. On May 1, 2020, the FDA authorized emergency use of remdesivir in adults and children hospitalized with severe disease (low oxygen saturation requiring either oxygen or mechanical ventilation) due to COVID-19. Remdesivir is not FDA-approved and hence access is limited to compassionate use programs, expanded access programs, and clinical studies [41] . As the initial uncertainty about availability and distribution of remdesivir was addressed, its price was fixed by the manufacturer for transparency [42] .

In a small study, convalescent plasma with neutralizing antibodies resulted in improvement in the clinical status of 5 patients with COVID-19 and ARDS [43] . Another comparatively larger study of 39 critically ill-hospitalized patients with COVID-19 from New York showed improved survival in those that received convalescent plasma, with more benefit seen in non-intubated patients compared to those on mechanical ventilation [44] .

Since there is an established role of low molecular weight heparin (LMWH) in critically ill patients for DVT/PE prophylaxis, all patients with COVID-19 who are hospitalized should receive it in absence of contraindication as coagulopathy is noted in sizeable number of patients [24] .

Rheumatologists deal with a wide variety of systemic immune-mediated disorders with complex manifestations and use agents ranging from nonsteroidal anti-inflammatory drugs (NSAID) and corticosteroids to potent immunosuppressive agents such as cyclophosphamide. These medications help suppress tissue inflammation, thereby preventing tissue/ organ damage in autoimmune diseases. Immunosuppressive agents can suppress cytokine storm, a feature observed in both, systemic autoimmune diseases and viral illnesses. However, it can sometimes cause serious harm when used during viral infection possibly due to factors like secondary bacterial infections [45, 46] .

Small, anecdotal studies have proposed that being on certain immunomodulatory regimens might have possibly conferred protection to rheumatologic patients against severe SARS-CoV-2 manifestations [47, 48] . However, there is a relative scarcity of studies that gives guidance regarding the use of immunosuppressant medications during COVID- 19 infection.

An early survey study done in Milan, Italy, by Favalli EG et al. showed that it is beneficial to continue all rheumatic medications in someone who has not had COVID-19 exposure, as it helps with disease stabilization and prevent flare-ups [47] . The study by Venerito V et al. concluded that patients with uncontrolled rheumatoid arthritis (RA) and SLE have a higher risk of acquiring infection than being on immunosuppressive regimen while the disease is in remission [48] . Disease flares and use of corticosteroids during disease flares may further increase the risk of infection. A cross-sectional study showed that > 90% patients followed their rheumatologists' recommendation and continued immunosuppressive therapy, irrespective of their treatment regimen [49] .

It is unclear whether continuing NSAIDs is beneficial due to its antipyretic and anti-inflammatory effect in less severe COVID-19 cases. Some advocate acetaminophen use, although it can complicate liver injury as seen in few cases [50, 51] .

Preliminary data from an ongoing large multi-center openlabel randomized trial (RECOVERY (randomized evaluation of COVID-19 therapy)) at University of Oxford, UK, suggested mortality benefit with dexamethasone in those who required supplemental oxygen or mechanical ventilation but not in those who did not require supplemental oxygen (ClinicalTrials.gov Identifier: NCT04381936). In a case series from Italy, younger patients in epidemic areas, who were on corticosteroids for cancer chemotherapy and had a history of solid organ transplant did escape severe COVID-19 [52] . A small hospital cohort study reported methylprednisone use in COVID-19-related ARDS led to a shorter intensive care unit (ICU) stay [53] and improved survival rates [34] . Corticosteroids are associated with a risk of bacterial and opportunistic infections [54] along with a possible reactivation of herpes zoster [55, 56] . A case series from China showed up to 50% of deaths associated with COVID-19 were linked to secondary bacterial infections [7] . American College of Rheumatology (ACR) COVID-19 taskforce recommended against the abrupt withdrawal of corticosteroids due to hypothalamic pituitary adrenal (HPA) axis suppression [32] . We conditionally recommend that corticosteroids be used in the smallest possible dose in patients on chronic steroids.

When used as monotherapy, conventional synthetic (cs)DMARDs are associated with minimal risk of serious infection. HCQ and CQ showed antiviral activity in vitro [9, 11, 12] ; however, to date, there is no definitive evidence reported Fig. 1 SARS-CoV2 port of entry is mostly at lungs and GI tract. As the virus infects the epithelium it gets endocytosed and the virus goes through proteolysis releasing its RNA (ribonucleic acid) at EPR (endoplasmic reticulum). With proteolysis, RNA is turned into amino-acids and gets reassembled with structural proteins at Golgi apparatus. After reassembly in cells, it gets exocytosed by cells at pulmonary/gastric epithelium. These reassembled viruses are ready to infect neighboring cells that it is effective for prevention and post-exposure prophylaxis. Gauderet et al. suggested that HCQ is beneficial in the treatment of COVID-19 [57] . However, the study was noted to have significant statistical limitations with small sample size as well as poor randomization and methodology [58] . Poor interpretation with over-simplification of one study by social media and lay press led to the active propagation of HCQ and CQ as "potential remedy of COVID-19." In certain countries, HCQ was propagated by authorities for prevention and post-exposure prophylaxis [59] . Divergence for using HCQ in COVID-19 led to its temporary shortage, which affected patients with RA and SLE [60] . HCQ and CQ are relatively safe medications and can be continued in patients having COVID-19; caution is advised about increased myocardial toxicity [61] and QT prolongation when used with agents like azithromycin [62] .

Targeted synthetic (ts)DMARD like JAK inhibitors and biologic (b)DMARD have a higher risk of serious bacterial and opportunistic infection [63] [64] [65] compared to csDMARD. There is also an increased risk of herpes zoster reactivation with JAK inhibitors [66, 67] . Baricitinib, a tsDMARD inhibiting JAK has shown to limit SARS-CoV-2 penetration in pulmonary epithelial cells [68] . Less protein-binding properties with minimal CYP interaction favors baricitinib to be combined with ritonavir and remdesivir [69] . However, a potential downside of baricitinib is that it can impair innate immunity by reducing interferon's response which is deemed critical to control viral replication [68] . In a case report, IL-6 inhibitor-tocilizumab possibly prevented development of severe COVID-19 complications in someone who had been taking it for scleroderma associated interstitial lung disease (ILD) [70] . Tocilizumab is currently being commonly used in figure) ; whereas the adaptive immune response (right side of dendrites/macrophage) occurs at lymphatic system. Each figure depicts various cells and its secretion. SARS-CoV2 infection triggers both innate and adaptive immunity. With innate immune response, the tissue injury/host infected cell is recognized by neutrophils, NK (null killer cells), macrophages, dendritic cells. Innate immunity focus on preventing instant spread of infection by recruiting more neutrophils, macrophages and NK cells. Dendritic and macrophage cell conveys message to antigen presenting cells, which in turn recruits pluripotent T cell. This pluripotent T cell secretes IL-12 (interleukin-12) and in turn gets differentiated into T-helper (CD4), cytotoxic T cell (CD8) and B cell. T-helper secrets IL-2 (interleukin-2) and IFN (interferon), whereas cytotoxic secrete IFN A, B (interferon A, B) and IL-12 (interleukin-12). Pharmacodynamics-red color-dotted lines indicate inhibition action of medications at specific site in a cell. Corticosteroids-inhibits phospholipase and thereby inhibiting leukotrienes, cycle-oxygenase production leading to less inflammation. NSAIDS-inhibits COX-2/ specific ones COX-1. CQ/HCQ (chloroquine/hydroxychloroquine)-inhibits Toll receptor/RLR receptors at intracellular level within macrophage, leading to decreased IFN production. Baricitinib-inhibits JAK/STAT pathway within T-helper cells, leading to further deactivation of adaptive immunity. Toclizumab-inhibits Interleukin-6 production by dendritic cells further delaying recruitment and inflammation critically ill patients with COVID-19 and has been associated with good outcomes [71, 72] .

In a small number of hospitalized patients with COVID-19, anakinra prevented cytokine storm, macrophage activation syndrome, and hemophagocytic lymphohistiocytosis [73] . A phase 3 multi-center, randomized, double-blind, placebocontrolled study is currently underway to evaluate safety and efficacy of colchicine in adults with COVID-19 infection and at least 1 high risk criteria (ClinicalTrials.gov ID: NCT04322682) [74] . Mycophenolate mofetil (MMF) is associated with improved survival rates after MERS-CoV [75] and cyclosporine prevents in vitro replication of coronavirus [76] ; however, their impact on SARS-CoV-2 infection risk is not fully understood.

For simplification, we classify FIVE broad categories of medications that most of them fall under-NSAIDs, corticosteroids, DMARDs (csDMARD, tsDMARD, and bDMARD), immunosuppressive agents, and miscellaneous anti-inflammatory agents like colchicine.

For better understanding, we categorize the patients with rheumatic illnesses as the following: no history of exposure, patients with exposure but not currently positive, patients exposed with confirmed infection, patients admitted in hospital including those in ICU, and those discharged from hospital after recovery (post-COVID-19).

We thoroughly reviewed the articles, guidelines, and recommendations so far published and created best practice guidance as shown in Table 1 :

The major cause of mortality in COVID-19 patients is excessive cytokine production which leads to unregulated inflammatory response. It is unclear whether there is any specific area in an immune response that can be inhibited without preventing the hosts' defense [77] . Although IgM and IgG antibodies are detected within a few days to weeks in most COVID-19 patients, it is not known why some patients with COVID-19 infection do not develop these antibodies [78] [79] [80] .

As of now, there is no known confirmed case of human reinfection of SARS-CoV-2 [81] , although viral PCR can remain positive for a long time even after the resolution of infection. Serologic assays that detect SARS-CoV-2 antibodies are increasingly becoming available, although it is not prudent to say currently that these subjects are immune against getting reinfected [81] . Except for a small animal study [82] that favors recovery and possible immunity to reinfection from SARS-CoV-2, there is currently paucity of data about it. In children, Kawasaki-like syndrome, which is provisionally called x* = side effects of SSZ (hepatitis, cytopenia) can be confused with SARS-CoV-2 +* = Closely monitor for myocardial injury and QT prolongation pediatric inflammatory multisystem syndrome (PIMS-TS), is temporally associated with SARS-CoV-2 [83] .

COVID-19 has posed important challenges to the management of autoimmune rheumatic diseases. We have attempted to address the dilemma faced by medical community about the commonly used immunosuppressive medications during COVID-19 crisis using the best available current evidence. Although it appears that almost all DMARDs can be continued in patients not exposed to COVID-19 and restarted after recovering from the infection, the level of evidence, at least at this point, is limited to few observational studies only, and prospective larger studies are needed to provide the definitive recommendations.

We are optimistic that while adhering to measures that has proven effective to prevent virus spread (frequent hand washing, wearing PPE like face masks and goggles, and social distancing), scientific community will continue its vigorous effort to mitigate this crisis.

Disclosures/Conflict of interest Amit P. Ladani-none Muruga Loganathan-none Abhijeet Danve-Advisory boards and honoraria: Janssen; Research Grants: Novartis

COVID-19 Public Health Emergency of International Concern (PHEIC) Global research and innovation forum

WHO declares COVID-19 a pandemic

Coronavirus genomics and bioinformatics analysis

A pneumonia outbreak associated with a new coronavirus of probable bat origin

On the origin and continuing evolution of SARS-CoV-2

Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

Triple combination of interferon beta-1b, lopinavir-ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial

Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro

Case of the index patient who caused tertiary transmission of coronavirus disease 2019 in Korea: the application of lopinavir/ritonavir for the treatment of COVID-19 pneumonia monitored by quantitative RT-PCR

Hydroxychloroquine, a less toxic derivative of chloroquine, is effective in inhibiting SARS-CoV-2 infection in vitro

In vitro antiviral activity and projection of optimized dosing design of hydroxychloroquine for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

A systematic review of the prophylactic role of chloroquine and hydroxychloroquine in coronavirus disease-19 (COVID-19)

A new clinical trial to test high-dose vitamin C in patients with COVID-19

Famotidine use and quantitative symptom tracking for COVID-19 in non-hospitalised patients: a case series

SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor

Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target

Cytokines in sepsis: potent immunoregulators and potential therapeutic targets-an updated view

Clinical features of patients infected with

Pathological findings of COVID-19 associated with acute respiratory distress syndrome

Chest CT manifestations of new coronavirus disease 2019 (COVID-19): a pictorial review

Systemic inflammation as a novel QT-prolonging risk factor in patients with torsades de pointes

Coagulation abnormalities and thrombosis in patients with COVID-19

Clinical features of haemophagocytic syndrome in patients with systemic autoimmune diseases: analysis of 30 cases

Reactive hemophagocytic syndrome in adult-onset Still disease: clinical features, predictive factors, and prognosis in 21 patients

The genetics of macrophage activation syndrome

for the China Medical Treatment Expert Group for COVID-19 (2020) Development and Validation of a clinical risk score to predict the occurrence of critical illness in hospitalized patients with COVID-19

Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72 314 cases from the Chinese Center for Disease Control and Prevention

Autopsy Findings and venous thromboembolism in patients with COVID-19: a prospective cohort study

SARS-CoV-2 viral load in upper respiratory specimens of infected patients

American College of Rheumatology guidance for the management of rheumatic disease in adult patients during the COVID-19 pandemic: version 1. Arthritis Rheumatol art

Clinical course of COVID-19 in a series of patients with chronic arthritis treated with immunosuppressive targeted therapies

Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease 2019 pneumonia in Wuhan

COVID-19) situation report -52 36. (2020) The novel coronavirus pneumonia emergency response epidemiology team. The epidemiological characteristics of an outbreak of

Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72314 cases from the Chinese Center for Disease Control and Prevention

Treating COVID-19-off-label drug use, compassionate use, and randomized clinical trials during pandemics

COVID-19, cytokines and immunosuppression: what can we learn from severe acute respiratory syndrome?

Emergency use authorization of remdesivir: the need for a transparent distribution process

Treatment of 5 critically ill patients with COVID-19 with convalescent plasma

Convalescent plasma treatment of severe COVID-19: a matched control study

The trinity of COVID-19: immunity, inflammation and intervention

Should we stimulate or suppress immune responses in COVID-19? Cytokine and anti-cytokine interventions

Incidence and clinical course of COVID-19 in patients with connective tissue diseases: a descriptive observational analysis

COVID-19, rheumatic diseases and immunosuppressive drugs: an appeal for medication adherence

A cross sectional study on patients with inflammatory rheumatic diseases in terms of their compliance to their immunsuppressive medication during COVID-19 pandemic

National Institute for Health and Care Excellence (NICE) in collaboration with NHS England and NHS Improvement (2020) Managing COVID-19 symptoms (including at the end of life) in the community: summary of NICE guidelines

Coronaviruses and immunosuppressed patients: the facts during the third epidemic

Clinical characteristics and treatment of patients infected with COVID-19 in Shishou

Infection risk and safety of corticosteroid use

Herpes zoster reactivation in patients with rheumatoid arthritis: analysis of disease characteristics and disease-modifying antirheumatic drugs

Herpes zoster in patients with systemic lupus erythematosus: clinical features, complications and risk factors

Hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an openlabel non-randomized clinical trial

Statistical review of hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an open-label non-randomized clinical trial

A rush to judgment? Rapid reporting and dissemination of results and its consequences regarding the use of hydroxychloroquine for COVID-19

health B reporter focused on the health-care economy's effects on patient, et al As Trump touts an unproven coronavirus treatment, supplies evaporate for patients who need those drugs

Association of coronavirus disease 2019 (COVID-19) with myocardial injury and mortality

Incidence of sustained ventricular tachycardia in patients with prolonged QTc after the administration of azithromycin: a retrospective study

The risk of infections associated with rheumatoid arthritis

Risk of serious infection in biological treatment of patients with rheumatoid arthritis: a systematic review and metaanalysis

Infections with biologics in rheumatoid arthritis and related conditions: a scoping review of serious or hospitalized infections in observational studies

Risk of herpes zoster in patients with rheumatoid arthritis treated with anti-TNF-α agents

Herpes zoster and tofacitinib: clinical outcomes and the risk of concomitant therapy

Baricitinib for COVID-19: a suitable treatment

COVID-19: combining antiviral and antiinflammatory treatments

COVID-19 in a patient with systemic sclerosis treated with tocilizumab for SSc-ILD

Tocilizumab in patients with severe COVID-19: a retrospective cohort study

Tocilizumab for treatment of patients with severe COVID-19: a retrospective cohort study

Continuous intravenous anakinra infusion to calm the cytokine storm in macrophage activation syndrome

Colchicine coronavirus SARS-CoV2 trial (COLCORONA) -Full Text View -ClinicalTrials

Treatment outcomes for patients with Middle Eastern Respiratory Syndrome Coronavirus (MERS CoV) infection at a coronavirus referral center in the Kingdom of Saudi Arabia

Cyclosporin A inhibits the replication of diverse coronaviruses

Coronavirus infections and immune responses

Antibody responses to SARS-CoV-2 in patients of novel coronavirus disease 2019

Virological assessment of hospitalized patients with COVID-2019

Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study

COVID-19 and postinfection immunity: limited evidence, many remaining questions

Reinfection could not occur

Kawasaki-like disease: emerging complication during the COVID-19 pandemic

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