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EULAR points to consider on pathophysiology and use of immunomodulatory therapies in COVID-19
  1. Alessia Alunno1,
  2. Aurélie Najm2,
  3. Pedro M Machado3,4,5,
  4. Heidi Bertheussen6,
  5. Gerd R Burmester7,
  6. Francesco Carubbi8,
  7. Gabriele De Marco9,
  8. Roberto Giacomelli10,
  9. Olivier Hermine11,12,
  10. John D Isaacs13,
  11. Isabelle Koné-Paut14,
  12. César Magro-Checa15,
  13. Iain McInnes2,
  14. Pier Luigi Meroni16,
  15. Luca Quartuccio17,
  16. Athimalaipet V Ramanan18,19,
  17. Manuel Ramos-Casals20,
  18. Javier Rodríguez Carrio21,
  19. Hendrik Schulze-Koops22,
  20. Tanja A Stamm23,
  21. Sander W Tas24,
  22. Benjamin Terrier25,
  23. Dennis G McGonagle9,
  24. Xavier Mariette26
  1. 1Rheumatology Unit, Department of Medicine, University of Perugia, Perugia, Italy
  2. 2Institute of Infection, Immunity and Inflammation, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, UK
  3. 3Centre for Rheumatology & Department of Neuromuscular Diseases, University College London, London, UK
  4. 4National Institute for Health Research (NIHR) Biomedical Research Centre (BRC), University College London Hospitals NHS Foundation Trust, London, UK
  5. 5Department of Rheumatology, Northwick Park Hospital, London North West University Healthcare NHS Trust, London, UK
  6. 6Oslo, Norway
  7. 7Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Freie Universität und Humboldt-Universität Berlin, Berlin, Germany
  8. 8Department of Medicine, ASL 1 Avezzano-Sulmona-L'Aquila, Internal Medicine and Nephrology Unit, Department of Life, Health & Environmental Sciences, University of L’Aquila, L'Aquila, Italy
  9. 9The Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK
  10. 10Rheumatology and Clinical Immunology Unit, University of Rome "Campus Biomedico" School of Medicine Rome, Rome, Italy
  11. 11Department of Haematology, Hôpital Necker, Assistance Publique - Hôpitaux de Paris, Paris, France
  12. 12INSERM UMR1183, Institut Imagine, Université de Paris, Paris, France
  13. 13Translational and Clinical Research Institute, Newcastle University and Musculoskeletal Unit, Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK
  14. 14Service de Rhumatologie Pédiatrique, Centre de Référence des Maladies Auto-Inflammatoires de l’enfant, Hôpital Bicêtre, AP HP, Université Paris Sud, Bicètre, France
  15. 15Department of Rheumatology, Zuyderland Medical Centre Heerlen, Heerlen, The Netherlands
  16. 16Experimental Laboratory of Immunological and Rheumatologic Researches, Istituto Auxologico Italiano, IRCCS, Milan, Italy
  17. 17Department of Medicine, Rheumatology Clinic, University of Udine, ASUFC Udine, Udine, Italy
  18. 18University Hospitals Bristol NHS Foundation Trust, Bristol, UK
  19. 19University of Bristol Translational Health Sciences, Bristol, UK
  20. 20Department of Autoimmune Diseases, ICMiD, Laboratory of Autoimmune Diseases Josep Font, IDIBAPS-CELLEX, Department of Autoimmune Diseases, ICMiD, University of Barcelona, Hospital Clínic, Barcelona, Spain
  21. 21Department of Functional Biology, Immunology Area, Faculty of Medicine, University of Oviedo, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain
  22. 22Division of Rheumatology and Clinical Immunology, Department of Internal Medicine IV, Ludwig-Maximilians University of Munich, Munchen, Germany
  23. 23Section for Outcomes Research, Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna and Ludwig Boltzmann Institute for Arthritis and Rehabilitation, Wien, Austria
  24. 24Department of Rheumatology and Clinical Immunology, Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centres, Amsterdam, The Netherlands
  25. 25Department of Internal Medicine, Cochin University Hospital, Paris, France; National Referral Centre for Systemic and Autoimmune Diseases, University Paris Descartes, Sorbonne Paris Cité, Paris, France
  26. 26Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, INSERM UMR1184, Department of Rheumatology, Université Paris-Saclay, Le Kremlin Bicêtre, France
  1. Correspondence to Professor Xavier Mariette, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, INSERM UMR1184, Department of Rheumatology, Université Paris-Saclay, 91190 Saint-Aubin, Île-de-France, France; xavier.mariette{at}


Objectives Severe systemic inflammation associated with some stages of COVID-19 and in fatal cases led therapeutic agents developed or used frequently in Rheumatology being at the vanguard of experimental therapeutics strategies. The aim of this project was to elaborate EULAR Points to consider (PtCs) on COVID-19 pathophysiology and immunomodulatory therapies.

Methods PtCs were developed in accordance with EULAR standard operating procedures for endorsed recommendations, led by an international multidisciplinary Task Force, including rheumatologists, translational immunologists, haematologists, paediatricians, patients and health professionals, based on a systemic literature review up to 15 December 2020. Overarching principles (OPs) and PtCs were formulated and consolidated by formal voting.

Results Two OPs and fourteen PtCs were developed. OPs highlight the heterogeneous clinical spectrum of SARS-CoV-2 infection and the need of a multifaceted approach to target the different pathophysiological mechanisms. PtCs 1–6 encompass the pathophysiology of SARS-CoV-2 including immune response, endothelial dysfunction and biomarkers. PtCs 7–14 focus on the management of SARS-CoV-2 infection with immunomodulators. There was evidence supporting the use of glucocorticoids, especially dexamethasone, in COVID-19 cases requiring oxygen therapy. No other immunomodulator demonstrated efficacy on mortality to date, with however inconsistent results for tocilizumab. Immunomodulatory therapy was not associated with higher infection rates.

Conclusions Multifactorial pathophysiological mechanisms, including immune abnormalities, play a key role in COVID-19. The efficacy of glucocorticoids in cases requiring oxygen therapy suggests that immunomodulatory treatment might be effective in COVID-19 subsets. Involvement of rheumatologists, as systemic inflammatory diseases experts, should continue in ongoing clinical trials delineating optimal immunomodulatory therapy utilisation in COVID-19.

  • therapeutics
  • inflammation
  • immune system diseases

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:

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Key messages

What is already known about this subject?

  • SARS-CoV-2 infection is potentially life threatening with severe disease being associated with immune system activation with severe pneumonia and pulmonary immunothrombosis that may be amenable to immunomodulatory treatments which have largely been pioneered in the rheumatology therapeutic arena.

  • The enormous amount of studies published in a very short timeframe and the continuous flow of new data leads to difficulties in summarising best evidence for clinical practice for severe COVID-19 treatment.

What does this study add?

  • Multifactorial pathophysiological mechanisms, including immune and non-immune cell abnormalities and loss of endothelial homeostasis, play a key role in COVID-19.

  • These are first EULAR–endorsed ‘points to consider’ (PtC) providing a framework to optimise the use of immunomodulatory therapies for the care of people with SARS-CoV-2 infection.

  • This article highlights areas of therapeutic success but also areas of uncertainty (eg, timing/add-in approach for glucocorticoids in combination with other immunomodulatory agents) that require to be addressed by further research and barriers to overcome in order to develop new therapeutic strategies for SARS-CoV-2 infection.

Key messages

How might this impact on clinical practice?

  • It is anticipated that clinicians will use these PtC as a basis for the optimal management of people with SARS-CoV-2 infection and for further strategies for optimal therapy.

  • These PtC will also support relevant stakeholders when evaluating new immunomodulatory therapeutic approaches to treat SARS-CoV-2 infection.


The rapid worldwide spread of the SARS-CoV-2 has led to an unpreceded pandemic. SARS-CoV-2 infection leads to heterogeneous disease phenotypes, from asymptomatic or mild disease associated with an uneventful recovery to severe disease leading to acute respiratory distress syndrome (ARDS), multiorgan failure and death.1 Immune mechanisms are critically involved in evolution of severe COVID-19, suggesting potential efficacy of immunomodulatory treatments.2 3

Since rheumatologists are at the vanguard of immunomodulatory therapy utilisation, they are well placed to provide insights in their usage, safety profile and timing towards potential mitigation of the severe inflammatory reactions associated with SARS-CoV-2 infection. Although an extremely large volume of publication is already available, most of the research is descriptive and definitive randomised controlled trials (RCTs) remains scarce. In this rapidly evolving landscape, and with the need to optimally define therapeutics solutions, it is considerably important to provide the medical and scientific community with guidance using the best available evidence. This is especially the case since antiviral agents have thus far failed to show a significant improvement of survival in COVID-19.4–6 The aim of this project was to elaborate EULAR points to consider (PtCs) on COVID-19 pathophysiology and immunomodulatory therapies from the rheumatology perspective through a systematic literature review (SLR)-based approach.


After approval by the EULAR Executive Committee, the convenors (XM and DGM) and the methodologist (PMM) led a multidisciplinary Task Force guided by the 2014 updated EULAR standardised operating procedures.7 The Task Force consisted of 24 members from 8 different countries, including rheumatologists, translational immunologists (two of them also representing the Emerging EULAR Network), haematologists, paediatric rheumatologists, a methodologist, one health professional and one patient representative. Four virtual meetings of the Task Force were held, one inJuly 2020 and three in November 2020. Two fellows (AA and AN), guided by the methodologist, performed an SLR, retrieving individual studies on pathophysiology of SARS-CoV-2 infection and its management with immunomodulatory therapies. Given the fast-paced publication of articles on treatment with potential impact on the formulation of PtCs, the last SLR update was performed on 11 December 2020. The SLR is published separately, however, it forms an integral part of the project.

Based on the presented evidence and expert opinion, and following a process of iterative discussion, the overarching principles (OPs) and PtCs were developed. According to EULAR guidance, the steering group (convenors, methodologist and fellows) prepared draft-statements based on the evidence from the SLRs and each statement was presented, discussed and voted on (informal voting). The statements were accepted if more than 75% of the Task Force approved the wording in the first round. If this was not reached, further discussion ensued and wording was refined. At least a 67% approval rate was required in the second voting round and more than 50% in the third round.8 The level of evidence (LoE) supporting each statement was assigned according to the Oxford Centre for Evidence Based Medicine 2011 LoE.9 Finally, each Task Force member anonymously indicated their level of agreement with each PtC online (numerical rating scale ranging from 0=‘completely disagree’ to 10=‘completely agree’). Based on the heterogeneity of studies gathered by the SLR and on the paucity of high-quality evidence (namely RCTs) despite the large amount of published articles, a research agenda was formulated. The final manuscript was reviewed and approved by all Task Force members, followed by ratification by the EULAR Executive Committee.


Two OP and 14 PtCs were formulated and encompass the pathophysiology of SARS-CoV-2 infection and its treatment with immunomodulatory agents (table 1). The PtC are intended to provide insights in pathogenesis and guidance on therapeutic aspects, and the target users are healthcare providers taking care of patients infected with SARS-CoV-2 as well as patients and policy-makers.

Table 1

Overarching principles and points to consider on COVID-19 pathophysiology and immunomodulatory treatment from the rheumatology perspective, with levels of evidence (LoE) and levels of agreement (LoA)

Overarching principles

OP-A: the phenotype of SARS-CoV-2 infection is heterogeneous, ranging from asymptomatic to fatal disease due to multiorgan damage

The Task Force recognised the importance of outlining this concept as OP to set the scenario for the PtCs. A heterogeneous clinical spectrum is a hallmark of SARS-CoV-2 infection and a challenge for the clinicians. Patients with severe manifestations, severe systemic inflammation and ARDS remain difficult to treat leading to a negative outcome in a high number of cases.

OP-B: SARS-CoV-2 infection may need different treatment approaches, including antiviral, oxygen therapy, anti-coagulation and/or immunomodulatory treatment at different stages of the disease

An increasing number of articles outlined the complexity of SARS-CoV-2 pathophysiology and recommendations issued by the WHO and other key stakeholders10–12 reflect the necessity to combine supportive therapy along with agents with different mechanisms of action, for example, antiviral treatment, oxygen therapy, anticoagulation and the inflammatory response along with other key mechanism involved in the process. However, it is not yet clear when and how to combine these various approaches (eg, combination vs sequential therapy).

PtCs: pathophysiology of COVID-19

PtC-1: genetically determined differences including, but not limited to, immune gene pathways may contribute to the variable immune response to SARS-CoV-2 and ultimately impact on the disease prognosis (LoE 3/4)

Genetic differences may contribute to the clinical heterogeneity of SARS-CoV-2 infection with the type 1 interferon (IFN) pathway emerging as the strongest genetic association in both genome wide association studies (GWAS) and from Mendelian genetic studies of critically ill patients.13 A GWAS study also reported associations with immune response genes such as C-C Motif Chemokine Receptor 9 and C-X-C Motif Chemokine Receptor 6, and severe COVID-19.14 The same study reported higher risk of severe disease in people with blood group A.14 Whole-exome sequencing reported variants of genes involved in IFN mediated immune response in a subset of patients with severe COVID-19 and patients showing these variants had hampered IFN immunity in vivo and in vitro.15–18 Data concerning (HLA) haplotypes are still conflicting.14 19 To note, low allelic variability of the ACE−2, whose binding by the SARS-CoV-2 spike protein facilitates cellular entry of the virus, was also observed in infected patients compared with normal subjects but was not associated with disease severity.20–22

PtC-2: cellular (LoE 3/4) and humoural (LoE 3) immune responses against SARS-CoV-2 vary across individuals, infection course and disease spectrum, but there is insufficient evidence to associate these directly with outcomes

The activation of phagocytes, antigen-sensitised T cells and B-cells have been extensively studied in SARS-CoV-2 infection. It is worth noting, however, that most studies assessed individual cell populations through extremely variable methods (ie, flow cytometry gating and sub-population definition) and measured specific anti-SARS-CoV-2 immunoglobulins with home-made assays using different viral proteins as substrate, thereby preventing definitive conclusions. Among the few studies using an unsupervised clustering approach through mass cytometry and other high throughput sequencing techniques (single cell RNA sequencing, Cellular Indexing of Transcriptomes and Epitopes, Assay for Transposase-Accessible Chromatin, among others) several cell populations where reported to be consistently altered. The lymphoid compartment disruption was mostly characterised by a reduction in CD4 and CD8 positive lymphocytes in patients with SARS-CoV-2 infection compared with healthy controls but also in patients displaying a severe disease vs milder phenotypes.23–32 In addition, this subset of patients displayed a higher amount of polyfunctional T cells along with an exhausted CD8+ phenotype as highlighted by a high PD-1+ expression.23 25 29 An alteration of cytotoxicity, as suggested by a reduction in granzymes A, B and perforin expression by CD8+ cells, was reported by one study.23 Natural killer and B-lymphocytes pools were also reduced in patients with SARS-CoV-2 infection when compared with healthy donors regardless of disease severity.25 27 In terms of myeloid response, an increase of classical CD14+ monocytes pool was consistently reported, along with a significant reduction of HLA-DR expression; as opposed to a reduction of dendritic cells in both mild and severe patients compared with healthy controls.23 26–28 33–36 In addition, the pool of immature neutrophils (pre and pro-neutrophils) was reported to be increased.35 36

With regard to the humoural response, a few studies used standardised, although based on different viral antigens, commercially available ELISA or chemiluminescence immunoassays.37–41 The authors reported appearance of anti-SARS-CoV-2 IgM within the first 2 weeks after the onset of symptoms but the fate of these antibodies is still controversial with studies reporting variable kinetics up to weeks 4–5 after the onset of symptoms. Conversely, anti-SARS-CoV-2 IgG variably appear either together with IgM in week 140 41 or in weeks 2-337 38 being still detectable up to week 4,38 week 637 40 or week 8.41 Data on the kinetics of neutralising antibodies are even more controversial. Additionally, results on other isotypes (IgA) are scarce, although potentially relevant for the clinical setting.

PtC-3: levels of many proinflammatory cytokines, especially serum interleukin-6, are elevated in COVID-19 and could be associated with outcome (LoE 3/4)

The cytokine expression profile during the course of SARS-CoV-2 infection has already been extensively studied. Since the level of proinflammatory cytokines is elevated in some stages of the disease, but not at very high levels, the group considered that the term severe systemic inflammatory state seems more appropriate than the frequently used ‘cytokine storm’.42 Of interest, while most studies used a targeted approach towards one cytokine or one family of cytokines subsequently leading to bias, only a few used multiparametric assays allowing the multivariable assessment of the expression of several cytokines at the same time. Among these, several studies reported a consistent elevation of interleukin (IL)-6, IL-1 beta and tumor necrosis factor along with Th1 associated cytokines (IFN-gamma, IL-18) in COVID-19 patients compared with healthy donors but the magnitude of cytokine elevations was greater in patients displaying more severe disease phenotypes compared with mild or moderate diseases.28 33 43–45

These results are concordant with the large amount of studies correlating IL-6 levels with disease severity and negative outcomes.46 In addition to these, anti-inflammatory cytokines and a broad range of chemokines and growth factors expression profiles were inconsistently reported to be disrupted to a variable extent according to disease severity and outcomes but these results were not felt consistent enough by the TF to lead to the formulation of a PtC.47 However, the extent of cytokinaemia in cases of severe and critical COVID-19 is less than that seen in other disorders associated with elevated cytokine production, such as chimeric antigen receptor T-cell-induced cytokine release syndrome and non-COVID-19 ARDS.42 48

PtC-4: hyperactivation of platelets, the complement system, endothelial damage and loss of endothelial homeostasis are pathophysiological mechanisms facilitating hypercoagulability and thrombosis during SARS-CoV-2 infection (LoE 4)

A large number of studies described an increased prevalence of thrombosis and thromboembolic disease in patients with SARS-CoV-2 infection.49 Controversy still exists as to whether hypercoagulability in SARS-CoV-2 infection may be immune driven or immunothrombotic in nature or may be linked to direct viral endothelitis (or both). Platelet aggregation and activation, as expected in the context of endothelial injury and immune activation were observed and were more pronounced in severe COVID-19.50–60

PtC-5: multiparameter algorithms including neutrophil-to-lymphocyte ratio and acute phase reactants (eg, C reactive protein, ferritin) may be helpful to predict survival, mortality or disease progression and severity (LoE 4)

In order to help clinicians in disease management, several studies aiming at creating algorithms for prediction of disease progression, severity or outcomes have been published.61–73 Among them, a few have used robust statistical approaches using uni- and multivariate analysis, followed by logistic regression or least absolute shrinkage and selection operator. Most of them included various parameters from clinical data (demographics, comorbidities, symptoms), biological results (acute phase reactants such as C reactive protein, ferritin, procalcitonin, calprotectin; coagulation markers such as platelets, D-dimer, prothrombin time; immune cell count such as neutrophils, lymphocytes or neutrophil-to-lymphocyte ratio) or imaging results (chest CT).

The relevance of combining different parameters for prognostic purposes in further underscored by the recent release of predictive criteria for COVID-19 severe systemic inflammatory state.74

PtC-6: primary infection with SARS-CoV-2 in children is largely a benign event. However, a small number of children develop a multisystem inflammatory syndrome which may reflect distinct pathophysiological mechanisms compared with adults (LoE 4/5)

Epidemiological data pertaining to SARS-CoV-2 infection in children are rather homogeneous describing mild to moderate symptoms in most cases.75 However, from the end of April 2020, a number of alerts have been raised in several countries about children with proven SARS-CoV-2 infection developing a multisystem inflammatory syndrome (MIS-C).76 More recently reports of MIS-C in young adults have been published.77 Studies comparing clinical and serological features of children and adults with SARS-CoV-2 infection are scarce and included small cohorts of patients hence they do not allow to draw definitive conclusions on similarities and differences of SARS-CoV-2 infection across the lifespan.78 However, the discussion on this PtC was led by the paediatric rheumatologists and resulted in an agreement to include expert opinion given the paucity of data from the SLR. In particular, the Task Force supported the hypothesis that this clinical heterogeneity may reflect distinct pathophysiological mechanisms, not yet fully elucidated, that occur in children and in adults with SARS-CoV-2 infection.

PtCs: immunomodulatory treatment

PtC-7: in non-hospitalised patients with SARS-CoV-2 infection there is currently no evidence to support the initiation of immunomodulatory therapy (LoE 2/3/4)

The literature assessing the efficacy of immunomodulatory therapies on reducing time to an undetectable viral load, reducing the duration of clinical symptoms or preventing clinical deterioration in patients presenting with mild or moderate forms including mild hypoxaemia not requiring hospitalisation remains scarce since most of the clinical research has included more severe patients. However, it is worth noting that among the few studies available, none provided evidence of treatment efficacy in this specific population. More specifically, none of the RCTs assessing the efficacy of hydroxychloroquine (HCQ) in non-hospitalised patients reported positive outcomes.79 80 It is possible that this phase of SARS-CoV-2 infection requires more efficient anti-viral drugs than immunomodulatory drugs.

PtC-8: In hospitalised patients with SARS-CoV-2 infection that do not need oxygen therapy there is currently no evidence to support the initiation of immunomodulatory therapy (LoE 2/3/4)

A large number of studies on hospitalised patients with SARS-CoV-2 infection and various disease severity investigated immunomodulatory therapy. However, none of the investigated compounds except leflunomide in one small RCT,81 specifically demonstrated to be effective if added to standard of care (SOC) in hospitalised patients with mild-to-moderate disease not requiring oxygen therapy compared with SOC only. Of note, in the large RECOVERY RCT, analysis of the subgroup of patients without oxygen support showed a possible (not statistically significant) deleterious effect of dexamethasone (DEX) on mortality: OR 1.22, 95% CI 0.93 to 1.61, p=0.14.82 Likewise, HCQ was clearly ineffective in three RCTs including patients with mild to moderate disease and it even showed a negative safety profile.79 80 Due to the lack of efficacy and the safety concerns also in patients with severe COVID-19, and the historical debate about the role of HCQ in SARS-CoV-2 infection, with HCQ shortages being reported during the SARS-CoV-2 pandemic, the group decided to elaborate a separate PtC for this drug.

PtC-9: HCQ should be avoided for treating any stage of SARS-CoV-2 infection since it does not provide any additional benefit to the SOC, and could worsen the prognosis in more severe patients particularly if coprescribed with azithromycin (LoE 2)

In the early phases of the SARS-CoV-2 pandemic, HCQ was extensively used for the management of infected patients due to its known antiviral and immunomodulatory effects.83 However, the initial promising data from prospective/retrospective studies have not been confirmed by RCTs. Data from eight RCTs on HCQ in patients with SARS-CoV-2 infection and different degrees of COVID-19 severity consistently showed that the addition of this compound to SOC did not provide any benefit at any stage of the disease.79 80 84–89 Importantly, the RECOVERY study reported that for some outcomes such as progression to invasive mechanical ventilation (IMV) or death, and probability to be discharged alive, the addition of HCQ to SOC led to even worse outcomes compared with SOC alone. Furthermore, safety concerns have been raised since patients treated with HCC+SOC displayed a higher rate of adverse events compared with SOC only at any disease stage, mainly if associated with azithromycin. For example, HCQ-treated patients with severe COVID-19 displayed prolongation of the corrected QT interval, elevation of liver-enzymes and higher risk of death from non–SARS-CoV-2 cardiac causes.86 87

PtC-10: in patients with COVID-19 requiring supplemental oxygen, non-IMV, systemic glucocorticoids should be used since they can decrease mortality; most evidence concerns the use of DEX (LoE 2/3)

This PtC was elaborated based on the results of 6 RCTs on patients with severe COVID-19. Two trials investigated DEX,82 90 two investigated methylprednisolone (MTP),91 92 and two investigated hydrocortisone.93 94 While the overall analysis of patients yielded conflicting results for the majority of outcomes, the evidence on mortality from subgroup analysis was striking and revealed the beneficial effect of DEX and MTP in specific subgroups of patients. The RECOVERY trial demonstrated that the addition of DEX to SOC reduced mortality only in patients requiring respiratory support.82 The addition of MTP to SOC reduced mortality only in patients aged 60 or over by mechanisms potentially including rescue of immunosenescence.91 The group agreed that the evidence was more consistent for DEX rather than for MTP. Based on this data, DEX has been included in most of the recommendations of treatment for critical intensive care unit (ICU) patients and for mild-to-moderate pneumonia needing oxygen in medical wards. Of note, in the latter population, there is no study to decipher the effect of glucocorticoids between the patients requiring a low rate of oxygen 1–2 L/min) and those requiring higher rate (3–15 L/min). It is an important point since the pathophysiology might be different in both groups.

PtC-11: an evolving RCT landscape cannot yet allow formal recommendation of the routine use of tocilizumab in patients with COVID-19 requiring oxygen therapy, non-invasive or invasive ventilation (LoE 2)

The SLR retrieved 104 articles evaluating tocilizumab (TCZ) in SARS-CoV-2 infection and only three were RCTs.95–97 A scenario similar to that reported above for HCQ occurred for TCZ. Based on the evidence of the severe systemic inflammation at some stages of the disease, where IL-6 is perceived to be ‘a leading actor’ and on results from early studies with low LoE, many of which lacking a control group, prompted initial widespread TCZ use. Two published RCT96 97 were negative but probably included mild patients, some of them not requiring oxygen support since day-28 mortality was low: 4.9% and 2.4%, respectively. The third published study (CORIMUNO-19)95 focusing on patients requiring at least 3 L/min oxygen but not in ICU showed a 33% reduction of non-invasive or invasive ventilation (NIV) or death at day 14, but day-28 mortality was not different between groups (around 12%). Of note, two studies in the preprint phase, the first one (EMPACTA) with the same inclusion criteria as CORIMUNO-19), and positive with the same composite primary outcome, the second one (COVACTA) negative for its primary outcome, but with positive results in the post hoc analysis of patients not in ICU. Lastly, in the patients recently admitted in ICU within 2 days, the REMAP-CAP study was prematurely stopped because of positive results on survival with TCZ98 and an emulated trial in the same population found an improvement of survival.99 Interestingly, safety of TCZ was good in all these studies with in some of them a decrease of the rate of serious infections in the TCZ arm versus placebo or usual care arm. To summarise, despite the encouraging signals in some subgroups, it remains impossible at the date of this paper to draw definitive conclusions and to formulate a PtC either recommending or discouraging the use of TCZ in severe COVID-19. Meta-analysis on aggregated or individual patient data and further clinical trials are warranted and results from these trials will inform about the potential benefit of TCZ, in selected patients. Observational studies suggested benefit of glucocorticoids in combination with TCZ, but RCTs are needed for the evaluation of TCZ in addition to DEX/MTP vs DEX/MTP alone. This will be an important step for determining the possible place of this drug as an ‘add on therapy’ in glucocorticoid non-responsive cases.

PtC-12: in COVID-19 there is no robust evidence to support the use of anakinra at any disease stage (LoE 2/4)

At present, the only RCT available on anakinra in SARS-CoV-2 infection was conducted by the CORIMUNO-19 Collaborative group in mild-to-moderate COVID-19 pneumonia requiring at least 3 L/min oxygen but not receiving NIMV or IMV ventilation at randomisation. The study was stopped early following the recommendation of the data and safety monitoring committee since no beneficial effect was observed.100 As far as moderate-to-severe COVID-19 is concerned, conflicting results have been reported from three retrospective controlled studies.101–103

PtC-13: in patients with COVID-19 requiring NIV or high-flow oxygen, the combination of remdesivir plus baricitinib could be considered since it can decrease time to recovery and accelerate improvement in clinical status (LoE 2)

At present, the only RCT available on baricitinib in SARS-CoV-2 infection compared remdesevir + baricitinib versus remdesevir +placebo.104 Patients receiving baricitinib had a median time to recovery of 7 days, as compared with 8 days with control (rate ratio for recovery, 1.16; 95% CI 1.01 to 1.32; p=0.03), except in the subgroup of patients with a baseline NIV (including high flow oxygen) in whom median time to recovery was 10 days with the combination, as compared with 18 days with control (rate ratio for recovery, 1.51; 95% CI 1.10 to 2.08). In light of these data, the main issue that emerged during the discussion pertained to the target population in which to recommend baricitinib + remdesivir. The majority of Task Force members agreed to suggest baricitinib + remdesivir only in the subgroup of patients with a baseline NIV since the small difference in time to recovery observed in the overall cohort was felt clinically not pertinent, although statistically significant.

PtC-14: in COVID-19 there is currently insufficient evidence to recommend the use of other immunomodulators, including ruxolitinib, IVIg, convalescent plasma therapy except in Ig-deficient patients, IFN kappa, IFN beta, leflunomide, colchicine (LoE 2), sarilumab, lenzilumab, eculizumab, cyclosporine, IFN alpha (LoE 3), canakinumab (LoE 4)

Various other immunomodulatory compounds have been investigated in SARS-CoV-2 infection. However, the available evidence to date is either too scarce/conflicting, although from RCTs, as in the case of ruxolitinib, IFN beta, IFN kappa, IVIg and convalescent plasma or with too low LoE/conflicting results as in the case of sarilumab, lenzilumab, eculizumab, IFN alpha, tumour necrosis factor alpha inhibitors and canakinumab (LoE 3/4). Hence, no recommendation either in favour or against the use of these compounds in SARS-CoV-2 infection could be formulated. The group did not comment on drugs for which published literature was not available, although being in the pipeline.


These are the first EULAR-endorsed PtCs on pathophysiology and immunomodulatory therapy of SARS-CoV-2 infection. Their aim is to serve as a reference for clinicians involved in the care of people with SARS-CoV-2 infection and the use of immunomodulatory therapy as seen from the translational rheumatology perspective. They have been proposed by a rheumatology/multidisciplinary team. Since rheumatologists are the experts on inflammatory systemic diseases and on the use of immunomodulatory therapy, they should be involved in mechanistic/pathophysiological studies and in the design, conduct and interpretation of trials with immunomodulatory therapies in COVID-19.

With the OPs, we recognised that the management of SARS-CoV-2 infection, with its heterogeneous nature, requires a multifaceted approach considering viral replication, hypercoagulability and the inflammatory response, the latter of which was our specific focus. In this regard, these PtCs focus on pathophysiology and immunomodulatory treatment and the discussion leading to formulation of these PtCs was based not only on the evidence obtained by the SLR but also on the opinion of experts of inflammation and immunomodulatory therapy.

These PtCs in no way attempt to undermine local regulations or guidelines released by overarching institutions such as the WHO. Rather, they seek to provide recommendations of good practice integrating evidence-based medicine and expert opinion, which can help clinicians analysing their own therapeutic strategy and inspire changes where appropriate. It is important to emphasise that our findings do not apply to people living with rheumatic and musculoskeletal diseases (RMDs) receiving immunomodulatory treatments where a dedicated EULAR Task Force has already developed provisional recommendations for the management of people with RMDs in the context of SARS-CoV-2 pandemic.105

One major pitfall encountered in the development of these PtCs was the extremely large bulk of literature that challenged its appraisal including a surprisingly high number of articles lacking original data, thus being uninformative to the discussion. Interestingly, the narrative around ‘cytokine storm’ and its specific therapy at the start of pandemic lacked evidence so was not included in the OP or PTC in the present recommendations. The rapidly evolving COVID-19 landscape along with the ongoing release of new studies represents a major challenge, since recommendations should only be elaborated on existing published peer-reviewed literature and following robust methodological procedures. To overcome these issues, we performed hand-search work throughout the entire SLR process and TF meetings, and based these PtCs on a very recent literature update. Based on the SLR results and the inputs from the group, a research agenda was also outlined (box 1).

Box 1

Research agenda

Pathophysiology of SARS-CoV-2 infection

  • To explore in depth the abnormalities of the immune system with mechanistic studies.

  • To better characterise the associations between immune alterations and SARS-CoV2 infection stages.

  • To elucidate the actual role of type I and type II interferons across the different stages and their potential use as therapeutic agents.

  • To elucidate the principles of effective immunity in agingageing individuals, namely in the context of SARS-CoV-2 infection.

  • To perform studies with unsupervised multiparametric approaches aimed at identifying reliable biomarkers for prediction of disease outcomes and response to immunomodulatory treatment.

  • To perform genome-wide association studies in patients with SARS-CoV-2 infection and various degrees of COVID-19 severity.

  • To perform comparative studies including large cohorts of adult and paediatric patients with different degree of severe systemic inflammation and disease severity, investigating not only clinical and serological assessment but also mechanistic aspects of the immune response.

  • To explore the possibility that SARS-CoV-2 infection may induce autoimmune diseases and/or flares of known conditions.

  • To better define subsets of severe COVID-19 patients with severe systemic inflammation and the possible application of immunomodulatory therapy in this subset.

Immunomodulatory treatment of SARS-CoV-2 infection

  • To define harmonised inclusion criteria and outcomes for both randomised controlled trials investigating immunomodulatory drugs and translational studies.

  • To conduct randomised controlled trials investigating immunomodulatory drugs that to date have been explored only in studies with lower level of evidence.

  • To conduct randomised controlled trials comparing the efficacy and safety of combining glucocorticoids and other immunomodulatory agents (eg, anticytokines) versus glucocorticoids alone.

In conclusion, these EULAR PtCs provide relevant guidance on the pathophysiology of SARS-COV-2 infection, especially immunomodulatory therapy utilisation from the rheumatology perspective. Indeed, the pathophysiology with an initial viral alveolitis and subsequent immunothrombosis and available evidence points towards a central role for immunomodulatory therapy, especially glucocorticoids, in improving disease survival in severe COVID-19. These first EULAR PtCs are intended to evolve and should be updated in response to the rapid increase of knowledge about the disease and the forthcoming vaccines.



  • Handling editor Désirée van der Heijde

  • Twitter @pedrommcmachado, @ProfJohnIsaacs

  • AA and AN contributed equally.

  • Contributors All authors contributed and finally approved the current manuscript. DGM and XM share last Authorship.

  • Funding This work was funded by European League Against Rheumatism (CLI122). PMM is supported by the National Institute for Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre (BRC). JDI is a NIHR Senior Investigator and his work is supported by the NIHR Newcastle Biomedical Research Centre in Ageing and Long-Term Conditions, and the Research Into Inflammatory Arthritis Centre versus Arthritis. AVR is a member of the paediatric steering committee of RECOVERY, the steering committee of COVINTOC study and the steering committee of baricitinib in COVID-19.

  • Disclaimer The views expressed are those of the authors and not necessarily those of the (UK) National Health Service, NIHR or the Department of Health.

  • Competing interests AA, AN, HB, FC, GDM, RG, CM-C and JRC have nothing to declare. PMM has received consulting and/or speaker’s fees from Abbvie, BMS, Celgene, Eli Lilly, Janssen, MSD, Novartis, Orphazyme, Pfizer, Roche and UCB, all unrelated to this manuscript. GRB has received consulting and/or speaker’s fees from Abbvie, Gilead, Lilly, Roche, Sanofi, Pfizer all unrelated to this manuscript. IK-P has received consulting and/or speaker’s fees from Novartis, SOBI, Amgen, CHUGAI, Pfizer, LFB, Novimmune, Abbvie and PAtent for AIDAI score AVR has received speaker fees/Honoraria from Abbvie, Lilly, Roche, UCB, SOBI and Novartis all unrelated to this manuscript. DGM has received consulting and/or speaker’s fees from Abbvie, BMS, Celgene, Eli Lilly, Janssen, MSD, Novartis, Pfizer, Roche and UCB, all unrelated to this manuscript. XM has received consulting and/or speaker’s fees from BMS, Eli Lilly, Galapagos, Gilead, GSK, Janssen, Novartis, Pfizer, Servier and UCB, all unrelated to this manuscript.

  • Patient and public involvement Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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