Chambers, RC

Dagna, L

Mehta, P

English

UCL Discovery

  Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website.  Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.  Commentwww.thelancet.com/rheumatology   Published online March 17, 2021   https://doi.org/10.1016/S2665-9913(21)00078-3 1Lancet Rheumatol 2021Published Online March 17, 2021 https://doi.org/10.1016/ S2665-9913(21)00078-3See Online/Articles https://doi.org/10.1016/ S2665-9913(21)00070-9Granulocyte-macrophage colony stimulating factor in COVID-19: friend or foe?A biphasic model of COVID-19 is now well-established, with an initial viraemic phase, followed by a host hyperinflammatory phase in a subgroup of patients with an inappropriate, excessive immune response associated with high mortality, which might respond to immunomodulatory therapy.1 Randomised controlled trials (eg, RECOVERY and REMAP-CAP) have shown the efficacy of corticosteroids2 and interleukin (IL)-6 blockade in reducing mortality in patients with severe COVID-19, although there have been mixed results with IL-6 inhibition.3 Granulocyte-macrophage colony stimulating factor (GM-CSF) is an immunoregulatory cytokine that exemplifies the complexity and challenges of drug trials in COVID-19, given its role in both the pro-inflammatory hyper cytokinaemia leading to monocyte and macro-phage activation, and in antiviral immunity. There is rationale for both therapeutic blockade and recombinant administration of GM-CSF,4,5 and there is accumulating evidence for targeting GM-CSF in patients with severe COVID-19. Bronchoalveolar lavage fluid analysis from patients with severe COVID-19 has shown clonally expanded tissue-resident memory-like Th17 cells with a potentially pathogenic profile of cytokine expression of GM-CSF and IL-17A; these memory-like Th17 cells are thought to interact with lung macrophages and cytotoxic CD8+ T cells, and are associated with disease severity and lung damage.6 High GM-CSF protein concentrations in the serum of patients with COVID-19 is associated with a more severe clinical course.6 Additionally, inhibiting GM-CSF might have advantages over targeting IL-6 with respect to safety, because there might be less pronounced pharmacodynamic suppression of C-reactive protein and fever, which can facilitate the detection of secondary infection. Cohort studies have shown an efficacy signal for drugs targeting GM-CSF (lenzilumab)7 or its receptor (mavrilimumab),8 but robust controlled trial data have been eagerly anticipated. In The Lancet Rheumatology, Paul Cremer and colleagues9 report the results of their double-blind, randomised trial of mavrilimumab in patients with severe COVID-19 pneumonia and systemic hyperinflammation (MASH-COVID). The study did not meet the primary endpoint (ie, proportion of patients free of supplemental oxygen support at day 14), which might be due to several factors, the smaller-than-planned sample size being probably the most important. Due to the slow recruitment rate, the study was terminated after enrolment of 20 patients per treatment group, instead of the 30 per group estimated to be needed based on preliminary case-control data. The study design has a badge of rigour that accompanies a double-blind, placebo-controlled trial (which is challenging in the COVID-19 pandemic). However, although the intended population was patients with severe COVID-19 pneumonia with hyperinflammation, enrolled patients probably had mild to moderate COVID-19 pneumonia with hypoxaemia (receipt of invasive mechanical ventilation was excluded) and a threshold C-reactive protein concentration of more than 5 mg/dL (ie, 50 mg/L), which might be set too low to identify a subgroup of patients with hyperinflammation.The efficacy of mavrilimumab might have also been masked by the heterogeneity of concomitant, permitted medications. Before random assignment, 26 (65%) of 40 patients were treated with corticosteroids and 30 (75%) patients were treated with remdesivir.9 After random assignment, an additional five patients were started on corticosteroids, ten patients received convalescent plasma, three patients received remdesivir, and two patients received tocilizumab.9 Although it seems that these additional medications had no significant influence on the primary and secondary outcomes, the actual contribution of all concomitant (especially when combined) and previous therapies is difficult to unpick and might confer potential confounding. Furthermore, patients were enrolled between May and September, 2020 (after the first COVID-19 surge), and standard of care definitions changed over time by virtue of the accrual of clinical experience, improved supportive care, and advances in background therapies. The changing standard of care in the placebo group could partially explain the finding that more patients than expected in this group were no longer in receipt of supplemental oxygen by day 14, and consequently the risk reduction with Comment2 www.thelancet.com/rheumatology   Published online March 17, 2021   https://doi.org/10.1016/S2665-9913(21)00078-3mavrilimumab was lower than predicted. Despite the negative primary outcome, patients who received mavrilimumab were numerically more likely to be alive and without respiratory failure by day 28, consistent at day 60 of follow-up, which might be more relevant clinical endpoints. Reassuringly, the adverse event rate was similar between the groups.The potential benefits of targeting GM-CSF in the context of a virally driven illness need to be carefully balanced with the potential risk associated with blocking the role of this cytokine in tissue homoeostasis, including maintenance of alveolar capillary barrier integrity, host defence (antiviral immunity), and epithelial repair. In February, 2021, there were two press releases describing two opposing therapeutic approaches in COVID-19. One was a phase 2 trial (OSCAR) of the anti-GM-CSF antibody otilimab, which did not meet the primary endpoint but supported the approach of blocking GM-CSF in a prespecified subgroup analysis of patients older than 70 years. The second was a clinical trial administering inhaled or intravenous recombinant GM-CSF (sargramostim), which did meet the primary endpoint of improvement oxygenation levels. The full publications of these trial findings following peer-review are awaited, and we agree with Cremer and colleagues that the results of the current study support further investigation in larger randomised controlled trials.9 It is likely that, analogous to other cytokine inhibitors,10 the value of therapies targeting (or perhaps even supplementing) the GM-CSF axis is likely to depend on patient selection and timing of intervention in the disease course.PM is a clinical training fellow with the Experimental Medicine Initiative to Explore New Therapies Consortium (EMINENT; funded by the Medical Research Council [MRC] and GlaxoSmithKline), with project funding outside the For the otilimab press release see https://www.gsk.com/en-gb/media/press-releases/gsk-announces-otilimab-data-for-treatment-of-covid-19 For the sargramostim press release see https://www.prnewswire.com/news-releases/sarpac-clinical-trial-of-leukine-sargramostim-rhu-gm-csf-in-hospitalized-covid-19-patients-meets-primary-endpoint-of-significant-improvement-in-lung-function-301236275.html submitted work; receives cofunding by the National Institute for Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre, outside the submitted work; and has received consultancy fees from Swedish Orphan Biovitrum (SOBI) outside the submitted work. RCC has received grant funding from UK Research and Innovation MRC and NIHR ULCH Biomedical Research Centre, and institutional research collaboration funding from GlaxoSmithKline, during the conduct of the study. LD has received consultancy fees from GlaxoSmithKline, Roche, SOBI, and Sanofi, outside the submitted work. Puja Mehta, Rachel C Chambers, *Lorenzo Dagnadagna.lorenzo@unisr.itCentre for Inflammation and Tissue Repair, Division of Medicine, University College London, London, UK (PM, RCC); Department of Rheumatology, University College London Hospital NHS Trust, London, UK (PM); Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Milan 20132, Italy (LD); Vita-Salute San Raffaele University, Milan, Italy (LD) 1 Mehta P, McAuley DF, Brown M, Sanchez E, Tattersall RS, Manson JJ. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet 2020; 395: 1033–34. 2 Sterne JAC, Murthy S, Diaz JV, et al. Association between administration of systemic corticosteroids and mortality among critically ill patients with COVID-19: a meta-analysis. JAMA 2020; 324: 1330–41. 3 Rubin EJ, Longo DL, Baden LR. Interleukin-6 receptor inhibition in COVID-19—cooling the inflammatory soup. N Engl J Med 2021; published online Feb 25. https://doi.org/10.1056/NEJMe2103108. 4 Mehta P, Porter JC, Manson JJ, et al. Therapeutic blockade of granulocyte macrophage colony-stimulating factor in COVID-19-associated hyperinflammation: opportunities and challenges. Lancet Respir Med 2020; 8: 822–30.5 Bonaventura A, Vecchié A, Wang TS, et al. Targeting GM-CSF in COVID-19 pneumonia: rationale and strategies. Front Immunol 2020; 11: 1625. 6 Zhao Y, Kilian C, Turner J-E, et al. Clonal expansion and activation of tissue-resident memory-like Th17 cells expressing GM-CSF in the lungs of severe COVID-19 patients. Sci Immunol 2021; 6: eabf6692.7 Temesgen Z, Assi M, Shweta FNU, et al. GM-CSF neutralization with lenzilumab in severe COVID-19 pneumonia: a case-cohort study. Mayo Clin Proc 2020; 95: 2382–94. 8 De Luca G, Cavalli G, Campochiaro C, et al. GM-CSF blockade with mavrilimumab in severe COVID-19 pneumonia and systemic hyperinflammation: a single-centre, prospective cohort study. Lancet Rheumatol 2020; 2: e465–73. 9 Cremer PC, Abbate A, Hudock K, et al. Mavrilimumab in patients with severe COVID-19 pneumonia and systemic hyperinflammation (MASH-COVID): an investigator initiated, multicentre, double-blind, randomised, placebo-controlled trial. Lancet Rheumatol 2021; published online March 17. https://doi.org/10.1016/S2665-9913(21)00070-9.10 Cavalli G, Dagna L. The right place for IL-1 inhibition in COVID-19. Lancet Respir Med 2021; 9: 223–24.

Granulocyte-macrophage colony stimulating factor in COVID-19: friend or foe?

https://discovery.ucl.ac.uk/10125696/1/Granulocyte-macrophage%20colony%20stimulating%20factor%20in%20COVID-19%20friend%20or%20foe.pdf

Granulocyte-macrophage colony stimulating factor in COVID-19: friend or foe?

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