Skip to main content
Critical Care logoLink to Critical Care
letter
. 2020 Oct 9;24:603. doi: 10.1186/s13054-020-03294-7

Infliximab can reduce mortality from 35 to 14% in critically ill patients with COVID-19: perhaps some potential confounders to consider

Patrick M Honore 1,, Leonel Barreto Gutierrez 1, Luc Kugener 1, Sebastien Redant 1, Rachid Attou 1, Andrea Gallerani 1, David De Bels 1
PMCID: PMC7545152  PMID: 33036639

We read with great interest the recent article by Stallmach et al. who reported data from a small retrospective case series of patients with COVID-19 that received infliximab compared to a contemporaneous cohort that received supportive care alone [1]. Infliximab (anti-TNF) was used to target proinflammatory cytokines that are associated with deterioration of organ function and poor outcomes in patients with COVID-19 [1, 2]. The authors reported that mortality was reduced from 35% in the control group to 14% in the infliximab group [1]. We would like to make some comments. Looking at the baseline characteristics of the patients, we can see that ferritin levels in the infliximab group were almost double those in the control group (2777.4 vs 1453 μg/L) [1]. It is possible that the patients in the treated group may have had secondary hemophagocytic lymphohistiocytosis (sHLH) syndrome induced by SARS-CoV-2 [3]. The HScore, one of the tools to diagnose HLH, assigns no points to a ferritin below 2000 μg/L, while a ferritin between 2000 and 6000 μg/L adds 35 points, showing that the limit of 2000 μg/L is really crucial [3]. Due to the massive cytokine release seen in patients with the condition, HLH is considered to be a cytokine storm syndrome [3]. In potential sHLH, early use of high-dose steroids alone can be successful, consistent with the recent findings regarding the efficacy of dexamethasone in patients with severe COVID-19 receiving any form of respiratory support [4]. Other drugs such as infliximab may be life-saving in this group of patients. In conclusion, on the basis of the difference in ferritin levels between the two groups and the potential diagnosis of sHLH, the two groups in this study are not well matched [3]. A diagnosis of sHLH could explain the enormous cytokine storm responding so well to infliximab [1] and may also explain why dexamethasone is so effective in patients with severe COVID-19 [4]. The sHLH-cytokine storm may be the main reason for the rapid deterioration seen in patients with COVID-19 [3]. It is advisable to measure baseline ferritin before starting any immunological treatment in order to improve the efficacy [5].

Acknowledgements

None.

Abbreviations

TNF

Tumor necrosis factor

IL-6

Interleukin-6

sHLH

Secondary hemophagocytic lymphohistiocytosis

HS

Hematophagocytic syndrome score

Authors’ contributions

PMH, SR, and DDB designed the paper. All authors participated in drafting and reviewing. The authors read and approved the final version of the manuscript.

Funding

None.

Availability of data and materials

Not applicable.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare to have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Patrick M. Honore, Email: Patrick.Honore@CHU-Brugmann.be

Leonel Barreto Gutierrez, Email: Leonel.BarretoGutierrez@chu-brugmann.be.

Luc Kugener, Email: Luc.Kugener@CHU-Brugmann.be.

Sebastien Redant, Email: Sebastien.Redant@CHU-Brugmann.be.

Rachid Attou, Email: Rachid.Attou@CHU-Brugmann.be.

Andrea Gallerani, Email: Andrea.Gallerani@CHU-Brugmann.be.

David De Bels, Email: David.DeBels@CHU-Brugmann.be.

References

  • 1.Stallmach A, Kortgen A, Gonnert F, Coldewey SM, Reuken P, Bauer M. Infliximab against severe COVID-19-induced cytokine storm syndrome with organ failure-a cautionary case series. Crit Care. 2020;24(1):444. doi: 10.1186/s13054-020-03158-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Liu J, Li S, Liu J, Liang B, Wang X, Wang H, et al. Longitudinal characteristics of lymphocyte responses and cytokine profiles in the peripheral blood of SARS-CoV-2 infected patients. EBioMedicine. 2020;55:102763. doi: 10.1016/j.ebiom.2020.102763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Soy M, Atagündüz P, Atagündüz I, Sucak GT. Hemophagocytic lymphohistiocytosis: a review inspired by the COVID-19 pandemic. Rheumatol Int. 2020:1–12. 10.1007/s00296-020-04636-y. [DOI] [PMC free article] [PubMed]
  • 4.The RECOVERY Collaborative Group. Dexamethasone in hospitalized patients with COVID-19 - preliminary report. N Engl J Med. 2020. 10.1056/NEJMoa2021436.
  • 5.Grangé S, Buchonnet G, Besnier E, Artaud-Macari E, Beduneau G, Carpentier D, et al. The use of ferritin to identify critically ill patients with secondary hemophagocytic lymphohistiocytosis. Crit Care Med. 2016;44(11):e1045–e1053. doi: 10.1097/CCM.0000000000001878. [DOI] [PubMed] [Google Scholar]
  • 6.George Dimopoulos et al. Favorable anakinra responses in severe COVID-19 patients with secondary hemophagocytic lymphohistiocytosis. Cell Host Microbe 2020;28(1):117–123.e1. doi: 10.1016/j.chom.2020.05.007. Epub 2020 May 14. [DOI] [PMC free article] [PubMed]
  • 7.Mehta P, McAuley DF, Brown M, et al. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet. 2020;395(10229):1033–1034. doi: 10.1016/S0140-6736(20)30628-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Shrestha GS, Paneru HR, Vincent J. Precision medicine for COVID-19: a call for better clinical trials. Crit Care. 2020;24:282. doi: 10.1186/s13054-020-03002-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
Crit Care. 2020 Oct 9;24:603.

Authors’ response

Andreas Stallmach 2, Andreas Kortgen 3, Falk Gonnert 4, Sina M Coldewey 3,5,6, Philipp Reuken 2, Michael Bauer 3,6

To the editor:

We thank Dr. Honore and colleagues for their thoughtful comments pointing towards a potential secondary hemophagocytic lymphohistocytosis (sHLH) characterized by pancytopenia, hyper-coagulation, acute kidney injury, and hepatobiliary dysfunction associated with COVID-19. Based on their suggestion, we applied the hemophagocytosis score (HScore) and obtained a median Hscore of 171 (136;186) for IFX-treated patients and 136 (77; 182) for controls (p = 0.393) reflecting that some but not all of the patients fulfilled the HScore criterium of sHLH, i.e., a score above 169. Nevertheless, all of the patients displayed a profound inflammatory state in particular in the IFX-treated patients, reflecting the experimental therapeutic approach. A recent proposal by a panel of experts suggested to screen all patients with severe COVID-19 both for a hyperinflammatory state using laboratory tests (e.g., ferritin, decreased platelet count or erythrocyte sedimentation rate) and for the HScore to identify the subgroup of patients for whom immunosuppressive therapies (e.g., infliximab or anakinra [6]) could improve outcome [7]. Whether severe COVID-19 indeed reflects a form of sHLH is still a matter of controversy; however, the evidence to support antiinflammatory interventions in the most severe cases is meanwhile supported by prospective randomized evidence for dexamethasone [4]. Though, research addressing the optimum immune modulating drug, e.g., depending on the severity of the cytokine response, is warranted [8].

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Data Availability Statement

    Not applicable.


    Articles from Critical Care are provided here courtesy of BMC

    RESOURCES