The use of anti-inflammatory drugs in the treatment of people with severe coronavirus disease 2019 (COVID-19): The Perspectives of clinical immunologists from China
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The pandemic outbreak of coronavirus disease 2019 (COVID-19) is rapidly spreading all over the world. Reports from China showed that about 20% of patients developed severe disease, resulting in a fatality of 4%. In the past two months, we clinical immunologists participated in multi-rounds of MDT (multidiscipline team) discussion on the anti-inflammation management of critical COVID-19 patients, with our colleagues dispatched from Chinese leading PUMC Hospital to Wuhan to admit and treat the most severe patients. Here, from the perspective of clinical immunologists, we will discuss the clinical and immunological characteristics of severe patients, and summarize the current evidence and share our experience in anti-inflammation treatment, including glucocorticoids, IL-6 antagonist, JAK inhibitors and choloroquine/hydrocholoroquine, of patients with severe COVID-19 that may have an impaired immune system.
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JAK1 and JAK2 inhibitors have the potential to inhibit signaling downstream of type I interferon, interleukin-6 and other gp130 family receptors, interferon-γ, and interleukin-2, among other cytokines.
“JAK1 and JAK2 inhibitors, which are approved for the treatment of a number of autoimmune and neoplastic conditions, have the potential to inhibit signaling downstream of type I interferon, interleukin-6 (and other gp130 family receptors), interferon-γ, and interleukin-2, among other cytokines.107”
From Cytokine storm (2020) · cites this paper as [107]
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- Authors
- Zhang, W., Zhao, Y., Zhang, F., Wang, Q., Li, T., Liu, Z., Wang, J., Qin, Y., Zhang, X., Yan, X., Zeng, X., & Zhang, S.
- Affiliations
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Corresponding author
- Yan, Xiaowei
- Zeng, Xiaofeng
- Zhang, Shuyang
- ORCID
- Venue
- Clinical Immunology
- Publisher
- Elsevier BV
- Published
- 2020-05
- Volume
- 214
- Pages
- 108393
- ISSN
- 1521-6616 (ISSN-L)
- PMC
- PMC7102614
- OpenAlex
- W3012655019
- Cited by
- 1,266
- References
- 48
- Citations by year
- 2026: 7 · 2025: 15 · 2024: 57 · 2023: 93 · 2022: 167 · 2021: 364 · 2020: 561 · 2019: 1
- FWCI
- 14.00
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Clinical Immunology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Basic Research Program of China (2016YFC0901500)
- Topics
- Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory Support and Mechanisms
- Keywords
- COVID-19 pandemic, severe COVID-19, anti-inflammatory therapy, glucocorticoids, IL-6 receptor inhibitor, JAK inhibitors, chloroquine, hydroxychloroquine, immunosuppression, critically ill patients, multidisciplinary discussion
- MeSH terms
- Betacoronavirus, COVID-19, SARS-CoV-2, Interleukin-6 Inhibitors, COVID-19 Drug Treatment, Anti-Inflammatory Agents, Chloroquine, Glucocorticoids, Humans, Hydroxychloroquine, Inflammation, Pneumonia, Viral, Thrombosis, Vasculitis, Interleukin-6, Cytokines, Coronavirus Infections, Janus Kinases, Pandemics, Antibodies, Monoclonal, Humanized
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