Anti-IL-17 monoclonal antibodies in hospitalized patients with severe COVID-19: A pilot study.
Anti-IL-17 monoclonal antibodies in hospitalized patients with severe COVID-19: A pilot study.
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DOI:
10.1016/j.cyto.2021.155627
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发表时间:
2021-10
期刊:
影响因子:
3.8
通讯作者:
Shmidt AE
中科院分区:
文献类型:
--
作者:
Avdeev SN;Trushenko NV;Tsareva NA;Yaroshetskiy AI;Merzhoeva ZM;Nuralieva GS;Nekludova GV;Chikina SY;Gneusheva TY;Suvorova OA;Shmidt AE
One of the main pathophysiological mechanisms underlying the severe course of COVID-19 is the hyper-inflammatory syndrome associated with progressive damage of lung tissue and multi-organ dysfunction. IL-17 has been suggested to be involved in hyper-inflammatory syndrome. To evaluate the efficacy and safety of the IL-17 inhibitor netakimab in patients with severe COVID-19. Study design. In our retrospective case-control study we evaluated the efficacy of netakimab in hospitalized patients with severe COVID-19 outside the intensive care unit (ICU). Patients in the experimental group were treated with standard of care therapy and netakimab at a dose of 120 mg subcutaneously. 171 patients with severe COVID-19 were enrolled in our study, and 88 of them received netakimab. On the 3 day of therapy, body temperature, SpO2/FiO2, NEWS2 score, and CRP improved significantly in the netakimab group compared to the control group. Other clinical outcomes such as transfer to ICU (11.4% vs 9.6%), need for mechanical ventilation (10.2% vs 9.6%), 28-day mortality (10.2% vs 8.4%), did not differ between the groups. In hospitalized patients with severe COVID-19, anti-IL-17 therapy might mitigate the inflammatory response and improve oxygenation, but do not affect the need for mechanical ventilation and mortality.
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DOI:
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影响因子:
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