PMID- 36445552 OWN - NLM STAT- MEDLINE DCOM- 20230228 LR - 20230530 IS - 1568-5608 (Electronic) IS - 0925-4692 (Print) IS - 0925-4692 (Linking) VI - 31 IP - 1 DP - 2023 Feb TI - Efficacy and safety of granulocyte-macrophage colony-stimulating factor (GM-CSF) antibodies in COVID-19 patients: a meta-analysis. PG - 275-285 LID - 10.1007/s10787-022-01105-9 [doi] AB - OBJECTIVE: This study aims to determine the efficacy and safety of granulocyte-macrophage colony-stimulating factor (GM-CSF) antibodies in COVID-19 patients. METHODS: We searched Cochrane Library, PubMed, Embase, and ClinicalTrials.gov databases until July 27, 2022. Both randomized control trials (RCTs) and cohort studies were included and analyzed separately. The outcomes included mortality, incidence of invasive mechanical ventilation (IMV), ventilation improvement rate (need oxygen therapy to without oxygen therapy), secondary infection, and adverse events (AEs). The odds ratio (OR) with a 95% confidence interval (CI) was calculated by a random-effects meta-analysis model. RESULTS: Five RCTs and 2 cohort studies with 1726 COVID-19 patients were recruited (n = 866 in the GM-CSF antibody group and n = 891 in the control group). GM-CSF antibodies treatment reduced the incidence of IMV, which was supported by two cohort studies (OR 0.16; 95% CI 0.03, 0.74) and three RCTs (OR 0.62; 95% CI 0.41, 0.94). GM-CSF antibodies resulted in slight but not significant reductions in mortality (based on two cohort studies and five RCTs) and ventilation improvement (based on one cohort study and two RCTs). The sensitive analysis further showed the results of mortality and ventilation improvement rate became statistically significant when one included study was removed. Besides, GM-CSF antibodies did not increase the risks of the second infection (based on one cohort study and five RCTs) and AEs (based on five RCTs). CONCLUSION: GM-CSF antibody treatments may be an efficacious and well-tolerant way for the treatment of COVID-19. Further clinical evidence is still warranted. CI - (c) 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG. FAU - Xi, An-Ran AU - Xi AR AD - Laboratory of Rheumatology and Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Binwen Road 548, Hangzhou, 310053, Zhejiang, China. FAU - Luo, Yi-Jun AU - Luo YJ AD - Laboratory of Rheumatology and Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Binwen Road 548, Hangzhou, 310053, Zhejiang, China. FAU - Guan, Jin-Tao AU - Guan JT AD - First People's Hospital of Taizhou, Taizhou, 318020, Zhejiang, China. FAU - Wang, Wei-Jie AU - Wang WJ AD - The Second Affiliated Hospital of Zhejiang, Chinese Medical University, Hangzhou, 310053, Zhejiang, China. FAU - Xu, Zheng-Hao AU - Xu ZH AUID- ORCID: 0000-0003-0033-525X AD - Laboratory of Rheumatology and Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Binwen Road 548, Hangzhou, 310053, Zhejiang, China. xuzhenghao@zcmu.edu.cn. AD - Key Laboratory of Neuropharmacology and Translational Medicine of Zhejiang Province, Zhejiang Chinese Medical University, Hangzhou, China. xuzhenghao@zcmu.edu.cn. LA - eng GR - No. LY22H280007/Natural Science Foundation of Zhejiang/ GR - 82174005/National Natural Science Foundation of China/ GR - No. Q2019Y02/Foundation of Zhejiang Chinese Medical University/ PT - Journal Article PT - Meta-Analysis PT - Review DEP - 20221129 PL - Switzerland TA - Inflammopharmacology JT - Inflammopharmacology JID - 9112626 RN - 83869-56-1 (Granulocyte-Macrophage Colony-Stimulating Factor) RN - 143011-72-7 (Granulocyte Colony-Stimulating Factor) RN - S88TT14065 (Oxygen) SB - IM MH - Humans MH - *Granulocyte-Macrophage Colony-Stimulating Factor/adverse effects MH - Granulocyte Colony-Stimulating Factor MH - *COVID-19 MH - Oxygen PMC - PMC9707187 OTO - NOTNLM OT - Antibody OT - COVID-19 OT - Granulocyte-macrophage colony-stimulating factor OT - Meta-analysis COIS- The authors declare that there is no conflict of interest. EDAT- 2022/11/30 06:00 MHDA- 2023/03/03 06:00 PMCR- 2022/11/29 CRDT- 2022/11/29 11:20 PHST- 2022/09/20 00:00 [received] PHST- 2022/11/17 00:00 [accepted] PHST- 2022/11/30 06:00 [pubmed] PHST- 2023/03/03 06:00 [medline] PHST- 2022/11/29 11:20 [entrez] PHST- 2022/11/29 00:00 [pmc-release] AID - 10.1007/s10787-022-01105-9 [pii] AID - 1105 [pii] AID - 10.1007/s10787-022-01105-9 [doi] PST - ppublish SO - Inflammopharmacology. 2023 Feb;31(1):275-285. doi: 10.1007/s10787-022-01105-9. Epub 2022 Nov 29.