Effect of degalactosylated bovine glycoprotein formulations MAF and M сapsules on lymphopenia and clinical outcomes in hospitalized COVID-19 patients: a randomized clinical trial

dc.contributor.authorGavrylov, Anatoliy
dc.contributor.authorInui, Toshio
dc.contributor.authorKruglova, Oksana
dc.contributor.authorMartynenko, Olga
dc.contributor.authorMartynenk, Kostiantyn
dc.contributor.authorTieroshyn, Vadym
dc.contributor.authorKubo, Kentaro
dc.contributor.authorYamakage, Hajime
dc.contributor.authorKutsyn, Borys
dc.contributor.authorKubashko, Alla
dc.contributor.authorVeklych, Zoryana
dc.contributor.authorTerashima, Yurika
dc.contributor.authorMette, Martin
dc.contributor.authorKutsyna, Galyna
dc.date.accessioned2024-06-05T09:28:02Z
dc.date.available2024-06-05T09:28:02Z
dc.date.issued2024-05
dc.description.abstractBackground Targeting mucosal immunity of the gut, which is known to provide antigen processing, while avoiding excessive or unnecessary inflammation, was tested as a way to modulate COVID-19 severity. Methods Randomized open-label trial in 204 adults hospitalized with non-critical COVID-19 who received for 14 days in addition to standard of care (SOC) degalactosylated bovine glycoproteins formulations of either MAF capsules (MAF group) or M capsules (M group) or SOC only (control group). Results Median recovery time when patients did not require supplemental oxygen was 6 days in both study groups compared to 9 days in the control (MAF vs. control; P=0.020 and M vs. control; P=0.004). A greater reduction in mortality was seen in the MAF group compared to the control by day 14 (8.3% vs. 1.6%; P=0.121) and by day 29 (15.3% vs. 3.2%; P=0.020), and similarly in the M group by day 14 (8.3% vs. 2.9%; P=0.276) and by day 29 (15.3% vs. 2.9%; P=0.017). The proportion of those who had baseline absolute lymphocyte count (ALC) lower than 0.8×109 /L was 13/63 (20.6%), 17/69 (24.6%), and 18/72 (25.0%) of patients in MAF, M, and control group respectively. Day 29 mortality among these lymphopenic patients was three times higher than for the intent-to-treat population (21% vs. 7%) and consisted in above subgroups: 2/13 (15%), 2/17 (12%), and 6/18 (33%) of patients. The decreased mortality in both study subgroups correlated with greater ALC restoration above 0.8×109/L level seen on day 14 in 91% (11/12) and 87.5% (14/16) of survivors in MAF and M subgroups respectively compared to 53.3% (8/15) of survivors in control subgroup. Incidences of any ALC decrease below the baseline level on day 14 occurred in 25.4% of patients in the MAF group and 29.0% of patients in the M group compared to 45.8% in control and ALC depletion by ≥50% from the baseline level consisted of 7.9%, 5.8%, and 15.3% of cases in these groups respectively. Conclusion This study showed that both study agents prevented ALC depletion and accelerated its restoration, which is believed to be one of the mechanisms of improved crucial clinical outcomes in hospitalized COVID-19 patients.en_US
dc.identifier.citationEffect of degalactosylated bovine glycoprotein formulations MAF and M сapsules on lymphopenia and clinical outcomes in hospitalized COVID-19 patients: a randomized clinical trial / T. Inui, O. Kruglova, O. Martynenko [et al.] // BMC Infectious Diseases. ─ 2024. ─ Vol. 24. ─ P. 519─535.en_US
dc.identifier.urihttps://repo.knmu.edu.ua/handle/123456789/33933
dc.language.isoen_USen_US
dc.subjectCOVID-19 treatmenten_US
dc.subjectsaisei MAF capsulesen_US
dc.subjectsaisei M capsulesen_US
dc.subjectlymphopeniaen_US
dc.subjectmortalityen_US
dc.subjectmucosal immunityen_US
dc.subject2024аen_US
dc.titleEffect of degalactosylated bovine glycoprotein formulations MAF and M сapsules on lymphopenia and clinical outcomes in hospitalized COVID-19 patients: a randomized clinical trialen_US
dc.typeArticleen_US

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