Vaccination reduces viral load and accelerates viral clearance in SARS-CoV-2 Delta variant-infected patients.
Vaccination reduces viral load and accelerates viral clearance in SARS-CoV-2 Delta variant-infected patients.
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DOI:
10.1080/07853890.2023.2166681
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发表时间:
2023-12
影响因子:
4.4
通讯作者:
中科院分区:
文献类型:
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作者:
The purpose of this study was to investigate vaccine effectiveness in relieving symptoms in patients with the SARS-CoV-2 delta (B.1.617.2) variant. In this retrospective study, 31 patients did not receive any vaccine (non-vaccination, NV), 21 patients received 1-dose of inactivated vaccine (one-dose vaccination, OV), and 60 patients received at least 2-dose inactivated vaccine (two-dose vaccination, TV). The baseline data, clinical outcomes and vaccination information were collected and analyzed. Patients in the OV group were younger than those in the other two groups (p = 0.001), but there was no significant difference in any of the other baseline data among the three groups. The TV group showed higher IgG antibody levels and cycle threshold values of SARS-CoV-2 than the NV and OV groups (p < 0.01), and time to peak viral load was shorter in the TV group (3.5 ± 2.3 d) than in the NV (4.8 ± 2.8 d) and OV groups (4.8 ± 2.9 d, p = 0.03). The patients in the TV group (18%) showed a higher recovery rate without drug therapy (p < 0.001). Viral clearance time and hospital stay were significantly shorter in the TV group than in the NV and OV groups (p < 0.01), and there were no significant differences in these parameters between the OV and NV groups, but IgG values were higher in the OV group (p = 0.025). No severe complications occurred in this study. In this study, our results shows that two-dose vaccination can reduce viral loads and accelerate viral clearance, and two-dose vaccination enhance the protection of IgG antibodies in vivo; however, one-dose vaccination did not confer protective effectiveness. Our results suggest that 2-dose vaccination can reduce viral load and accelerate viral clearance in patients with the delta variant and enhance the protection afforded by IgG antibodies in vivo.
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影响因子:
82.9
作者:
Levine-Tiefenbrun, Matan;Yelin, Idan;Kishony, Roy
通讯作者:
Kishony, Roy
DOI:
10.1016/j.ijid.2021.03.083
发表时间:
2021-05
期刊:
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
影响因子:
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作者:
Trachootham D;Thongyen S;Lam-Ubol A;Chotechuang N;Pongpirul W;Prasithsirikul W
通讯作者:
Prasithsirikul W
影响因子:
8.1
作者:
Ward MP;Liu Y;Xiao S;Zhang Z
通讯作者:
Zhang Z
影响因子:
5.5
作者:
Raman R;Patel KJ;Ranjan K
通讯作者:
Ranjan K
DOI:
10.1111/ajt.16641
发表时间:
2022-01
期刊:
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
影响因子:
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作者:
通讯作者:
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