Tα1 |
269/317 |
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▪
The level of NLR increased
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▪
Patients with severe COVID-19 are not suitable for the treatment of glucocorticoid, immunoglobulin, thymosin, and ammonium glycyrrhizinate
|
2022 [76] |
306/1026 |
-
▪
Tα1 use in COVID-19 was associated with poor clinical outcomes
-
▪
Tα1 use at a later stage was significantly associated with a higher non-recovery rate than Tα1 use at an earlier stage
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▪
The duration to use Tα1 had a less significant effect on recovery rate
|
2021 [74] |
126/275 |
|
2021 [71] |
232/1388 |
|
2021 [68] |
27/47 |
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▪
The reduction rate of complement C3 level and C-reactive protein level was higher than that of the control group (p = 0.01, 0.04), but it has no obvious positive effect on virus elimination
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▪
Continuous monitoring of complement C3 levels and nucleic acid load are helpful for early assessment of discharge indications
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▪
The immune system is closely related to the severity of COVID-19 and clinical outcomes
|
2021 [77] |
327/771 |
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▪
The treatment of Tα1 was not associated with a difference in 28-day mortality in patients with COVID-19 after adjustment for baseline confounders
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▪
Subgroup analysis and phenotype analysis did not show benefits in 28-day mortality with Tα1 therapy
|
2021 [75] |
78/127 |
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▪
The male patients in the treatment group showed higher CRP and IL-6 levels after treatment, but the PCT level decreased significantly
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▪
Gender differences may be a factor in sustaining the immunity respond of COVID-19 to Tα1
|
2020 [76] |
36/76 |
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▪
Tα1 supplement significantly reduce mortality of severe COVID-19 patients
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▪
COVID-19 patients with counts of CD8+ T cells or CD4+ T cells in circulation lower than 400/μL or 650/μL, respectively, gain more benefits from Tα1
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▪
Tα1 reverses T cell exhaustion and recovers immune reconstitution through promoting thymus output during SARS-CoV-2 infection
|
2020 [70] |
102/334 |
|
2020 [78] |