Table 1. Antiviral effects of different immunobiotics used in clinical studies.
Immunobiotics | Experimental Challenge | Study population | Study design | Antiviral outcomes | Ref |
Lactobacillusrhamnosus GG | COVID-19 infection | 1132 subjects tested positive for COVID-19 | Double-blinded, randomised, placebo-controlled trial. Daily oral administration of LGG or placebo 28 days |
Reduction of secondary infection and moderation of immunity in patients | [52] |
Bifidobacterium, Lactobacillus, Enterococcus and Bacillus | COVID-19 infection | 311 patientsAge ≥ 18 years | Single-center retrospective analysis 1.5 g (tablet) 28 days |
Reduction of severity of disease and associated with beneficial changes in gut microbiome composition | [53] |
Lactiplantibacillus plantarum KABP022, KABP023, KAPB033, Pediococcus acidilactici KABP021 | COVID-19 infection | 300 adult Covid19 outpatients Media age: 37 years |
Single-center, quadruple-blinded, randomized trial 2 × 109 CFU/day or placebo 30 days |
Reduction of nasopharyngeal viral load, lung infiltrates Increase of specific IgM and IgG level |
[54] |
Bifidobacterium longum Lactobacillus bulgaricus Streptococcus thermophilus | COVID-19 infection | 156 patients | Randomized controlled trial 4 x 0.5 × 106 CFU, 3 times a day | Significant decrease of time to achieving a negative nucleic acid test and inflammation indexes | [55] |
Bifidobacteria strains, galactooligosaccharides xylooligosaccharide, resistant dextrin | COVID-19 infection | 55 patients Age ≥ 18 years | Open-label, proof-of-concept study 10 x 1011 CFU/day 28 days |
Significant reduction in pro-inflammatory markers (IL-6, MCP-1, M-CSF, TNF-α and IL-1RA) compared with controls | [56] |
Heat-killed Pediococcus acidilactici K15 | Viral respiratory tract infections | 172 children Age 3–6 years | Randomized, double-blind, placebo-controlled 5 × 1010 bacteria4 months |
Duration of a fever significantly decreased sIgA level significantly higher | [57] |
Lactiplantibacillus plantarum HEAL9 and Lacticaseibacillus paracasei 8700:2 | Common colds | 448 Age 18–70 years | Double-blind study 109 CFU/day 12 weeks |
Reduction of symptom severity IFN-γ production enhancement |
[58] |
Bacillus spores (LiveSpo Navax) | Acute respiratory tract infections | 46 children | Nasal-spraying of spores 5 × 109 spores 6 days |
Symptoms improvement Reduction of load and level of pro-inflammatory cytokines | [59] |
Bifidobacterium animalis subsp. lactis Bl-04 (1) | Respiratory and gastro intestinal infections | 241 males; age 35 years and 224 females; age 36 years | Randomized double-blind placebo-controlled trial. 2.0 × 109 CFU/day 3–4 months |
Significant decrease in respiratory illness episode compared to placebo. | [60] |
Lactobacillus plantarum HEAL9 and Lactobacillus paracasei 8700:2 | Common cold | 131 childrenAge 1–6 years | Randomized, double blind placebo-controlled trial. 109 CFU/day 3 months |
Significant decrease of symptom severity | [61] |
Loigolactobacillus coryniformis K8 CECT 5711 | Immune response generated by the COVID-19 mRNA vaccine | 200 subjects > 60 years | Randomized, placebo-controlled, double-blind trial 3 months |
Levels of IgG were significantly higher | [62] |
Lactobacillus rhamnosus HN001 | Acute respiratory infections | 398 children Age 1–5 years | Double-blind placebo-controlled trial. 1010 CFU/day 3 months |
High level of Lactobacillus Significant increase of sIgA levels in treated group | [63] |
Saccharomyces cerevisiae | Cold and flu-like symptoms | 116 subjects 57% femalesAge 18–94 years | Randomized double-blind placebo-controlled trial 500 mg (dried)/day 12-week |
Significant decrease in incidence, no significant reduction in duration, no impact on severity of illness | [64] |