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. 2022 Jul 14;10(7):1428. doi: 10.3390/microorganisms10071428

Table 2.

Murine models and clinical trials on the use of probiotics in AD.

Study Model Treatment Effect Ref.
Dust-mite-induced AD in NC⁄Nga mice Lactiplantibacillus plantarum CJLP55, CJLP133 and CJLP136 Decrease in AD-like skin lesions, IgE levels, eosinophil and mast cell infiltration, and IL-4 and IL-5 production; increase in IL-10 and IFN-γ and Treg cells [153]
Ovalbumin-induced AD in SKH-1/Hr mice Lacticaseibacillus rhamnosus Lcr35® Decrease in AD-like skin lesions, IgE levels, inflammatory cell infiltration, and IL-4 and TSLP production; increase in Treg cells [152]
Dust-mite-induced AD in NC⁄Nga mice Lacticaseibacillus rhamnosus IDCC32 tyndallized Improvement in AD symptoms and decrease in mast cell infiltration, IgE levels, and IL-4 production [154]
DCNB-induced AD in NC⁄ Nga mice Faecalibacterium prausnitzii EB-FPDK11 and Akkermansia muciniphila EB-AMDK19 Improvement in AD symptoms, skin lesions, and Th1/Th2 ratio; decrease in IgE levels, eosinophil and mast cell infiltration, and IL-4 and TSLP production; increase in filaggrin, ZO-1, and claudin-1 [155]
DNFB-induced AD in C57BL/6 mice Bifidobacterium longum CCFM1029 Increased indole-3-carbaldehyde production. Inhibition of Th2 immune response; decreased TSLP, IL-4, and IL-5 production [156]
Randomized, double-blind, placebo-controlled trial in pregnant women and infants Lacticaseibacillus rhamnosus GG, Lacticaseibacillus rhamnosus LC705, Bifidobacterium breve Bb99, and Propionibacterium freudenreichii subsp.
shermanii JS
Prevention of AD development [150]
Randomized, double-blind, placebo-controlled trial in pregnant women Bifidobacterium bifidum BGN4, Bifidobacterium lactis AD011, and Lactobacillus acidophilus AD031 Prevention of AD development [151]
Randomized, double-blind trial in neonates Lacticaseibacillus rhamnosus LCS-742 and Bifidobacterium longum subsp. infantis M63 Prevention of AD development [149]
Cohort of pregnant women and infants Probiotic milk containing Lactobacillus acidophilus LA-5, Bifidobacterium lactis Bb12, and Lacticaseibacillus rhamnosus GG Reduction in AD incidence [147]
Open trial in pregnant women and infants Bifidobacterium breve M-16V and Bifidobacterium longum BB536 Prevention of AD development [148]
Randomized, double-blind, placebo-controlled trial in AD patients Ligilactobacillus salivarius LS01 and Bifidobacterium breve BR03 Improvement in AD symptoms and in Th17/Treg and Th1/Th2 ratios; reduction in microbial translocation and immune activation [160]
Randomized, double-blind, placebo-controlled trial in children with AD Lacticaseibacillus rhamnosus IDCC32 tyndallized Improvement in AD symptoms; decrease in eosinophil cationic protein and IL-31 [162]
Randomized, double-blind, placebo-controlled trial in children with AD Bifidobacterium animalis subsp. lactis CECT 8145, Bifidobacterium longum CECT 7347, and Lacticaseibacillus casei CECT 9104 Improvement in AD symptoms [158]
Randomized, double-blind, placebo-controlled trial in AD patients Lactiplantibacillus plantarum PBS067, Limosilactobacillus reuteri PBS072, and Lacticaseibacillus rhamnosus LRH020 Improvement in AD symptoms; decrease in TNFα, TSLP, and CCL17 levels [159]
Randomized, double-blind, placebo-controlled trial in AD patients Bifidobacterium longum CCFM1029 Improvement in AD symptoms; increased indole-3-carbaldehyde production; decreased IgE levels [156]