- cross-posted to:
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- science
- cross-posted to:
- [email protected]
- science
I get sad when I see daycare/school yards full of concrete, asphalt and sand. My kindergarten had huge trees, grass, moss, bushes, boulders etc… on top of all the swings, carouselles and slides.
Just having some shrubs that a kid can crawl into will give the kids hours and hours worth of entertainment. We used to arrange the barnches in a way that there were tunnels inside the bushes and a “big” empty area in the middle.
I’m sure crawling in there made changes to my system but the biggest plus for me was just the playing. I was never on the basketball court or the ice hockey rink. I was always climbing the trees or doing shenanigans in the bushes.
Ha ha we had a forest with this enormous boulder (left there by the ice retreating like 100.000 years ago) like 8 meters tall and cracked in two so there was this grotty part between the two pieces. So fun climbing, we were there like whenever we had a chance to.
No deaths only maybe a broken bone every other year or so :-p.
From the study:
Objective
We aimed to perform the first placebo-controlled double-blinded test that investigates the effect of biodiversity on immune tolerance.
Methods
In the intervention group, children aged 3–5 years were exposed to playground sand enriched with microbially diverse soil, or in the placebo group, visually similar, but microbially poor sand colored with peat (13 participants per treatment group). Children played twice a day for 20 min in the sandbox for 14 days. Sand, skin and gut bacterial, and blood samples were taken at baseline and after 14 days. Bacterial changes were followed for 28 days. Sand, skin and gut metagenome was determined by high throughput sequencing of bacterial 16 S rRNA gene. Cytokines were measured from plasma and the frequency of blood regulatory T cells was defined as a percentage of total CD3 +CD4 + T cells.
Results
Bacterial richness (P < 0.001) and diversity (P < 0.05) were higher in the intervention than placebo sand. Skin bacterial community, including Gammaproteobacteria, shifted only in the intervention treatment to resemble the bacterial community in the enriched sand (P < 0.01). Mean change in plasma interleukin-10 (IL-10) concentration and IL-10 to IL-17A ratio supported immunoregulation in the intervention treatment compared to the placebo treatment (P = 0.02). IL-10 levels (P = 0.001) and IL-10 to IL-17A ratio (P = 0.02) were associated with Gammaproteobacterial community on the skin. The change in Treg frequencies was associated with the relative abundance of skin Thermoactinomycetaceae 1 (P = 0.002) and unclassified Alphaproteobacteria (P < 0.001). After 28 days, skin bacterial community still differed in the intervention treatment compared to baseline (P < 0.02).
Conclusions
This is the first double-blinded placebo-controlled study to show that daily exposure to microbial biodiversity is associated with immune modulation in humans. The findings support the biodiversity hypothesis of immune-mediated diseases. We conclude that environmental microbiota may contribute to child health, and that adding microbiological diversity to everyday living environment may support immunoregulation.