Benefits
Common Cold Incidence (Borderline, Manufacturer-Funded)
In a 12-week trial of 199 healthy adults (4.5 g/day), the primary outcome of common cold incidence was not statistically significant (p = 0.055); a secondary count, the number of participants who caught a cold, was significantly lower on ResistAid (p = 0.038). Symptom severity at episode onset was actually higher on ResistAid. The trial was funded by the manufacturer, and no effect on influenza has been shown.
Vaccine Antibody Response (Selective, Surrogate)
In a 45-person pilot trial, ResistAid raised the IgG response to the pneumococcal vaccine for only 2 of 7 tested subtypes (18C and 23F); the other five were not significant. In a separate 75-person trial it raised tetanus IgG at 1.5 g/day but not at the higher 4.5 g/day dose, and had no effect on influenza antibodies. Both trials were manufacturer-funded and measured antibody titers, not fewer infections.
Gut Microbiome Modulation
In a 30-person crossover trial (15 g/day for 6 weeks) the fecal Firmicutes-to-Bacteroidetes ratio fell; Bifidobacterium only tended to increase and overall microbial diversity decreased. Lactobacillus was not shown to rise. The trial was manufacturer-funded and measured microbiome composition, not a clinical gut outcome.
NK Cell Activity (Proposed Mechanism, Not Shown in Trials)
Natural killer cell activation is a proposed mechanism from laboratory studies. In the human ResistAid vaccine trial the innate immune markers that were measured (white blood cell count, inflammatory cytokines, complement) did not change, so this remains a mechanism rather than a demonstrated human effect.
Sustainable Larch Source
Larch arabinogalactan extracted from sustainably-sourced North American larch chips using water-based extraction (no chemical solvents). Clean-label positioning.
Soluble Fiber / Prebiotic
ResistAid is a soluble fiber that bypasses upper GI digestion; fermented in the colon to produce short-chain fatty acids (in the human ResistAid trial the specific profile did not show a butyrate increase, and some minor fecal fatty acids fell).
Mechanism of action
Innate Immune Activation
Arabinogalactan binds to immune cell receptors; activates macrophages, dendritic cells, NK cells; enhances first-line immune response.
Adaptive Immune Support
ResistAid enhances B-cell antibody production — improved adaptive immune response to pathogens and vaccines.
Prebiotic Fermentation
Soluble fiber resists upper GI digestion; fermented in colon by beneficial bacteria; produces short-chain fatty acids supporting gut barrier and gut-immune axis.
Gut Microbiome Modulation
Selective stimulation of beneficial bacteria (Bifidobacterium, Lactobacillus); shifts microbiome composition toward healthier profile.
Larch Source Distinction
Larch arabinogalactan distinct from acacia gum arabic — different polysaccharide structure; specific immune evidence base.
Clinical trials
Clinical trial of ResistAid 4.5 g/day for 12 weeks during cold season in healthy adults.
199 healthy adults during cold season.
Common cold incidence, the primary outcome, was not statistically significant (p = 0.055); the number of participants affected by a cold was significantly lower on ResistAid (p = 0.038), significant in the per-protocol set. Symptom severity at onset was higher on ResistAid. Manufacturer-funded.
Clinical trial of ResistAid effects on pneumococcal vaccine antibody response.
Adults receiving pneumococcal vaccine.
IgG response to the 23-valent pneumococcal vaccine was significantly greater on ResistAid for 2 of 7 subtypes (18C and 23F); the other five subtypes and salivary IgA were not significant. An antibody-titer surrogate, not fewer infections. Manufacturer-funded pilot (n=45).
Randomized double-blind crossover trial (n=30) of ResistAid 15 g/day for 6 weeks on fecal microbiome composition and short-chain fatty acids in healthy adults.
Healthy adults.
At 15 g/day for 6 weeks the fecal Firmicutes-to-Bacteroidetes ratio fell and Bifidobacterium tended to rise, but overall microbial diversity decreased. No immune markers were measured. Manufacturer-funded crossover (n=30).