FLORATOPIC
Dermatology
Promotes a balanced gut microbiota in patients with atopic dermatitis (AD)
Counteracts AD-associated increased pathogen load and LPS levels
Promotes a balanced Th1/Th2 immune response
Supports improvement of atopic dermatitis symptoms in infants, children and adults
Ligilactobacillus salivarius LS01 (DSM 22775)
Atopic dermatitis (AD) is a prevalent inflammatory skin condition characterized by recurrent episodes, dry skin, erythema, and itching [1]. The incidence of AD has been increasing, particularly with the rise of industrialization and urbanization, and it now affects 15-30% of children and 10% of adults globally [2]. AD's pathophysiology is multifaceted, involving an altered immune response towards Th2 immunity and defects in the innate immune system. Predisposing factors for AD include smaller family size, urban living, and a Western diet, all of which impact both skin and gut microbiota [2]. AD typically begins in early childhood and often marks the onset of the "atopic march," which may progress to asthma, allergic rhinitis, and allergic conjunctivitis.
FLORATOPIC® has been specifically formulated and clinically tested to address AD in infants, adults, and children, utilizing the immunomodulatory properties of Ligilactobacillus salivarius LS01 [3-6]. The clinical and immunological efficacy of LS01 in AD is attributed to its regulation of the Th1/Th2 cytokine ratio, rather than a mere increase in the expression of Th1 cytokines. LS01 is known to enhance the production of IL-12, critical for Th1 development.
In two clinical studies involving both adults and children with AD (including moderate/severe cases in adults), 16 weeks of FLORATOPIC® supplementation led to significant improvements in the Dermatology Life Quality Index (DLQI), SCORAD score, and itching index [4,5]. These improvements persisted for 4 weeks after the end of probiotic supplementation. Furthermore, in a double-blind, placebo-controlled randomized controlled trial (RCT) in adults, FLORATOPIC® supplementation:
Rebalanced the intestinal microflora: significantly decreased fecal staphylococci load and LPS plasma concentration (with effects persisting post-treatment), while increasing fecal LS01 content (LS01 was recovered in all subjects after treatment).
Improved Th1 cytokine stability, even during pollen season.
1. Langan SM, et al. Atopic dermatitis. Lancet. 2020 Aug 1;396(10247):345-360. doi: 10.1016/S0140-6736(20)31286-1
2. Ricci G, et al. Long-term follow-up of atopic dermatitis: retrospective analysis of related risk factors and association with concomitant allergic diseases. J Am Acad Dermatol. 2006 Nov;55(5):765-71. doi: 10.1016/j.jaad.2006.04.064
3. Drago L. et al. Effects of Lactobacillus salivarius LS01 (DSM 22775) treatment on adult atopic dermatitis: a randomized placebo-controlled study. Int J Immunopathol Pharmacol. 2011; 24(4):1037-48. DOI: 10.1177/039463201102400421
4. Drago L. et al. Changing of fecal flora and clinical effect of L. salivarius LS01 in adults with atopic dermatitis. J Clin Gastroenterol. 2012; 46 Suppl:S56-63. DOI: 10.1097/MCG.0b013e318265ef38
5. Niccoli A. et al. Preliminary results on clinical effects of probiotic Lactobacillus salivarius LS01 in children affected by atopic dermatitis. J Clin Gastroenterol. 2014; 48 Suppl:S34-36. DOI: 10.1097/MCG.0000000000000233
6. Drago L. et al. Treatment of atopic dermatitis eczema with a high concentration of Lactobacillus salivarius LS01 associated with an innovative gelling complex. J Clin Gastroenterol. 2014; 48 Suppl:S47-511. DOI: 10.1097/MCG.0000000000000249