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The role played by the human microbiota in immune development and its responses is increasingly well understood, reports Dr Fernando Schved, Vice President R&D and CSO, Galam.
Likewise, the contribution played by probiotics, prebiotics and synbiotics and their effects on the microbiota have gained much attention.
Short-chain fructo-oligosaccharides (sc-FOS) are among the most researched non-digestible soluble prebiotic dietary fibres consumed by humans.
A myriad of beneficial attributes has been documented for prebiotics; for example, the ability of prebiotics such as sc-FOS to affect our immune system is of great importance and may play a key role in sustaining the bodys immune system.
The immunomodulating action of prebiotics such as sc-FOS is primarily mediated (but not only) via effects on the "innate immune system" by both direct and indirect mechanisms.
A commensal microflora provides intrinsic protection against potentially pathogenic bacteria by competing for both nutrients and controlling the colonisation of prospective pathogens (by lowering the pH of the colon, for example).
The human colon plays a central role in our immunity via mechanisms including mucosal barriers and the GALT system (gut-associated lymphoid tissue), which is the largest human immune tissue.
In mammals, intestinal immunity is largely maintained by interactions between gut microbiota and the GALT. GALT stimulation may be mediated by the bifidogenic effect of prebiotics such as sc-FOS; as such, its role is crucial to the digestive tract of newborns and infants by promoting the maturation of B-type immune cells.
In animal models, dietary sc-FOS increased the intestinal immunoglobulin A (IgA) response in the small intestine as well as in the colon.
Short oligosaccharide components of sc-FOS (namely kestose and nystose) have been reported to be rapidly and preferably used by Bifidobacteria and certain Lactobacillus species because of the unique enzymatic abilities that are innate to these bacteria.
Indeed, sc-FOS is characterised by a relatively low threshold bifidogenic dose of only 2.5 g/day. The stimulatory action of prebiotics (such as sc-FOS) on the immune system may occur via two mechanisms:
Activation pathways by which sc-FOS positively affects components of the colonic immune system may include
Moreover, the mucosal barrier (local immune system) separates and protects colonocytes facing the colon lumen and serves as a first line of defence by reducing full systemic immunity.
SCFAs (mainly butyric acid) have been reported to induce mucin secretion and enhancing physiological protection.
SCFAs (such as acetate) may also provide benefits to colon health by improving both the blood flow and oxygenation of the colonic mucosa, resulting in increased barrier integrity.
Butyrate may increase mucosal depth by enhancing cell differentiation at the bottom level, reducing apoptosis at the apex of the villi as demonstrated in a piglet study.
Prebiotics such as sc-FOS may also contribute immunoprotective activity in cases of respiratory infections such as common flu, which are often a result of viral agents such as Influenza.
For example, in a human study, fructo-oligosaccharides were included as a constituent of a nutritional formula (9%) for seniors (183-day follow-up, age >65).
This study demonstrated a positive enhancement of the immune function as measured by antibody and lymphocyte proliferation (day count reduction) with symptoms of upper respiratory tract infection following an influenza vaccination.
In an animal trial, the addition of sc-FOS has been shown to bind "toxin A" alongside changes in the composition of mucosal immune cells (an increased number of macrophages in the lamina propia).
An important aspect of immunity enhancement by sc-FOS is the prevention of infectious diarrhoea and/or alleviation of its symptoms.
In children (1–14 years of age) suffering from acute diarrhoea, Juffrie showed that sc-FOS — dosed at 2.5–5 g/day — was able to reduce the duration of diarrhoea events compared with the control group.
sc-FOS has been reported to reduce the concentrations of potential procarcinogens produced in the colon.
A 42-day human clinical study (12 healthy subjects, both genders, age 20–34) explored the effects of sc-FOS supplementation at 4 g/day (as chewable tablets and a drink) on faecal flora and certain activities of reductive enzymes associated with the conversion of procarcinogens to carcinogens (β-glucuronidase and glycocholic acid hydroxylase).
Moreover, sc-FOS has been shown to neutralise the activity of ROS (reactive oxygen species) such as hydroxyl radicals. Pejin and colleagues demonstrated the capacity of sc-FOS components (1-kestose and nystose) to scavenge hydroxyl radicals (•OH), suggesting their potential immunoprotective role.
Therefore, sc-FOS may help to reduce the damage derived from oxidative stress and inflammation caused by improper nutrition.
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