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veNTIlATIoN - Green Cross Publishing

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probiotics<br />

36<br />

Part 4<br />

deIrdre JordAN bsc ANutr (SCIENCE OFFICER, yAKULT IRELAND)<br />

lINdA v ThomAs bsc Phd FIFsT (SCIENCE DIRECTOR, yAKULT UK LTD)<br />

There is now a reasonable body of evidence to<br />

indicate that certain probiotic strains may help<br />

support the immune system and, in general, the<br />

body’s natural defences. In this four part series<br />

on probiotics we have looked at the evidence for<br />

probiotics (i) as a risk reduction measure against antibioticassociated<br />

diarrhoea and Clostridium difficile infection; (ii)<br />

in reducing the effects of irritable bowel syndrome and<br />

associated symptoms, and more recently (iii) in the general<br />

health benefits of probiotics for the elderly. A fundamental<br />

aspect of regular probiotic consumption is their modification<br />

of the intestinal microflora such that numbers of beneficial<br />

bacteria are maintained or increased, and the effects or<br />

numbers of harmful or pathogenic bacteria are decreased. This<br />

is associated with a range of positive effects on the health and<br />

functioning of the digestive system, as well as modulation of<br />

immune function. 1 Probiotics can also have many related and<br />

more specific modes of action. By supporting the beneficial<br />

bacteria in the commensal flora, they may help inhibit the<br />

growth and reduce any harmful effects of other bacteria,<br />

antigens, toxins and carcinogens in the gut. In addition,<br />

and very importantly, probiotics can influence the immune<br />

system via the gut-associated lymphoid tissue, with positive<br />

modulation reported for the innate and even the acquired<br />

immune system (Box 1).<br />

The gut is the most vulnerable site in the body, which is<br />

why the majority of the immune system is based there in the<br />

form of the gut-associated lymphoid tissue (Figure: GALT).<br />

The small intestine contains hundreds of Peyer’s patches<br />

(concentrations of lymphoid tissues), but lymph nodes are<br />

found through the whole length of the gut (in fact, 85% of<br />

the body’s lymph nodes are estimated to be in the gut). This<br />

immune network must recognise and tolerate the commensal<br />

microflora (otherwise inflammation results), and it must also<br />

tolerate food antigens. But importantly, it must recognise and<br />

deal with pathogenic microbes. Studies with germ-free animals<br />

have clearly shown that the commensal microflora is important<br />

in educating and supporting the immune system; animals<br />

without any gut bacteria have a poorly developed immune<br />

The immune<br />

system and<br />

your gut:<br />

a closer look at an<br />

intricate relationship<br />

(Part 4 of a 4 part series)<br />

system with significantly fewer antibody-producing cells.<br />

Probiotics can support the work of the commensal flora<br />

in interacting and supporting the immune system, which<br />

explains why certain probiotics have been shown to benefit<br />

the health of the whole body, not just that of the gut.<br />

box 1: Innate and acquired immune system<br />

• The innate or non-specific immune response<br />

defends the host from infection in a non-specific<br />

manner. Cell surface receptors (Toll-like receptors)<br />

on tissue recognise and bind different microbial<br />

components. This can trigger phagocytosis and<br />

production of pro-inflammatory cytokines, which<br />

attract a local increase in white blood cells. The innate<br />

immunity is an immediate response but it does not<br />

confer long-lasting or protective immunity. Example<br />

constituents of this system are natural killer (NK)<br />

cells and phagocytic cells such as neutrophils and<br />

macrophages. Examples of Toll-like receptors are TLR-4<br />

(recognises lipopolysaccharide, the cell wall of Gramnegative<br />

bacteria) and TLR-9 (recognises bacterial<br />

DNA).<br />

• The acquired/adaptive or specific immune<br />

response recognises and remembers specific<br />

pathogens and is thus able to mount a rapid and<br />

stronger defence when the pathogen is next<br />

encountered. Lymphocytes (T and B cells) recognise<br />

specific and different parts of a pathogen, and then<br />

can activate different pathways against it. Humoral<br />

immunity is an antibody-mediated specific response<br />

by B cell production of immunoglobulins (antibodies)<br />

such as IgA, IgG and IgE. (Humoral refers to the bodily<br />

fluids and comes from the old idea of ‘humors’ of the<br />

body). The other response is cell-mediated, mainly<br />

involving antigen-specific T cells.

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