Immunomodulation by food: promising concept for mitigating allergic disease? (original) (raw)

Introduction

The importance of a properly functioning and well-balanced immune system for maintaining health has become strikingly evident over the past few decades. There has been, roughly since World War II, an apparent decrease in the prevalence of “traditional” infectious diseases, such as tuberculosis, mumps, or measles, with a concomitant increase in immune-related disorders, such as multiple sclerosis, irritable bowel disease, type 1 diabetes and various allergic diseases. In addition, a “gradient” in disease incidence can be observed, decreasing in the north–south direction in the Northern Hemisphere, and vice versa in the Southern Hemisphere [1]. Such observations suggest a relationship with nongenetic factors, such as (changes in) health care and medical practice, (changes in) living environment and lifestyle, level of welfare, dietary habits, and the like. In particular, it has been hypothesised that the strong increases in rates of asthma and allergic disease are related to the increased use of hygienic practices and the subsequently reduced exposure to microbes, which supposedly results in an “undereducated” immune system [2]. This includes food hygienic practice, the tremendous virtues of which cannot be disputed, but which may have contributed to impaired or delayed immune maturation. Also, the rise in food products that are composed of highly refined ingredients has led to the decreased consumption of micronutrients, which may be relevant to immune maturation [3]. Interestingly, the incidence of tuberculosis was reported to be inversely related to the incidence of asthma and rhinoconjunctivitis, confirming the importance of a vigilant Th1 compartment in disease aetiology, as mycobacteria elicit particularly strong Th1 responses [4]. Not just in atopic disorders, but in many other chronic diseases—for instance cardiovascular diseases, neoplastic malformations, and metabolic syndrome—chronic inflammatory processes are involved, possibly causally, in the development of subsequent related health problems, also suggesting an important role for immune interventions [5–9]. The prophylactic and therapeutic relevance of immune modulation is confirmed by the possibility of developing antitumor strategies via vaccination, such as as has been described for _Mycobacterium_-based vaccines and lung tumours, an effect supposedly based on selective enhancement of Th1-mediated immunity [10], and the claimed prophylactic effect of the Th1-stimulating mushroom-derived β-glucan lentinan on malaria [11], which all adds to the evidence that a better comprehension of and capacity to maintain immune homeostasis is of extreme importance to both individual and public health.

Immune modulation, for example via dietary strategies, may hold promise as well for maintaining immune homeostasis in the healthy population. Immunity, described as the activities of its various compartments, strongly varies throughout life. For instance, there is a decline in the functional capacity to elicit generalised and specific immune responses with increasing age, and regulatory cells show a decrease in production and response to regulatory signals. Overall, these developments result in the impairment with age of innate and adaptive immune responses, increased self-antigen reactivity, increased incidence of infection, and increased vulnerability to the development of neoplastic malformations. Overall, the implications of such immune phenomena associated with senescence are that susceptibility to specific health conditions may vary with age, with immune impairment eventually leading to increased risk of mortality [12–16]. Although still in its infancy, the use of dietary factors, notably vitamin E and ω-3-PUFAs, as tools to circumvent this age-related decline in immune function is a focus of research [17].

Dietary components and immunity

The question “which food components impact on the functioning of specific immune compartments?” could perhaps better be phrased as “which food components do not have an impact on immune function?”. Protein energy malnutrition (PEM), for instance, affects all aspects of immune function, with these effects being even more pronounced in the elderly. The functioning of T-cell and B-cell subsets and functions and of innate immunity are strongly related to protein nutritional status. Immune responses can be restored by relieving this protein shortage, but at a slower speed in patients that suffer from inflammatory processes. The imbalance between normal macrophage functions and decreased T-cell function is partly responsible for chronic inflammatory processes in vulnerable patients. Acute phase responses are, for these reasons, more detrimental to nutritional status and nutrient reserves in elderly patients than in adults [18, 19]. The dietary protein:carbohydrate ratio appears to be important in maintaining immune responsiveness; maintaining low protein and high carbohydrate levels for prolonged intervals seems to be beneficial, as evidenced in a rat model [20].

The concept of dietary components being of paramount importance to immune function is also tangible in the formulation of so-called immunonutrition, specific nutritional preparations for clinical use in critically ill patients with jeopardised immune function. Such preparations contain specific amino acids such as arginine and glutamine, nucleotides, and specific polyunsaturated fatty acids, notably ω-3 PUFAs [21, 22].

Immune function is the target for the development of functional foods. In particular, vitamins, such as A, C, D and E, and minerals as Zn and Se are focal points for this, next to PUFAs such as docosahexaenoic acid (22:6n-3; DHA) and eicosapentaenoic acid (20:5n-3; EPA). A detailed essay on the immunomodulatory properties of each of these nutrients is beyond the scope of this paper, so the reader is referred to a number of recent reviews and research papers that deal with these matters [21–26], and references therein. For a number of other nutrients and products, research is still in a less advanced stage—at the stage of in vitro or animal models at best—and some research issues in this field will be dealt with below.

Therefore, there seems to be a role for food and nutrition in supporting and maintaining immune homeostasis for various groups of individuals. It should be realised, however, that research into the possible role of functional foods in mitigating (human) immune function is still in its infancy, and that controversy around health claims will remain the rule rather than the exception so long as there is no improvement in (for example) the identification of suitable biomarkers, and in our comprehension of individual responses (genetics and imprinting) and the underlying physiological and biochemical mechanisms associated with nutrients.

The conclusion that modulating immune response may well serve as the basis for the development of functional foods appears at hand. Before such approach can achieve its full potential, however, it is essential to realise that functional foods should be regarded as food products with specific health benefits (above those of average consumption levels) for targeted groups of consumers. Therefore, the specific needs of individuals or groups of individuals must be matched with the immunomodulatory properties of specific products. Products that may be of benefit to, for example, allergic consumers do not necessarily have a beneficial effect on other consumers with different requirements for immune mitigation; requirements for neonates likely differ from those of the elderly, and so on: one size does not fit all!

Objective and rationale

The objectives of the research area are to develop immunity-related markers for health effects of food, and to develop dietary or food products to support vital and balanced immune function throughout life.

Immunological read-outs are used to determine possible health effects because:

• A variety of chronic health threats that have an enormous economic impact and also impact on quality of life are directly related to immune function, such as autoimmune diseases, allergies and asthma, and immune deficiencies.
• The immune system plays a role in the pathology of chronic and age-related anomalies; in some cases a causal one (or perhaps only partially so).
• There is increasing evidence (from randomised double-blind intervention studies and clinical trials too) of the capacity of food components to modulate the response of the immune system, both positively (immune-potentiating) and negatively (e.g. food allergy).

The analysis of the capacity and activity of the immune system offers advantages that may facilitate the translation from an experimental setting to possible application and implementation, because of the pivotal role of the immune system that has been acknowledged in health analysis and clinical practice:

• For many immune functions, diagnostically validated in vitro or in vivo test systems are available
• For many immune functions, animal models and cell lines for in vitro analysis are available
• The role of the immune system in clinical practice and the pathology of many chronic anomalies is relatively well documented.
• There is an increased interest in linking individual immune reactivity to lifestyle- and age-associated factors, where food and nutrition show the best documented effects.

The current lack of mechanistic underpinning of the health effects of food intake results in sometimes contradictory claims and statements, confusion, and a loss of trust and confidence amongst consumers. Addressing this lacuna will contribute to a solid basis for health claims, and consequently to the concept of “health promotion via nutrition”. Immune modulation offers unique perspectives for meeting such requirements.

Types of products with immunomodulatory claims that are currently on the market

Despite the relative infancy of the state of scientific understanding of interactions between immunity, food and diet at present, there are already a number of products on the market for either clinical, food or feed-related applications. Since this paper is not an “advertorial”, no specific products will be mentioned, but some product groups with more or less specific applications will be indicated:

• “_Immunonutrition_”. Immunonutrition-type products are typically meant for clinical use for critically ill or surgical patients, to fortify hampered immune function. Application routes can be either parenteral or enteral; the optimal route may depend on patient and disease characteristics. Typical components included in such products are specific amino acids (notably glutamine and arginine), nucleotides, ω-3 PUFAs, minerals such as Zn and Se, and various compounds with antioxidative properties [21–31]. Since immunonutrition is used in relatively well-described clinical cases, with relatively well-defined end-points, there is a rather well-elaborated scientific basis for its application.
• Pro- and prebiotics. Probiotics are, by definition, “nonpathogenic microorganisms that when given in adequate numbers exert beneficial effects on the host”, whereas prebiotics are a category of functional food defined as “nondigestible food ingredients that beneficially affect the host by selectively stimulating the growth and/or activity of one or a limited number of bacteria in the colon, and thus improve host health” [32]. A number of beneficial health effects have been claimed for the pro-pre-biotic product category, including effectiveness against antibiotic-associated or travellers diarrhoea, improved stools, as well as an array of immunity-related health claims, also in relation to allergic disease.
  Fructose oligosaccharide and galactose oligosaccharide fortified infant formulas are currently on the market; these are intended to support the developing immune systems of neonates (see below for more detail, and [33] for an extensive review of various health-related claims).
• Hypoallergenic infant formulas. A product category that has the immunomodulatory property that it does not activate a potentially anomalously reacting immune response. Hydrolysed preparations of milk proteins are in the market, and these are aimed in particular at circumventing clinical reactions in individuals allergic to cow’s milk. The degree of protection is usually quite good, and dependent on the degree of hydrolysis [34]. Again, this concerns a category of relatively well-defined patients with a relatively well-understood clinical history.
• β-Glucan-containing preparations for feed applications. In an attempt to limit the use of antibiotics in animal husbandry, spent brewer’s yeast is added to feed in order to increase natural resistance. This effect is attributed to β-glucans, which are present in yeast cell walls, and are supposed to interfere with and enhance immunity (see e.g. [35]). Preparations that claim an enhanced accessibility of β-glucans to the immune system are even marketed.
• Various supplements. A plethora of various kinds of food supplements are available on the market, which are too large in number and too variable in composition (if they can be defined at all) to be discussed comprehensively here. However, they often have a common denominator, in the sense that there is only very meagre underpinning of claims, and indications of who should or could take such preparations and when are scarce.

Research into immunomodulation by food, with a focus on allergy

Probiotics

Probiotic bacteria are nonpathogenic microorganisms that are thought to exert positive health effects on the host. In by far the majority of cases, Lactobacillus or Bifidobacterium spp. are the microorganisms endowed with the supposed beneficial effects; nevertheless, it should be noted that the distinction between “good” and “bad” organisms is a rather arbitrary one, and is strongly dependent on where in the digestive tract, and to whom, they are applied [36]. Some years ago, relationships between the composition of intestinal microbiota and the occurrence and incidence of allergic diseases were noted [37–39]. In particular, a comparison between Estonian and Swedish school children demonstrated that allergic children were less often colonised with Lactobacilli and more often with aerobic coliforms and Staphylococcus aureus [37, 38], or lower Bifidobacterium counts and higher Clostridium colonisation numbers were found [39]. This was supposed to be relevant to the proper maturation of intestinal immunity, and in particular to impact on the balance between Th1 and Th2 cells [38, 39], thus suggesting options for nutritional and dietary intervention, via probiotics, for this type of condition.

Indeed, when Lactobacilli (LGG) was given to 159 pregnant women (at risk of allergy) for two weeks and to their babies for six months, 50% fewer infants in the LGG group than in the placebo group demonstrated atopic eczema at two years of age [40]. Similarly, LGG and Bifidobacterium lactis Bb12 were shown to decrease the severity of atopic eczema [41]. In a similar study, serum tolerance-related cytokine IL-10 was elevated significantly in the LGG group [42]. Furthermore, administering L. casei Shirota was found to significantly suppress the production of IL-5, IL-6 and IFN-γ compared to placebo in PBMCs of (adult) sufferers from seasonal allergic rhinitis [43]. However, results sometimes were reproducible elsewhere [44], or they were not, e.g. in the development of atopic dermatitis [45]. Also, in a group of teenagers and young adults, the application of Lactobacillus rhamnosis did not alleviate birch-pollen allergy symptoms [46]. Furthermore, dietary LGG supplementation a few weeks before delivery did not appear to have an effect on the proliferative response of PBMCs from atopic or control neonates, thus suggesting that there was no impact on sensitisation potential [47].

In conclusion, results in allergy prevention are still variable and heavily debated. In vitro observations suggest that a possible mechanism for positive effects on allergy-related immunity is the restoration of imbalances between various T-cell subsets, perhaps indirectly via TLR signalling in innate immune cells. In vivo results may be strongly strain dependent, as a variety of immune effects, e.g. IL-10 inducing (tolerance enhancing?) or Th1 skewing, may be observed during the in vitro screening of probiotic strain collections [Vissers et al., publications in preparation]. However, effects on gut permeability or intestinal allergen processing cannot be excluded. Also, responses may depend on individual patient characteristics as well, such as whether allergies have already fully developed or not. Recently, interactions between (inducible) Lactobacillus S-layer protein and gut DCs were described that may contribute to the mechanism of action [48], primarily in relation to innate immunity.

In addition to allergic disease, probiotics are being investigated in for example celiac disease, gastroenteritis, IBD, colon and colorectal cancer, and antibiotic-associated diarrhoea [33].

However, above all, the conclusion is that stringent requirements for experimental design are imperative to avoid contradictory data, and to further this promising area of research.

β-Glucans

β-(1→3)-(1→6)-Glucans are rather ubiquitous polymers of glucose with a β-(1→3) backbone and β-(1→6) crosslinks, with typical Mr values in the range of several hundreds of kDa, indicating Dp values of several thousands of glucose units, and are the subject of research in relation to their anticipated effects on immunity, in particular via binding to cells from the innate immune compartment such as macrophages and to NK cells [47, 48]. This type of glucan can be found in bacteria, yeasts, fungi [51], seaweed [52] and cereals (the latter mainly containing (1→4) crosslinks [53]).

Kimura et al. described a mitigating effect of (orally administered) β-glucans on food allergic reactions in mouse models. Adding 0.5–1.0% of a β-glucan from Aureobasidium pullulans strain A1 to the diet of ovalbumin-allergic Balb/C mice considerably reduced ova-specific IgE and stimulated IL-4, IFN- and IL-12 production in ConA-stimulated splenocytes from the mice [54]. Oral application of finely dispersed shiitake β-glucan (lentinan) in human patients allergic to cedar pollen significantly alleviated the symptoms of Japanese cedar pollen-induced rhinitis, sneezing, nasal congestion, and conjunctivitis, and its oral uptake before symptom onset exhibited preventive effects. Allergic symptoms were relieved not only for seasonal allergies to cedar pollen but also for perennial allergies. Oral ingestion of β-(1→3)-glucan in individuals with allergic tropism could reduce the spontaneous increase in both allergen-specific and total IgE titers, and the clinical responses to treatment were well correlated with the capacity of monocytes to bind to β-(1→3)-glucan [55]. Both the route of application (nasal application of β-glucans, resulting in the glucans acting as an allergen [54]) and the degree of dispersion appeared important, as nondispersed lentinan did not give the desired effects [55].

Similar (peanut) allergy relieving effects were observed in C3H/HeJ mice, for an orally applied complex herbal preparation in which β-glucans (from the fungus Ganoderma lucidum) were undoubtedly present [56]. Also, again orally applied, G. lucidum preparations were effective in a mouse model for house dust mite allergy [57].

β-Glucans appear to exert their immunomodulatory effects via the activation of innate pathways, e.g. in macrophages ([49, 50] Fig. 1). β-Glucans were found to stimulate the production of TNF-α, IFN-γ and IL-12 when injected into ICR mice [58], as was also found in models of human peripheral blood mononuclear cells in which various fungal extracts were screened [59], although there is also a report that shows a somewhat different picture for Aureobasidium pullulans; in that report, IL-8 production in PBMCs and in a monocyte cell line was detected [60]. Activation of T-cells in PBMC cultures is probably an indirect effect of the stimulation of innate cells, and reaction cascades may depend on typical characteristics of β-glucans such as Mr (the Aureobasidium glucan being relatively small, ca. 100 kDa, and highly branched (50–80%) [54]), which can perhaps account for (some of) the differences in observations. A number of receptors for β-glucans (dectin-1, complement receptor 3, TLR2 and TLR6, scavenger receptors and lactosylceramide) have been described. Dectin-1 is particularly commonly expressed on immune cells, such as dendritic cells, macrophages, monocytes, neutrophils, eosinophils, some T-cells and in humans on B-cells too. The possible expression of dectin-1 on intestinal cells is under debate [49]. The interaction of dectin-1 and TLR2 upon β-glucan binding leads to synergistic effects on the production of cytokines such as TNF-α and IL12, a process in which NF-kB [59] and spleen tyrosine kinase are claimed to be involved [62].

Fig. 1

Conceptual model for the interaction between β-glucans and innate immune receptors as expressed on macrophages. Interaction between dectin-1 and the TLRs leads to synergistic responses

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Receptor binding studies in which the Ig-labelled polysaccharide-binding domains of dectin-1 were used to detect glucan binding have demonstrated that dectin-1 preferentially binds to the β-(1→3) part of the glucan, and that the minimal length required to allow binding to dectin-1 is 10–11 glucose residues [63]. It should be realised that these observations were derived from an abstracted experimental model, leaving the physiological significance of the β-(1→6)-branches as yet unanswered. As the binding of β-glucans to dectin and TLR-2 shows synergistic effects, perhaps there is a role for the β-(1→6)-branched structure in this effect [61]. Single-chain β-glucans appear to induce stronger responses (NF-kB, iNO production, TNF-α) in (murine) macrophages than oligomeric chains do [50]. Increasing the solubility of β-glucans, for instance by preparing sulfated, carboxymethylated, methylated, hydroxyethylated or hydroxypropylated derivatives, increased their activity against Sarcoma-180 tumour cells [64], the effectiveness of which in relation to allergy mitigation can only be speculated on.

Taken altogether, there appear to be clear indications, from both animal models and from a human study, that orally applied β-glucans or glucan-containing preparations can be of help for relieving various allergy-related symptoms. Applications of Th1 stimulation are anticipated not only in allergy mitigation but also in the stimulation of cell-mediated immunity and increased infection resistance. It appears as if these compounds activate (indirectly via primary innate activation) Th1-mediated immunity, primarily via activation through TLR/CLR (dectin) signalling.

More details on their mode of action, such as for instance how and where interactions between ß-glucans and immune cells take place (via intestinal microfold-(M-) cells? Via, into the intestinal lumen protruding, dendritic cells? Transport via tight junctions (para-cellular transport), as well as structure-function studies and research on application and delivery methods, for instance incorporation into food products or supplements, will be essential to further develop this promising research direction.

Fungal immunomodulatory proteins (FIPs)

FIPs are 15 kDa proteins of (as far as we are aware so far) fungal origin. A number of FIPs have been described in some detail, including those from Flammulina velutipes (golden needle mushroom; FIP-fve), Volvariella volvacea ((paddy) straw mushroom; FIP-vvo), Ganoderma lucidum and G. tsugae (Japanese lacquer mushroom; LZ-8 and FIP-gts, resp.), which are composed of 114 (FIP-fve), 110 (LZ-8 and FIP-Gts) and 112 (FIP-vvo) amino acids, respectively, and share high sequence homology ([65] and Fig. 2). FIP-fve was crystallised and its X-ray structure determined [65, 66]; it was found to be a homodimer where each subunit comprises a pair of N-terminal secondary structural elements, an α-helix followed by a β-strand linked to a domain consisting almost exclusively of β-sheets adopting an Ig-like fold, with α-helix, β-strand and loop fractions of respectively 11.3, 42.6 and 46.1% [66]. The α-helices HA and HB are amphipathic and the side chains of the amino acids on the hydrophobic face of one helix pack well against those of the other α-helix, enabling them to bind via hydrophobic interactions. Lin et al. [68] predicted that the N-terminal residues 1–13 of FIP-Gts formed an α-helix, and they found that recombinant mutants of FIP-Gts in which residues 1–13 (the N-terminal α-helix) were deleted were incapable of dimerisation. Triple mutants in which Leu5, Phe7 and Leu9 were deleted lost their amphipathic character, the ability to form dimers with themselves and with the wild-type FIP-Gts protein, suggesting that this property was important for immunomodulatory activity [67, 68]. FIPs show lectin-like properties, as they are able to agglutinate erythrocytes, and it was suggested that they should be classified as such [67].

Fig. 2

Sequence alignment of FIPs from various sources, demonstrating homology; see text

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The biological relevance of FIPs for allergy mitigation lies in the observation that they were able to inhibit food-allergic and respiratory-allergic reactions in mouse models when applied orally or nasally. When fed (at 200 mcg/mouse, i.e. ca. 4 mg kg−1, every other day) to ovalbumin-allergic Balb/c-mice, allergy symptoms (symptom score, histamine release, intestinal damage) were strongly suppressed, and the Th2-dominant phenotype shifted towards a strongly elevated Th1 response (measured in splenocytes) upon FIP feeding, showing its potential in allergy prophylaxis [69]. Liu et al. found that FIP-fve could be applied in local nasal immune therapy to suppress allergic responses to house dust mite allergy in Balb/c mice [70], and a shift in cytokine profile towards a stronger Th1-response was also noted in this study.

Not many details on the putative mode of action of FIPs have been published, other than that FIP-fve appeared to stimulate IFN-γ production in human PBMCs via p38-MAPK activation [71]. Our own observations ([72], and unpublished results) indicate that natural FIPs or cloned FIPs from Flammulina or Ganoderma have a limited effect on NO production in RAW 264.7 cells (a murine monocyte cell line), and a Th1-skewing effect in human PBMC cultures from healthy volunteers. This was partly corroborated by observations for a immunomodulatory protein from Auricularia (Jew’s ear) mushroom, a protein that perhaps (although this is not yet confirmed) should also be considered a FIP, of Th1 skewing but not NO production in RAW 264.7 cells [73].

One interesting aspect, considering their potential application as food-derived immunomodulatory compounds, is the apparent resistance of the biological activity of these FIPs to common food processing conditions, such as freezing, thawing, dehydration, and acid/alkali conditions [74, 75].

Questions as to their digestion stability, and on the signalling mechanisms (again: absorption via tight junctions (para-cellular transport), DCs, M-cells, signalling via GALT?) remain to be answered.

Perspectives

Based on the above, the option of immunomodulation via diet appears to be a realistic option, with advantages for specific immune-related conditions such as allergies at the very least, although perhaps also in other application areas too, such as in maintaining immune homeostasis and vigilance. Considering the pivotal role of immune homeostasis in general health, and the very relevant and significant societal and economic perspectives, this research avenue seems to be a very worthwhile one, to say the least. It appears as if different food components can exhibit effects on specific immune compartments, thus offering the potential for use in a variety of applications, depending on the characteristics of the deviating chronic processes and the characteristics of the consumers or patients. Foods can thus play a significant role in fortifying and balancing immune responses.

As it becomes more and more clear that the aetiology and course of a given “disease” varies from person to person, it also appears increasingly obvious that treatments (or, if possible and appropriate, supportive dietary measures) should be tuned more towards individual needs. This means that, in the “functional foods” domain, uniform approaches will probably not be maximally effective, thus emphasising the need for greater knowledge on individual consumer’s responses and the (deviations in) metabolism that underlie the development of chronic anomalies. This may not be a nice message for food producers, because markets may fragment, but so be it; once more insight into the underlying mechanisms has been obtained, a better perspective on the chances of product development will be obtained.

With respect to the impact of immunomodulatory foods and food components on allergic reactions, as described in this manuscript, it is striking that in all of the described cases, a skewing of cytokine profiles from Th2 dominance towards a more rebalanced state (read: an enhanced Th1 response) was observed. Secondly, in all cases the active products or ingredients were microorganisms or products derived from them. This leads to the hypothesis that, if indeed an overly hygienic living environment and lifestyle is the basis for the increase in allergic reactions, this situation can perhaps be (partly) restored by exposure to specific microbial constituents, likely activating innate immunity and subsequently skewing adaptive immunity towards a strengthened cell-mediated response: a little bit of dirt does not seem to be bad!

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