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Atopic dermatitis is a chronic inflammatory skin disease associated with cutaneous hyperreactivity to environmental triggers and is often the first step in the atopic march that results in asthma and allergic rhinitis. The clinical phenotype that characterizes atopic dermatitis is the product of interactions between susceptibility genes, the environment, defective skin barrier function, and immunologic responses. This review summarizes recent progress in our understanding of the pathophysiology of atopic dermatitis and the implications for new management strategies.
Atopic dermatitis (AD) is a chronic inflammatory skin disease associated with cutaneous hyperreactivity to environmental triggers that are innocuous to normal nonatopic individuals (1). Although written descriptions of AD date back to the early 1800s, an objective laboratory test does not exist for AD. The diagnosis of AD is based on the following constellation of clinical findings: pruritus, facial and extensor eczema in infants and children, flexural eczema in adults, and chronicity of the dermatitis.
AD usually presents during early infancy and childhood, but it can persist into or start in adulthood (2). The lifetime prevalence of AD is 10–20% in children and 1–3% in adults. Its prevalence has increased two- to threefold during the past three decades in industrialized countries but remains much lower in countries with predominantly rural or agricultural areas. Wide variations in prevalence have been observed within countries inhabited by groups with similar genetic backgrounds, suggesting that environmental factors play a critical role in determining expression of AD.
A precise understanding of the mechanisms underlying AD is critical for development of more effective management strategies (Table (Table1).1). Various studies indicate that AD has a complex etiology, with activation of multiple immunologic and inflammatory pathways (3). The clinical phenotype that characterizes AD is the product of complex interactions among susceptibility genes, the host’s environment, defects in skin barrier function, and systemic and local immunologic responses. An understanding of the relative role of these factors in the pathogenesis of AD has been made possible by a variety of approaches, including the analysis of cellular and cytokine gene expression in AD skin lesions in humans as well as gene knockout and transgenic mouse models of candidate genes in AD. The current review will summarize progress in our understanding of the pathophysiology of AD and implications for therapy.
Several observations suggest that AD is the cutaneous manifestation of a systemic disorder that also gives rise to asthma, food allergy, and allergic rhinitis (1, 2). These conditions are all characterized by elevated serum IgE levels and peripheral eosinophilia. AD is often the initial step in the so-called “atopic march,” which leads to asthma and allergic rhinitis in the majority of afflicted patients. In experimental models of AD, the induction of allergic skin inflammation by epicutaneous application of allergens has been found to augment the systemic allergic response and airway hyperreactivity characteristic of asthma (4).
At least two forms of AD have been delineated: an “extrinsic” form associated with IgE-mediated sensitization involving 70–80% of the patients, and an “intrinsic” form without IgE-mediated sensitization involving 20–30% of the patients (5). Both forms of AD have associated eosinophilia. In extrinsic AD, memory T cells expressing the skin homing receptor, cutaneous lymphocyte-associated antigen (CLA), produce increased levels of Th2 cytokines. These include IL-4 and IL-13, which are known to induce isotype switching to IgE synthesis, as well as IL-5, which plays an important role in eosinophil development and survival. These CLA+ T cells also produce abnormally low levels of IFN-γ, a Th1 cytokine known to inhibit Th2 cell function. Intrinsic AD is associated with less IL-4 and IL-13 production than extrinsic AD.
Clinically unaffected skin in AD is not normal. It frequently manifests increased dryness and a greater irritant skin response than healthy controls. Unaffected AD skin contains a sparse perivascular T cell infiltrate not seen in normal healthy skin (see Figure Figure1).1). Analyses of biopsies from clinically unaffected skin of AD patients, as compared with normal nonatopic skin, demonstrate an increased number of Th2 cells expressing IL-4 and IL-13, but not IFN-γ, mRNA (6).
Acute eczematous skin lesions present clinically as intensely pruritic, erythematous papules associated with excoriation and serous exudation. In the dermis of acute lesions, there is a marked infiltration of CD4+ activated memory T cells. When compared to normal skin or uninvolved skin of AD patients, acute skin lesions have a significantly greater number of IL-4, IL-5, and IL-13 mRNA–expressing cells, but few IFN-γ or IL-12 mRNA–expressing cells. APCs (e.g., Langerhans cells [LCs], inflammatory dendritic epidermal cells [IDECs], and macrophages) in lesional and, to a lesser extent, in nonlesional skin bear IgE molecules (7).
Chronic lichenified skin lesions have undergone tissue remodeling (Figure (Figure2)2) due to chronic inflammation and are characterized by thickened plaques with increased markings (lichenification) and dry, fibrotic papules. There is an increased number of IgE-bearing LCs and IDECs in the epidermis, and macrophages dominate the dermal mononuclear cell infiltrate. Eosinophils also contribute to the inflammatory response, and T cells remain present, although in smaller numbers than seen in acute AD. Chronic AD skin lesions have significantly fewer IL-4 and IL-13 mRNA–expressing cells, but greater numbers of IL-5, GM-CSF, IL-12, and IFN-γ mRNA–expressing cells, than in acute AD. Recent studies suggest that collagen deposition during chronic AD is due to increased gene expression of the profibrotic cytokine, IL-11 (8).
The evolution of AD skin lesions is orchestrated by the local tissue expression of proinflammatory cytokines and chemokines. Cytokines such as TNF-α and IL-1 from resident cells (keratinocytes, mast cells, and DCs) bind to receptors on vascular endothelium, activating cellular signaling including the NF-κB pathway and inducing expression of vascular endothelial cell adhesion molecules. These events initiate the process of tethering, activation, and adhesion to the endothelium followed by extravasation of inflammatory cells. Once the inflammatory cells have infiltrated into the tissue, they respond to chemotactic gradients established by chemoattractant cytokines and chemokines, which emanate from sites of injury or infection (9). These molecules play a central role in defining the nature of the inflammatory infiltrate in AD (10). IL-16, an LC-derived chemoattractant cytokine for CD4+ T cells, is increased in acute AD skin lesions. C-C chemokine ligand 27 is highly upregulated in AD and preferentially attracts CLA+ T cells into the skin. As compared to psoriasis, the C-C chemokines, RANTES, monocyte chemotactic protein-4, and eotaxin (Figure (Figure3)3) are increased in AD skin lesions and likely contribute to the chemotaxis of C-C chemokine receptor 3–expressing (CCR3-expressing) eosinophils, macrophages, and Th2 lymphocytes into AD skin. Selective recruitment of CCR4-expressing Th2 cells into AD skin may also be mediated by macrophage-derived chemokine and thymus and activation–regulated cytokine, which are increased in AD. Persistent skin inflammation in chronic lesions may be due to elevated IL-5 and GM-CSF expression in the skin leading to enhanced survival of eosinophils and monocyte-macrophages as well as LCs. In addition, extracellular matrix molecules deposited into chronic skin lesions have been found to enhance the survival of memory T cells (11).
The key role of immune effector T cells in AD is supported by the observation that individuals with primary T cell immunodeficiency disorders frequently have elevated serum IgE levels and eczematous skin lesions which clear following successful bone marrow transplantation. Furthermore, in animal models of AD, the eczematous rash does not occur in the absence of T cells. Use of the atopy patch test technique as a model for the induction of eczema in patients with AD has shown that house dust mite (HDM) allergen–induced skin lesions display two phases: an initial phase with predominantly IL-4 producing Th2 cells and a subsequent phase after 24 to 48 hours characterized by IFN-γ producing Th1 cells (1). This switch is thought to be initiated by the local production of IL-12 from infiltrating eosinophils and/or IDECs (3). Activated T cells expressing Fas ligand have also been shown to induce keratinocyte apoptosis contributing to the spongiosis found in acute AD (12). This process is mediated by IFN-γ, which upregulates Fas on keratinocytes.
The important role that Th1 and Th2 cytokines play in the skin inflammatory response has been demonstrated in experimental models of allergen-induced allergic skin inflammation in mice with targeted deletions or overexpression of these cytokines. In this regard, transgenic mice genetically engineered to overexpress IL-4 in their skin develop inflammatory pruritic skin lesions similar to AD, suggesting that local skin expression of Th2 cytokines plays a critical role in AD (13). Allergen-sensitized skin from IL-5 knockout mice has been found to have no detectable eosinophils and exhibits decreased thickening; skin from IL-4 knockout mice displays normal thickening of the skin layers, but has a reduction in eosinophils, while skin of IFN-γ knockout mice is characterized by reduced dermal thickening (14).
AD skin, as compared to nonatopic skin, contains an increased number of IgE-bearing LCs and IDECs expressing the high affinity IgE receptor Fcε receptor I (FcεRI) (7). The increased expression of FcεRI on DCs in atopic skin is due to enhanced expression of the FcεRIγ chain and is preserved by increased IgE levels (15). LCs and IDECs play an important role in allergen presentation to Th2 and Th1 cells, respectively (3). FcεRI-bound IgE on LCs facilitates the capture and internalization of allergens prior to their processing and antigen presentation to T cells in atopic skin. FcεRI+/IgE+ LCs may also migrate to the lymph nodes and stimulate naive T cells to expand the pool of Th2 cells. The clinical importance of these cells is supported by the observation that, using an experimental model of aeroallergen-induced patch test reactions on atopic skin, the presence of FcεRI+/IgE+ LC is required to provoke eczematous skin lesions. IL-10 expression by APCs and T cells has recently been demonstrated to play a key role in Th2 cell development in an animal model of AD (16).
Epidermal keratinocytes from AD patients produce a unique profile of chemokines and cytokines following mechanical stimulation, e.g., scratching, or exposure to proinflammatory cytokines, including abnormally high levels of RANTES following stimulation with TNF-α and IFN-γ. They are also an important source of thymic stromal lymphopoietin, which activates DCs to prime naive Th cells to produce IL-4 and IL-13. These observations may explain the link between scratching and the triggering of Th2-mediated skin inflammation in AD. As discussed below, keratinocytes in AD are also deficient in their ability to synthesize antimicrobial peptides needed for innate immune responses against microbes (17, 18).
AD is characterized by dry skin and even involves nonlesional skin and increased transepidermal water loss. This impairment of the skin barrier function in AD leads to increased antigen absorption contributing to the cutaneous hyperreactivity characteristic of AD. In particular, ceramides serve as the major water-retaining molecules in the extracellular space of the cornified envelope, and the barrier function of these complex structures is provided by a matrix of structural proteins that are bound to ceramides (19). A reduced content of ceramides has been reported in the cornified envelope of both lesional and nonlesional skin in AD patients. The increased susceptibility to irritants in AD may therefore represent a primary defect of epidermal differentiation compounded by the presence of inflammation-induced skin damage.
AD is a genetically complex disease that has a high familial occurrence. Twin studies of AD have shown concordance rates of 0.72–0.86 in monozygotic, and 0.21–0.23 in dizygotic, twin pairs, indicating that genetic factors play an important role in the development of this disease (20). Relevant to AD as part of a systemic atopic disorder, candidate genes involving IgE and Th2 cytokines have been identified. There has been particular focus on chromosome 5q31-33, as it contains a clustered family of Th2 cytokine genes, i.e., IL-3, IL-4, IL-5, IL-13, and GM-CSF (21). Case-control comparisons have suggested a genotypic association between the T allele of the -590C/T polymorphism of the IL-4 gene promoter region and AD. The fact that this allele is associated with increased IL-4 gene promoter activity suggests that it may increase allergic responses in AD. Similarly, IL-13 coding region variants, a gain-of-function polymorphism in the α subunit of the IL-4 receptor (located on chromosome 16q12), and a functional mutation in the promoter region of RANTES (located on chromosome 17q11) have been reported in AD. There have been controversial linkage findings between AD and markers on chromosome 11q13, including the gene encoding for the β-chain of the high affinity receptor for IgE (FcεRIβ). Most of these studies included patients with elevated IgE levels, i.e., patients with extrinsic AD. Thus, studies of so-called “pure” or intrinsic AD are needed to identify AD genes unrelated to IgE biology. Importantly, linkages to AD have generally not corresponded to loci associated with asthma, suggesting the presence of separate or additional genes in AD that may not act through atopic mechanisms.
Genome screens have been performed to identify susceptibility loci for AD. One screen in families of German and Scandinavian children found a linkage for AD on chromosome 3q21 (20). This region encodes the costimulatory molecules CD80 and CD86 and therefore may modulate T cell responses. A second screen reported linkage of AD to loci on chromosomes 1q21, 17q25, and 20p. Interestingly, these same regions are known to contain psoriasis susceptibility genes, which suggests common candidate genes involved in the control of skin inflammation. Although AD and psoriasis are distinct skin diseases, both conditions involve dry, scaly skin and disrupted epidermal differentiation.
A Glu420Lys polymorphism variant in the SPINK5 gene, which encodes serine proteinase inhibitor, Kazal type 5, has shown significant association with AD in two independent cohorts (22). This gene is expressed in the outermost layers of the skin and has been implicated in Netherton disease, an autosomal recessive disorder characterized by ichthyosis and atopy. It may have a protective role against allergens that are serine proteinases.
The rapid rise in prevalence of atopic diseases has been ascribed to the so-called hygiene hypothesis. According to this theory, early infections or exposure to microbial-derived material, such as LPS, early in life prevent the development of Th2-driven allergic disease. Thus, polymorphisms of genes involved in the recognition of microbial material may alter the balance between Th1- and Th2-driven immune responses and could change an individual’s susceptibility to development of allergic diseases. Indeed, polymorphisms of a number of innate immunity genes such as CD14 and Toll-like receptors have been associated with the development of allergy. Recently, a polymorphism (G2722C) that results in functional impairment of caspase recruitment domain–containing protein 15, an intracellular receptor for LPS involved in NF-κB activation, has been associated with a twofold increased risk for development of AD (23). Thus, not only reduced microbial exposure in the environment, but also impaired molecular recognition of microbial molecules, may give rise to enhanced Th2 responses.
The skin represents the interface between the body and the surrounding environment. It is therefore subjected to numerous insults, which act as triggers of inflammation. These include irritants as well as allergens. These factors trigger the scratching that ensues to induce and sustain the inflammatory cascade initiated by release of proinflammatory cytokines from atopic keratinocytes. Stress itself has been found to induce immunologic changes and combined with scratching will trigger the exacerbation of AD.
Placebo-controlled, food challenge studies have demonstrated that food allergens can induce eczematoid skin rashes in nearly 40% of children with moderate to severe AD. In a subset of these patients, urticarial reactions, or noncutaneous symptoms, are elicited, which can trigger the itch-scratch cycle that flares this skin condition. Children with food allergies generally have positive immediate skin tests or serum IgE directed to various foods, particularly eggs, milk, wheat, soy, and peanuts. Importantly, food allergen–specific T cells have been cloned from the skin lesions of patients with AD, providing direct evidence that foods can contribute to skin inflammation. In mouse models of AD, oral sensitization with foods results in the elicitation of eczematous skin lesions on repeat oral food challenges.
After the age of 3, children frequently outgrow food allergy but may become sensitized to inhalant allergens. Pruritus and skin lesions can develop after intranasal or bronchial inhalation challenge with aeroallergens in sensitized AD patients. Epicutaneous application of aeroallergens (e.g., HDMs, weeds, animal danders, and molds) by atopy patch test on uninvolved skin of AD patients elicits eczematoid reactions in 30–50% of patients with AD. A combination of effective HDM-reduction measures has been reported to improve AD. The degree of IgE sensitization to aeroallergens is directly associated with the severity of AD. The isolation from AD skin lesions and allergen patch test sites of T cells that selectively respond to Dermatophagoides pteronyssinus and other aeroallergens supports the concept that immune responses in AD skin can be elicited by environmental aeroallergens.
Patients with severe AD have been reported to generate IgE antibodies directed against human proteins. The autoallergens identified to date have been intracellular proteins, which can be detected in IgE immune complexes of AD sera. These data suggest that while IgE immune responses are initiated by environmental allergens, allergic inflammation can be maintained by the release of human proteins derived from damaged skin in chronic AD.
Most patients with AD are colonized with Staphylococcus aureus and suffer relapses of their skin disease following overgrowth of this organism (24). The importance of S. aureus is supported by the observation that, in AD patients with secondary infection, treatment with a combination of antistaphylococcal antibiotics and topical corticosteroids results in greater clinical improvement than treatment with topical corticosteroids alone. One strategy by which S. aureus exacerbates AD is by secreting toxins called superantigens, which stimulate activation of T cells and macrophages. Most AD patients make specific IgE antibodies directed against staphylococcal superantigens (25), and these IgE antisuperantigens correlate with skin disease severity. Superantigens also induce corticosteroid resistance, suggesting that several mechanisms exist by which superantigens increase AD severity.
Increased binding of S. aureus to skin is driven by underlying AD skin inflammation. This is clinically supported by studies demonstrating that treatment with topical corticosteroids or tacrolimus reduces S. aureus counts on atopic skin. In experimental animal models, S. aureus binding was significantly greater at skin sites with Th2- as compared to Th1-mediated skin inflammation due to IL-4–induced expression of fibronectin. AD skin has also been found to be deficient in antimicrobial peptides needed for host defense against bacteria, fungi, and viruses (17, 18). Thus, once S. aureus binds to AD skin, inadequate host defense allows bacteria to colonize and grow. The lack of skin innate immune responses may predispose these patients to infection as well to fungi and viruses. Patients with AD have an increased propensity toward disseminated infections with herpes simplex or vaccinia virus. As such, smallpox vaccination is contraindicated in patients with AD unless there is imminent danger of exposure to smallpox.
Successful management of AD requires a multipronged approach. This includes the avoidance of irritants and specific immunologic stimuli, including foods and aeroallergens, which can either induce the dermatitis or trigger the itch-scratch cycle that results in AD (1). Skin hydration and use of emollients to repair the impaired skin barrier function is a key part of management. Addition of a “ceramide-dominant” emollient to standard therapy results in both clinical improvement and decreased transepidermal water loss and improvement of stratum corneum integrity in children with “stubborn-to-recalcitrant” AD (26). Although viral or fungal infection can trigger AD, S. aureus colonization or infection is the most common cause of increased AD severity. In such patients a course of antibiotics, in combination with anti-inflammatory therapy, will lead to better control of skin disease. The key to successful long-term management of AD is the introduction of effective anti-inflammatory therapy.
This class of drugs is the mainstay of anti-inflammatory treatment, showing efficacy in the control of both acute and chronic skin inflammation. Corticosteroids mediate their anti-inflammatory effects through a cytoplasmic glucocorticoid receptor (GCR) in target cells. Upon ligand binding, the corticosteroid/GCR complex translocates into the nucleus where it mediates its anti-inflammatory effects via two major actions. First, the GCR complex can induce gene transcription by binding of GCR dimers to glucocorticoid response elements (a process known as transactivation) in the promoter regions of target genes. Transactivation is mainly responsible for the unwanted side effects of glucocorticoids. The major mechanism by which GCR mediates its anti-inflammatory effects is via a process called transrepression, which is independent of GCR DNA binding. In this process, ligand-bound GCR binds to various transcription factors, including activator protein-1 and NF-κB, via protein-protein interactions to inhibit the transcriptional activity of various proinflammatory genes encoding proinflammatory proteins such as cytokines (IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-11, IL-13, TNF-α, and GM-CSF), chemokines (IL-8, RANTES, macrophage inflammatory protein–1α [MIP-1α], monocyte chemotactic protein-1 [MCP-1], MCP-3, MCP-4, and eotaxin), and adhesion molecules (ICAM-1,VCAM-1, and E-selectin).
Due to concerns about potential side effects associated with chronic use, topical corticosteroids have not been used for maintenance therapy, especially on nonlesional skin, in AD. However, normal-appearing skin in AD is associated with subclinical inflammation, suggesting that maintenance anti-inflammatory therapy may be required to prevent relapse. Indeed, several studies with fluticasone propionate have shown that once control of clinical disease is achieved, long-term control can be maintained with twice weekly therapy (27).
Topical FK506 and pimecrolimus have recently been FDA-approved for the treatment of AD. Both agents act by binding with high affinity to the 12 kDa macrophilin and inhibit the phosphatase activity of the calcium-dependent serine/threonine phosphatase, calcineurin. In the presence of these calcineurin inhibitors, the transcription factor, nuclear factor of activated T cell protein (NF-ATp), is not dephosphorylated and therefore cannot translocate into the nucleus to activate transcription of various Th1 and Th2 cytokine genes. Tacrolimus and pimecrolimus inhibit the activation of a number of key effector cells involved in AD, including T cells and mast cells.
Short-term, multicenter, blinded, vehicle-controlled trials, in both adults and children, have shown both topical tacrolimus and pimecrolimus to be effective. In a minority of patients, stinging and local irritation have been reported with this new class of drugs, but overall they have been found to be quite safe. Long-term studies with both drugs have been performed in adults and children, with demonstrated sustained efficacy and no significant side effects. Unlike topical glucocorticoids, topical calcineurin inhibitors are not atrophogenic and have been used safely for facial and eyelid eczema. Several studies with pimecrolimus cream have also found that introducing the medication at the earliest signs of clinical disease results in significantly less need for corticosteroid “rescue” therapy.
The approval of topical calcineurin inhibitors for the treatment of AD represents a significant advance in our management options for this disease. The distinction between pimecrolimus and tacrolimus is that pimecrolimus is a cream that is somewhat weaker than tacrolimus but less irritating. Tacrolimus is currently marketed as an ointment that is more potent but also more irritating. Importantly, there are situations in which topical calcineurin inhibitors may be advantageous over topical corticosteroids and may be useful as first-line therapy. These would include treatment of patients who are poorly responsive to topical steroids or have steroid phobia, and treatment of face and neck dermatitis where ineffective, low-potency topical corticosteroids are usually used due to fears of steroid-induced skin atrophy. The potential use of topical calcineurin inhibitors as maintenance therapy is also intriguing for prevention of AD flares and progression of the atopic march (28, 29). However, although systemic absorption of these compounds is low, there is a need for careful surveillance to rule out the possibility that skin cancers and increased viral skin infections will appear when such agents are used long-term.
UV light therapy can be a useful treatment modality for chronic recalcitrant AD. The photoimmunologic effects target key cells in atopic inflammation, such as LCs and keratinocytes, interfering with cytokine production and decreasing the expression of activation markers such as HLA-DR and IL-2 receptor on CLA+ T cells. Unlike traditional UVA-UVB phototherapy, which appears less effective for acute exacerbations and acts primarily in the epidermis, high-dose UVA1 therapy has been shown to significantly decrease dermal IgE-binding cells, including mast cells, LCs, and DCs. UVA1 also inhibits LC migration out of the epidermis.
Cyclosporin A is a potent systemic calcineurin inhibitor. A number of studies have demonstrated its efficacy in both children and adults with severe, refractory AD, although toxicity, primarily renal, limits its chronic use. Preliminary data with oral pimecrolimus suggest that it may have a greater safety margin than either systemic cyclosporin or tacrolimus, which could make treatment more acceptable to some patients and reach inflammatory targets not accessible to topical medications (30). Antimetabolites, including mycophenolate mofetil, a purine biosynthesis inhibitor, methotrexate, and azathiaprine, have also been utilized for recalcitrant AD, although the potential for systemic toxicities restricts their use and requires close monitoring.
Although a number of anecdotal and case reports suggest clinical benefit from allergen-specific desensitization in AD, double-blinded, controlled trials have failed to show consistent efficacy of immunotherapy compared to placebo in the treatment of AD. Recently, omalizumab, a humanized IgG1 monoclonal antibody against IgE that recognizes and masks an epitope in the CH3 region of IgE responsible for binding to the high-affinity FcεR on mast cells and basophils, has been shown to be effective in treatment of allergic asthma and allergic rhinitis. Thus, it could potentially neutralize the effects of IgE in AD. However, the high serum IgE levels seen in AD may limit the usefulness of this antibody, although it may have a role in food-induced AD. In this respect, treatment of a population of peanut-allergic patients with anti-IgE significantly increased their threshold of sensitivity to peanuts on oral food challenge, suggesting protection against unintended ingestion of the food allergen (31).
Insights into the role that certain cells and cytokines play in AD create opportunities for the development of targeted therapy. However, given the complexity of the biological processes involved, none of the tested compounds to date has proven to be the magic bullet. Some promising agents have been limited by associated toxicity. In this respect, several studies with recombinant human IFN-γ demonstrated clinical efficacy that correlated with a decrease in blood eosinophilia, even with long-term therapy. Early treatment with microbial probiotics may be more beneficial by boosting Th1 immune responses in AD (32). Additional approaches include cytokine modulation (e.g., soluble IL-4 receptor; anti–IL-5 monoclonal antibody; TNF inhibitors), blockade of inflammatory cell recruitment (chemokine receptor antagonists, CLA inhibitors, ref. 33), inhibition of T cell activation (alefacept, efalizumab, ref. 34), and use of synthetic antimicrobial peptides (Table (Table22).
Our challenge for the future will be the development of more effective and safer drugs in the treatment of AD. Given the complexity of immune pathways that lead to AD, it is possible that more selective anti-inflammatory or immunomodulatory agents will be less effective. Thus, it will be important to better characterize the key immune pathways leading to the different phenotypes of AD, as medications may vary in their effectiveness for treatment of different forms of AD. For example, it is important to resolve whether the immune pathways leading to so-called intrinsic (or pure) vs. extrinsic (IgE-mediated) AD are fundamentally different. The role that IgE plays in allergic disease is still debated. Animal models of allergy can occur in IgE-knockout mice. This molecule may primarily act to facilitate allergen processing for Th2 cell activation and immediate reaction at extremely low environmental concentrations of allergens. Immune responses to allergen may occur in the absence of IgE in intrinsic AD but require higher allergen concentrations for T cell activation in the absence of immediate reaction. Indeed, atopy patch tests can be positive in a subset of AD patients lacking IgE responses to the relevant allergen. The relative role of microbes and autoantigens in the initiation and progression of AD also requires further clarification.
New advances are likely to require better definitions for the various clinical phenotypes of AD, including identification of the susceptibility genes leading to the different forms of AD and delineation of the relative role of immunoregulatory abnormalities and structural skin barrier defects underlying AD skin. New treatment paradigms are needed for preventing disease progression of AD to more severe forms of this skin disease and halting the so-called atopic march, which results in development of asthma. The factors that determine the chronicity, skin remodeling, and natural history of this disease remain poorly characterized. An understanding of the genes responsible for individual variation in response to therapy will be tied to the development of pharmacogenetics and the targeting of effective therapies to the different phenotypes of AD.
Nonstandard abbreviations used: atopic dermatitis (AD); cutaneous lymphocyte-associated antigen (CLA); Fcε receptor I (FcεRI); glucocorticoid receptor (GCR); house dust mite (HDM); inflammatory dendritic epidermal cell (IDEC); Langerhans cell (LC); macrophage inflammatory protein (MIP); monocyte chemotactic protein (MCP).
Conflict of interest: D.Y.M. Leung is a consultant, grant recipient, and member of the Speaker’s Bureau for Novartis, Fujisawa, and Glaxo/SKB. The remaining authors have declared that no conflict of interest exists.