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The importance of vitamin D levels in autoimmune diseases

Abstracts

In addition to its role in calcium homeostasis, it is believed that the active form of vitamin D has immunomodulatory effects on cells of the immune system, particularly T lymphocytes, as well as on the production and action of several cytokines. The interaction of vitamin D with the immune system has been the target of a growing number of publications in recent years. Current studies have linked the deficiency of vitamin D with different autoimmune diseases, including insulin-dependent diabetes mellitus (IDDM), multiple sclerosis (MS), inflammatory bowel disease (IBD), systemic lupus erythematosus (SLE), and rheumatoid arthritis (RA). This article reviews the physiology and immunomodulatory role of vitamin D, emphasizing its involvement in rheumatic diseases such as SLE and RA.

vitamin D; immune system; autoimmune diseases; systemic lupus erythematosus; rheumatoid arthritis


Além do seu papel na homeostase do cálcio, acredita-se que a forma ativa da vitamina D apresenta efeitos imunomoduladores sobre as células do sistema imunológico, sobretudo linfócitos T, bem como na produção e na ação de diversas citocinas. A interação da vitamina D com o sistema imunológico vem sendo alvo de um número crescente de publicações nos últimos anos. Estudos atuais têm relacionado a deficiência de vitamina D com várias doenças autoimunes, como diabetes mellitus insulino-dependente (DMID), esclerose múltipla (EM), doença inflamatória intestinal (DII), lúpus eritematoso sistêmico (LES) e artrite reumatoide (AR). O artigo faz uma revisão da fisiologia e do papel imunomodulador da vitamina D, enfatizando sua participação nas doenças reumatológicas, como o lúpus e a artrite reumatoide.

vitamina D; sistema imunológico; doenças autoimunes; lúpus eritematoso sistêmico; artrite reumatoide


REVIEW ARTICLE

The importance of vitamin D levels in autoimmune diseases

Cláudia Diniz Lopes MarquesI; Andréa Tavares DantasII; Thiago Sotero FragosoIII; Ângela Luzia Branco Pinto DuarteIV

IRheumatologist, specialist in Public Health, and Tutor of Escola Pernambucana de Medicina - FBV/IMIP

IIFormer resident of the Rheumatology Department of HC-UFPE and student of the Postgraduate Program in Health Sciences of UFPE

IIIPediatric Rheumatology Resident of HC-UFPE and student of the Postgraduate Program in Health Sciences of UFPE

IVFull Professor and Chief of the Rheumatology Department of HC-UFPE

Correspondence to

ABSTRACT

In addition to its role in calcium homeostasis, it is believed that the active form of vitamin D has immunomodulatory effects on cells of the immune system, particularly T lymphocytes, as well as on the production and action of several cytokines. The interaction of vitamin D with the immune system has been the target of a growing number of publications in recent years. Current studies have linked the deficiency of vitamin D with different autoimmune diseases, including insulin-dependent diabetes mellitus (IDDM), multiple sclerosis (MS), inflammatory bowel disease (IBD), systemic lupus erythematosus (SLE), and rheumatoid arthritis (RA). This article reviews the physiology and immunomodulatory role of vitamin D, emphasizing its involvement in rheumatic diseases such as SLE and RA.

Keywords: vitamin D, immune system, autoimmune diseases, systemic lupus erythematosus, rheumatoid arthritis.

INTRODUCTION

Vitamin D and its prohormones have been the focus of a growing number of studies in past years, demonstrating their function not only in calcium metabolism and bone formation, but also their interaction with the immune system, which is not surprising, since vitamin D receptors are expressed in different tissues, such as brain, heart, skin, bowel, gonads, prostate, breasts, and immune cells, as well as bones, kidneys, and parathyroid glands.1

Current studies have related vitamin D deficiency with several autoimmune disorders, including insulin-dependent diabetes mellitus (IDDM), multiple sclerosis (MS), inflammatory bowel disease (IBD), systemic lupus erythematosus (SLE), and rheumatoid arthritis (RA).1-4 In view of those associations, it has been suggested that vitamin D is an extrinsic factor capable of affecting the prevalence of autoimmune diseases.5

Vitamin D seems to interact with the immune system through its actions on the regulation and differentiation of cells like lymphocytes, macrophages, and natural killer cells (NK), besides interfering in the in vivo and in vitro production of cytokines. Among the immunomodulatory effects demonstrated we should mention: a reduction in the production of interleukin-2 (IL-2), gamma interferon (INFγ), and tumor necrosis factor (TNF); inhibition of the expression of IL-6; and inhibition of the secretion and production of autoantibodies by B lymphocytes.6,7

VITAMIN D PHYSIOLOGY

Vitamin D, or cholecalciferol, is a steroidal hormone whose main function is the regulation of calcium homeostasis, and bone formation and reabsorption through the interaction with the parathyroid glands, kidneys, and bowel.8

The main source of vitamin D comes from the endogenous production in the skin after exposure to ultraviolet B light.8-10 The diet is an alternative, but less effective, source of vitamin D, which is responsible for only 20% of the body needs, but it assumes a major role in the elderly, institutionalized people, and those living in temperate climates.

Upon exposure to ultraviolet radiation, the cutaneous precursor of vitamin D, 7-dehydrocholesterol, undergoes photochemical cleavage, giving rise to previtamin-D3. Within 48 hours, this heat-susceptible molecule undergoes temperature-dependent molecular rearrangement, resulting in the formation of vitamin-D3 (cholecalciferol). Previtamin-D3 can also undergo isomerization, originating biologically inactive compounds (lumisterol and tachysterol), and this mechanism is important to prevent overproduction of vitamin D after prolonged exposure to sunlight. The degree of skin pigmentation is another limiting step in the production of vitamin D, since ultraviolet rays have limited penetration in dark skin.9

In the blood, vitamin D is bound, mainly, to a vitamin D-binding protein, although a small fraction is bound to albumin.9 In a cytochrome P450-like enzyme-mediated reaction, vitamin D is hydroxylated in the liver and converted in 25-hydroxyvitamin D [25(OH)D], the most abundant circulating form, which is biologically inactive.8,9 Hepatic hydroxylation is poorly regulated and, therefore, blood levels of 25(OH)D reflect the amount of vitamin D entering the circulation, which is proportional to the amount of vitamin D ingested and produced in the skin.9,10

The additional hydroxylation in the cells of the convulated proximal tubule of the kidneys, originating 1.25-dihydroxyvitamin D [1.25(OH)2D3], the biologically active form,8,9 is the final step in the production of the hormone.

Extra-renal hydroxylation of vitamin D, originating a vitamin with autocrine and paracrine effects that inhibits cellular proliferation, promotes cellular differentiation, and immune regulation, is currently accepted. Regulation of renal 1-α-hydroxylase depends on the ingestion of calcium and phosphate, circulating levels of 1.25(OH)2D3 metabolites, and parathyroid hormone (PTH). On the other hand, the extra-renal regulation of hydroxylase is determined by local factors, such as the production of cytokines and growing factors, and by the levels of 25(OH)D, making it the most sensitive pathway to vitamin D deficiency.10

The increase in the intestinal absorption of calcium by participating in the stimulation of the active transportation of this ion in enterocytes, is main function of vitamin D.9,11 It also participates in calcium mobilization from the bones, in the presence of PTH, and it increases the renal reabsorption of calcium from the distal tubule.12 Prolonged vitamin D deficiency causes rickets and osteomalacia, and, in adults, when associated with osteoporosis, it increases the risk of fractures.13

Other actions of vitamin D in the positive regulation of bone formation include: inhibits the synthesis of type 1 collagen; induces the synthesis of osteocalcine; and promotes the in vitro differentiation of monocytes-macrophages precursors into osteoclasts. It also stimulates the production of RANK ligand (RANK-L), which facilitates maturation of osteoclast precursors into osteoclasts, which, in turn, mobilize calcium storage in the bones to maintain calcium homeostasis.8,9 Vitamin D exerts its biological actions through the binding of nuclear receptors, vitamin D receptors (VDR), which, similar to steroid, thyroid hormone, and retinoid receptors, regulate the transcription of DNA into RNA.9,11 Those receptors are expressed by a variety of cells, including the epithelium of the small bowel and renal tubules, osteoblasts, osteoclasts, hematopoietic cells, lymphocytes, epidermal cells, pancreatic cells, myocytes, and neurons.11

More recently, noncalcemic actions of vitamin D mediated by VDR, such as cellular proliferation and differentiation, besides immunomodulation, have been recognized. Vitamin D receptor is widely expressed in the majority of immune cells, including monocytes, macrophages, dendritic cells, NK cells, and T and B lymphocytes.14 However, it concentration is higher in immature immune cells in the thymus and immature CD8 lymphocytes, regardless of their activation status.8,12 Table 1 shows a summary of the main effects of vitamin D in the immune system.

DETERMINATION OF THE SERUM LEVELS OF VITAMIN D

Although 1.25OH2D3 is the active form of this vitamin, it should not be used to evaluate serum levels, since it has a half-life of only four hours and its concentration is 1,000 times lower than that of 25(OH)D. Besides, vitamin D deficiency is associated with a compensatory increase of PTH secretion, which stimulated the kidneys to produce more 1.25OH2D3. Thus, when 25(OH)D levels fall due to vitamin D deficiency, the concentrations of 1.25OH2D3 remain within normal limits and, in some cases, they might even be elevated.9,15

To determine whether adequate levels of vitamin D are present, one should measure the concentration of 25(OH)D, the predominant circulating form, with a half-life of approximately two weeks.9

A consensus on the ideal serum level of vitamin D does not exist. The majority of the specialists agree that the levels of vitamin D should remain with a concentration range that does not induce an increase in PTH levels.10,15 Normal levels vary according to the commercial assay used, from 25-37.5 nmol/L (10-15 ng/mL) to 137.5-162.5 nmol/L (55-65 mg/ mL).13 Recent reviews have suggested that 50 to 80 nmol/L should be the ideal concentration, while others recommend levels between 75 and 125 nmol/L.16 Using the elevation of PTH levels as a biomarker that reflects low levels of vitamin D, deficiency should be defined as a serum concentration below 32 ng/mL (80 nmol/L).16

The ideal level of vitamin D necessary to guarantee the immune system will work properly has not been defined. It is most likely that this level should be different than that necessary to prevent vitamin D deficiency or maintain calcium homeostasis.5

EFFECTS OF VITAMIN D ON THE IMMUNE SYSTEM

Based on the ectopic production of vitamin D in cells of the immune system and the presence of VDR in tissues that are not related with bone physiology, the immunoregulatory properties of vitamin D have been better characterized.17 Epidemiological studies have shown that deficiency of this vitamin could be associated with an increased risk of colon and prostate cancer, cardiovascular disease, and infections.13,15,17,18

Several mechanisms have been proposed to explain the role of vitamin D in the physiology of the immune system, as can be seen in Table 1.

Among the main functions of vitamin D in the immune system, we could mention: regulation of the differentiation and activation of CD4 lymphocytes;5,11,19 increase in the number and function of regulatory T cells (Treg);11 in vitro inhibition of the differentiation of monocytes in dendritic cells;8,11 reduction in the production of cytokines, interferon-g, IL-2, and TNF-α by Th1 cells, and stimulation of the function of Th2 helper cells;5,8,11,17 inhibition of the production of IL-17 by Th1 cells;20 and in vivo and in vitro stimulation of NK T cells.21

VITAMIN D AND AUTOIMMUNE DISEASES

As a rule, the effects of vitamin D in the immune system translate into an enhancement of innate immunity associated with a multifaceted regulation of acquired immunity.22 A relationship between vitamin D deficiency and the prevalence of some autoimmune diseases like IDDM, MS, RA, SLE, and IBD has been demonstrated.5,13

It has been suggested that vitamin D and its analogues not only prevent the development of autoimmune diseases, but they could also be used in their treatment.11 Vitamin D supplementation has been shown to be therapeutically effective in different experimental animal models, such as allergic encephalomyelitis, collagen-induced arthritis, type 1 diabetes mellitus, inflammatory bowel disease, autoimmune thyroiditis, and SLE.8

Low serum levels of vitamin D could also be related with factors other than nutritional, such as reduction in physical capacity, decreased exposure to sunlight, increased frequency of polymorphisms of VDR genes, and side effects of drugs.10,11

Rheumatoid arthritis

Rheumatoid arthritis is an autoimmune disorder with a very complex physiology. It is believed that the first event is the activation of antigen-dependent T cells triggering an immune response essentially of the Th1 type. This activation has multiple effects, including activation and proliferation of endothelial and synovial cells, recruitment and activation of proinflammatory cells, secretion of cytokines and proteases by macrophages and fibroblast-like synovial cells, and production of auto-antibodies.23

As mentioned before, vitamin D deficiency is associated with an exacerbation of Th1 immune response. Thus, in the last few years, the possible role of vitamin D in the pathogenesis, activity, and treatment of RA has been raised based on the results and observations of clinical and laboratorial studies.5

The rationale for relating vitamin D deficiency and RA is based on two facts: evidence indicate that patients with RA have vitamin D deficiency and the presence of 1.25(OH)2D3 and VDR in macrophages, chondrocytes, and synovial cells in the joints of those patients.14,24

The relationship between polymorphisms of the VDR gene and the onset of RA activity has been demonstrated in a study in which patients with BB or Bb genotypes for VDR had higher indices in the HAQ, erythrocyte sedimentation rate (ESR), cumulative dose of corticosteroids, and number of disease-modifying antirheumatic drugs (DMARDs) when compared to patients with the BB genotype.25

In collagen-induced arthritis models, dietarian supplementation or oral administration of vitamin D prevented the development or delayed the progression of arthritis.1,26 Similarly, a study with 29,386 women showed that the risk of developing RA was inversely related to higher ingestion of vitamin D.27 However, in another large prospective study that evaluated 186,389 women from 1980 to 2002, an association between the increased ingestion of vitamin D and the risk of developing RA or SLE was not observed.28 Corroborating this result, a study with 79 blood donors evaluated the serum levels of vitamin D; differences between the basal levels of vitamin D of patients who later developed RA and the control group were not observed.29 Those findings demonstrate that this is still a very controversial subject, lacking a consensus among the authors on the real relationship between vitamin D and RA.

In an open study with 19 patients with RA treated with traditional DMARDs, oral supplementation with high doses of alfacalcidol for three months reduced the severity of the symptoms in 89% of the patients, 45% of which achieved complete remission and 44% had satisfactory results. Higher incidence of side effects, such as hypercalcemia, was not observed.30

There also seem to be an inverse relationship between disease activity and the concentration of vitamin D metabolites in patients with inflammatory arthritis.31 In basal, pre-treatment conditions, a proportional inverse relationship among the levels of 25(OH) vitamin D and the number of painful joints, DAS28, and HAQ is observed. For each increase in 10 ng/mL in vitamin D serum levels, the DAS28 reduced by 0.3 points and the levels of CRP by 25%.31

Systemic lupus erythematosus

Several authors have demonstrated a higher prevalence of vitamin D deficiency in SLE patients when compared to individuals with other rheumatologic diseases and healthy individuals.3,32,34 In a transversal study, Muller et al.33 observed that the levels of vitamin D were significantly lower in SLE patients (mean 13 ng/mL) when compared to patients with RA (24 ng/mL), osteoarthritis (32 ng/mL), and healthy controls (27 ng/mL). Huisman et al.34 observed that 50% of SLE patients had vitamin D deficiency (cut off <50 nmol/L or 20 ng/mL). However, when those individuals were compared to those with fibromyalgia, differences in PTH, 25(OH)D, and 1.25(OH2)D3 levels were not observed.

Patients with systemic lupus erythematosus have multiple risk factors for 25(OH)D deficiency. Photosensitivity, characteristic of the disease, and the recommendation to apply sunscreen are responsible for lower sun exposure, decreasing the production of vitamin D in the skin. Chronic treatment with corticosteroids and hydroxichloroquine seems to affect vitamin D metabolism, although evidence are not so clear yet. Besides, severe renal involvement, which can be seen in patients with lupus nephritis, can affect the hydroxylation step of 25(OH)D.13

The higher incidence and severity of SLE in individuals of African descent has been well documented. It is believed that this is a consequence of not only genetic factors, but it is speculated that lower serum concentrations of 25(OH)D, due to the lower cutaneous conversion rate secondary to skin color, would be another important factor.19

It has been observed that critical levels of vitamin D (<10 ng/mL) are more common in patients with renal involvement and photosensitive skin lesions.3 The association between low serum levels of vitamin D and disease activity scores, according to the SLEDAI (Systemic Lupus Erythematosus Disease Activity Index) and ECLAM (European Consensus Lupus Activity Measurement) has been documented.19,35 Thudi et al.35 demonstrated that functional assessment using combined scores (modified HAQ, global VAS by the patient, and fatigue scale) was worse in patients with probable or confirmed diagnosis of lupus and vitamin D deficiency. However, this study did not demonstrate an association between vitamin D deficiency and the levels of auto-antibodies, including anti-DNA.

The association between vitamin D deficiency and disease activity was demonstrated in a Brazilian study with 36 patients: levels of 25(OH)D were lower (mean 17.4 ± 12.5 ng/mL) in patients with high disease activity (SLEDAI > 12) when compared to those with mild disease activity (SLEDAI < 3) and the control group36. In a Spanish study with 92 SLE patients, the authors observed low levels of vitamin D (< 30 ng/mL) in 75% of the patients and deficiency (< 10 ng/mL) in 45% of them. In this study, 45% of the patients with low levels and 35% of those with deficiency were on calcium and vitamin D supplementation at the time of the evaluation. This study also showed higher degree of fatigue in patients with vitamin D deficiency, although a relationship between disease duration, SLEDAI, or SLIC-ACR was not observed.13

Carvalho et al.37 investigated the presence of anti-vitamin D antibodies in the serum of SLE patients to better explain vitamin D deficiency in autoimmune diseases. One-hundred and seventy-one SLE patients were investigated and 4% of them had vitamin D antibodies but the levels of 25(OH)D were similar in patients with or without those autoantibodies. Among the clinical and laboratorial associations investigated, the presence of anti-dsDNA was the only one that showed a strong relationship with anti-vitamin D antibodies (P = 0.0004).

Undifferentiated connective tissue disease (UCTD)

Astudy by Zold et al.38 demonstrated the presence of a seasonal variation in the levels of 25(OH)D in patients with UCTD and that those levels were lower in this population than in the control population. In this same study, 21.7% of patients with UCTD and vitamin D deficiency developed established connective tissue disease (especially RA, SLE, Sjögren's syndrome, and mixed connective tissue disease); their level of vitamin D was lower than that of patients who remained with undifferentiated disease.

Inflammatory bowel disease (IBD)

Inflammatory bowel disease (Ulcerative Colitis and Crohn's disease) is an immunomediated disorder whose pathophysiology involves Th1 cells, with the production of IL-2, TNF-α, and IFN-γ.14 Low serum levels of 25(OH) D have been described in IBD. In a study by Jahnsen et al.,39 the authors observed vitamin D deficiency in 27% of the patients with Crohn's disease and in 15% of those with ulcerative colitis.

It seems that a combination of factors, such as low ingestion and malabsorption of vitamin D, and decreased exposure to the sun, are responsible for the higher frequency of vitamin D deficiency in IBD.8

In experimental IBD with IL-10 knockout rats, vitamin D deficiency accelerated the disease, with earlier development of diarrhea and cachexia and higher mortality rate.14 On the other hand, treatment with 1.25(OH)2D3 prevented the development of symptoms, besides reducing the progression and activity of the disease.1,3

Multiple sclerosis

Multiple sclerosis is an autoimmune disease of the central nervous system characterized by inadequate recognition of auto-epitopes in myelinated nerve fibers by cells of the acquired immune system, generating an inflammatory immune response mediated by lymphocytes and macrophages, resulting in localized areas of inflammation and demyelnation.14

Some studies have also demonstrated the association of vitamin deficiency and MS and its role not only in the reduction of relapse rates, as well as in the prevention of its development.40,41 The risk of MS decreases considerably (up to 40%) in Caucasian individuals with a high ingestion of vitamin D. The same benefit was not observed in individuals of African descent and Hispanics.40

In a study with experimental models of MS, the administration of vitamin D prevented the onset of autoimmune allergic encephalitis and slowed down the progression of the disease.42

Type I diabetes mellitus

Several effector mechanisms that lead to cell destruction, including the presence of CD8+ lymphocytes and macrophages, which regulate the differentiation of Th1 cells through Il-12, are involved in the pathophysiology of type 1 diabetes mellitus (DM1).43 In experimental models using non-obese diabetic mice (NOD mice), vitamin D deficiency accelerated the onset of DM1.44 Using this same model, early supplementation of 1.25 (OH)2D3, before the progression of a mononuclear infiltrate within pancreatic cells, reduced autoimmune insulitis and prevented the development of diabetes.45

Epidemiological studies have demonstrated that dietary supplementation of vitamin D in childhood can reduce the risk of developing DM1. A Finish study with a 30-year follow-up observed a significant reduction in the prevalence of DM1 in children who received daily vitamin D supplementation (RR = 0.12).46

Inflammatory cutaneous diseases

Dysfunction of cathelicidins, antimicrobial peptides (AMPs) present in the skin, is relevant in the pathogenesis of several cutaneous diseases, including atopic dermatitis, rosacea, and psoriasis.47,48 A recent study demonstrated that vitamin D3 is one of the main factors responsible for regulating the expression of cathelicidins, involving epigenetic alterations, such as histone acetylation.49 Thus, treatments aimed at the metabolism and signaling of vitamin D3 could be beneficial in cutaneous inflammatory diseases.48,53

In psoriasis, blocking the expression of human peptides of cathelicidins (LL-37) can inhibit the activation of dendritic cells and cutaneous inflammation.53 Paradoxically, vitamin D3 analogues were used for a long time in the treatment of psoriasis. Those compounds bind vitamin D receptors, activating them, therefore increasing the levels of cathelicidins in the keratinocytes and, presumably, worsening inflammation. However, the opposite occurs: improvement of cutaneous inflammation and reversion of the morphological changes in damaged skin.53

The use of vitamin D3 and its analogues in the treatment of psoriasis has been studied for several years, demonstrating the effects of calcitriol on the improvement of psoriatic lesions. However, due to hypercalcemia and hypercalciuria, long-term use of those agents is limited. Those findings led to the investigation of other vitamin D3 analogues that could have the antipsoriatic effects of vitamin D3 without the undesirable side effects in calcium homeostasis. Calcipotriene (also known as calcipotriol), one of those compounds, has an effect of differentiation and inhibition of the proliferation of keratinocytes in vitro, while the effects in calcium metabolism were 100 to 200 times smaller than those of calcitriol.54 Currently, topical synthetic vitamin D analogues represent one of the safest and most effective alternatives for the treatment of mild to moderate psoriasis, comparable to high-potency topical corticosteroids.55,56

Vitamin D supplementation in the prophylaxis and treatment of autoimmune diseases

Despite clinical and experimental evidence that vitamin D deficiency is an important factor responsible for increasing the prevalence of specific autoimmune diseases and the proven immunomodulatory effects of this compound,5 as described above, little is known about the effects of vitamin D supplementation in the prevention and treatment of those disorders; however, it is believed that its supplementation is relevant for the control of graft rejection and in the prevention and treatment of autoimmune diseases.22

Most studies available have used experimental models MS,57,58 IBD,59 of lupus,6 arthritis,60,61 and type 1 DM,45,62 and all have demonstrated the beneficial effects of vitamin D supplementation in modulating the components of the immune system responsible for the inflammation, such as the expression of cytokines, growth factors, nitrous oxide, and metalloproteinases.

Only small and non-controlled studies have been carried out in humans; however, they also seem to indicate the beneficial effects of vitamin D supplementation in preventing the development of autoimmune diseases, as well as in reducing the severity of pre-existing disease.63-69

FINAL CONSIDERATIONS

Evidence suggest that vitamin D deficiency can play an important role in regulating the immune system and, probably, in the prevention of immune-mediated diseases. However, further studies are necessary to determine the risks and benefits of vitamin D supplementation, when and in which patients the levels of 25(OH)D should be measured, which reference levels should be considered deficiency/insufficiency, clinical actions, and the real impact of this association in daily clinical practice.

REFERENCES

  • 1
    Jones BJ, Twomey PJ. Issues with vitamin D in routine clinical practice. Rheumatology 2008; 47:1267-68.
  • 2
    Cantorna MT. Vitamin D and autoimmunity: is vitamin D status an environmental factor affecting autoimmune disease prevalence? Proc Soc Exp Biol Med 2000; 223:230-3.
  • 3
    Kamen DL, Cooper GS, Bouali H, Shaftman SR, Hollis BW, Gilkeson GS. Vitamin D deficiency in systemic lupus erythematosus. Autoimmun Rev 2006; 5:114-7.
  • 4
    Lipps, P. Which circulating level of 25-hydroxyvitamin D is appropriate? J Steroid Biochem Mol Biol 2004: 611-4.
  • 5
    Cantorna MT, Mahon B. Mounting evidence for vitamin D as an environmental factor affecting autoimmune disease prevalence. Exp Bio Med (Maywood) 2004; 229(11):1136-42.
  • 6
    Lemire JM, Ince A, Takashima M. 1,25-Dihydroxyvitamin D3 attenuates the expression of experimental murine lupus of MRL/I mice. Autoimmunity 1992; 12(2):143-8.
  • 7
    Linker-Israeli M, Elstner E, Klinenberg JR, Wallace DJ, Koeffler HP. Vitamin D(3) and its synthetic analogs inhibit the spontaneous in vitro immunoglobulin production by SLE-derived PBMC. Clin Immunol 2001; 99:82-93.
  • 8
    Arnson Y, Amital H, Shoenfeld Y. Vitamin D and autoimmunity: new etiological and therapeutic considerations. Ann Rheum Dis 2007; 66:1137-42.
  • 9
    Bringhurst FR, Demay MB, Kronenberg HM. Hormones and Disorders of Mineral Metabolism. In: Kronenberg HM, Melmed S, Polonsky KS, Larsen PR editors. Williams Textbook of Endocrinology, 11 ed. Philadelphia: Elsevier, 2008.
  • 10
    Leventis P, Patel S. Clinical aspects of vitamin D in the management of rheumatoid arthritis. Rheumatology 2008; 47:1617-21.
  • 11
    Szodoray P, Nakken B, Gaal J, Jonsson R, Szegedi A, Zold E et al The complex role of vitamin D in autoimmune diseases. Scand J Immunol 2008; 68(3):261-9.
  • 12
    Deluca HF, Cantorna MT. Vitamin D - its role and uses in immunology. FASEB Journal 2001; 15:2579-85.
  • 13
    Ruiz-Irastorza G, Egurbide MV, Olivares N, Martinez-Berriotxoa A, Aguirre C. Vitamin D deficiency in systemic lupus erythematosus: prevalence, predictors and clinical consequences. Rheumatology 2008; 47:920-3.
  • 14
    Nagpal S, Na S, Rathnachalam R. Noncalcemic actions of vitamin D receptor ligands. Endocrine Reviews 2005; 26(5):662-87.
  • 15
    Bandeira F, Griz L, Dreyer P, Eufrazino C, Bandeira C, Freese E. Vitamin D deficiency: a global perspective. Arq Bras Endocrinol Metabol 2006; 50(4):640-6.
  • 16
    Lamb EJ, Wong T, Smith DJ, Simpson DE, Coakley AJ, Moniz C. Metabolic bone disease is present at diagnosis in patients with inflammatory bowel disease. Aliment Pharmacol Ther 2002; 16(11):1985-92.
  • 17
    Cutolo M. Vitamin D and autoimmune rheumatic diseases. Rheumatology 2009; 48: 210-2.
  • 18
    Holick MF. Vitamin D: importance in the prevention of cancers, type 1 diabetes, heart disease and osteoporosis. Am J Clin Nutr 2004; 79:362-71.
  • 19
    Cutolo M, Otsa K. Review: vitamin D, immunity and lupus. Lupus 2008; 17:6-10.
  • 20
    Steinman L. A brief history of TH17, the first major revision in the TH1/TH2 hypothesis of T cell-mediated tissue damage. Nat Med 2007; 13:139-45.
  • 21
    Yu S, Cantorna MT. The vitamin D receptor is required for iNKT cell development. Proc Natl Acad Sci USA 2008; 105:5207-12.
  • 22
    Adorini A, Penna G. Control of autoimmune diseases by the vitamin D endocrine system. Nat Clin Pract Rheumatol 2008; 4:404-12.
  • 23
    Harris Jr ED, Schur PH. Pathogenesis of rheumatoid arthritis. In: UpToDate, Basow, DS (Ed), UpToDate, Waltham, MA, 2007.
  • 24
    Manolagas SC, Werntz DA, Tsoukas CD, Provvedini DM, Vaughan JH. 1,25-dihydroxyvitamin D3 receptors in lymphocytes from patients with rheumatoid arthritis. J Lab Clin Med 1986; 108:596-600.
  • 25
    Gomez-Vaquero C, Fiter J, Enjuanes A, Nogues X, Diez-Perez A, Nolla JM. Influence of the Bsml polymorphism of the vitamin D receptor gene on rheumatoid arthritis clinical activity. J Rheumatol 2007; 34:1823-6.
  • 26
    Tsuji M, Fujii K, Nakano T, Nishii Y. 1994 1a-hydroxyvitamin D3 inhibits type II collagen-induced arthritis in rats. FEBS Lett 1994; 337:248-50.
  • 27
    Merlino LA, Curtis J, Mikuls TR, Cerhan JR, Criswell LA, Saag KG. Vitamin D intake is inversely associated with rheumatoid arthritis. Arthritis Rheum 2004; 50(1):72-7.
  • 28
    Costenbader KH, Feskanich D, Holmes M, Karlson EW, Benito-Garcia E. Vitamin D intake and risks of systemic lupus erythematosus and rheumatoid arthritis in women. Ann Rheum Dis 2008; 67:530-5.
  • 29
    Nielen MMJ, Schaardenburg D, Lems WF, van de Stadt RJ, de Koning MHM, Reesink HW et al Vitamin D deficiency does not increase the risk of rheumatoid arthritis: comment on the article by Merlino et al Arthritis Rheum 2006; 54(11): 3719-24.
  • 30
    Andjelkovic Z, Vojinovic J, Pejnovic N, Popovic M, Dujic A, Mitrovic D. Disease modifying and immunomodulatory effects of high dose 1a(OH) D3 in rheumatoid arthritis patients. Clin Exper Rheumatol 1999; 17:453-6.
  • 31
    Patel S, Farragher T, Berry J, Bunn D, Silman A, Symmons D. Association between serum vitamin D metabolite levels and disease activity in patients with early inflammatory polyarthritis. Arthritis Rheum 2007; 56:2143-9.
  • 32
    Bultink IE, Lems WF, Kostense PJ, Dijkmans BAC, Voskuyl AE. Prevalence of and risk factors for low bone mineral density and vertebral fractures in patients with systemic lupus erythematosus. Arthritis Rheum 2005; 52:2044-50.
  • 33
    Muller K, Kriegbaum NJ, Baslund B, Sørensen OH, Thymann M, Bentzen K. Vitamin D3 metabolism in patients with rheumatic diseases: low serum levels of 25-hydroxyvitamin D3 in patients with systemic lupus erythematosus. Clin Rheumatol 1995; 14:397-400.
  • 34
    Huisman AM, White KP, Algra A, Harth M, Vieth R, Jacobs JW. Vitamin D levels in women with systemic lupus erythematosus and fibromyalgia. J Rheumatol 2001; 28:2535-39.
  • 35
    Thudi A, Yin S, Wandstrat AE, Li QZ, Olsen NJ. Vitamin D levels and disease status in Texas patients with systemic lupus erythematosus. Am J Med Sci 2008; 335:99-104.
  • 36
    Borba VZC, Vieira JGH, Kasamatsu T, Radominski SC, Sato EI, Lazaretti-Castro M. Vitamin D deficiency in patients with active systemic lupus erythematosus. Osteoporos Int 2009; 20:427-33.
  • 37
    Carvalho JF, Blank M, Kiss E, Tarr T, Amital H, Shoenfeld Y. Antivitamin D in SLE: preliminary results. Ann N Y Acad Sci 2007; 1109:550-7.
  • 38
    Zold E, Szodoray P, Gaal J, Kappelmayer J, Csathy L, Gyimesi E. Vitamin D deficiency in undifferentiated connective tissue disease. Arthritis Res Ther 2008; 10: R123.
  • 39
    Jahnsen J, Falch JA, Mowinckel P, Aadland E. Vitamin D status, parathyroid hormone and bone mineral density in patients with inflammatory bowel disease. Scand J Gastroenterol 2002; 37:192-9.
  • 40
    Munger KL, Zhang SM, O'Reilly E, Hernán MA, Olek MJ, Willett WC. Vitamin D intake and incidence of multiple sclerosis. Neurology 2004; 62:60-5.
  • 41
    Goldberg P, Fleming MC, Picard EH. Multiple sclerosis: decreased relapse rate through dietary supplementation with calcium, magnesium and vitamin D. Med Hypotheses 1986; 21:193-200.
  • 42
    Mark BL, Carson JA. Vitamin D and autoimmune disease-implications for practice from the multiple sclerosis literature. J Am Diet Assoc 2006; 106:418-24.
  • 43
    Salomon B, Lenschow DJ, Rhee L, Ashourian N, Singh B, Sharpe A. B7/CD28 costimulation is essential for the homeostasis of the CD4' CD25' immunoregulatory T cells that control autoimmune diabetes. Immunity 2000; 12(4): 431-40.
  • 44
    Giulietti A, Gysemans C, Stoffels K, van Etten E, Decallonne B, Overbergh L. Vitamin D deficiency in early life accelerates Type 1 diabetes in non-obese diabetic mice. Diabetologia 2004; 47(3):451-62.
  • 45
    Mathieu C, Laureys J, Sobis H, Vandeputte M, Waer M, Bouillon R. 1,25-Dihydroxyvitamin D3 prevents insulitis in NOD mice. Diabetes 1992; 41:1491-5.
  • 46
    EURODIAB study group; Vitamin D supplement in early childhood and risk for type I (insulin-dependent) diabetes mellitus. Diabetologia 1999; 42(1):51-4.
  • 47
    Schauber J, Gallo R. The vitamin D pathway: a new target for control of the skin's immune response? Exp Dermatol 2008; 17:633-9.
  • 48
    Schauber J, Oda Y, Büchau AS, Yun QC, Steinmeyer A, Zügel U. Histone acetylation in keratinocytes enables control of the expression of cathelicidin and CD14 by 1,25-Dihydroxyvitamin D(3). J Invest Dermatol 2008: 128:816-24.
  • 49
    Schwarz T. 25 years of UV-induced immunosuppression mediated by T cells-from disregarded T suppressor cells to highly respected regulatory T cells. Photochem Photobiol 2008: 84:10-18.
  • 50
    Lehmann B, Genehr T, Knuschke P, Pietzsch J, Meurer M. UVB induced conversion of 7-dehydrocholesterol to 1alpha,25- dihydroxyvitamin D3 in an in vitro human skin equivalent model. J Invest Dermatol 2001; 117:1179-85.
  • 51
    Wang TT, Nestel F, Bourdeau V, Nagai Y, Wang Q, Liao J. Cutting edge: 1,25-dihydroxyvitamin D3 is a direct inducer of antimicrobial peptide gene expression. J Immunol 2004; 173:2909-12.
  • 52
    Jansen T, Krug S, Kind P, Plewig G, Messer G. BsmI polymorphism of the vitamin D receptor gene in patients with the fulminant course of rosacea conglobata (rosacea fulminans). J Dermatol 2004; 31:244-6.
  • 53
    Lebwohl M, Menter A, Koo J, Feldman SR. Combination therapy to treat moderate to severe psoriasis. J Am Acad Dermatol 2004; 50:416-30.
  • 54
    Stwart DB, Lewis H. Vitamin D analogues and psoriasis. J Clin Pharm Ther 1996; 21:143-8.
  • 55
    Carrascosa JM, Vanaclocha F, Borrego L, Fernández-López E, Fuertes A, Rodríguez-Fernández-Freire L. Update of the topical treatment of psoriasis. Actas Dermosifiliogr 2009; 100(3):190-200.
  • 56
    Ashcroft DM, Po AL, Williams HC, Griffiths CE. Systematic review of comparative efficacy and tolerability of calcipotriol in treating chronic plaque psoriasis. BMJ. 2000; 320:963-97.
  • 57
    Cantorna M, Woodward W, Hayes C, De Luca H. 1,25-Dihydroxyvitamin D3 is a positive regulator for the two anti-encephalitogenic cytokines TGF-b1 and IL-4. J Immunol 1998; 160:5314-9.
  • 58
    Garcion E, Nataf S, Berod A, Darcy F ,Brachet P. 1,25-Dihydroxyvitamin D3 inhibits the expression of inducible nitric oxide synthase in rat central nervous system during experimental allergic encephalomyelitis. Brain Res 1997; 45:255-67.
  • 59
    Bregenholt S, Claesson MH. Increased intracellular Th1 cytokines in scid mice with inflammatory bowel disease. Eur J Immunol 1998; 28:379-89.
  • 60
    Cantorna MT, Hayhes CE, DeLuca HF. 1,25-Dihydroxycholecalciferol inhibits the progression of arthritis in murine models of human arthritis. J Nutr 1998; 128:68-72.
  • 61
    Tetlow LC, Woolley DE. The effects of 1 alpha,25-dihydroxyvitamin D(3) on matrix metalloprotease and prostaglandin E(2) production by cells of the rheumatoid lesion. Arthritis Res 1999; 1:63-70.
  • 62
    Casteels KM, Mathieu C, Waer M, Valckx D, Overbergh L, Laureys JM. Prevention of type I diabetes in nonobese diabetic mice by late intervention with nonhypercalcemic analogs of 1,25-dihydroxyvitamin D3 in combination with a short induction course of cyclosporin A. Endocrinology 1998; 139:95-102.
  • 63
    Yamauchi Y, Tsunematsu T, Konda S, Hoshino T, Itokawa Y, Hoshizaki H. A double blind trial of alfacalcidol on patients with rheumatoid arthritis (RA). Ryumachi 1989; 29:11-24.
  • 64
    Perez A, Raab R, Chen TC, Turner A, Holick MF. Safety and efficacy of oral calcitriol (1,25-dihydroxyvitamin D3) for the treatment of psoriasis. Br J Dermatol 1996; 134:1070-8.
  • 65
    El-Azhary RA, Peters MS, Pittelkow MR, Kao PC, Muller SA. Efficacy of vitamin D3 derivatives in the treatment of psoriasis vulgaris: a preliminary report. Mayo Clin Proc 1993; 68:835-41.
  • 66
    Morimoto S, Yoshikawa K, Kozuka T, Kitano Y, Imanaka S, Fukuo K. Treatment of psoriasis vulgaris with oral 1 alpha,25dihydroxyvitamin D3 - report of two cases. J Dermatol 1987; 14:59-62.
  • 67
    Elst EF, Van Suijlekom-Smit LW, Oranje AP. Treatment of linear scleroderma with oral 1,25-dihydroxyvitamin D3 (calcitriol) in seven children. Pediatr Dermatol 1999; 16:53-8.
  • 68
    Kumar S, Davies M, Zakaria Y. Improvement in glucose tolerance and beta-cell function in a patient with vitamin D deficiency during treatment with vitamin D. Postgrad Med J 1994; 70:440-3.
  • 69
    Taylor AV, Wise PH. Vitamin D replacement in Asians with diabetes may increase insulin resistance. Postgrad Med J 1998; 74:365-6.
  • Endereço para correspondência:
    Ângela Pinto Duarte
    Serviço de Reumatologia - Hospital das Clinicas
    Av. Professor Morais Rego, s/n, sala 133
    CEP: 50670-420. Cidade Universitária, Recife - PE
    Tel: (81) 3454-0155
    E-mail:
  • Publication Dates

    • Publication in this collection
      10 Mar 2010
    • Date of issue
      Feb 2010

    History

    • Accepted
      26 Nov 2009
    • Received
      22 June 2009
    Sociedade Brasileira de Reumatologia Av Brigadeiro Luiz Antonio, 2466 - Cj 93., 01402-000 São Paulo - SP, Tel./Fax: 55 11 3289 7165 - São Paulo - SP - Brazil
    E-mail: sbre@terra.com.br