Open Access Research article

CD209 in inflammatory bowel disease: a case-control study in the Spanish population

Concepción Núñez1, Javier Oliver2, Juan Luis Mendoza3, María Gómez-García4, Carlos Taxonera3, Luis M Gómez2, Miguel A López-Nevot5, Emilio G de la Concha1, Elena Urcelay1, Alfonso Martínez1* and Javier Martín2

Author Affiliations

1 Servicio de Inmunología Clínica, Hospital Clínico San Carlos, Madrid, Spain

2 Instituto de Parasitología y Biomedicina, CSIC, Granada, Spain

3 Unidad de Enfermedad Inflamatoria Intestinal, Hospital Clínico San Carlos, Madrid, Spain

4 Unidad de Enfermedad Inflamatoria Intestinal, Hospital Virgen de las Nieves, Granada, Spain

5 Servicio de Inmunología, Hospital Virgen de las Nieves, Granada, Spain

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BMC Medical Genetics 2007, 8:75  doi:10.1186/1471-2350-8-75

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2350/8/75


Received:29 August 2007
Accepted:10 December 2007
Published:10 December 2007

© 2007 Núñez et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

The etiology of Ulcerative Colitis (UC) and Crohn's Disease (CD), considered together as Inflammatory Bowel Diseases (IBD), involves environmental and genetic factors. Although some genes are already known, the genetics underlying these diseases is complex and new candidates are continuously emerging. The CD209 gene is located in a region linked previously to IBD and a CD209 functional polymorphism (rs4804803) has been associated to other inflammatory conditions. Our aim was to study the potential involvement of this CD209 variant in IBD susceptibility.

Methods

We performed a case-control study with 515 CD patients, 497 UC patients and 731 healthy controls, all of them white Spaniards. Samples were typed for the CD209 single nucleotide polymorphism (SNP) rs4804803 by TaqMan technology. Frequency comparisons were performed using χ2 tests.

Results

No association between CD209 and UC or CD was observed initially. However, stratification of UC patients by HLA-DR3 status, a strong protective allele, showed that carriage of the CD209_G allele could increase susceptibility in the subgroup of HLA-DR3-positive individuals (p = 0.03 OR = 1.77 95% CI 1.04–3.02, vs. controls).

Conclusion

A functional variant in the CD209 gene, rs4804803, does not seem to be influencing Crohn's disease susceptibility. However, it could be involved in the etiology or pathology of Ulcerative Colitis in HLA-DR3-positive individuals but further studies are necessary.

Background

Inflammatory bowel diseases comprise two distinct entities, Crohn's disease (CD) and Ulcerative Colitis (UC). Both forms are characterized by a chronic inflammation of the intestine, but several clinical and immunological profiles differ between them. IBD is a multifactorial disease: environmental factors seem to be involved in disease onset in genetically susceptible individuals. Common susceptibility genetic components exist for both diseases as evidenced apparently by the higher risk of developing UC in relatives of patients with CD or vice versa, but also specific genes seem to play an important role in the development or course of each disease. For CD, CARD15 mutations are the main susceptibility factors described in Caucasian populations [1]. On the other hand, HLA genes show stronger effects on UC in our population, specifically HLA-DR3 seems to have a protective role in the development of this disease [2]. However, a complex genetic contribution exists in both diseases and new etiological genes remain to be discovered.

DC-SIGN (dendritic cell-specific ICAM3-grabbing non-integrin), also named CD209, is a type II membrane protein member of the C-type lectin receptor superfamily. It is expressed by dendritic cells and is involved in pattern recognition and immunoregulation [3]. The gene coding for this protein, CD209, is located in the region 19p13, where a linkage peak to IBD resulted from a genomewide scan performed in Canadian families [4]. A promoter variant of this gene, rs4804803, affects its transcriptional activity in vitro and it has been associated to susceptibility or severity to some infections [5]. Recently, this polymorphism has been also associated to susceptibility to a subset of celiac disease patients, another inflammatory condition sharing with IBD alterations in mucosal immunoregulation [6].

The aim of this study was to evaluate the relevance of the rs4804803 polymorphism in susceptibility to IBD.

Methods

Samples

A total of 515 Crohn's disease patients and 497 ulcerative colitis patients were collected from two Hospitals in Spain (Hospital Clínico San Carlos, Madrid; Hospital Virgen de las Nieves, Granada). All the patients were of Spanish white origin. Diagnosis of UC and CD was based on standard clinical, radiological, endoscopic, and histological criteria. Demographic and clinical characteristics of IBD patients are shown in Table 1. A total of 731 healthy individuals were used as controls, all of them ethnically matched, they were blood donors and staff members. Written informed consent was obtained from all the participants in the study, which was approved by the Ethical Committee of Hospital Clínico San Carlos and the Ethical Committee of Hospital Virgen de las Nieves.

Table 1. Clinical characteristics of IBD patients

Genotyping

One single nucleotide polymorphism (SNP), rs4804803, was analyzed by TaqMan technology as previously described [6]. The two SNPs studied in the CARD15 gene were analyzed using C__11717468_20 (R702W, rs2066844) and C__11717466_20 (G908R, rs2066845) assays on Demand from Applied Biosystems (Foster City, CA). The 1007fs deletion (rs2066847) in the same gene was studied by an Assay by Design, also from Applied Biosystems. HLA-DR typing had been previously performed in the UC and CD patients, respectively, as well as in controls, as described before [7].

Statistical Analysis

Allelic and genotypic frequencies were compared between groups by means of χ2 tests. Statistical analyses were performed using the statistical package EpiInfo v5.00 (CDC, Atlanta, USA).

Results

No significant differences were observed when genotypic or allelic frequencies of the CD209 polymorphism studied were compared between CD or UC patients and controls (Table 2). However, the stratification of UC patients by HLA-DR3, a genetic factor protective for UC (p = 0.00002; OR = 0.48), showed association of the CD209 SNP with UC only in HLA-DR3-positive patients (Table 3). When HLA-DR3-positive patients were compared with controls a similar association emerged (p = 0.03 OR = 1.77 95% CI 1.04–3.02). Stratification of CD patients by the presence of CARD15 mutations did not show any significant result (data not shown). Similarly, no association was found after location was considered (left-sided vs. extensive colitis for UC, and ileal vs. colonic for CD).

Table 2. Genotypic and allelic frequencies of CD209 rs4804803 in CD and UC patients and in controls

Table 3. Genotypic and allelic frequencies in Ulcerative Colitis patients stratified by HLA-DR3 status

Discussion

We have studied the influence of the functional polymorphism rs4804803 of CD209 in susceptibility to UC and CD in the Spanish population. This gene seems to be increasing UC susceptibility in a subgroup of patients, those carrying HLA-DR3. It is known that HLA-DR3 is a strong protective factor for the development of the disease (HLA-DR3 allele: 7% in UC patients vs. 13% in controls, p = 5.7*10-7 OR = 0.48 95% CI 0.36–0.63). Thus, HLA-DR3-positive patients, i.e., those patients with minimal HLA genetic contribution to susceptibility, might present some additional susceptibility factors when compared with HLA-DR3-negative patients. Albeit the association described here barely reaches statistical significance, it seems rather interesting because a most similar effect of this gene has been recently described in other intestinal inflammatory pathology, celiac disease [6]. The CD209 gene was found to be increasing celiac disease susceptibility only in HLA-DQ2-negative patients, i.e., those lacking the main genetic susceptibility factor described to celiac disease. Allele rs4804803_G seems to be involved in susceptibility to both diseases. A similar hypothesis to the one proposed in relation to celiac disease could be working in this case; the lower transcriptional activity consequence of the rs4804803_G allele would imply minor surveillance capacity of dendritic cells and probably increased persistence of pathogens in the gut. In these conditions, a chronic inflammation could ensue. A role of pathogens in initiation or maintaining of the inflammatory process in IBD has been repeatedly proposed [8]; CD209 could be one of the receptors involved in the recognition of some of those pathogens. This role of CD209 in UC is compatible with the stronger impact of environmental factors described in UC compared to CD [9].

However, the weak statistical significance obtained makes necessary further analyses to confirm the influence of the CD209 rs4804803_G allele in susceptibility to HLA-DR3 positive UC patients in other populations and specially to investigate the involvement of this functional polymorphism in other chronic inflammatory conditions, mainly in those in whose origin pathogens could be involved. As a matter of fact, it is known that several common genes are underlying different autoimmune diseases [10].

Ulcerative colitis has been often proposed to be a heterogeneous group of diseases included together because of their clinical similarities [11]. Therefore, it is not surprising to find particular genes affecting only a previously well-defined genetic subset of patients. This kind of findings could be rewarding from a therapeutic perspective since patients potentially responding to a specific treatment could be previously selected.

Conclusion

We reported a new susceptibility factor affecting to an ulcerative colitis subgroup of patients, those carrying HLA-DR3. Because CD209 is involved in pathogen recognition and the rs4804803_G CD209 allele results in lower transcriptional activity, the presence of this allele might generate an increased persistence of pathogens in the gut and consequently a chronic inflammation.

Abbreviations

caspase recruitment domain 15 (CARD15); Crohn's Disease (CD); Human leukocyte antigen (HLA); Inflammatory Bowel Diseases (IBD); Single nucleotide polymorphism (SNP); Ulcerative Colitis (UC).

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

CN and JA carried out the genotyping of the samples, participated in the statistical analysis and drafted the manuscript. LMG participated in the statistical analysis and revised the manuscript. JLM, MGG, CT and MALP made the diagnosis, collaborated in collection of samples and revised critically the manuscript. EGC coordinated the study and critically revised the manuscript. EU, AM and JM conceived the study, participated in the statistical analysis and completed the writing of the manuscript.

Acknowledgements

This work was supported by grants SAF2003-08522 and SAF2006-00398. Concepción Núñez and Alfonso Martínez have a FIS contract (CA06/0163 and CP04/00175, respectively) and Elena Urcelay works for the "Fundación para la Investigación Biomédica-Hospital Clínico San Carlos".

References

  1. Gaya DR, Russell RK, Nimmo ER, Satsangi J: New genes in inflammatory bowel disease: lessons for complex diseases?

    Lancet 2006, 367(9518):1271-1284. PubMed Abstract | Publisher Full Text OpenURL

  2. de la Concha EG, Fernandez-Arquero M, Martinez A, Vigil P, Vidal F, Lopez-Nava G, Diaz-Rubio M, Garcia-Paredes J: Amino acid polymorphism at residue 71 in HLA-DR beta chain plays a critical role in susceptibility to ulcerative colitis.

    Dig Dis Sci 1999, 44(11):2324-2329. PubMed Abstract | Publisher Full Text OpenURL

  3. Zhou T, Chen Y, Hao L, Zhang Y: DC-SIGN and immunoregulation.

    Cell Mol Immunol 2006, 3(4):279-283. PubMed Abstract | Publisher Full Text OpenURL

  4. Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, McLeod RS, Griffiths AM, Green T, Brettin TS, Stone V, Bull SB, Bitton A, Williams CN, Greenberg GR, Cohen Z, Lander ES, Hudson TJ, Siminovitch KA: Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.

    Am J Hum Genet 2000, 66(6):1863-1870. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  5. Sakuntabhai A, Turbpaiboon C, Casademont I, Chuansumrit A, Lowhnoo T, Kajaste-Rudnitski A, Kalayanarooj SM, Tangnararatchakit K, Tangthawornchaikul N, Vasanawathana S, Chaiyaratana W, Yenchitsomanus PT, Suriyaphol P, Avirutnan P, Chokephaibulkit K, Matsuda F, Yoksan S, Jacob Y, Lathrop GM, Malasit P, Despres P, Julier C: A variant in the CD209 promoter is associated with severity of dengue disease.

    Nat Genet 2005, 37(5):507-13. Epub 2005 Apr 17.. PubMed Abstract | Publisher Full Text OpenURL

  6. Nunez C, Rueda B, Martinez A, Maluenda C, Polanco I, Lopez-Nevot MA, Ortega E, Sierra E, Gomez de la Concha E, Urcelay E, Martin J: A functional variant in the CD209 promoter is associated with DQ2-negative celiac disease in the Spanish population.

    World J Gastroenterol 2006, 12(27):4397-4400. PubMed Abstract | Publisher Full Text OpenURL

  7. de la Concha EG, Fernandez-Arquero M, Lopez-Nava G, Martin E, Allcock RJ, Conejero L, Paredes JG, Diaz-Rubio M: Susceptibility to severe ulcerative colitis is associated with polymorphism in the central MHC gene IKBL.

    Gastroenterology 2000, 119(6):1491-1495. PubMed Abstract | Publisher Full Text OpenURL

  8. Subramanian S, Campbell BJ, Rhodes JM: Bacteria in the pathogenesis of inflammatory bowel disease.

    Curr Opin Infect Dis 2006, 19(5):475-484. PubMed Abstract | Publisher Full Text OpenURL

  9. Russell RK, Satsangi J: IBD: a family affair.

    Best Pract Res Clin Gastroenterol 2004, 18(3):525-539. PubMed Abstract | Publisher Full Text OpenURL

  10. Pearce SH, Merriman TR: Genetic progress towards the molecular basis of autoimmunity.

    Trends Mol Med 2006, 12(2):90-98. PubMed Abstract | Publisher Full Text OpenURL

  11. Targan SR, Karp LC: Defects in mucosal immunity leading to ulcerative colitis.

    Immunol Rev 2005, 206:296-305. PubMed Abstract | Publisher Full Text OpenURL

Pre-publication history

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http://www.biomedcentral.com/1471-2350/8/75/prepub