New genes associated with rheumatoid arthritis identified by gene expression profiling.

Abstract:

:In this study, we aimed to find new genes associated with rheumatoid arthritis (RA) so that more comprehensive genes would be used for monitoring and/or diagnosing patients. Illumina digital gene expression profiling was applied in two sample types - peripheral blood mononuclear cells (PBMCs) and synovial cells to compare the gene expression pattern between 17 patients with RA and three control groups (six osteoarthritis patients, three ankylosing spondylitis patients and 17 healthy controls). Bioinformatics was performed on pathway analysis and protein-protein interaction networks. Four novel genes from PBMCs - DHRS3, TTC38, SAP30BP and LPIN2 - were found to be associated with RA and further confirmed through quantitative real-time polymerase chain reaction. Five new differentially expressed genes (EPYC, LIFR, GLDN, TADA3 and ZNRF3) found in synovial cells were not confirmed. Pathway analyses revealed 10 significantly enriched pathways, and a protein-protein interaction network analysis showed that four novel PBMC-derived genes were connected to previously reported genes by four intermediate genes. Therefore, we proposed that four newly identified PBMC-derived genes could be integrated with previously reported RA-associated genes to monitor and/or diagnose RA.

journal_name

Int J Immunogenet

authors

Wang H,Guo J,Jiang J,Wu W,Chang X,Zhou H,Li Z,Zhao J

doi

10.1111/iji.12313

subject

Has Abstract

pub_date

2017-06-01 00:00:00

pages

107-113

issue

3

eissn

1744-3121

issn

1744-313X

journal_volume

44

pub_type

杂志文章
  • Analysis of polymorphic sites in the promoter of the nitric oxide synthase 2 gene in Brazilian patients with leprosy.

    abstract::Leprosy is one of the most neglected infectious tropical diseases of the skin and the nerves caused by the intracellular pathogen Mycobacterium leprae. The inducible NOS isoform encoded by NOS2A plays a vital role in host defence against bacterial infections. The functional promoter polymorphisms in NOS2A are associat...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12108

    authors: Messias-Reason IJ,van Tong H,Velavan TP

    更新日期:2014-06-01 00:00:00

  • IFN-γ +874T/A polymorphism increases susceptibility to post-traumatic osteomyelitis.

    abstract::Immunological inflammatory reaction is one of the key links in the occurrence and development of post-traumatic osteomyelitis after microbial invasion. Growing evidence suggests complex interactions between IFN-γ and bone remodelling cells. However, potential association of IFN-γ gene polymorphism with susceptibility ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12462

    authors: Zhao XQ,Jiang N,Hu YJ,Yu B

    更新日期:2020-04-01 00:00:00

  • No evidence for association of the TP53 12139 and the BAX-248 polymorphisms with endemic pemphigus foliaceus (fogo selvagem).

    abstract::Pemphigus foliaceus (PF) is an autoimmune bullous epidermal disease, characterized by autoantibodies specific to the desmosomal protein desmoglein 1 (dsg1) and by acantholysis, the rupture of the cellular junctions among keratinocytes. Known also as fogo selvagem (wild fire) in Brazil, the disease has distinct epidemi...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00585.x

    authors: Köhler KF,Petzl-Erler ML

    更新日期:2006-04-01 00:00:00

  • No association of SUMO4 M55V with autoimmune diabetes in Asian-Indian patients.

    abstract::Autoimmune diabetes [type 1 diabetes mellitus (T1DM), latent autoimmune diabetes in adults (LADA) and part of malnutrition-related diabetes] has been shown to have genetic predisposition. Studies in IDDM 5 have lead to the discovery of a novel polymorphism 163 A-->G, of SUMO4 (small ubiquitin-related modifier) gene, a...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00668.x

    authors: Sedimbi SK,Kanungo A,Shastry A,Park Y,Sanjeevi CB

    更新日期:2007-04-01 00:00:00

  • Association between interferon lambda 3 rs12979860 polymorphism and clinical outcome in dengue virus-infected children.

    abstract::Single nucleotide polymorphisms (SNPs) in immune-related genes have been shown to play a role in driving the development of the severe phenotypes of dengue virus (DENV) infection. We assessed the association between IFNL3 gene SNP (rs12979860) and dengue clinical outcomes in children. Patients with dengue-related symp...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12477

    authors: da Silva Cezar RD,da Silva Castanha PM,Matos Freire N,Mola C,Feliciano do Carmo R,Tenório Cordeiro M,Baptista P,Silva Vasconcelos LR,Moura P,da Silva Teixeira VG

    更新日期:2020-08-01 00:00:00

  • HLA-DPB1, -DRB1, and -DQB1 polymorphism defined in Ewenki ethnic minority of China Inner Mongolia Autonomous Region.

    abstract::In the present study, DNA typing for human leucocyte antigen (HLA)-DPB1, -DRB1, and -DQB1 was performed using polymerase chain reaction-sequence-based-typing (PCR-SBT) method on 94 randomly selected, healthy, unrelated individuals from the Ewenki ethnic population in Inner Mongolia Autonomous Region of China. A total ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00718.x

    authors: Su X,Bi L,Hai R,Qimuge S,Ying M,Bahring S,Gong M

    更新日期:2007-12-01 00:00:00

  • Phenotypic and allelic profile of ABO and Rhésus D blood group system among blood donor in Antananarivo.

    abstract::This study assessed the phenotypic and allelic profiles of ABO and Rhesus D blood group system among first time blood donors at the National Centre of Blood Supply of Antananarivo. We collected through this retrospective study all data registered during 7 years of practice (from 2003 to 2009). Age and sex were analyse...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01120.x

    authors: Randriamanantany ZA,Rajaonatahina DH,Razafimanantsoa FE,Rasamindrakotroka MT,Andriamahenina R,Rasoarilalamanarivo FB,Hanitriniala SP,Herisoa FR,Rasamindrakotroka A,Rakoto Alson OA

    更新日期:2012-12-01 00:00:00

  • Variations in genes involved in regulation of the nuclear factor - κB pathway and the risk of acute myeloid leukaemia.

    abstract::Genes involved in regulation of the nuclear factor - kappa B (NF-κB) pathway are suggested to play a role in the pathogenesis of acute myeloid leukaemia (AML). The present study aimed to assess the association between the NF-κB1, TRAF3 and TLRs genes single nucleotide polymorphisms (SNPs) and disease susceptibility as...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12255

    authors: Rybka J,Gębura K,Wróbel T,Wysoczańska B,Stefanko E,Kuliczkowski K,Bogunia-Kubik K

    更新日期:2016-04-01 00:00:00

  • Influence of HLA-DR2 on perforin-positive cells in pulmonary tuberculosis.

    abstract::Perforin is one of the key effector molecules of cytotoxic T cells and natural killer cells. The influence of HLA-DRB1 alleles on peripheral blood perforin-positive CD4, CD8, CD16 and CD 56 cells was studied by flow cytometry. HLA-DRB1 typing was done in normal healthy subjects (NHS: n = 156) and patients with pulmona...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00703.x

    authors: Rajeswari DN,Selvaraj P,Raghavan S,Jawahar MS,Narayanan PR

    更新日期:2007-10-01 00:00:00

  • Association study of polymorphisms within matrix metalloproteinase 9 with bronchial asthma.

    abstract::Matrix metalloproteinase 9 plays an important role in the development of bronchial asthma. We were interested in whether the polymorphisms -T1702A, -C1562T, R279Q and +C6T within the matrix metalloproteinase 9 (MMP-9) gene were associated with asthma in a population of 231 asthmatic children. However, we found no asso...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2005.00516.x

    authors: Ganter K,Deichmann KA,Heinzmann A

    更新日期:2005-08-01 00:00:00

  • Characterization of tumour necrosis factor-alpha genetic variants and mRNA expression in patients with severe sepsis.

    abstract::Tumour necrosis factor-alpha (TNFalpha) has been implicated in the pathogenicity of severe sepsis by both genetic association studies and animal models. Conflicting functional data have emerged in relation to genetic variants and TNFalpha protein production. Therefore, we assessed the functionality of TNFalpha genetic...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2008.00773.x

    authors: O'Dwyer MJ,Mankan AK,Ryan AW,Lawless MW,Stordeur P,Kelleher D,McManus R,Ryan T

    更新日期:2008-08-01 00:00:00

  • Cytokine typing: SNP allele frequencies in the Iranian population.

    abstract::Single nucleotide polymorphisms within the promoter or other regulatory sequences of cytokine genes were evaluated and compared between an Iranian population and populations of different ethnic/geographical background. In 40 healthy Iranian subjects, cytokine typing was performed by polymerase chain reaction-sequence-...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,收录出版

    doi:10.1111/j.1744-313X.2006.00595.x

    authors: Bagheri M,Abdi-Rad I,Omrani D,Khalkhali HR

    更新日期:2006-06-01 00:00:00

  • The clinical implications of HLA mismatches in unrelated donor haematopoietic cell transplantation.

    abstract::Haematopoietic stem cell transplantation (HSCT), using unrelated donors (UD), is now a common modality of treatment for individuals with a variety of different diseases. HLA matching has been shown to have a significant impact on patient outcome. This study includes 423 unrelated UK patient/donor pairs. The patients a...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2008.00793.x

    authors: Shaw BE

    更新日期:2008-08-01 00:00:00

  • Vascular endothelial growth factor +405 G/C,-460 T/C and -2578 A/C polymorphisms are not associated with insulin resistance in polycystic ovary syndrome.

    abstract::Insulin resistance (IR) and pancreatic beta-cell dysfunction are usual comorbidities in polycystic ovary syndrome (PCOS). Vascular endothelial growth factor (VEGF) is known to play an important role in the pathogenesis of PCOS. This study examined firstly the possible association of common +405 G/C,-460 T/C and -2578 ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00915.x

    authors: Vural P,Küskü-Kiraz Z,Doğru-Abbasoğlu S,Cil E,Karadağ B,Uysal M

    更新日期:2010-08-01 00:00:00

  • MBL1 genotypes in wild boar populations from Sweden, Austria, the Czech Republic, and Japan.

    abstract::The single nucleotide polymorphism (SNP) G949T in the mannose-binding lectin ( MBL ) 1 gene has been associated with low MBL-A concentration in serum and detected at different frequencies in various European pig populations. However, the origin of this SNP is not known. Part of the MBL1 gene was sequenced in 12 wild b...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01132.x

    authors: Bergman IM,Sandholm K,Ekdahl KN,Okumura N,Uenishi H,Guldbrandtsen B,Essler SE,Knoll A,Heegaard PM,Edfors I,Juul-Madsen HR

    更新日期:2013-04-01 00:00:00

  • Association between CCL2 haplotypes and knee osteoarthritis.

    abstract::We examined five single nucleotide polymorphisms (SNPs) and reconstructed 5-locus haplotypes of the CCL2 gene, in knee osteoarthritis (OA) cases and in controls. The CCL2 rs2857657 variant (G) allele was observed more frequently in female knee OA cases than in controls. One haplotype (H5) was observed exclusively in t...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12015

    authors: Hulin-Curtis SL,Bidwell JL,Perry MJ

    更新日期:2013-08-01 00:00:00

  • Characterization of a novel HLA-DRB1*04 allele (DRB1*0460) in the Italian population.

    abstract::We report the identification of a novel HLA-DRB1*04, officially named DRB1*0460. It was detected during performing HLA-DRB1 high resolution typing by DNA sequencing-based method. The exon 2 nucleotide sequence of DRB1*0460 is identical to that of DRB1*040301 except at codon 63 (AGC-->AAC), changing the encoded serine ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00641.x

    authors: Frison S,Rinaldini C,Pagoda M,Brambilla C,Poli F

    更新日期:2007-02-01 00:00:00

  • HLA genotyping using the Illumina HLA TruSight next-generation sequencing kits: A comparison.

    abstract::Illumina first introduced their TruSight human leucocyte antigen (HLA) next-generation sequencing (NGS) typing kit in 2015 and subsequently followed up with a new version in 2016. Here we report on our experience comparing the two versions of the Illumina HLA NGS kits. ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12322

    authors: Profaizer T,Lázár-Molnár E,Pole A,Delgado JC,Kumánovics A

    更新日期:2017-08-01 00:00:00

  • Promoter polymorphism of IL-18 gene in pulmonary tuberculosis in South Indian population.

    abstract::Interleukin-18 (IL-18) plays a vital role in both innate and acquired immunity. We analysed polymorphisms at -607(C/A) and -137(G/A) in the promoter region of IL-18 gene by allele-specific polymerase chain reaction in normal healthy subjects (n = 173) and patients with pulmonary tuberculosis (n = 165). Allele, genotyp...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00714.x

    authors: Harishankar M,Selvaraj P,Rajeswari DN,Anand SP,Narayanan PR

    更新日期:2007-10-01 00:00:00

  • Using ESTs database to predict and validate single polymorphisms at the HLA system.

    abstract::We propose a bioinformatics pipeline in which we use an ESTs database to predict and validate single-nucleotide polymorphisms (SNPs) directly linked to gene-coding regions at the HLA class I genes (HLA-A, HLA-B and HLA-C). Annotation originated from our analysis revealed various classes of possible new variations that...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01076.x

    authors: Figueiredo TC,de Oliveira JR

    更新日期:2012-06-01 00:00:00

  • Characterization of the novel HLA-DQB1*06:48 allele by group-specific sequencing.

    abstract::HLA-DQB1*06:48 has single nucleotide polymorphisms within codons 70 and 62 of exon 2 (GGG>AGG and AAG>AAC) relative to HLA-DQB1*06:02:01 and HLA-DQB1*06:37. This results in amino acid differences (G>R and K>N) that will change the polarity and charge of the encoded antigen and may therefore affect its peptide repertoi...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12004

    authors: Foster L,Tate D,Poulton K

    更新日期:2013-08-01 00:00:00

  • The distributions of HLA-A, HLA-B, HLA-C, HLA-DRB1 and HLA-DQB1 allele and haplotype at high-resolution level in Zhejiang Han population of China.

    abstract::The distributions of HLA allele and haplotype are variable in different ethnic populations and the data for some populations have been published. However, the data on HLA-C and HLA-DQB1 loci and the haplotype of HLA-A, HLA-B, HLA-C, HLA-DRB1 and HLA-DQB1 loci at a high-resolution level are limited in Zhejiang Han popu...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12411

    authors: Chen N,Wang W,Wang F,Dong L,Zhao S,Zhang W,He J,Huang H,Zhu F

    更新日期:2019-02-01 00:00:00

  • Study on the polymorphisms of HLA-ABCDQB1DRB1 alleles and haplotypes in Hubei Han population of China.

    abstract::The present study aimed to analyse the frequencies of human leukocyte antigen HLA-ABCDQB1 and HLA-DRB1 alleles and haplotypes in a subset of 3,732 Han population from Hubei of China. All samples were typed in the HLA-ABCDQB1 and HLA-DRB1 loci using the sequence-based typing method; subsequently, the HLA polymorphisms ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12516

    authors: Zou J,Shen G,Qiang W,Zhu YY,Li WX

    更新日期:2021-02-01 00:00:00

  • The complement-mediated prozone effect in the Luminex single-antigen bead assay and its impact on HLA antibody determination in patient sera.

    abstract::The Luminex xMAP system has become an important tool for HLA antibody screening and identification in sera of transplant patients. Recently, the Luminex single antigen bead assay was shown to be prone to an artefact, the so called prozone phenomenon: Sera with high titer HLA antibodies gave negative results when teste...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/j.1744-313X.2012.01147.x

    authors: Weinstock C,Schnaidt M

    更新日期:2013-06-01 00:00:00

  • HLA class II eplet mismatch load improves prediction of dnDSA development after living donor kidney transplantation.

    abstract::HLA donor-specific antibodies developed de novo after transplant remain a major cause of chronic allograft dysfunction. Our study main purpose was to determine whether HLA MM, assessed traditionally and by HLA total and AbVer eplet mismatch load (EptMM and EpvMM) assessed with HLAMatchMaker, had impact on dnDSA develo...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12519

    authors: Tafulo S,Malheiro J,Santos S,Dias L,Almeida M,Martins S,Pedroso S,Mendes C,Lobato L,Castro-Henriques A

    更新日期:2021-02-01 00:00:00

  • Identification of a novel MICB allele, MICB*030, by cloning and sequencing.

    abstract::A novel MICB allele, MICB*030, has been identified in a healthy Chinese individual of Mongol ethnicity residing in northern China by polymerase chain reaction sequence-based typing (PCR-SBT) and confirmed by cloning and sequencing. MICB*030 was linked to HLA-B*35. Aligned with MICB*005:02, MICB*030 has a nonsynonymous...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12207

    authors: Wang WY,Wang F,Tian W

    更新日期:2015-08-01 00:00:00

  • A comparison of methods for determining genotypes at the tumour necrosis factor-alpha-308, interleukin (IL)-1beta+3953, IL-6 -174 and IL-10 -1082/-819/-592 polymorphic loci.

    abstract::Induced heteroduplex genotyping (IHG) is one of many methods that can be used to determine single nucleotide polymorphisms (SNPs). It is relatively new in comparison to other polymerase chain reaction (PCR)-based techniques. The aim of this study was to compare the results of genotyping using IHG with the results of g...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2005.00494.x

    authors: Bown MJ,Weston S,Horsburgh T,Nicholson ML,Bell PR,Sayers RD

    更新日期:2005-04-01 00:00:00

  • HLA-A*11:53 is shown to be identical to the corrected A*11:02:01 allele sequence.

    abstract::According to the IMGT/HLA Database, the DNA sequence of A*11:53 is identical to A*11:02:01 in exons 2, 3, 4 and 5 except at codon 276. A*11:53 was reported as a rare variant of A*11, while A*11:02:01 was understood to be the second most frequently observed variant of A*11 after A*11:01:01 in Taiwanese. We sequenced HL...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01121.x

    authors: Yang KL,Chu CC,Marsh SG,Lin PY

    更新日期:2012-12-01 00:00:00

  • Molecular approaches to transfusion medicine in Polynesians and Maori in New Zealand.

    abstract::In recent years, with the application of genotyping technology, there has been a substantial increase in the number of reported blood group alleles. This survey was designed to evaluate new molecular blood group genotyping methods and compile reference blood group data sets for Polynesian and Maori subjects. Subsequen...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12073

    authors: Edinur HA,Dunn PP,Lea RA,Chambers GK

    更新日期:2013-12-01 00:00:00

  • Frequency of ABO/Rhesus (D) blood groupings and ethnic distribution in the Greater-Accra region of Ghana, towards effective blood bank inventory.

    abstract::Knowledge on blood group phenotypes is of key importance in clinical practice. It used in blood transfusion practice to determine the direction of recruitment of voluntary donors as required for each population within a country, and for disease association and population genetics studies. This study aimed at reporting...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12412

    authors: Doku GN,Agbozo WK,Annor RA,Kisseh GD,Owusu MA

    更新日期:2019-04-01 00:00:00