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Investigation of the association between the genetic polymorphisms of the co-stimulatory system and systemic lupus erythematosus
by
Chen, Ding-Ping
, Yu, Kuang-Hui
, Lin, Wei-Tzu
in
Antigens
/ association
/ autoimmune disease (AD)
/ Autoimmune diseases
/ Case-Control Studies
/ CD28 antigen
/ CD28 Antigens - genetics
/ co-stimulatory/co-inhibitory molecules
/ CTLA-4 Antigen - genetics
/ CTLA-4 protein
/ Disease
/ Gene polymorphism
/ Genes
/ Genetic Predisposition to Disease
/ Haplotypes
/ Histocompatibility antigen HLA
/ HLA Antigens
/ Humans
/ Immunology
/ Immunoregulation
/ Lupus
/ Lupus Erythematosus, Systemic - genetics
/ Lymphocytes
/ Lymphocytes B
/ OX40 Ligand - genetics
/ Pathogenesis
/ Polymorphism
/ Polymorphism, Single Nucleotide
/ Proteins
/ Risk factors
/ single nucleotide polymorphism (SNP)
/ Single-nucleotide polymorphism
/ Systemic lupus erythematosus
/ systemic lupus erythematosus (SLE)
/ Womens health
2022
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Investigation of the association between the genetic polymorphisms of the co-stimulatory system and systemic lupus erythematosus
by
Chen, Ding-Ping
, Yu, Kuang-Hui
, Lin, Wei-Tzu
in
Antigens
/ association
/ autoimmune disease (AD)
/ Autoimmune diseases
/ Case-Control Studies
/ CD28 antigen
/ CD28 Antigens - genetics
/ co-stimulatory/co-inhibitory molecules
/ CTLA-4 Antigen - genetics
/ CTLA-4 protein
/ Disease
/ Gene polymorphism
/ Genes
/ Genetic Predisposition to Disease
/ Haplotypes
/ Histocompatibility antigen HLA
/ HLA Antigens
/ Humans
/ Immunology
/ Immunoregulation
/ Lupus
/ Lupus Erythematosus, Systemic - genetics
/ Lymphocytes
/ Lymphocytes B
/ OX40 Ligand - genetics
/ Pathogenesis
/ Polymorphism
/ Polymorphism, Single Nucleotide
/ Proteins
/ Risk factors
/ single nucleotide polymorphism (SNP)
/ Single-nucleotide polymorphism
/ Systemic lupus erythematosus
/ systemic lupus erythematosus (SLE)
/ Womens health
2022
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Investigation of the association between the genetic polymorphisms of the co-stimulatory system and systemic lupus erythematosus
by
Chen, Ding-Ping
, Yu, Kuang-Hui
, Lin, Wei-Tzu
in
Antigens
/ association
/ autoimmune disease (AD)
/ Autoimmune diseases
/ Case-Control Studies
/ CD28 antigen
/ CD28 Antigens - genetics
/ co-stimulatory/co-inhibitory molecules
/ CTLA-4 Antigen - genetics
/ CTLA-4 protein
/ Disease
/ Gene polymorphism
/ Genes
/ Genetic Predisposition to Disease
/ Haplotypes
/ Histocompatibility antigen HLA
/ HLA Antigens
/ Humans
/ Immunology
/ Immunoregulation
/ Lupus
/ Lupus Erythematosus, Systemic - genetics
/ Lymphocytes
/ Lymphocytes B
/ OX40 Ligand - genetics
/ Pathogenesis
/ Polymorphism
/ Polymorphism, Single Nucleotide
/ Proteins
/ Risk factors
/ single nucleotide polymorphism (SNP)
/ Single-nucleotide polymorphism
/ Systemic lupus erythematosus
/ systemic lupus erythematosus (SLE)
/ Womens health
2022
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Investigation of the association between the genetic polymorphisms of the co-stimulatory system and systemic lupus erythematosus
Journal Article
Investigation of the association between the genetic polymorphisms of the co-stimulatory system and systemic lupus erythematosus
2022
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Overview
Human leukocyte antigen genes have been shown to have the strongest association with autoimmune disease (AD). However, non-HLA genes would be risk factors of AD. Many genes encoding proteins that are related to T- and B-cell function have been identified as susceptibility genes of systemic lupus erythematosus (SLE). In this study, we explored the correlation between SLE and the genetic polymorphisms of co-stimulatory/co-inhibitory molecules, including CTLA4, CD28, ICOS, PDCD1, and TNFSF4. We found that there were nine single-nucleotide polymorphisms (SNPs) associated with SLE, namely, rs11571315 (TT vs. CT vs. CC: p < 0.001; TT vs. CT: p = 0.001; p = 0.005; TT vs. CT +CC: p < 0.001; TT+CT vs. CC: p = 0.032), rs733618 (CC vs. CT vs. TT: p = 0.002; CC vs. CT: p = 0.001; CC vs. TT: p = 0.018; CC vs. CT + TT: p = 0.001), rs4553808 (AA vs. AG: p < 0.001), rs62182595 (GG vs. AG vs. AA: p < 0.001; GG vs. AG: p < 0.001; GG vs. AG+AA: p < 0.001), rs16840252 (CC vs. CT vs. TT: p < 0.001; CC vs. CT: p < 0.001; CC vs. CT + TT: p < 0.001), rs5742909 (CC vs. CT: p = 0.027; CC vs. CT + TT: p = 0.044), rs11571319 (GG vs. AG vs. AA: p < 0.001, GG vs. AG: p < 0.001; GG vs. AG+AA: p < 0.001), rs36084323 (CC vs. CT vs. TT: p = 0.013, CC vs. TT: p = 0.004; CC vs. CT + TT: p = 0.015; CC +CT vs. TT: p = 0.015), and rs1234314 (CC vs. CG vs. GG: p = 0.005; CC vs. GG: p=0.004; CC+ CG vs. GG: p=0.001), but not in CD28 and ICOS by using the chi-square test. Additionally, rs62182595 and rs16840252 of CTLA and rs1234314 and rs45454293 of TNFSF4 were also associated with SLE in haplotypes. These SLE-related SNPs also had an association with several diseases. It was indicated that these SNPs may play an important role in immune regulation and pathogenic mechanisms.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
/ co-stimulatory/co-inhibitory molecules
/ Disease
/ Genes
/ Genetic Predisposition to Disease
/ Histocompatibility antigen HLA
/ Humans
/ Lupus
/ Lupus Erythematosus, Systemic - genetics
/ Polymorphism, Single Nucleotide
/ Proteins
/ single nucleotide polymorphism (SNP)
/ Single-nucleotide polymorphism
/ Systemic lupus erythematosus
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