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Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity
by
Candotti, Fabio
, Liu, Chaohong
, Miller, Heather
, Ren, Anwen
, Lee, Pamela
, Gong, Quan
, Westerberg, Lisa S.
, Park, Chan-Sik
, Chen, Yan
, Yin, Wei
in
Amino acids
/ Anemia
/ Animals
/ Antibiotics
/ Autoimmunity
/ Bacterial infections
/ Cardiovascular disease
/ CD122 antigen
/ CD137 antigen
/ Cells
/ Cytomegalovirus
/ Disease prevention
/ DNA methylation
/ Epstein-Barr virus
/ Genetic Diseases, Inborn - genetics
/ Humans
/ hyperinflammation
/ immune dysregulation
/ Immune system
/ Immune System Diseases - genetics
/ Immunity
/ Immunity (Disease)
/ Immunoglobulins
/ Immunology
/ inborn errors of immunity
/ Inflammation
/ Inflammatory bowel disease
/ Lymphocytes
/ Lymphoma
/ lymphoproliferation
/ Medical prognosis
/ Mutation
/ Pathology, Molecular
/ Phenotype
/ Phosphorylation
/ primary immune dysregulation disease
/ Proteins
/ Purpura
/ Steroids
/ Streptococcus infections
/ Transforming growth factor-b1
/ Vitiligo
/ Whole Exome Sequencing
/ Whole genome sequencing
2021
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Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity
by
Candotti, Fabio
, Liu, Chaohong
, Miller, Heather
, Ren, Anwen
, Lee, Pamela
, Gong, Quan
, Westerberg, Lisa S.
, Park, Chan-Sik
, Chen, Yan
, Yin, Wei
in
Amino acids
/ Anemia
/ Animals
/ Antibiotics
/ Autoimmunity
/ Bacterial infections
/ Cardiovascular disease
/ CD122 antigen
/ CD137 antigen
/ Cells
/ Cytomegalovirus
/ Disease prevention
/ DNA methylation
/ Epstein-Barr virus
/ Genetic Diseases, Inborn - genetics
/ Humans
/ hyperinflammation
/ immune dysregulation
/ Immune system
/ Immune System Diseases - genetics
/ Immunity
/ Immunity (Disease)
/ Immunoglobulins
/ Immunology
/ inborn errors of immunity
/ Inflammation
/ Inflammatory bowel disease
/ Lymphocytes
/ Lymphoma
/ lymphoproliferation
/ Medical prognosis
/ Mutation
/ Pathology, Molecular
/ Phenotype
/ Phosphorylation
/ primary immune dysregulation disease
/ Proteins
/ Purpura
/ Steroids
/ Streptococcus infections
/ Transforming growth factor-b1
/ Vitiligo
/ Whole Exome Sequencing
/ Whole genome sequencing
2021
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Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity
by
Candotti, Fabio
, Liu, Chaohong
, Miller, Heather
, Ren, Anwen
, Lee, Pamela
, Gong, Quan
, Westerberg, Lisa S.
, Park, Chan-Sik
, Chen, Yan
, Yin, Wei
in
Amino acids
/ Anemia
/ Animals
/ Antibiotics
/ Autoimmunity
/ Bacterial infections
/ Cardiovascular disease
/ CD122 antigen
/ CD137 antigen
/ Cells
/ Cytomegalovirus
/ Disease prevention
/ DNA methylation
/ Epstein-Barr virus
/ Genetic Diseases, Inborn - genetics
/ Humans
/ hyperinflammation
/ immune dysregulation
/ Immune system
/ Immune System Diseases - genetics
/ Immunity
/ Immunity (Disease)
/ Immunoglobulins
/ Immunology
/ inborn errors of immunity
/ Inflammation
/ Inflammatory bowel disease
/ Lymphocytes
/ Lymphoma
/ lymphoproliferation
/ Medical prognosis
/ Mutation
/ Pathology, Molecular
/ Phenotype
/ Phosphorylation
/ primary immune dysregulation disease
/ Proteins
/ Purpura
/ Steroids
/ Streptococcus infections
/ Transforming growth factor-b1
/ Vitiligo
/ Whole Exome Sequencing
/ Whole genome sequencing
2021
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Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity
Journal Article
Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity
2021
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Overview
With the expansion of our knowledge on inborn errors of immunity (IEI), it gradually becomes clear that immune dysregulation plays an important part. In some cases, autoimmunity, hyperinflammation and lymphoproliferation are far more serious than infections. Thus, immune dysregulation has become significant in disease monitoring and treatment. In recent years, the wide application of whole-exome sequencing/whole-genome sequencing has tremendously promoted the discovery and further studies of new IEI. The number of discovered IEI is growing rapidly, followed by numerous studies of their pathogenesis and therapy. In this review, we focus on novel discovered primary immune dysregulation diseases, including deficiency of SLC7A7, CD122, DEF6, FERMT1, TGFB1, RIPK1, CD137, TET2 and SOCS1. We discuss their genetic mutation, symptoms and current therapeutic methods, and point out the gaps in this field.
Publisher
Frontiers Media SA,Frontiers Media S.A
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