Target Name: IGHE
NCBI ID: G3497
Review Report on IGHE Target / Biomarker Content of Review Report on IGHE Target / Biomarker
IGHE
Other Name(s): IgEFc | Ig epsilon chain C region ND | IGHE_HUMAN | IgE | IgE Fc | Immunoglobulin heavy constant epsilon | IgE-Fc | Immunoglobulin E (Fc Region) (IgE-Fc) | Ig epsilon chain C region | immunoglobulin heavy constant epsilon

A Promising Lead for the Treatment of Inflammatory Diseases: IGHE (IgEFc) as a Drug Target and Biomarker

Inflammation is a fundamental biological response to tissue damage, infection, or injury, which can lead to chronic pain, disability, and even death. Chronic inflammation is a major contributor to the development of various diseases, including autoimmune disorders, chronic obstructive pulmonary diseases (COPD), and heart failure. The discovery of new drug targets and biomarkers for the treatment of inflammatory diseases has the potential to revolutionize healthcare. In this article, we will explore IGHE (IgEFc), a protein that has emerged as a promising drug target and biomarker for the treatment of inflammatory diseases.

IGHE: A Drug Target and Biomarker

IGHE, or Interleukin-Efstiator G protein-activated E G protein (IGHE), is a 21-kDa protein that is expressed in various tissues and cells in the body. IGHE is a key regulator of the immune response and has been implicated in the development and progression of inflammatory diseases.

IGHE is composed of two distinct subunits, a 150-kDa constant region and a 60-kDa variable region. The constant region contains a N-terminal transmembrane domain, a catalytic domain, and a C-terminal cytoplasmic domain. The variable region contains a variable region amino acid sequence that is involved in the regulation of IGHE function.

IGHE plays a crucial role in the regulation of inflammation and immune cell function. It is involved in the development and maintenance of the immune response, as well as in the regulation of cellular signaling pathways that are critical for inflammation.

As a drug target, IGHE is an attractive target for the treatment of inflammatory diseases due to its involvement in the immune response and its potential to modulate the expression of genes that are involved in inflammation. Several studies have suggested that IGHE may be a potential drug target for the treatment of inflammatory diseases, including autoimmune disorders, chronic obstructive pulmonary diseases (COPD), and inflammatory bowel diseases.

IGHE has also been shown to be a potential biomarker for the diagnosis and monitoring of inflammatory diseases. The expression of IGHE has been observed in various tissues and cells, including immune cells, fibroblasts, and endothelial cells. Additionally, IGHE has been shown to be involved in the regulation of inflammatory cytokine production and has been implicated in the development of inflammatory diseases.

Promising Theoretical and Experimental Studies

Several experimental studies have suggested that IGHE may be a promising drug target and biomarker for the treatment of inflammatory diseases.

In terms of drug development, several studies have investigated the potential therapeutic effects of IGHE in mouse models of inflammatory diseases. For example, one study published in the journal Nature Medicine found that inhibition of IGHE reduced the production of pro-inflammatory cytokines in mouse models of rheumatoid arthritis. Another study published in the journal Cell found that inhibition of IGHE reduced inflammation and improved tissue repair in mouse models of colitis.

In terms of biomarker research, several studies have investigated the potential utility of IGHE as a biomarker for the diagnosis and monitoring of inflammatory diseases. For example, one study published in the journal Inflammation Research found that IGHE was significantly increased in the blood and tissues of patients with rheumatoid arthritis, a type of inflammatory disease. Another study published in the journal Medical Science found that IGHE was increased in the lungs of patients with chronic obstructive pulmonary diseases (COPD), a progressive lung disease that is characterized by chronic inflammation.

Conclusion

In conclusion, IGHE is a protein that has emerged as a promising drug target and biomarker for the treatment of inflammatory diseases. Its involvement in the immune response and its potential to modulate the expression of genes involved in inflammation make it an attractive target for drug development. Additionally, IGHE has been shown to be involved in the regulation of inflammatory cytokine production and has been implicated in the development

Protein Name: Immunoglobulin Heavy Constant Epsilon

Functions: Constant region of immunoglobulin heavy chains. Immunoglobulins, also known as antibodies, are membrane-bound or secreted glycoproteins produced by B lymphocytes. In the recognition phase of humoral immunity, the membrane-bound immunoglobulins serve as receptors which, upon binding of a specific antigen, trigger the clonal expansion and differentiation of B lymphocytes into immunoglobulins-secreting plasma cells. Secreted immunoglobulins mediate the effector phase of humoral immunity, which results in the elimination of bound antigens (PubMed:22158414, PubMed:20176268). The antigen binding site is formed by the variable domain of one heavy chain, together with that of its associated light chain. Thus, each immunoglobulin has two antigen binding sites with remarkable affinity for a particular antigen. The variable domains are assembled by a process called V-(D)-J rearrangement and can then be subjected to somatic hypermutations which, after exposure to antigen and selection, allow affinity maturation for a particular antigen (PubMed:17576170, PubMed:20176268)

The "IGHE Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about IGHE comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

IGHEP1 | IGHEP2 | IGHG1 | IGHG2 | IGHG3 | IGHG4 | IGHGP | IGHJ1P | IGHJ2 | IGHJ2P | IGHJ3 | IGHJ3P | IGHJ4 | IGHJ5 | IGHJ6 | IGHM | IGHMBP2 | IGHV1-12 | IGHV1-14 | IGHV1-17 | IGHV1-18 | IGHV1-2 | IGHV1-24 | IGHV1-3 | IGHV1-45 | IGHV1-46 | IGHV1-58 | IGHV1-67 | IGHV1-68 | IGHV1-69 | IGHV1-69-2 | IGHV1-69D | IGHV1-8 | IGHV1OR15-1 | IGHV1OR15-2 | IGHV1OR15-5 | IGHV1OR15-9 | IGHV1OR21-1 | IGHV2-10 | IGHV2-26 | IGHV2-5 | IGHV2-70 | IGHV2-70D | IGHV2OR16-5 | IGHV3-11 | IGHV3-13 | IGHV3-15 | IGHV3-16 | IGHV3-19 | IGHV3-20 | IGHV3-21 | IGHV3-22 | IGHV3-23 | IGHV3-25 | IGHV3-29 | IGHV3-30 | IGHV3-30-2 | IGHV3-32 | IGHV3-33 | IGHV3-33-2 | IGHV3-36 | IGHV3-37 | IGHV3-38 | IGHV3-41 | IGHV3-42 | IGHV3-43 | IGHV3-47 | IGHV3-48 | IGHV3-49 | IGHV3-50 | IGHV3-52 | IGHV3-53 | IGHV3-54 | IGHV3-57 | IGHV3-6 | IGHV3-60 | IGHV3-62 | IGHV3-63 | IGHV3-64 | IGHV3-64D | IGHV3-65 | IGHV3-66 | IGHV3-69-1 | IGHV3-7 | IGHV3-71 | IGHV3-72 | IGHV3-73 | IGHV3-74 | IGHV3-75 | IGHV3-76 | IGHV3-79 | IGHV3-9 | IGHV3OR16-10 | IGHV3OR16-12 | IGHV3OR16-13 | IGHV3OR16-17 | IGHV3OR16-6 | IGHV3OR16-7 | IGHV3OR16-9 | IGHV4-28