Target Name: HLA Class II Histocompatibility Antigen DM (HLA-DM)
NCBI ID: P40589
Other Name(s): HLA-DM | HLA Class II Histocompatibility Antigen DM

HLA-DM: Key Player in T Cell Development and Function

HLA Class II Histocompatibility Antigen DM (HLA-DM) is a protein that is expressed in the major histocompatibility complex (MHC) and is involved in the immune response. It is a key player in the regulation of T cell development and function and has been implicated in a number of diseases, including cancer, autoimmune disorders, and neurodegenerative diseases. In this article, we will discuss the biology and implications of HLA-DM and its potential as a drug target.

HLA-DM is a type of transmembrane protein that is composed of two main regions: the constant region and the variable region. The constant region is the portion of the protein that is constant throughout and is involved in maintaining the stability and structure of the protein. The variable region is the portion of the protein that is variable and is involved in the recognition of antigens by T cells.

HLA-DM is expressed in a variety of tissues and cells, including spleen, thymus, spleen lymphocytes, and human skin samples. It is highly conserved across different species and has a high degree of sequence identity between different isoforms. HLA-DM has been implicated in the regulation of T cell development and function by regulating the expansion and differentiation of T cells, as well as by regulating immune responses to infections.

One of the key functions of HLA-DM is its role in regulating the development and function of T cells. T cells are a critical part of the immune system and play a key role in detecting and responding to foreign antigens. T cell development and function are regulated by a complex interplay of genetic and environmental factors, including the interactions between HLA-DM and other immune molecules.

HLA-DM has been shown to play a key role in regulating the development and function of T cells by regulating the expansion and differentiation of T cells intoCD4+ and CD8+ T cells. CD4+ T cells are responsible for cell-to-cell communication and play a key role in immune surveillance of the body, while CD8+ T cells are involved in antigen presentation and elimination. HLA-DM has been shown to regulate the expansion and differentiation of T cells by regulating the interactions between T cells and other immune molecules, including the cytoskeleton and the T cell receptor (TCR).

HLA-DM has also been shown to play a key role in regulating the immune response to infections. In response to an infection, T cells are activated and their activity is regulated by HLA-DM. HLA-DM has been shown to regulate the production of IFN-纬, a key mediator of the immune response, by regulating the activity of STAT3, a transcription factor that is involved in the regulation of gene expression.

In addition to its role in regulating T cell development and function, HLA-DM has also been implicated in the regulation of a variety of other immune processes, including inflammation and neurodegenerative diseases. For example, HLA-DM has been shown to be involved in the regulation of inflammation by regulating the production of pro-inflammatory cytokines, such as TNF-伪 and IL-12. HLA-DM has also been shown to be involved in the regulation of neurodegenerative diseases by regulating the production of neurotoxins and promoting the clearance of neurodegenerate protein aggregates.

HLA-DM has also been shown to have potential as a drug target. One of the main advantages of HLA-DM as a drug target is its high degree of conservation across different species, which makes it more likely to be effective in humans. Additionally, HLA-DM has been shown to be involved in a variety of immune processes and its dysfunction has been implicated in a number of diseases, which makes it a promising target for the development of new therapeutics.

HLA-DM has been shown to be involved in the regulation of

Protein Name: HLA Class II Histocompatibility Antigen DM (HLA-DM)

More Common Targets

HLA class II histocompatibility Antigen DO (HLA-DO) | HLA class II histocompatibility antigen DP (HLA-DP) | HLA Class II Histocompatibility Antigen DQ8 | HLA class II histocompatibility antigen DR (HLA-DR) | HLA Class II Histocompatibility Antigen, DQ (HLA-DQ) | HLA class II histocompatibility antigen, DRB1-7 beta chain, transcript variant X1 | HLA complex group 16 (non-protein coding), transcript variant X2 | HLA complex group 8 | HLA-A | HLA-B | HLA-C | HLA-DMA | HLA-DMB | HLA-DOA | HLA-DOB | HLA-DPA1 | HLA-DPA2 | HLA-DPA3 | HLA-DPB1 | HLA-DPB2 | HLA-DQA1 | HLA-DQA2 | HLA-DQB1 | HLA-DQB1-AS1 | HLA-DQB2 | HLA-DRA | HLA-DRB1 | HLA-DRB2 | HLA-DRB3 | HLA-DRB4 | HLA-DRB5 | HLA-DRB6 | HLA-DRB7 | HLA-DRB8 | HLA-DRB9 | HLA-E | HLA-F | HLA-F-AS1 | HLA-G | HLA-H | HLA-J | HLA-K | HLA-L | HLA-N | HLA-P | HLA-U | HLA-V | HLA-W | HLCS | HLF | HLTF | HLX | HM13 | HMBOX1 | HMBS | HMCES | HMCN1 | HMCN2 | HMG20A | HMG20B | HMGA1 | HMGA1P2 | HMGA1P4 | HMGA1P7 | HMGA1P8 | HMGA2 | HMGA2-AS1 | HMGB1 | HMGB1P1 | HMGB1P10 | HMGB1P19 | HMGB1P37 | HMGB1P38 | HMGB1P46 | HMGB1P5 | HMGB1P6 | HMGB2 | HMGB2P1 | HMGB3 | HMGB3P1 | HMGB3P14 | HMGB3P15 | HMGB3P19 | HMGB3P2 | HMGB3P22 | HMGB3P24 | HMGB3P27 | HMGB3P30 | HMGB3P6 | HMGB4 | HMGCL | HMGCLL1 | HMGCR | HMGCS1 | HMGCS2 | HMGN1 | HMGN1P16 | HMGN1P30 | HMGN1P37 | HMGN1P8