Immunoglobulin superfamily protein (IgSF), Type-1 membrane glycoprotein, B7 receptor family member, Cell surface molecule, Receptor ligand (for CD200 receptor, CD200R)
01
Overview
CD200 is a broadly expressed cell surface glycoprotein with two immunoglobulin-like domains, functioning primarily to suppress myeloid cell activity via interaction with the CD200 receptor (CD200R), which is highly expressed on macrophages and other myeloid cells. This ligand-receptor axis is a key checkpoint in both innate and adaptive immunity, regulating inflammatory responses and maintaining self-tolerance. Increased or aberrant expression of CD200 is linked to immune evasion in cancers, while viral orthologs of CD200 are used by pathogens to reduce host defense. Soluble forms and splice variants of CD200 add to its complexity in clinical contexts. CD200 is a validated immunological target in oncology, neuroinflammation, and infectious disease research, recognized for its role in immune checkpoint regulation.
Other names
OX-2 membrane glycoproteinCD200MOX1MOX2My033MRCOX-2CD200 antigenantigen identified by monoclonal antibody MRC OX-2
02
Mechanism of action
For experimental anti-CD200 agents and antibodies: Blockade of CD200-CD200R interaction to restore immune activation in cancer or minimize immune suppression. CD200R engagement by CD200 leads to tyrosine phosphorylation and recruitment of DOK1/DOK2 adaptors, resulting in downstream inhibition of MAPK/ERK pathway, reduced proinflammatory cytokine production, suppressed immune cell activation, and prevention of mast cell degranulation.
03
Biological functions
Immune response regulationInhibition of myeloid cell activation (macrophages, neutrophils, mast cells)Maintenance of self-toleranceModulation of inflammatory responsesShift cytokine profile (Th2 response)Regulation of NK cell cytotoxicityControl of T-cell activation thresholdIndoleamine-2,3-dioxygenase production in macrophagesRegulatory T cell expansionInhibition of basophil function
04
Disease associations
Cancer (chronic lymphocytic leukemia, acute myeloid leukemia, multiple myeloma, renal carcinoma, colon carcinoma, glioblastoma multiforme, melanoma, testicular cancer)Inflammation/excessive inflammatory responsesNeurodegenerative diseases (implicated via tissue-specific regulation and neural expression)Infection (CD200 orthologs are used by viruses such as herpesviruses and cytomegalovirus to evade immunity)Other (expansion of myeloid-derived suppressor cells, tumor microenvironment immunosuppression)
05
Safety considerations
Potential risk of excessive immunosuppression (linked to tumor immune escape or worsened infection)Challenges in selectively targeting only pathological CD200 expression, as it also maintains immune tolerance under physiological conditionsPossible impact on central nervous system homeostasis due to CD200's neural expression
06
Interacting drugs
No widely approved drugs directly targeting CD200 are currently listed in major clinical drug databases. Experimental agents (e.g., anti-CD200 antibodies) are explored in oncology and immunology research contexts
1 more in the full profile.
07
Biomarkers
Serum soluble CD200 (sCD200): Elevated levels are associated with poor prognosis in leukemia (CLL), glioblastoma multiforme, ependymoma, and medulloblastomaCD200 tumor cell expression: Used as a diagnostic or prognostic marker in certain hematologic malignancies
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