αAβ–Gas6
Identification
- Summary
αAβ–Gas6 is a chimeric fusion protein being investigated for Alzheimer's disease.
- Generic Name
- αAβ–Gas6
- DrugBank Accession Number
- DB17069
- Background
αAβ–Gas6 is a chimeric fusion protein being investigated in preclinical studies as an immunotherapeutic agent for Alzheimer's disease (AD). It is made of a single chain variable fragment (scFv) of an Amyloid β (Aβ)-targeting monoclonal antibody fused with a truncated receptor binding domain of growth arrest-specific 6 (Gas6), which is a ligand for receptor kinases expressed in glial cells.1,2 αAβ–Gas6 is a phagocyte inducer of Aβ,1 which is the main component of the amyloid plaques found in individuals with AD and is considered to contribute to the pathophysiology of AD.3 This experimental drug gained attention because it was associated with fewer inflammatory side effects than the previously-approved Aβ antibody-based immunotherapy, aducanumab.6
- Type
- Biotech
- Groups
- Experimental
- Biologic Classification
- Protein Based Therapies
Fusion proteins - Protein Chemical Formula
- Not Available
- Protein Average Weight
- Not Available
- Sequences
- Not Available
- Synonyms
- Not Available
Pharmacology
- Indication
Not Available
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- Pharmacodynamics
Not Available
- Mechanism of action
TAM (TYRO3, AXL, and MERTK) receptors are receptor tyrosine kinases expressed ubiquitously,4 including microglia and astrocytes of the nervous system.1 They play a critical role in homeostatic processes such as phagocytosis of apoptotic cells and membranous organelles, and regulation of inflammatory responses and inflammation.5,4
αAβ-Gas6 targets TAM receptors by binding to growth arrest-specific 6 (Gas6), a ligand for TAM receptors.2 By activating the TAM receptor signalling pathway, αAβ-Gas6 promotes TAM receptor-dependent phagocytosis to selectively eliminate Aβ plaques without affecting NF-kB-mediated inflammatory responses or reactive gliosis.1
- Absorption
Not Available
- Volume of distribution
Not Available
- Protein binding
Not Available
- Metabolism
- Not Available
- Route of elimination
Not Available
- Half-life
Not Available
- Clearance
Not Available
- Adverse Effects
- Improve decision support & research outcomesWith structured adverse effects data, including: blackbox warnings, adverse reactions, warning & precautions, & incidence rates. View sample adverse effects data in our new Data Library!Improve decision support & research outcomes with our structured adverse effects data.
- Toxicity
Not Available
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs
- Not Available
Interactions
- Drug Interactions
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.Not Available
- Food Interactions
- Not Available
Categories
- Drug Categories
- Not Available
- Chemical TaxonomyProvided by Classyfire
- Description
- Not Available
- Kingdom
- Organic Compounds
- Super Class
- Organic Acids
- Class
- Carboxylic Acids and Derivatives
- Sub Class
- Amino Acids, Peptides, and Analogues
- Direct Parent
- Peptides
- Alternative Parents
- Not Available
- Substituents
- Not Available
- Molecular Framework
- Not Available
- External Descriptors
- Not Available
- Affected organisms
- Not Available
Chemical Identifiers
- UNII
- Not Available
- CAS number
- Not Available
References
- General References
- Jung H, Lee SY, Lim S, Choi HR, Choi Y, Kim M, Kim S, Lee Y, Han KH, Chung WS, Kim CH: Anti-inflammatory clearance of amyloid-beta by a chimeric Gas6 fusion protein. Nat Med. 2022 Sep;28(9):1802-1812. doi: 10.1038/s41591-022-01926-9. Epub 2022 Aug 4. [Article]
- Shankar SL, O'Guin K, Cammer M, McMorris FA, Stitt TN, Basch RS, Varnum B, Shafit-Zagardo B: The growth arrest-specific gene product Gas6 promotes the survival of human oligodendrocytes via a phosphatidylinositol 3-kinase-dependent pathway. J Neurosci. 2003 May 15;23(10):4208-18. [Article]
- Thal DR, Walter J, Saido TC, Fandrich M: Neuropathology and biochemistry of Abeta and its aggregates in Alzheimer's disease. Acta Neuropathol. 2015 Feb;129(2):167-82. doi: 10.1007/s00401-014-1375-y. Epub 2014 Dec 23. [Article]
- Lemke G: Biology of the TAM receptors. Cold Spring Harb Perspect Biol. 2013 Nov 1;5(11):a009076. doi: 10.1101/cshperspect.a009076. [Article]
- Lemke G, Rothlin CV: Immunobiology of the TAM receptors. Nat Rev Immunol. 2008 May;8(5):327-36. doi: 10.1038/nri2303. [Article]
- SciTechDaily: A New, More Effective Alzheimer’s Drug With No Inflammatory Side Effects [Link]
- External Links
- Not Available
Clinical Trials
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
- Not Available
- Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Not Available
- Experimental Properties
- Not Available
Drug created at October 13, 2022 14:30 / Updated at December 01, 2022 11:34