Target intelligence / Profile preview

Kidney injury molecule-1 (KIM-1)

Target
KIM-1
Molecular classification
Type I membrane protein, Transmembrane glycoprotein, Receptor, Scavenger receptor
01

Overview

Kidney injury molecule-1 (KIM-1) is a type I transmembrane protein and scavenger receptor predominantly expressed by proximal tubular epithelial cells of the kidney after injury. It is normally undetectable in healthy kidneys, but its expression is markedly upregulated in response to acute or chronic tubular injury, including ischemia, toxic injury, and inflammation. KIM-1 mediates the phagocytosis of apoptotic and necrotic cells by binding to phosphatidylserine and oxidized phospholipids, thereby promoting tissue remodeling and resolution of injury. KIM-1 is also involved in antigen presentation and modulation of immune tolerance in the kidney. It serves as a highly sensitive and specific noninvasive biomarker in urine and blood for early detection, prognosis, and therapeutic monitoring of a variety of kidney disorders, including acute kidney injury, chronic kidney disease, diabetic nephropathy, and various glomerulopathies. It is being investigated as both a therapeutic target (to facilitate tissue repair and limit injury) and a prognostic biomarker in renal cell carcinoma. KIM-1 is also known as HAVCR1 or TIM-1, with some roles described outside the kidney in immune regulation.

Other names
HAVCR1 (Hepatitis A virus cellular receptor 1)TIM-1 (T-cell immunoglobulin and mucin domain-containing protein 1)Hepatitis A virus receptor 1
02

Mechanism of action

Drugs or compounds targeting KIM-1 would be likely to act by modulating immune responses, enhancing tubular repair, or reducing apoptotic cell accumulation, but no drugs with established mechanism of action against KIM-1 in clinical use as of now.

03

Biological functions

Phagocytosis of apoptotic and necrotic cellsImmune response regulationAntigen presentation and maintenance of immune toleranceRenal tubular repair and epithelial cell migration/proliferation via ERK/MAPK signalingAutophagy in kidney tubular epitheliumEndocytosis and binding of oxidized lipidsMarker for dedifferentiated proximal tubular epithelial cells in damaged regions
04

Disease associations

Acute kidney injury (AKI)Chronic kidney disease (CKD)Diabetic nephropathyGlomerulonephritis (e.g., ANCA-associated vasculitis)Renal cell carcinoma (prognostic marker)Inflammatory/autoimmune kidney diseasesKidney transplant dysfunction
05

Safety considerations

No direct safety concerns for targeting KIM-1 are reported; main challenges are sensitivity/specificity as a biomarker, and the translation of preclinical findings to clinical interventions.
06

Interacting drugs

No direct therapeutic drugs widely established as interacting with KIM-1 yet; it is primarily a biomarker and research target at present.
07

Biomarkers

Urinary KIM-1 (for early detection and monitoring of AKI, CKD, nephropathy, drug-induced nephrotoxicity, ANCA-GN, etc.)Blood KIM-1 (recently recognized for association with kidney injury severity)FDA-recognized preclinical biomarker for renal injury

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