Anti-histone antibodies
Anti-histone antibodies
Anti-histone antibodies are autoantibodies directed against histones, which are proteins that help package DNA into structural units called nucleosomes. These antibodies are often associated with certain autoimmune diseases, particularly systemic lupus erythematosus (SLE) and drug-induced lupus erythematosus.
Structure and Function of Histones
Histones are a group of basic proteins found in the cell nucleus. They are essential components of chromatin, the complex of DNA and protein that makes up chromosomes. Histones play a critical role in the regulation of gene expression by controlling the accessibility of DNA to transcription factors and other DNA-binding proteins.
There are five main types of histones: H1, H2A, H2B, H3, and H4. The core histones (H2A, H2B, H3, and H4) form an octamer around which DNA is wrapped to form a nucleosome, the fundamental unit of chromatin structure. The linker histone H1 binds to the DNA between nucleosomes, helping to compact the chromatin into higher-order structures.
Role in Autoimmune Diseases
Anti-histone antibodies are most commonly associated with drug-induced lupus erythematosus, a condition that resembles systemic lupus erythematosus but is triggered by certain medications. These antibodies can also be found in patients with idiopathic SLE, although they are less specific for this condition compared to other autoantibodies such as anti-double-stranded DNA antibodies.
In drug-induced lupus, the presence of anti-histone antibodies is a key diagnostic marker. Common drugs that can induce lupus-like symptoms include procainamide, hydralazine, and isoniazid.
Detection and Clinical Significance
The detection of anti-histone antibodies is typically performed using enzyme-linked immunosorbent assay (ELISA) or immunofluorescence techniques. The presence of these antibodies can aid in the diagnosis of drug-induced lupus and can also be a feature of idiopathic SLE.
In clinical practice, the identification of anti-histone antibodies can help differentiate between drug-induced lupus and idiopathic SLE, as well as monitor disease activity and response to treatment.
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Contributors: Prab R. Tumpati, MD