Anti-DNase B (Streptococcal) Antibodies
The Anti-DNase B test measures serum antibodies to an extracellular deoxyribonuclease enzyme of group A streptococci, providing serological evidence of recent infection. Titres rise within one to two weeks and peak at four to six weeks; the response is particularly robust after skin infection.
1
Biomarkers
Blood (serum)
Sample
2–4 business days
Turnaround
No
Fasting
What is the Anti-DNase B test?
The Anti-DNase B test detects antibodies to an extracellular enzyme of group A streptococci, offering serological proof of recent infection when the organism is no longer recoverable from the throat or skin. Practitioners order it almost exclusively in the context of suspected post-streptococcal immune-mediated complications — acute rheumatic fever and acute post-streptococcal glomerulonephritis — where establishing temporal association with a streptococcal infection is a diagnostic prerequisite. Anti-DNase B complements rather than replaces the anti-streptolysin O (ASO) assay: ASO is more sensitive after pharyngitis, while anti-DNase B is more sensitive after skin infection and remains elevated longer. Dual testing increases the cumulative sensitivity for detecting recent infection to well above 90 per cent, so when a post-streptococcal sequela is suspected and ASO is normal or equivocal, anti-DNase B often resolves the diagnostic uncertainty.
What does the Anti-DNase B test measure?
Deoxyribonuclease B is an extracellular deoxyribonuclease enzyme produced by group A streptococci (Streptococcus pyogenes). During and after pharyngeal or cutaneous infection, the host mounts a specific antibody response to DNase B; titres rise within one to two weeks of infection, peak at four to six weeks, and then decline slowly over months. The response is particularly robust following skin infection (pyoderma, impetigo), where anti-streptolysin O (ASO) may be weak or absent because lipid-rich skin inactivates streptolysin O.
Anti-DNase B antibodies are serological evidence of recent group A streptococcal infection. Clinicians order the test when a post-streptococcal sequela — acute rheumatic fever or acute post-streptococcal glomerulonephritis — is suspected and to corroborate a streptococcal aetiology in patients with a negative or borderline ASO. Because the antibody response is more reliable after skin infection, anti-DNase B is especially useful for glomerulonephritis cases following impetigo, and dual testing (ASO plus anti-DNase B) captures the majority of true streptococcal exposures.
Why is the Anti-DNase B test ordered?
- Investigation of suspected acute rheumatic fever in a patient presenting with migratory polyarthritis, carditis, chorea, erythema marginatum, or subcutaneous nodules, to fulfil the Jones criteria for recent streptococcal infection
- Evaluation of acute post-streptococcal glomerulonephritis when haematuria, proteinuria, oedema, and hypertension appear one to three weeks after a skin or throat infection, particularly if that infection was pyoderma
- Patients with a negative or borderline ASO titre in whom a post-streptococcal aetiology remains clinically suspected, to improve diagnostic sensitivity
- Serial follow-up of confirmed post-streptococcal disease, though falling titres are expected and a persistently elevated titre alone does not imply ongoing active disease
- Outbreak or epidemiological investigation of group A streptococcal infections in institutional or close-contact settings, when throat culture is no longer practical
- Paediatric cases where skin infection predominates, since ASO may be falsely negative after impetigo
Sample collection and turnaround
Sample type
Blood (serum)
Fasting required
No
Collection method
Venipuncture at patient service centre
Turnaround
2–4 business days
Collection notes
Phlebotomy at LabCorp draw site; no special preparation. When acute rheumatic fever or glomerulonephritis is suspected, collect the specimen as soon as possible after presentation, and consider a convalescent specimen two weeks later if the initial result is equivocal, to demonstrate a rising titre.
Specimen requirements
Minimum 0.5 mL serum. Separate from cells promptly; stable refrigerated for up to one week or frozen for longer storage. Submit alongside or shortly after an ASO specimen for dual streptococcal serology.
What can affect Anti-DNase B results?
Titres begin rising one to two weeks after infection, peak at four to six weeks, and decline over months; a specimen drawn too early in the acute phase may be falsely negative, while one drawn months later may have returned to baseline.
Repeated group A streptococcal exposure, especially in children in crowded settings, can sustain a moderately elevated titre without current disease, so clinical correlation is essential.
Early antibiotic therapy may blunt or delay the antibody response, though titres usually still rise; a negative result does not exclude infection if treatment was prompt.
Children and adolescents have higher baseline and upper-limit thresholds than adults because of frequent streptococcal exposures; reference ranges must be age-adjusted.
Anti-DNase B response is particularly strong and sustained after skin infection (impetigo, pyoderma), whereas ASO may be weak because skin lipids inactivate streptolysin O; this makes anti-DNase B the preferred marker for post-impetigo glomerulonephritis.
What do Anti-DNase B results mean?
Elevated
An elevated or rising titre is serological evidence of recent group A streptococcal infection within the preceding weeks to months. In the appropriate clinical context — migratory arthritis, carditis, glomerulonephritis, low complement, erythema marginatum — it supports a diagnosis of acute rheumatic fever or post-streptococcal glomerulonephritis. A single elevated titre indicates exposure but not necessarily active disease; clinical correlation, timing, and the presence of compatible sequelae are required for diagnosis.
Normal
A normal or negative anti-DNase B in the setting of suspected post-streptococcal disease makes recent infection less likely but does not exclude it, especially if ASO is also negative and clinical suspicion is high. In that situation consider repeat serology in one to two weeks to capture a rising titre, or review the clinical diagnosis.
Reduced
A titre below the laboratory threshold is interpreted as negative and indicates no serological evidence of recent streptococcal infection. It does not, however, exclude infection if the specimen was drawn too early (first week) or if the patient received early antibiotic treatment that blunted the response.
Note: Anti-DNase B must be interpreted with the timing of the suspected infection, the clinical syndrome, and the ASO result. Dual testing (ASO plus anti-DNase B) achieves the highest sensitivity. A persistently elevated titre after documented infection is common and does not itself indicate recurrent or ongoing disease. Reference limits differ by age, assay, and laboratory, so note the performing lab for serial comparisons.
Frequently asked questions
Anti-DNase B is an antibody to an enzyme produced by group A streptococci. It is measured to confirm recent streptococcal infection when a post-streptococcal complication such as acute rheumatic fever or glomerulonephritis is suspected, especially after the organism is no longer present in throat or skin.
How to access the Anti-DNase B test
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Published: October 7, 2026
Last reviewed: October 7, 2026
- Gerber MA, et al. Prevention of rheumatic fever and diagnosis and treatment of acute streptococcal pharyngitis: a scientific statement from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee. (2009)
- Carapetis JR, et al. Acute rheumatic fever. Lancet. (2005)
- Rodriguez-Iturbe B, Musser JM. The current state of poststreptococcal glomerulonephritis. J Am Soc Nephrol. (2008)
- Ayoub EM, Wannamaker LW. Evaluation of the streptococcal deoxyribonuclease B and diphosphopyridine nucleotidase antibody tests in acute rheumatic fever and acute glomerulonephritis. Pediatrics. (1962)
This content is for licensed healthcare practitioners only and does not constitute medical advice. Clinical decisions should be based on the full clinical picture and not on any single test result.