Candida albicans Antibody, IgM
Code:17039
| Includes | Candida albicans IgM antibody |
|---|
Analysis details
Methodology
- Enzyme-linked immunosorbent assay (ELISA)
Expected Turnaround Time
1–2 days
Special Instructions
- Do not eat for 2–3 hours before the blood draw; water is allowed.
- Do not smoke during the 30 minutes before specimen collection.
How to use
Candida albicans Antibody, IgM (also known as a Candida antibody assay or candidiasis serology) is used as an adjunct in the assessment of suspected Candida infection. It helps characterize recent or primary exposure by identifying IgM antibodies to C. albicans and can be followed over time to observe serologic trends during therapy. Results are correlated with history, examination, and direct detection methods—such as microscopy, culture, molecular assays, and antigen testing—because colonization may produce seropositivity, and sensitivity is reduced in the early 1–2 week window after exposure and in immunosuppressed patients.
Limitations
Candida albicans is a commensal yeast of skin and mucosal surfaces that can cause mucocutaneous disease or progress to invasive candidiasis under permissive conditions. Laboratory evaluation encompasses potassium hydroxide (KOH) microscopy, wet mounts for vulvovaginitis, culture, molecular tests (PCR), antigen detection, and serology. Serologic assays detect host antibodies formed in response to Candida antigens. IgM is typically the earliest antibody detected after a primary encounter with C. albicans, with peak levels developing within 1–2 weeks and declining as infection resolves. Upon re-exposure, IgG rises quickly, whereas the IgM response is comparatively attenuated. Because mucosal colonization is common and can stimulate antibody production, an isolated IgM-positive result does not distinguish colonization from clinically significant infection and functions as supportive evidence for mucocutaneous disease, secondary to clinical assessment and direct microscopy. Species-level identification remains clinically relevant due to variable antifungal susceptibilities; IgM assays directed at C. albicans do not detect non-albicans Candida species. In invasive candidiasis, no single diagnostic test is definitive; IgM serology may contribute within a multimodal strategy but is limited by reduced sensitivity in immunosuppressed patients and by the 1–2 week delay required to mount a detectable antibody response.
| Reference interval |
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|---|---|---|---|---|---|
| Indications | Symptoms consistent with mucocutaneous candidiasis (oral thrush, vulvovaginal or cutaneous disease), including pruritus, pain, erythema, and white curd-like plaques, Persistent febrile neutropenia not responding to broad-spectrum antibacterial therapy, raising concern for invasive candidiasis, Recipient of a hematopoietic stem cell transplant or a solid-organ transplant, Marked immunosuppression due to high-dose corticosteroids, cytotoxic chemotherapy, or radiation therapy, History of severe burns, major trauma, or extensive surgical procedures associated with higher risk of invasive Candida infection |
Possible Causes of Abnormal Results
Increased levels
- colonization with candida albicans
Decreased levels
- early infection (≤1–2 weeks after exposure)
- immunosuppression
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
References
Quindós G, Moragues MD, Pontón J. Is there a role for antibody testing in the diagnosis of invasive candidiasis? Rev Iberoam Micol. 2004 Mar;21(1):10-4.
Ellepola AN, Morrison CJ. Laboratory diagnosis of invasive candidiasis. J Microbiol. 2005 Feb;43 Spec No:65-84.
Jones JM. Laboratory diagnosis of invasive candidiasis. Clin Microbiol Rev. 1990 Jan;3(1):32-45.