Chlamydia Antibody Panel, IgM by IFA
Also known as: V CHLAM M
Use
The Chlamydia Antibody Panel, IgM by IFA is used to differentiate between Chlamydophila species, including C. psittaci, C. pneumoniae, and nine serotypes of C. trachomatis, excluding LGV strains. It is intended to identify early IgM response to infection and distinguish it from persistent low-level titers. Serological cross-reactions can occur, with C. pneumoniae-specific reactions potentially displaying titers twofold or greater compared to C. trachomatis or C. psittaci. This test provides limited diagnostic value for most oculogenital chlamydial infections.
Special Instructions
Not provided.
Limitations
The test is not FDA cleared or approved, and its performance characteristics were determined by ARUP Laboratories. The assay does not include LGV strains of C. trachomatis and is not suitable for diagnosing most oculogenital chlamydial infections. Seroconversion, a fourfold or greater increase in antibody titer between acute and convalescent sera, is considered strong evidence of recent infection. Interpret results carefully due to potential cross-reactivity between species.
New York Approved
Methodology
Immunoassay (Other)
Biomarkers
LOINC Codes
- 6914-6 - C pneum IgM Titr Ser IF
- 6920-3 - C trach IgM Titr Ser IF
- 6917-9 - C psittaci IgM Titr Ser IF
- 59464-8 - Microbiologist review
Result Turnaround Time
1-4 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.4 mL
Container
ARUP standard transport tube
Collection Instructions
Separate serum from cells ASAP or within 2 hours of collection and transfer to the transport tube.
Storage Instructions
Refrigerated storage is preferred. Avoid repeated freeze/thaw cycles.
Causes for Rejection
Contaminated, hemolyzed, or hyperlipemic sera.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
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