Test Code Billings Clinic: 6828 Mayo: TPPA Syphilis Antibody, Treponema pallidum Particle Agglutination, Serum
Reporting Name
Syphilis Ab by TP-PA, SPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
An aid to resolve discrepant results between screening treponemal and non-treponemal assays
This test is not recommended for general screening purposes for syphilis.
This test should not be used to evaluate response to therapy.
This test is not intended for medical-legal use.
Method Name
Particle Agglutination
Ordering Guidance
This assay is recommended by the Centers for Disease Control and Prevention for sera testing positive by a screening treponemal assay and negative by rapid plasma reagin (RPR). The results of this assay assist in determining whether the results of a screening treponemal test are truly or falsely positive.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Specimen Type
SerumSpecimen Minimum Volume
0.3 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 14 days | |
Frozen | 14 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Reference Values
Negative
Interpretation
Syphilis screening at Mayo Clinic is performed by using the reverse algorithm, which first tests sera for Treponema pallidum specific IgG antibodies using an automated immunoassay. Antibodies to syphilis can remain elevated despite appropriate antimicrobial treatment and a reactive result does not distinguish between recent or past infection. To further evaluate disease and treatment status, samples that are reactive by the syphilis screening test are reflexed to the rapid plasma reagin (RPR) assay, which detects antibodies to cardiolipin, a lipoidal antigen released from host cells damaged by T pallidum. Unlike treponemal-specific antibodies, RPR titers decrease and usually become undetectable following appropriate treatment and can be used to monitor response to therapy.
In some patients, the results of the treponemal screening test and RPR may be discordant (eg, syphilis IgG positive and RPR negative). To discriminate between a falsely reactive screening result and past syphilis, a second treponemal-specific antibody test is recommended using a method that is different from the initial screening test (eg, T pallidum particle agglutination: TP-PA).
In the setting of a positive syphilis IgG screening result and a negative RPR, a positive TP-PA result is consistent with one of the following:
1. Past, successfully treated syphilis
2. Early syphilis with undetectable RPR titers
3. Late/latent syphilis in patients who do not have a history of treatment for syphilis
Further historical evaluation is necessary to distinguish between these scenarios (Table).
In the setting of a positive syphilis IgG screening result and a negative RPR, a negative TP-PA result is most consistent with a falsely reactive syphilis IgG screen (Table). If syphilis remains clinically suspected, a second specimen should be submitted, order SYPH1 / Syphilis IgG with Reflex, Enzyme Immunoassay, Serum.
Table. Interpretation and follow-up of reverse screening results
Patient history |
Test and result |
Interpretation |
Follow-up |
||
EIA/CIA/MFI |
RPR |
TP-PA |
|||
Unknown history of syphilis |
Nonreactive |
N/A |
N/A |
No serologic evidence of syphilis |
None, unless clinically indicated (eg, early/acute/ primary syphilis) |
Unknown history of syphilis |
Reactive |
Reactive |
N/A |
Untreated or recently treated syphilis |
See Centers for Disease Control and Prevention treatment guidelines  |
Unknown history of syphilis |
Reactive |
Nonreactive |
Nonreactive |
Probable false-positive screening test |
No follow-up testing, unless clinically indicated (eg, acute/primary syphilis) |
Unknown history of syphilis |
Reactive |
Nonreactive |
Reactive |
Possible syphilis (eg, early or latent) or previously treated syphilis |
Historical and clinical evaluation required |
Known history of syphilis |
Reactive |
Nonreactive |
Reactive or N/A |
Past, successfully treated syphilis |
None |
CIA, chemiluminescence immunoassay; EIA, enzyme immunoassay; N/A, not applicable; RPR, rapid plasma reagin; TP-PA, Treponema pallidum particle agglutination.
Day(s) Performed
Monday through Friday
Report Available
Same day/1 to 4 daysTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86780
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
TPPA | Syphilis Ab by TP-PA, S | 24312-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
61480 | Syphilis Ab by TP-PA, S | 24312-1 |
Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.
Testing Algorithm
For more information see Syphilis Serology Algorithm.