Test Catalog

Test Id : TPPA

Syphilis Antibody, Treponema pallidum Particle Agglutination, Serum

Useful For
Suggests clinical disorders or settings where the test may be helpful

An aid to resolve discrepant results between screening treponemal (eg, enzyme immunoassay [EIA], multiplex flow immunoassay) and non-treponemal (eg, rapid plasma regain) 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.

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

See Syphilis Serology Algorithm in Special Instructions.

Special Instructions
Library of PDFs including pertinent information and forms related to the test

Method Name
A short description of the method used to perform the test

Particle Agglutination

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Syphilis Ab by TP-PA, S

Aliases
Lists additional common names for a test, as an aid in searching

Syphilis

Treponema pallidum

Treponemal

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

See Syphilis Serology Algorithm in Special Instructions.

Specimen Type
Describes the specimen type validated for testing

Serum

Ordering Guidance

This assay is recommended by the Centers for Disease Control and Prevention for specimens 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
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Specimen Volume: 0.5 mL

Special Instructions
Library of PDFs including pertinent information and forms related to the test

Forms

If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

0.3 mL

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

Gross hemolysis Reject
Gross lipemia Reject

Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 14 days
Frozen 14 days

Useful For
Suggests clinical disorders or settings where the test may be helpful

An aid to resolve discrepant results between screening treponemal (eg, enzyme immunoassay [EIA], multiplex flow immunoassay) and non-treponemal (eg, rapid plasma regain) 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.

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

See Syphilis Serology Algorithm in Special Instructions.

Clinical Information
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Syphilis is a disease caused by infection with the spirochete Treponema pallidum. The infection is systemic and the disease is characterized by periods of latency. These features, together with the fact that T pallidum cannot be isolated in culture, mean that serologic techniques play a major role in the diagnosis and follow-up of treatment for syphilis.

 

Syphilis is categorized by an early primary infection in which patients may have nonspecific symptoms and, potentially, genital lesions. Patients tested by serology during the primary phase may be negative for antibodies, especially if testing is performed during the first 1 to 2 weeks after symptom onset. As the disease progresses into the secondary phase, antibodies to T pallidum reach peak titers and may persist indefinitely regardless of the disease state or prior therapy. Therefore, detection of antibodies to non-treponemal antigens, such as cardiolipin (a lipoidal antigen released by host cells damaged by T pallidum) may help to differentiate between active and past syphilis infection. Non-treponemal antibodies are detected by the rapid plasma reagin (RPR) assay, which is typically positive during current infection and negative following treatment or during late/latent forms of syphilis.

 

For prenatal syphilis screening, the syphilis IgG test (SYPGN / Syphilis Total Antibody, Serum) is recommended. Testing for IgM-class antibodies to T pallidum should not be performed during routine pregnancy screening unless clinically indicated.

 

Historically, the serologic testing algorithm for syphilis included an initial non-treponemal screening test, such as the RPR or the venereal disease research laboratory (VDRL) tests. Because these tests measure the host's antibody response to non-treponemal antigens, they may lack specificity. Therefore, a positive result by RPR or VDRL requires confirmation by a treponemal-specific test, such as fluorescent treponemal antibody absorption (FTA-ABS) or T pallidum particle agglutination (TP-PA). Although the FTA-ABS and TP-PA are technically simple to perform, they are labor intensive and require subjective interpretation by testing personnel.

 

Due to the low prevalence of syphilis in the United States, the increased specificity of treponemal assays, and the objective interpretation of automated treponemal enzyme immunoassay (EIA) and multiplex flow immunoassay (MFI), many large clinical laboratories have switched to screening for syphilis using a reverse algorithm. Per this algorithm, serum samples are first tested by an automated treponemal assay (eg, EIA or MFI). Specimens testing positive by these assays are then reflexed to the RPR assay to provide an indication of the patient's disease state and history of treatment. Recently, the Centers for Disease Control and Prevention recommended that specimens testing positive by a screening treponemal assay and negative by RPR be tested by a second treponemal test (eg, TP-PA). The results of TP-PA assist in determining whether the results of a screening treponemal test are truly or falsely positive.

Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Negative

Interpretation
Provides information to assist in interpretation of the test results

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 multiplex flow immunoassay (MFI).(1) IgG 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 IgG 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.(2) 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 (syphilis IgG) and RPR may be discordant (eg, syphilis IgG positive and RPR negative). To discriminate between a falsely reactive screening result and past syphilis, the Centers for Disease Control and Prevention recommends performing a second treponemal-specific antibody test using a method that is different from the initial screening test (eg, T pallidum particle agglutination; TP-PA).(2)

 

In the setting of a positive syphilis IgG screening result and a negative RPR, a positive TP-PA result is consistent with either 1) past, successfully treated syphilis, 2) early syphilis with undetectable RPR titers, or 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 1).

 

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 1). If syphilis remains clinically suspected, a second specimen should be submitted, order SYPHT / Syphilis Total Antibody with Reflex, Serum.

 

Table 1. 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

Non-reactive

N/A

N/A

No serologic evidence of syphilis

None, unless clinically indicated  (eg, early syphilis)

Unknown history of syphilis

Reactive

Reactive

N/A

Untreated or recently treated syphilis

See CDC treatment guidelines 

Unknown history of syphilis

Reactive

Non-reactive

Non-reactive

Probable false-positive screening test

No follow-up testing, unless clinically indicated

Unknown history of syphilis

Reactive

Non-reactive

Reactive

Possible syphilis (eg, early or latent) or previously treated syphilis

Historical and clinical evaluation required

Known history of syphilis

Reactive

Non-reactive

Reactive or N/A

Past, successfully treated syphilis

None

CIA, chemiluminescence immunoassay; EIA, enzyme immunoassay; MFI, multiplex flow immunoassay; N/A, not applicable; RPR, rapid plasma reagin; TP-PA, Treponema pallidum particle agglutination.

Cautions
Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Testing by only Treponema pallidum particle agglutination (TP-PA) is not recommended for general screening purposes for syphilis. TP-PA should only be requested when:

1. The results of a treponemal screening test (eg, enzyme immunoassay [EIA] or multiplex flow immunoassay; MFI) and rapid plasma reagin (RPR) are discordant (eg, syphilis IgG-positive, RPR-negative)

2. A laboratory screens for syphilis using RPR and is in need of a treponemal confirmatory test.

 

Interpretation of results obtained with the Serodia TP-PA syphilis antibody test must be used in conjunction with the patient's clinical symptoms, medical history and other clinical and laboratory findings.

 

Serodia TP-PA assay is less sensitive than the fluorescent treponemal antibody absorption (FTA-ABS) test in untreated primary syphilis but compares favorably in all other stages of syphilis.

 

Serodia TP-PA assay should not be used to evaluate response to therapy since treponemal tests tend to remain reactive following treatment for syphilis.

 

Serodia TP-PA assay may be reactive in a small percentage (<1%) of normal or healthy persons. These false-positive results are often transient with unknown cause. False-positive results may occur in association with other underlying illnesses.

 

Serodia TP-PA may be reactive in persons from areas endemic for yaws or pinta.

 

Serodia TP-PA performs best in populations at risk for T pallidum infection.

 

False-positive or inconclusive results for this assay may be seen in patients with HIV, leprosy, toxoplasmosis, or Helicobacter pylori.

Supportive Data

Accuracy:

The Treponema pallidum particle agglutination (TP-PA) assay was compared to the BioPlex 2200 syphilis IgG multiplex flow immunoassays (MFI) assay using 1200 serum specimens (1100 prospective and 100 previously characterized sera). The results are summarized in Table 2:

 

Table 2. Comparison of the BioPlex 2200 syphilis IgG and TP-PA assays using serum samples (n=1,200)

 

 

BioPlex syphilis IgG MFI assay

Fujirebio

TP-PA

 

Positive

Negative

No result

Positive

101

3

0

Negative

11

1083

1

Indeterminate

0

1

0

 

Sensitivity = 90.18%; (95% CI, 83.15%-94.61%)

Specificity = 99.6%; (95% CI, 99.0%-99.9%)

Overall percent agreement = 98.7%; (95% CI, 96.3%-100%)

 

All discrepant samples tested negative by rapid plasma reagin (RPR)

 

Precision:

For interassay precision, 1 negative (TP-PA titer <1:80), 1 low-positive (1:80), 1 mid-positive (1:320), and 1 high-positive (1:1280) serum specimen were tested by TP-PA over 10 separate days and showed 100% agreement with the expected result for each category of results.

 

For intraassay precision, a negative, low-positive, and high-positive serum specimen were tested 20 times in a single run and showed 100% agreement for each category of results.

 

Reference Range:

The expected result is negative for this test. To validate reference range, testing of sera collected from 50 healthy blood donors showed a reactive rate of 2% (1/50) by TP-PA. The positive sample was also determined to be positive by the BioPlex syphilis IgG assay.

 

Reportable Range:

The TP-PA is reported as positive, negative, or indeterminate.

 

Analytic Specificity:

Testing of sera (n=58) known to be positive for antibodies to other microorganisms/conditions (n =30) or from pregnant females (n=28) showed a positive rate of 0% (0/58) by TP-PA. See Table 3 for a list of samples included in the cross-reactivity panel.

 

Table 3. Cross-reactivity panel tested by TP-PA to assess analytical specificity

 

Antibody or condition tested:

Number of samples tested by TP-PA

Epstein Barr VCA IgG

5

Epstein Barr VCA IgM

5

HSV IgG

5

HSV IgM

2

Lyme IgM/IgG

5

Heterophile antibody

5

Rheumatoid factor

3

Pregnancy

28

Clinical Reference
Recommendations for in-depth reading of a clinical nature

1. Binnicker MJ, Jespersen DJ, Rollins LO: Direct comparison of the traditional and reverse syphilis screening algorithms in a population with a low prevalence of syphilis. J Clin Microbiol. 2012 Jan;50(1):148-150

2. Center of Disease Control and Prevention (CDC): Discordant results from reverse sequence syphilis screening-five laboratories, United States, 2006-2010. MMWR Morb Mortal Wkly Rep. 2011;60(5):133-137

3. Radolf JD, Tramont EC, Salazar JC: Syphilis (Treponema pallidum). In Bennett JE, Dolin R, Blaser MJ, eds. Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases. 9th ed. Elsevier; 2020:2865-2892

Special Instructions
Library of PDFs including pertinent information and forms related to the test

Method Description
Describes how the test is performed and provides a method-specific reference

The Serodia TP-PA test is based on the agglutination of colored gelatin particle carriers sensitized with Treponema pallidum (Nichols Strain) antigen. Serum samples are serially diluted in microplate wells. Sensitized gelatin particles are added to respective wells and the contents of the plate mixed. The mixture is incubated for 2 hours at ambient temperature. Serum containing specific antibodies will react with the antigen-sensitized colored gelatin particles to form a smooth mat of agglutinated particles in the microplate well. A compact button formed by the settling of the nonagglutinated particles characterizes negative reactions. The agglutination patterns are read visually to determine interpretation.(Package insert: Serodia TP-PA. Fujirebio Diagnostics, Inc; 8/13/2017)

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information

No

Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Monday through Friday

Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

Same day/1 to 4 days

Specimen Retention Time
Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

14 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test

Rochester

Fees
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

  • Authorized users can sign in to Test Prices for detailed fee information.
  • Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
  • Prospective clients should contact their Regional Manager. For assistance, contact Customer Service.

Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

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
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

86780

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports