Test Code TXPAB Toxoplasma gondii Antibody, IgM and IgG, Serum
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.7 mL
Collection Instructions: Centrifuge and aliquot serum into plastic vial.
Useful For
Qualitative detection of IgM and quantitative detection of IgG antibodies to Toxoplasma gondii in human serum
Profile Information
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| TXPM | Toxoplasma Ab, IgM, S | Yes | Yes |
| TXPG | Toxoplasma Ab, IgG, S | Yes | Yes |
Testing Algorithm
For more information see Meningitis/Encephalitis Panel Algorithm.
Method Name
Electrochemiluminescence Immunoassay (ECLIA)
Reporting Name
Toxoplasma Ab, IgM and IgG, SSpecimen Type
SerumSpecimen Minimum Volume
0.7 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 21 days |
| Frozen | 90 days | |
| Ambient | 72 hours |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | Reject |
| Additives (eg, biocides, antioxidants) | Reject |
Reference Values
Toxoplasma IgM
Negative
Toxoplasma IgG
Negative
<1 IU/mL Negative
≥1-<3 IU/mL Borderline
≥3 IU/mL Positive
Reference values apply to all ages.
Interpretation
Negative: No IgM or IgG antibodies to Toxoplasma gondii detected. False negative results may occur in immunocompromised patients or if testing performed within 1 to 2 weeks of initial exposure and repeat testing may be helpful. A single negative result should not be used to rule-out toxoplasmosis, and repeat testing is recommended for patients at high risk for infection.
Borderline: Repeat testing on a new sample collected in 2 to 3 weeks is recommended to assess for seroconversion. Further confirmatory testing may be necessary at a Toxoplasma reference laboratory in borderline results persist following repeat testing.
Positive: Toxoplasma gondii IgM antibodies detected. Specimens with positive results should be confirmed by a laboratory with expertise in the diagnosis of toxoplasmosis. T gondii IgG antibodies detected, indicating recent or past infection. A significant change in T gondii IgG levels suggests recent infection. For confirmation of toxoplasmosis, the US Food and Drug Administration issued a Public Health Advisory (07/25/1997) that recommends sera found to be positive for T gondii IgM antibodies should be sent to a Toxoplasma reference laboratory.
Day(s) Performed
Monday through Saturday
Report Available
Same day/1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test 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
86778-Toxoplasma IgM
86777-Toxoplasma IgG
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| TXPAB | Toxoplasma Ab, IgM and IgG, S | 88746-3 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| GTXP | Toxoplasma Ab, IgG, S | 40677-7 |
| MTXP | Toxoplasma Ab, IgM, S | 40678-5 |
| DEX04 | Toxoplasma IgG Value | 8039-0 |