Test Code LAB792 Diphtheria/Tetanus Antibody Panel, Serum
Useful For
Assessing antibody response to tetanus and diphtheria toxoid vaccines, which should be performed at least 3 weeks after immunization
Aiding in the evaluation of immunodeficiency
This test should not be used to diagnose tetanus infection
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
DIPGS | Diphtheria Toxoid IgG Ab, S | Yes | Yes |
TTIGS | Tetanus Toxoid IgG Ab, S | Yes | Yes |
Reporting Name
Diphtheria/Tetanus Ab Panel, SSpecimen Type
SerumSpecimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into plastic vial.
Specimen Minimum Volume
0.8 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 30 days | |
Frozen | 30 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Heat Inactivated specimen | Reject |
Reference Values
DIPHTHERIA TOXOID IgG ANTIBODY
Vaccinated: Positive (≥0.01 IU/mL)
Unvaccinated: Negative (<0.01 IU/mL)
Reference values apply to all ages.
TETANUS TOXOID IgG ANTIBODY
Vaccinated: Positive (≥0.01 IU/mL)
Unvaccinated: Negative (<0.01 IU/mL)
Reference values apply to all ages.
Supportive Data
Diphtheria:
A total of 211 serum samples prospectively submitted to our reference laboratory for routine testing for antidiphtheria toxoid IgG antibodies by the Binding Site Anti-Diphtheria Toxoid IgG enzyme-linked immunosorbent assay (ELISA) were also evaluated by the EuroImmun Anti-Diphtheria Toxoid IgG ELISA and results are summarized in Table 1.
Table 1. Comparison of the EuroImmun and Binding Site Anti-Diphtheria Toxoid IgG ELISAs
|
Binding Site IgG ELISA |
|
||
Positive |
Negative |
Total |
||
EuroImmun IgG ELISA |
Positive |
206 |
0 |
206 |
Negative |
4(a) |
1 |
5 |
|
|
Total |
210 |
1 |
2011 |
a) 1 of 4 samples tested positive by the ARUP Quantitative Multiplex Bead assay for antidiphtheria toxoid IgG
% Positive Agreement: 98.1% (206/210); 95% CI: 95.0-99.4%
% Negative Agreement: 100% (1/1); 95% CI: 16.8-100%
% Overall Agreement: 98.1% (207/211); 95% CI: 95.1-99.4%
Tetanus:
A total of 227 serum samples prospectively submitted to our laboratory for routine antitetanus toxoid IgG testing by the Binding Site Anti-Tetanus Toxoid IgG ELISA were also evaluated by the EuroImmun Anti-Tetanus Toxoid IgG ELISA. Results are summarized in Table 2:
Table 2. Comparison of the EuroImmun and Binding Site Anti-Tetanus Toxoid IgG ELISAs
|
Binding Site IgG ELISA |
|
||
Positive |
Negative |
Total |
||
EuroImmun IgG ELISA |
Positive |
220 |
0 |
220 |
Negative |
6(a) |
1 |
7 |
|
|
Total |
226 |
1 |
227 |
a) 3 of the 6 samples tested positive by the anti-Tetanus Toxoid IgG Quantiative Multiplex Bead Assay at ARUP
% Positive Agreement: 97.4% (220/226); 95% CI: 94.2-98.9%
% Negative Agreement: 100% (1/1); 95% CI: 16.8-100%
% Overall Agreement: 97.4% (221/227); 95% CI: 94.2-98.9%
Day(s) Performed
Monday through Friday
Report Available
Same day/1 to 4 daysSpecimen Retention Time
14 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
86317 x 2
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
DTABS | Diphtheria/Tetanus Ab Panel, S | 101791-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
TETG | Tetanus IgG Ab | 26643-7 |
DIPG | Diphtheria IgG Ab | 45166-6 |
DEXDP | Diphtheria IgG Value | 48654-8 |
DEXTG | Tetanus IgG Value | 53935-3 |
Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.