Test ID LPMGF Lymphocyte Proliferation to Mitogens, Blood
Useful For
Assessing T-cell function in patients on immunosuppressive therapy, including solid-organ transplant patients
Evaluating patients suspected of having impairment in cellular immunity
Evaluation of T-cell function in patients with primary immunodeficiencies, either cellular (DiGeorge syndrome, T-negative severe combined immunodeficiency: SCID, etc) or combined T- and B-cell immunodeficiencies (T- and B-negative SCID, Wiskott-Aldrich syndrome, ataxia telangiectasia, common variable immunodeficiency, among others) where T-cell function may be impaired
Evaluation of T-cell function in patients with secondary immunodeficiency, either disease related or iatrogenic
Evaluation of recovery of T-cell function and competence following bone marrow transplantation or hematopoietic stem cell transplantation
Method Name
Flow Cytometry
Reporting Name
Lymphocyte Proliferation, MitogensSpecimen Type
WB Sodium HeparinShipping Instructions
Testing performed Monday through Friday. Specimens not received by 4 p.m. Central time on Friday may be canceled.
Specimens arriving on the weekend and observed holidays may be canceled.
Collect and package specimen as close to shipping time as possible. Ship specimen overnight in an Ambient Shipping Box-Critical Specimens Only (T668) following the instructions in the box. It is recommended that specimens arrive within 24 hours of collection.
Necessary Information
1. Date and time of collection are required.
2. The ordering healthcare professional's name and phone number are required.
Specimen Required
Supplies: Ambient Shipping Box-Critical Specimens Only (T668)
Container/Tube: Green top (sodium heparin)
Specimen Volume: 20 mL
See tables for information on recommended volume based on absolute lymphocyte count
Pediatric Volume:
<3 months: 1 mL
3-24 months: 3 mL
25 months-18 years: 5 mL
Collection Instructions: Send whole blood specimen in original tube. Do not aliquot.
Additional Information: For serial monitoring, it is recommended that specimen collection be performed at the same time of day.
Table. Blood Volume Recommendations Based on Absolute Lymphocyte Count (ALC)
Mitogen only |
|||
ALC x 10(9)/L |
Blood volume for minimum phytohemagglutinin (PHA) only |
Blood volume for minimum PHA and pokeweed mitogen (PWM) |
Blood volume for full assay |
<0.5 |
>6.5 mL |
>8.5 mL |
>22 mL |
0.5-1.0 |
6.5 mL |
8.5 mL |
22 mL |
1.1-1.5 |
3.0 mL |
4.0 mL |
10 mL |
1.6-2.0 |
2.0 mL |
2.5 mL |
7 mL |
2.1-3.0 |
1.5 mL |
2.0 mL |
6 mL |
3.1-4.0 |
1.0 mL |
1.5 mL |
4 mL |
4.1-5.0 |
0.8 mL |
1.0 mL |
3 mL |
>5.0 |
0.5 mL |
0.8 mL |
2 mL |
Mitogen and antigen |
||
ALC x 10(9)/L |
Blood volume for minimum of each assay |
Blood volume for full assay |
<0.5 |
>28 mL |
>60 mL |
0.5-1.0 |
28 mL |
60 mL |
1.1-1.5 |
12 mL |
30 mL |
1.6-2.0 |
8.5 mL |
20 mL |
2.1-3.0 |
6.5 mL |
15 mL |
3.1-4.0 |
4.5 mL |
10 mL |
4.1-5.0 |
3.5 mL |
8 mL |
>5.0 |
2.5 mL |
6 mL |
Specimen Minimum Volume
See Specimen Required
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
WB Sodium Heparin | Ambient | 48 hours | GREEN TOP/HEP |
Reference Values
Viability of lymphocytes at day 0: ≥75.0%
Maximum proliferation of phytohemagglutinin as % CD45: ≥49.9%
Maximum proliferation of phytohemagglutinin as % CD3: ≥58.5%
Maximum proliferation of pokeweed mitogen as % CD45: ≥4.5%
Maximum proliferation of pokeweed mitogen as % CD3: ≥3.5%
Maximum proliferation of pokeweed mitogen as % CD19: ≥3.9%
Day(s) Performed
Monday through Friday
Performing Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
86353
86353 (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
LPMGF | Lymphocyte Proliferation, Mitogens | 69018-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
32317 | Interpretation | 69052-9 |
32318 | Viab of Lymphs at Day 0 | 33193-4 |
32321 | Max Prolif of PWM as % CD45 | 69019-8 |
32322 | Max Prolif of PWM as % CD3 | 69020-6 |
32323 | Max Prolif of PWM as % CD19 | 69037-0 |
32319 | Max Prolif of PHA as % CD45 | 69038-8 |
32320 | Max Prolif of PHA as % CD3 | 57741-1 |
32324 | Mitogen Comment | 48767-8 |
Test Classification
This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.Report Available
8 to 11 daysNY State Approved
YesReflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
MGSTM | Additional Flow Stimulant, LPMGF | No, (Bill Only) | No |
Testing Algorithm
To ensure the most reliable results, if insufficient peripheral blood mononuclear cells are isolated from the patient's sample due to low white blood cell counts or specimen volume received, selected dilutions or stimulants may not be tested at the discretion of the laboratory.
Testing with one stimulant will always be performed. When adequate specimen is available for both stimulants to be tested, the second stimulant will be evaluated at an additional charge.
Disease States
- Ataxia telangiectasia
- Common variable immunodeficiency