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Test ID BLOD1336 Lymphocyte Proliferation to Mitogens, Blood

Reporting Name

Lymphocyte Proliferation, Mitogens

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

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

WB Sodium Heparin


Shipping 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

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.

CPT Code Information

86353

86353 (if appropriate)

 

Report Available

8 to 11 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject

Method Name

Flow Cytometry

Reflex 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.

Secondary ID

60591
Sanford Laboratories - Bemidji Additional Information:

Sanford Interface Build Information

Result Code Result Code Description
16428 Interpretation
16429  Viab of Lymphs at Day 0
16430 Max Prolif of PWM as % CD45
16431 Max Prolif of PWM as % CD3
16432 Max Prolif of PWM as % CD19
16433 Max Prolif of PHA as % CD45
16434 Max Prolif of PHA as % CD3
16435 Mitogen Comment