Phytohemagglutinin (PHA)-induced Lymphocyte Proliferation

Phytohemagglutinin (PHA)-induced Lymphocyte Proliferation

Test Code

91980
86353
CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
91980
86353
CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to confirm Test Code for the lab that services your account or to find available tests you can order.
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Phytohemagglutinin (PHA)-induced Lymphocyte Proliferation - Measurement of human lymphocytes' proliferative responses to various stimuli is a fundamental technique used to assess their biological status and functions. Mitogens, such as plant lectins phytohemagglutinin (PHA), concanavalin A (Con A) and pokeweed mitogen (PWM), are able to nonspecifically stimulate lymphocyte proliferation and used to evaluate patient immune responsiveness.

Test Resources

None found for this test
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Test Details

Methodology

Cell Culture (CC) • Scintillation Counter

Assay Category

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

⁠⁠⁠⁠⁠⁠⁠PHA, CPM

Males73700-265000 Net CPM
Females53000-200000 Net CPM

PHA, SINot established
Cell Viability80-100%

Alternative Name(s)

Mitogen-induced Cell Proliferation,Lymphocyte Stimulation

LOINC® Codes, Performing Laboratory

Methodology

Cell Culture (CC) • Scintillation Counter
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

⁠⁠⁠⁠⁠⁠⁠PHA, CPM
Males73700-265000 Net CPM
Females53000-200000 Net CPM

PHA, SINot established
Cell Viability80-100%

Alternative Name(s)

Mitogen-induced Cell Proliferation,Lymphocyte Stimulation

Preferred Specimen(s)

5 mL whole blood collected in a sodium heparin (green-top) tube

Minimum Volume

3 mL

Collection Instructions

Whole blood must be transported at room temperature and delivered to the testing laboratory within 48 hours after collection.
Maintain and transport blood at room temperature. Avoid temperatures <15° C and >37° C. In hot weather, it may be necessary to pack the specimen in a container with insulating material around it and place this container inside another one that contains a cold pack (ice pack) and absorbent material. This method will help retain the specimen at ambient temperature. For longitudinal studies, draw specimens at the same time of day to minimize diurnal variation.

Clients: Contact the lab prior to ordering for special logistics arrangements.
PSC: Follow Short Stability Protocol.

Test available by prior arrangement only. Special sample collection and transportation arrangements must be made prior to ordering the test. Contact your local Customer Service Department and request to speak to someone in Referral Testing Department for specific instructions.
Submit Monday-Thursday only. Do not draw day before a holiday. Samples received in testing lab >48 hours after collection will be rejected. Date and time of draw are required and must be provided.

Transport Container

Sodium heparin (green-top) tube

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 48 hours
  • Refrigerated: Unacceptable
  • Frozen: Unacceptable

Reject Criteria

Hemolysis • Received refrigerated • Received frozen • Clotted specimens • Samples collected in lithium heparin tubes

Setup Schedule

5 mL whole blood collected in a sodium heparin (green-top) tube
3 mL
Whole blood must be transported at room temperature and delivered to the testing laboratory within 48 hours after collection.
Maintain and transport blood at room temperature. Avoid temperatures <15° C and >37° C. In hot weather, it may be necessary to pack the specimen in a container with insulating material around it and place this container inside another one that contains a cold pack (ice pack) and absorbent material. This method will help retain the specimen at ambient temperature. For longitudinal studies, draw specimens at the same time of day to minimize diurnal variation.

Clients: Contact the lab prior to ordering for special logistics arrangements.
PSC: Follow Short Stability Protocol.

Test available by prior arrangement only. Special sample collection and transportation arrangements must be made prior to ordering the test. Contact your local Customer Service Department and request to speak to someone in Referral Testing Department for specific instructions.
Submit Monday-Thursday only. Do not draw day before a holiday. Samples received in testing lab >48 hours after collection will be rejected. Date and time of draw are required and must be provided.
Sodium heparin (green-top) tube
Room temperature
Room temperature: 48 hours
Refrigerated: Unacceptable
Frozen: Unacceptable
Hemolysis • Received refrigerated • Received frozen • Clotted specimens • Samples collected in lithium heparin tubes
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to confirm Test Code for the lab that services your account or to find available tests you can order.
In-home collection may be available in your area for purchase through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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