T-Cell Activation Profile, CD8 Subsets
T-Cell Activation Profile, CD8 Subsets
    
Number
505750
CPTCPT - Updated December 31 2007
86356 (x3); 86359; 86360
Test Includes
Percentage and absolute values CD3+, CD3+CD4+, CD3+CD8+, CD3+CD25+, CD8+CD38+, CD8+HLA-DR+, CD4:CD8 ratio; CBC with differential
Special Instructions
State date and time of collection on the request form and on the specimen tube.
Specimen
Whole blood
Volume
7 mL EDTA whole blood and 7 mL ACD-A whole blood
Container
Lavender-top (EDTA) tube and yellow-top (ACD-A) tube
Collection
To preserve cellular viability, collect specimen so it will arrive in the laboratory Monday through Friday and within 24 hours of collection. Please indicate date and time of venipuncture on the tube(s) and on the request form.
Storage Instructions
Maintain specimen at room temperature. Do not freeze or refrigerate.
Causes for Rejection
Hemolysis; specimen refrigerated or frozen; clotted specimen; contaminated specimen
Reference Interval
Reference intervals are established by the laboratory. See table.
Adult Reference Intervals for Lymphocyte Immunophenotyping


CD 95% Confidence Interval 
Percentage Cells/mm3 
Minimum Maximum Minimum Maximum 
CD3+ 58 86 622 2402 
CD3+CD4+ 31 59 359 1519 
CD3+CD8+ 12 36 109 897 
CD3+CD25+ 26 79 535 
T4:T8 ratio 0.92 3.72   
CD8+CD38+ 18 381 
CD8+HLA-DR+ 117 
Use
Expanded profile for AIDS monitoring and prognosis. An increase in activation markers is associated with poor prognosis.
Limitations
This procedure may be considered by Medicare and other carriers as investigational and, therefore, may not be payable as a covered benefit for patients.
Methodology
Flow cytometry
References

Landay AL, Jessop C, Lennette ET, et al, “Chronic Fatigue Syndrome: Clinical Condition Associated With Immune Activation,” Lancet, 1991, 338(8769):707-12.

Sadler D and Keren DF, “Surface Marker Assays in Immunodeficiency Diseases,” Flow Cytometry and Clinical Diseases, Chapter 9, Keren DF, Hanson CA, and Hurtubise PE, eds, Chicago, IL: ASCP Press, 1994.


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