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Sorted By Test Name - Mayo Medical Laboratories

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coincides with associated thymic recovery. For patients with DiGeorge syndrome (DGS)-a cellular<br />

immunodeficiency associated with other congenital problems including cardiac defects, facial<br />

dysmorphism, hypoparathyroidism, and secondary hypocalcemia, and chromosome 22q11.2 deletion (in a<br />

significant proportion of patients)-measurement of thymic function provides valuable information on the<br />

functional phenotype, ie, complete DGS (associated with thymic aplasia) or partial DGS (generally<br />

well-preserved thymic function). Thymus transplants have been performed in patients with complete DGS<br />

but are not required in partial DGS.<br />

Useful For: Evaluating thymic reconstitution in patients following hematopoietic stem cell<br />

transplantation, chemotherapy, biological or immunomodulatory therapy, and immunosuppression<br />

Evaluating thymic recovery in HIV-positive patients on highly active antiretroviral therapy (HAART)<br />

Evaluating thymic output in patients with DiGeorge syndrome or other cellular immunodeficiencies<br />

Assessing the naive T-cell compartment in a variety of immunological contexts (autoimmunity, cancer,<br />

immunodeficiency, and transplantation) The CD8 RTE test has limited value in the clinical interpretation<br />

of recent thymic output in adults (see Cautions), and is likely to be of more clinical relevance in pediatric<br />

individuals<br />

Interpretation: The absence or reduction of CD31+CD4 recent thymic emigrants (RTEs) and<br />

CD8+CD103+ RTEs correlates with loss or reduced thymic output and changes in the naive CD4 T-cell<br />

compartment. CD4 RTEs measured along with CD8 RTEs and TREC (TREC/87959 T-Cell Receptor<br />

Excision Circles [TREC] Analysis for Immune Reconstitution) provides a comprehensive assessment of<br />

thymopoiesis. Conversely, increases in CD8 RTEs are of no clinical significance, and do not indicate a<br />

pathologic finding. Since CD8 RTEs is a rare population, small changes in serial measurements may<br />

result in some values being above the reference range; however, as noted, increases in CD8 RTEs do not<br />

have clinical significance. To evaluate immune reconstitution or recovery of thymopoiesis post-T-cell<br />

depletion due to HSCT, immunotherapy, or other clinical conditions, it is essential to serially measure<br />

CD4, CD8 RTE, and TREC levels. A consultative report is provided.<br />

Reference Values:<br />

CD4 T-CELL RECENT THYMIC EMIGRANTS (RTE)<br />

CD4 Absolute<br />

Males<br />

1 month-17 years: 153-1,745 cells/mcL<br />

18-70 years: 290-1,175 cells/mcL<br />

Females<br />

1 month-17 years: 582-1,630 cells/mcL<br />

18-70 years: 457-1,766 cells/mcL<br />

Reference values have not been established for patients that are 70 years of age.<br />

CD4 RTE %<br />

Males<br />

1 month-17 years: 19.4-60.9%<br />

18-25 years: 6.4-51.0%<br />

26-55 years: 6.4-41.7%<br />

56-70 years: 6.4-27.7%<br />

Females<br />

1 month-17 years: 25.8-68.0%<br />

18-25 years: 6.4-51.0%<br />

26-55 years: 6.4-41.7%<br />

56-70 years: 6.4-27.7%<br />

Reference values have not been established for patients that are 70 years of age.<br />

CD4 RTE Absolute<br />

Males<br />

1 month-17 years: 50.0-926.0 cells/mcL<br />

18-70 years: 42.0-399.0 cells/mcL<br />

Females<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1737

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