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Updated: Jan 18, 2026

Simultaneous Quantification of T-Cell Receptor Excision Circles TRECs and K-Deleting Recombination Excision Circles KRECs by Real-time PCR
Published on: December 6, 2014
Circulating T-Cell Receptor Excision Circles at Birth and Risk of Childhood Cancers
Jun Tao1, Paul S Albert1, Nellie Gottlieb2
1Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20850, USA.
Low T-cell receptor excision circles (TRECs) at birth, even within normal ranges, were investigated for links to childhood cancer. This study found no consistent association between TREC levels and childhood cancer risk.
Area of Science:
- Immunology
- Pediatric Oncology
- Public Health
Background:
- T-cell receptor excision circles (TRECs) are vital for newborn screening to detect severe combined immunodeficiency (SCID).
- This study explored if lower, but normal, TREC levels at birth correlate with increased childhood cancer susceptibility.
- Investigating TRECs offers insights into early immune system development and its relation to pediatric cancers.
Purpose of the Study:
- To determine the association between newborn T-cell receptor excision circle (TREC) levels and the risk of developing childhood cancers.
- To assess if TREC levels, even within the normal range, can serve as an indicator for compromised immunity related to cancer risk.
- To analyze TREC data from large newborn screening and cancer registry datasets in California and Texas.
Main Methods:
- A case-control study design was employed, linking newborn screening data with cancer registry information.
- The study included a substantial number of childhood cancer cases and matched controls from California and Texas.
- Statistical analyses were performed to compare TREC levels between cancer cases and control groups within each state.
Main Results:
- In California, acute myeloid leukemia cases showed significantly lower TREC levels than controls (p=0.0051).
- In Texas, acute lymphocytic leukemia cases exhibited significantly higher TREC levels compared to controls (p=0.0034).
- These state-specific findings were not replicated in the other state, and no significant differences were observed for other cancer types.
Conclusions:
- No consistent association was found between birth TREC levels and overall childhood cancer risk.
- The complex nature of childhood cancer etiology may explain the lack of clear TREC level differences.
- Further longitudinal studies incorporating additional immune biomarkers are recommended to elucidate the immunologic basis of childhood cancer.
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