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Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)

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Significance of T-receptor and kappa-deletion recombina- tion excision rings as molecular markers in the assessment of newborns of different gestational ages

https://doi.org/10.21508/1027-4065-2024-69-4-31-36

Abstract

   Currently, there is a large number of studies indicating that preterm infants have reduced levels of T-receptor and kappa-deletion recombination excision rings (TREC and KREC) as indicators of impaired T- and/or B-cell immunity. Studies aimed at in-depth study of the causative factors that led to the decrease in the estimated indicators remain relevant.

   Purpose. Determination of the influence of somatometric parameters and prenatal factors on the level of TREC and KREC in newborns, as well as evaluation of the dynamics of these indicators from gestational age.

   Material and methods. The study included 203 neonates with gestational ages ranging from 22 to 41 weeks. TREC and KREC were isolated by PCR from dried blood spots on Guthrie cards. Blood sampling was performed as part of neonatal screening. The estimated parameters were analyzed according to gestational age, somatometric data and prenatal factors (mode of delivery, number of fetuses in pregnancy). Statistical analysis was performed using the StatTech v. 4.1.4 software.

   Results. It was found that the increase in gestational age by 1 week increases the KREC level by 44.610·105 (rxy = 0.271, p < 0.001), TREC level by 27.274·105 (rxy = 0.264, p = 0.002). Linear regression analysis showed weak direct relationships between TREC and KREC levels and anthropometric data. Children from multiple pregnancies had significantly higher TREC values than infants from singleton pregnancies (p < 0.001).

   Conclusion. The immune system of premature newborns is capable of producing adequate amounts of TREC and KREC. Between 22 and 28 weeks of age, the most intense increase in the assessed indicators occurs, after which their levels relatively stabilize. Since TREC and KREC levels tend to decrease in preterm newborns, a comprehensive evaluation of the dynamics of these indicators depending on significant prenatal and somatometric data is extremely important.

About the Authors

E. N. Volkova
Voronezh Regional Clinical Hospital No. 1
Russian Federation

Voronezh



L. I. Ippolitova
Voronezh Burdenko State Medical University
Russian Federation

Voronezh



References

1. Marinova M., Georgyeva А., Yordanova V., Ivanov N., Atanasova V., Naumova E. et al. Implementation of TREC/KREC detection protocol for newborn SCID screening in Bulgaria: a pilot study. Cent Eur J Immunol 2022; 47(4): 339–349. DOI: 10.5114/ceji.2022.124396

2. Cheremokhin D., Shinwari K., Deryabina S., Bolkov M., Tuzankina I., Kudlay D. Analysis of the TREC and KREC Levels in the Dried Blood Spots of Healthy Newborns with Different Gestational Ages and Weights. Acta Naturae 2022; 14(1): 101–108. DOI: 10.32607/actanaturae.11501

3. Currier R., Puck J. SCID newborn screening: What we’ve learned Allergy. Clin Immunol 2021; 147(2): 417–426. DOI: 10.1016/j.jaci.2020.10.020

4. Korsunskiy I., Blyuss O., Gordukova M., Davydova N., Zaikin A., Zinovieva N. et al. Expanding TREC and KREC Utility in Primary Immunodeficiency Diseases Diagnosis. Front Immunol 2020; 11: 320. DOI: 10.3389/fimmu.2020.00320

5. Dasouki M., Jabr A., AlDakheel G., Elbadaoui F., Alazami A., Al-Saud B. Et al. TREC and KREC profiling as a representative of thymus and bone marrow output in patients with various inborn errors of immunity. Clin Exp Immunol 2020; 202(1): 60–71. DOI: 10.1111/cei.13484

6. Remaschi G., Ricci S., Cortimiglia M., De Vitis E., lannuzzi L., Boni L. et al. TREC and KREC in very preterm infants: reference values and effects of maternal and neonatal factors. J Matern Fetal Neonatal 2021; 34(23): 3946–3951. DOI: 10.1080/14767058.2019.1702951

7. Mauracher A., Pagliarulo F., Faes L., Vavassori S., Gingör I., Bachmann L. et al. Causes of low neonatal T-cell receptor excision circles: A systematic review. J Allergy Clin Immunol Pract 2017; 5(5): 1457–1460. DOI: 10.1016/j.jaip.2017.02.009

8. Currier R., Puck J. SCID newborn screening: What we’ve learned. J Allergy Clin Immunol 2021; 147(2): 417–426. DOI: 10.1016/j.jaci.2020.10.020

9. Dasouki M., Jabr A., AlDakheel G., Elbadaoui F., Alazami A., Al-Saud B. et al. TREC and KREC profiling as a representative of thymus and bone marrow output in patients with various inborn errors of immunity. Clin Exp Immunol 2020; 202(1): 60–71. DOI: 10.1111/cei.13484

10. Mauracher A., Pagliarulo F., Faes L., Vavassori S., Gingör I., Bachmann L. et al. Causes of low neonatal T-cell receptor excision circles: A systematic review. J Allergy Clin Immunol Pract 2017; 5(5): 1457–1460. DOI: 10.1016/j.jaip.2017.02.009

11. Kutlug S., Alpaslan M., Hancioglu G., Okan S., Yesilirmak D., Bulut H. et al. Multiplex PCR-Based Newborn Screening for Severe T and B-Cell Lymphopenia: The first Pilot Study in Turkey. Sisli Etfal Hastan Tip Bul 2021; 55(4): 551–559. DOI: 10.14744/SEMB.2020.09623

12. Gul K., Strand J., Pettersen R., Brun H., Abrahamsen T. T-cell Receptor Excision Circles in Newborns with Heart Defects. Pediatr Cardiol 2020; 41(4): 809–815. DOI: 10.1007/s00246–020–02317-y

13. Morton S., Schnur M., Kerper R., Young V., O’Connell А. Premature Infants Have Normal Maturation of the T Cell Receptor Repertoire at Term. Front Immunol 2022; 30:13:854414. DOI: 10.3389/fimmu.2022.854414


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For citations:


Volkova E.N., Ippolitova L.I. Significance of T-receptor and kappa-deletion recombina- tion excision rings as molecular markers in the assessment of newborns of different gestational ages. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2024;69(4):31-36. (In Russ.) https://doi.org/10.21508/1027-4065-2024-69-4-31-36

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ISSN 1027-4065 (Print)
ISSN 2500-2228 (Online)