First pilot study for newborn screening of severe T and B lymphopenias in Colombia

Sebastián Gutiérrez-Hincapié , Carlos Muskus-López , Isaura Pilar Sánchez , José Luis Franco-Restrepo , Claudia M. Trujillo-Vargas, .

Keywords: neonatal screening, lymphopenia, T-lymphocytes, B-lymphocytes, severe combined immunodeficiency

Abstract

Introduction. Congenital lymphopenias cause increased susceptibility to infections in children apparently healthy at birth. Earlier detection of these conditions would facilitate prompt treatment, prevent potentially serious disease complications and early deaths, and save healthcare resources.
Objective. To perform a pilot study for neonatal screening of congenital lymphopenias by the quantification of TREC and KREC –T- and B-cell receptor excision circles– in peripheral blood samples from newborns in Medellín, Colombia.
Materials and methods. Blood samples from 1,092 newborns and six referred patients with suspected lymphopenia were collected by heel or toe-finger prick and dropped onto a filter paper. Thereafter, DNA was extracted and levels of TRECs and KRECs were measured by qPCR.
Results. The six patients with suspected lymphopenia showed undetectable or very low TREC levels. All newborns screened presented normal TREC and KREC levels. A positive correlation was found between TREC or KREC values quantified from two different filter papers. Detectable levels of the receptor excision circles decrease considerably after 24 weeks of the dried blood spot sample storage. We identified a positive association between low TREC levels and low birth weight; and a negative correlation between KREC values and prematurity. Finally, no statistical differences were found between TREC or KREC levels and delivery method.
Conclusion. We describe the first preliminary study for the early detection of lymphopenias in Colombia. We proposed to use a cut-off value of 119 and 69 copies/μl blood of TREC and KREC, respectively for future newborn screening programs in our country.

Downloads

Download data is not yet available.
  • Sebastián Gutiérrez-Hincapié Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia https://orcid.org/0000-0002-1576-595X
  • Carlos Muskus-López Programa de Estudio y Control en Enfermedades Tropicales – PECET, Universidad de Antioquia, Medellín, Colombia https://orcid.org/0000-0003-4280-5627
  • Isaura Pilar Sánchez Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia; Grupo de Investigaciones Biomédicas UniRemington, Facultad de Ciencias de la Salud, Corporación Universitaria Remington, Medellín, Colombia https://orcid.org/0000-0002-1415-0785
  • José Luis Franco-Restrepo Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia https://orcid.org/0000-0001-5664-6415
  • Claudia M. Trujillo-Vargas Grupo de Inmunodeficiencias Primarias, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia https://orcid.org/0000-0001-8546-2666

References

Bousfiha AA, Jeddane L, Ailal F, Benhsaien I, Mahlaoui N, Casanova JL, et al. Primary immunodeficiency diseases worldwide: More common than generally thought. J Clin Immunol. 2013;33:1-7. https://doi.org/10.1007/s10875-012-9751-7

Quinn J, Modell V, Orange JS, Modell F. Growth in diagnosis and treatment of primary immunodeficiency within the global Jeffrey Modell Centers Network. Allergy Asthma Clin Immunol. 2022;18:19. https://doi.org/10.1186/s13223-022-00662-6

Dorsey MJ, Wright NAM, Chaimowitz NS, Dávila-Saldaña BJ, Miller H, Keller MD, et al. Infections in infants with SCID: Isolation, infection screening, and prophylaxis in PIDTC centers. J Clin Immunol. 2021;41:38-50. https://doi.org/10.1007/s10875-020-00865-9

Barry JC, Crowley TB, Jyonouchi S, Heimall J, Zackai EH, Sullivan KE, et al. Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. J Clin Immunol. 2017;37:476-85. https://doi.org/10.1007/s10875-017-0403-9

Tangye SG, Al-Herz W, Bousfiha A, Cunningham-Rundles C, Franco JL, Holland SM, et al. Human inborn errors of immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee. J Clin Immunol. 2022;42:1473-507. https://doi.org/10.1007/s10875-022-01289-3

Lev A, Somech R, Somekh I. Newborn screening for severe combined immunodeficiency and inborn errors of immunity. Curr Opin Pediatr. 2023;35:692-702. https://doi.org/10.1097/MOP.0000000000001291

Eissa H, Thakar MS, Shah AJ, Logan BR, Griffith LM, Dong H, et al. Post-transplantation late complications increase over time for patients with SCID: A Primary Immune Deficiency Treatment Consortium (PIDTC) landmark study. J Allergy Clin Immunol. 2024;153:287-96. https://doi.org/10.1016/j.jaci.2023.09.027

Douek DC, Vescio RA, Betts MR, Brenchley JM, Hill BJ, Zhang L, et al. Assessment of thymic output in adults after haematopoietic stem-cell transplantation and prediction of T-cell reconstitution. Lancet. 2000;355:1875-81. https://doi.org/10.1016/S0140-6736(00)02293-5

Chan K, Puck JM. Development of population-based newborn screening for severe combined immunodeficiency. J Allergy Clin Immunol. 2005;115:391-8. https://doi.org/10.1016/j.jaci.2004.10.012

Routes JM, Grossman WJ, Verbsky J, Laessig RH, Hoffman GL, Brokopp CD, et al. Statewide newborn screening for severe T-cell lymphopenia. JAMA. 2009;302:2465-70. https://doi.org/10.1001/jama.2009.1806

Dorsey MJ, Puck JM. Newborn screening for severe combined immunodeficiency in the United States: Lessons learned. Immunol Allergy Clin North Am. 2019;39:1-11. https://doi.org/10.1016/j.iac.2018.08.002

van Zelm MC, Szczepanski T, van der Burg M, van Dongen JJ. Replication history of B lymphocytes reveals homeostatic proliferation and extensive antigen-induced B cell expansion. J Exp Med. 2007;204:645-55. https://doi.org/10.1084/jem.20060964

Kanegae MPP, Barreiros LA, Sousa JL, Brito MAS, de Oliveira Junior EB, Soares LP, et al. Newborn screening for severe combined immunodeficiencies using TRECS and KRECS: Second pilot study in Brazil. Rev Paul Pedriatr. 2017;35:25-32. https://doi.org/10.1590/1984-0462/;2017;35;1;00013

Tagliaferri L, Kunz JB, Happich M, Esposito S, Bruckner T, Hübschmann D, et al. Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC). Clin Immunol. 2017;175:51-5. https://doi.org/10.1016/j.clim.2016.11.016

Giraldo GA, Suárez-Obando F, Mora L, Sánchez P, Prieto JC. Evaluation of TSH levels in the program of congenital hypothyroidism newborn screening in a pilot study of preterm newborns in Bogotá, Colombia. J Inborn Errors Metab Screen. 2015;3. https://doi.org/10.1177/2326409815597706

Sottini A, Serana F, Bertoli D, Chiarini M, Valotti M, Vaglio-Tessitore M, et al. Simultaneous quantification of T-cell receptor excision circles (TRECs) and K-deleting recombination excision circles (KRECs) by real-time PCR. J Vis Exp. 2014;94:52184. https://doi.org/10.3791/52184

Baker MW, Grossman WJ, Laessig RH, Hoffman GL, Brokopp CD, Kurtycz DF, et al. Development of a routine newborn screening protocol for severe combined immunodeficiency. J Allergy Clin Immunol. 2009;124:522-7. https://doi.org/10.1016/j.jaci.2009.04.007

Kwan A, Hu D, Song M, Gomes H, Brown DR, Bourque T, et al. Successful newborn screening for SCID in the Navajo Nation. Clin Immunol. 2015;158:29-34. https://doi.org/10.1016/j.clim.2015.02.015

Esquerda M, Palau F, Lorenzo D, Cambra FJ, Bofarull M, Cusi V, et al. Ethical questions concerning newborn genetic screening. Clin Genet. 2021;99:93-8. https://doi.org/10.1111/cge.13828

Evans A, Bonhomme N, Goodman A, Terry SF. Newborn screening and health communications. Genet Test Mol Biomarkers. 2018;22:507-8. https://doi.org/10.1089/gtmb.2018.0234

van der Spek J, Groenwold RH, van der Burg M, van Montfrans JM. TREC based newborn screening for severe combined immunodeficiency disease: A systematic review. J Clin Immunol. 2015;35:416-30. https://doi.org/10.1007/s10875-015-0152-6

Kimizu T, Nozaki M, Okada Y, Sawada A, Morisaki M, Fujita H, et al. Multiplex real-time PCR-based newborn screening for severe primary immunodeficiency and spinal muscular atrophy in Osaka, Japan: Our results after 3 years. Genes (Basel). 2024;15:314. https://doi.org/10.3390/genes15030314

Taylor JL, Lee FK, Yazdanpanah GK, Staropoli JF, Liu M, Carulli JP, et al. Newborn blood spot screening test using multiplexed real-time PCR to simultaneously screen for spinal muscular atrophy and severe combined immunodeficiency. Clin Chem. 2015;61:412-9. https://doi.org/10.1373/clinchem.2014.231019

De Felipe B, Olbrich P, Goycochea-Valdivia W, Delgado-Pecellin C, Sánchez-Moreno P, Sánchez B, et al. Newborn screening for primary T- and B-cell immune deficiencies—A prospective study in Andalucía. Int J Neonatal Screen. 2017;3:27. https://doi.org/10.3390/ijns3040027

Rechavi E, Lev A, Simon AJ, Stauber T, Daas S, Saraf-Levy T, et al. First year of Israeli newborn screening for severe combined immunodeficiency – Clinical achievements and insights. Front Immunol. 2017;8:1448. https://doi.org/10.3389/fimmu.2017.01448

Zhao Q, Dai R, Li Y, Wang Y, Chen X, Shu Z, et al. Trends in TREC values according to age and gender in Chinese children and their clinical applications. Eur J Pediatr. 2022;181:529-38. https://doi.org/10.1007/s00431-021-04223-8

Ward CE, Baptist AP. Challenges of newborn severe combined immunodeficiency screening among premature infants. Pediatrics. 2013;131:e1298-302. https://doi.org/10.1542/peds.2012-1921

Audrain M, Thomas C, Mirallie S, Bourgeois N, Sebille V, Rabetrano H, et al. Evaluation of the T-cell receptor excision circle assay performances for severe combined immunodeficiency neonatal screening on Guthrie cards in a French single center study. Clin Immunol. 2014;150:137-9. https://doi.org/10.1016/j.clim.2013.11.012

Gaviglio A, Lasarev M, Sheller R, Singh S, Baker M. Newborn screening for severe combined immunodeficiency: Lessons learned from screening and follow-up of the preterm newborn population. Int J Neonatal Screen. 2023;9:68. https://doi.org/10.3390/ijns9040068

Wirbelauer J, Thomas W, Rieger L, Speer CP. Intrauterine growth retardation in preterm infants ≤ 32 weeks of gestation is associated with low white blood cell counts. Am J Perinatol. 2010;27:819-24. https://doi.org/10.1055/s-0030-1254547

Olearo E, Oberto M, Oggè G, Botta G, Pace C, Gaglioti P, et al. Thymic volume in healthy, small for gestational age and growth-restricted fetuses. Prenat Diagn. 2012;32:662-7. https://doi.org/10.1002/pd.3883

Schlinzig T, Johansson S, Stephansson O, Hammarström L, Zetterström RH, von Döbeln U, et al. Surge of immune cell formation at birth differs by mode of delivery and infant characteristics – A population-based cohort study. PloS ONE. 2017;12:e0184748. https://doi.org/10.1371/journal.pone.0184748

Neu J, Rushing J. Cesarean versus vaginal delivery: Long-term infant outcomes and the hygiene hypothesis. Clin Perinatol. 2011;38:321-31. https://doi.org/10.1016/j.clp.2011.03.008

Kristensen K, Henriksen L. Cesarean section and disease associated with immune function. J Allergy Clin Immunol. 2016;137:587-90. https://doi.org/10.1016/j.jaci.2015.07.040

Barreiros LA, Sousa JL, Geier C, Leiss-Piller A, Kanegae MPP, França TT, et al. SCID and other inborn errors of immunity with low TRECs – The Brazilian Experience. J Clin Immunol. 2022;42:1171-92. https://doi.org/10.1007/s10875-022-01275-9

Kumarasamy G, Khairiz K, Chang WL, Aye TT, Ali A. Paving the way in implementation of SCID newborn screening in developing nations: Feasibility study and strategies to move forward in Malaysia. Front Immunol. 2024;15:1400247. https://doi.org/10.3389/fimmu.2024

Huang J, Shankar A, Hurden I, Thomas R, Hill J, Seth D, et al. Increased mortality in infants with abnormal T-cell receptor excision circles. Pediatr Res. 2024;96:199-207. https://doi.org/10.1038/s41390-024-03121-7

Shih ST, Keller E, Wiley V, Wong M, Farrar MA, Chambers GM. Economic evaluation of newborn screening for severe combined immunodeficiency. Int J Neonatal Screen. 2022;8:44. https://doi.org/1010.3390/ijns8030044

How to Cite
1.
Gutiérrez-Hincapié S, Muskus-López C, Sánchez IP, Franco-Restrepo JL, Trujillo-Vargas CM. First pilot study for newborn screening of severe T and B lymphopenias in Colombia. Biomed. [Internet]. 2024 Dec. 23 [cited 2025 Jun. 3];44(Sp. 2):94-106. Available from: https://revistabiomedicaorg.biteca.online/index.php/biomedica/article/view/7568

Some similar items:

Published
2024-12-23

Altmetric

Article metrics
Abstract views
Galley vies
PDF Views
HTML views
Other views
Crossref Cited-by logo
QR Code