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Am J Perinatol 2023; 40(07): 748-752
DOI: 10.1055/s-0041-1731044
Original Article

Neonatal Lymphopenia Screening Is Important for Early Diagnosis of Severe Combined Immunodeficiency

Aykut Poyraz 
1   Department of Pediatrics, Erciyes University, School of Medicine, Kayseri, Turkey
,
Murat Cansever 
2   Division of Allergy and Immunology, Department of Pediatrics, Erciyes University, School of Medicine, Kayseri, Turkey
,
Ipek Muderris 
3   Department of Gynecology and Obstetrics, Erciyes University, School of Medicine, Kayseri, Turkey
,
Turkan Patiroglu 
4   Division of Hematology and Oncology, Immunology, Department of Pediatrics, Erciyes University, School of Medicine, Kayseri, Turkey
› Institutsangaben Funding This work was supported by the Scientific Research Projects Unit (grant number: TSA2017/7127).
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Abstract

Objective T-cell receptor excision circles are expensive for neonatal severe combined immunodeficiency screening in developing countries. We aimed to detect immunodeficiencies presenting with lymphopenia to enable screening in the general population and to improve awareness regarding lymphopenia among clinicians.

Study Design This study was conducted prospectively. In all newborns included, complete blood count from umbilical cord blood samples was recorded. Absolute lymphopenia was defined as absolute lymphocyte count <3,000/mm3 in umbilical cord blood sample. Complete blood count was repeated at month 1 in cases found to have lymphopenia.

Results Overall, 2,000 newborns were included in the study. Absolute lymphopenia was detected in 42 newborns (2.1%), while lymphocyte count was >3,000/mm3 in 1,958 newborns (97.9%). Two infants with persisted lymphopenia at the end of the first month; therefore, further evaluations such as lymphocyte subsets for severe combined immunodeficiency (SCID) were done. In the first infant, the lymphocyte subgroups were detected as compatible with T (−), B (−), natural killer cells (NK) (+) SCID phenotype RAG defect. Sanger sequencing revealed that NM_000448 c.2209C > T (p.R737C) homozygous mutation of RAG1 gene. In the other infant, the lymphocyte subgroups were found as considered with T (−), B (+) NK (−) SCID phenotype JAK3 defect. Both patients underwent hematopoietic stem cell transplantation from human leukocyte antigen-matched family member.

Conclusion Absolute lymphopenia by complete blood count is a more simpler, relatively noninvasive and inexpensive screening methodfor detection of SCID in newborns compared with T-cell receptor excision circles technique.

Key Points

  • Our study was conducted with a much smaller number of study groups compared with the previous ones.

  • However, SCID was found at a higher rate compared with other studies.

  • Our study for this disease that is common in our country where consanguineous marriages are common

Keywords

neonatal lymphopenia - severe combined immunodeficiency - RAG1 deficiency - JAK3 deficiency


Publikationsverlauf

Eingereicht: 04. März 2021

Angenommen: 30. April 2021

Artikel online veröffentlicht:
11. Juni 2021

© 2021. Thieme. All rights reserved.

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