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      First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency—Clinical Achievements and Insights

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          Abstract

          Severe combined immunodeficiency (SCID), the most severe form of T cell immunodeficiency, is detectable through quantification of T cell receptor excision circles (TRECs) in dried blood spots obtained at birth. Herein, we describe the results of the first year of the Israeli SCID newborn screening (NBS) program. This important, life-saving screening test is available at no cost for every newborn in Israel. Eight SCID patients were diagnosed through the NBS program in its first year, revealing an incidence of 1:22,500 births in the Israeli population. Consanguine marriages and Muslim ethnic origin were found to be a risk factor in affected newborns, and a founder effect was detected for both IL7Rα and DCLRE1C deficiency SCID. Lymphocyte subset analysis and TREC quantification in the peripheral blood appear to be sufficient for confirmation of typical and leaky SCID and ruling out false positive (FP) results. Detection of secondary targets (infants with non-SCID lymphopenia) did not significantly affect the management or outcomes of these infants in our cohort. In the general, non-immunodeficient population, TREC rises along with gestational age and birth weight, and is significantly higher in females and the firstborn of twin pairs. Low TREC correlates with both gestational age and birth weight in extremely premature newborns. Additionally, the rate of TREC increase per week consistently accelerates with gestational age. Together, these findings mandate a lower cutoff or a more lenient screening algorithm for extremely premature infants, in order to reduce the high rate of FPs within this group. A significant surge in TREC values was observed between 28 and 30 weeks of gestation, where median TREC copy numbers rise by 50% over 2 weeks. These findings suggest a maturational step in T cell development around week 29 gestation, and imply moderate to late preterms should be screened with the same cutoff as term infants. The SCID NBS program is still in its infancy, but is already bearing fruit in the early detection and improved outcomes of children with SCID in Israel and other countries.

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          Most cited references22

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          Changes in thymic function with age and during the treatment of HIV infection.

          The thymus represents the major site of the production and generation of T cells expressing alphabeta-type T-cell antigen receptors. Age-related involution may affect the ability of the thymus to reconstitute T cells expressing CD4 cell-surface antigens that are lost during HIV infection; this effect has been seen after chemotherapy and bone-marrow transplantation. Adult HIV-infected patients treated with highly active antiretroviral therapy (HAART) show a progressive increase in their number of naive CD4-positive T cells. These cells could arise through expansion of existing naive T cells in the periphery or through thymic production of new naive T cells. Here we quantify thymic output by measuring the excisional DNA products of TCR-gene rearrangement. We find that, although thymic function declines with age, substantial output is maintained into late adulthood. HIV infection leads to a decrease in thymic function that can be measured in the peripheral blood and lymphoid tissues. In adults treated with HAART, there is a rapid and sustained increase in thymic output in most subjects. These results indicate that the adult thymus can contribute to immune reconstitution following HAART.
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            Timely and spatially regulated maturation of B and T cell repertoire during human fetal development.

            Insights into the ontogeny of the human fetal adaptive immune system are of great value for understanding immunocompetence of the developing fetus. However, to date, this has remained largely uncharted territory, in large part because blood samples from healthy, early gestation fetuses have been hard to come by. In a comprehensive study, we analyzed levels of T cell receptor excision circles (TRECs), signal-joint κ receptor excision circles (sjKRECs), and intron recombination signal sequence-K-deleting element (iRSS-Kde) rearrangement, and T and B lymphocyte repertoire clonality in human fetuses from 12 to 26 weeks of gestational age. Using next-generation sequencing, we analyzed the diversity and complexity of T cell receptor β (TRB) and immunoglobulin heavy chain (IGH) repertoires in four fetuses at 12, 13, 22, and 26 weeks of gestation and in healthy full-term infants. We report the progressive increase of TREC, sjKREC, and iRSS-Kde levels over time and confirm that B cell development precedes T cell development in the human fetus. Temporally and spatially regulated maturation of B and T cell repertoire diversity and complexity during human fetal development was observed, including evidence that immunoglobulin somatic hypermutation and class switch recombination occur already during intrauterine life. Our results help define physiological levels of immunodeficiency in premature infants and may serve as a reference for future studies aimed at investigating the impact of intrauterine pathologies on fetal immune development and function.
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              Newborn screening for SCID in New York State: experience from the first two years.

              To describe the process and assess outcomes for the first 2 years of newborn screening for severe combined immunodeficiency (SCID NBS) in New York State (NYS).
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                06 November 2017
                2017
                : 8
                : 1448
                Affiliations
                [1] 1Pediatric Department A and the Immunology Service, Jeffrey Modell Foundation Center, Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Affiliated to the Sackler Faculty of Medicine, Tel Aviv University , Tel Aviv, Israel
                [2] 2The National Center for Newborn Screening, Israel Ministry of Health , Tel-HaShomer, Israel
                [3] 3Pediatric Immunology Clinic, Soroka University Medical Center, Faculty of Health Sciences, Ben-Gurion University of the Negev , Beer Sheva, Israel
                [4] 4The Jeffrey Modell Foundation Israeli Network for Primary Immunodeficiency , New York, NY, United States
                [5] 5Allergy and Immunology Unit, Schneider Children’s Medical Center of Israel, Felsenstein Medical Research Center, Petach Tikva, Sackler Faculty of Medicine, Tel Aviv University , Tel Aviv, Israel
                [6] 6Ruth Children Hospital, Rappaport Faculty of Medicine, Technion – Israel Institute of Technology , Haifa, Israel
                [7] 7Bone Marrow Transplantation Department, Hadassah Hebrew University Medical Center, Hadassah-Hebrew University Medical School , Jerusalem, Israel
                [8] 8Allergy and Clinical Immunology Clinic, Department of Pediatrics, Shaare Zedek Medical Center, Hadassah-Hebrew University Medical School , Jerusalem, Israel
                [9] 9Pediatric Allergy Unit, Wolfson Medical Center , Holon, Israel
                [10] 10Pediatric Department, Wolfson Medical Center , Holon, Israel
                [11] 11Sackler Faculty of Medicine, Tel Aviv University , Tel Aviv, Israel
                [12] 12The National Lab for Diagnosing SCID – The Israeli Newborn Screening Program, Israel Ministry of Health , Tel-Hashomer, Israel
                Author notes

                Edited by: Menno C. van Zelm, Monash University, Australia

                Reviewed by: Stuart Paul Adams, Great Ormond Street Hospital, United Kingdom; Peter Schielen, National Institute for Public Health and the Environment, Netherlands

                These authors have contributed equally to this article and are equal corresponded.

                Specialty section: This article was submitted to Primary Immunodeficiencies, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2017.01448
                5682633
                29167666
                6122e792-2ea1-48b1-895d-187fe46bb170
                Copyright © 2017 Rechavi, Lev, Simon, Stauber, Daas, Saraf-Levy, Broides, Nahum, Marcus, Hanna, Stepensky, Toker, Dalal, Etzioni, Almashanu and Somech.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 July 2017
                : 17 October 2017
                Page count
                Figures: 4, Tables: 3, Equations: 0, References: 30, Pages: 10, Words: 6836
                Categories
                Immunology
                Original Research

                Immunology
                severe combined immunodeficiency,newborn screening,t cell development,preterm,immunodeficiency

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