Evidence map›Paper›PMID 40892369›Full record

ArticleCell biochemistry and biophysics2026

T-Cell Receptor Excision Circle/Kappa-Deleting Recombination Excision Circle-Based Newborn Screening Program for Severe Combined Immunodeficiency in Kumamoto, Japan.

Yuya Kinoshita, Jun Kido, Takaaki Sawada, Keishin Sugawara, Fumiko Nozaki, Tomoyuki Mizukami, Madoka Nishimura, Shinichiro Yoshida, Ryutaro Tsuru, Kimitoshi Nakamura

Abstract read
In one paragraph

Article in Cell biochemistry and biophysics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yuya KinoshitaDepartment of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Jun KidoDepartment of Pediatrics, Kumamoto University Hospital, Kumamoto, Japan.
Takaaki SawadaDepartment of Pediatrics, Kumamoto University Hospital, Kumamoto, Japan. sawada.takaki@kuh.kumamoto-u.ac.jp.
Keishin SugawaraDepartment of Pediatrics, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Fumiko NozakiDepartment of Pediatrics, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Tomoyuki MizukamiDepartment of Pediatrics, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Madoka NishimuraDepartment of Pediatrics, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Shinichiro YoshidaKM Biologics Co., Ltd, Kumamoto, Japan.
Ryutaro TsuruKM Biologics Co., Ltd, Kumamoto, Japan.
Kimitoshi NakamuraDepartment of Pediatrics, Kumamoto University Hospital, Kumamoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe combined immunodeficiency (SCID) is a life-threatening hereditary disorder that requires early diagnosis and intervention. Therefore, this study aimed to evaluate the utility of T-cell receptor excision circle (TREC) and kappa-deleting recombination excision circle (KREC) measurements in newborn screening (NBS) for SCID and other primary immunodeficiencies in Kumamoto Prefecture, Japan. In a TREC-based NBS program (February 2019–March 2022, N = 43,658), six newborns (0.014%) underwent immunological testing, and three (0.007%) were diagnosed with T-cell lymphopenia. In a subsequent combined TREC/KREC-based NBS program (April 2022–March 2023, N = 12,335), eight newborns (0.065%) required further testing, and one (0.008%) was diagnosed with X-linked agammaglobulinemia. Decreased KREC levels were observed in two newborns exposed to maternal azathioprine (AZP). The TREC levels tended to be lower in more premature infants, whereas the KREC levels showed no clear correlation with gestational age (GA). Both the TREC and KREC levels were reduced in infants with low birth weights (BWs). These findings indicate that the combined TREC/KREC-based NBS program is an effective approach for detecting T- and B-cell immunodeficiencies. However, clinical factors such as maternal AZP exposure, low GA, and low BW may affect TREC and/or KREC levels, necessitating careful interpretation of results from dried blood spot samples.

Indexed as

Neonatal ScreeningReceptors, Antigen, T-CellSevere Combined ImmunodeficiencyFemaleGestational AgeHumansInfant, NewbornJapanMaleRecombination, GeneticT-LymphocytesReceptors, Antigen, T-CellKappa-deleting recombination excision circleNewborn screeningSevere combined immunodeficiencyT-cell receptor excision circle

Identifiers

PMID40892369
PMCPMC12967461

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.