Evidence map›Paper›PMID 41749119›Full record

ArticleBMC infectious diseases2026

Neutrophil-to-lymphocyte ratio as a correlative factor of severe SARS-CoV-2 infection in neonates: associations with lymphocyte subsets alterations.

Guangliang Bi, Qingyan Xiao, Jie He, Shuzhe Xiao, Jie Yang

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Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Guangliang BiDepartment of Neonatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, PR China.
Qingyan XiaoDepartment of Neonatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, PR China.
Jie HeDepartment of Neonatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, PR China.
Shuzhe XiaoDepartment of Neonatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, PR China.
Jie YangDepartment of Neonatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, PR China. jieyang0830@126.com.

Funding

National Key Research and Development Program of China 2021YFC2701700Natural Science Foundation of Guangdong Province 2022A1515012021
6 · The paper itself

Abstract

backgroundThe SARS-CoV-2 remains prevalent, and neonates remain susceptible. This study aims to explore the potential of the Neutrophil-to-Lymphocyte Ratio (NLR) as a valuable tool for assessing the severity of SARS-CoV-2 infection in term neonates in the late neonatal period (8-28 days of life). Additionally, it seeks to examine the underlying immune characteristics associated with this ratio.

methodsA retrospective cohort study was conducted from November 1, 2022, to February 1, 2023 in four hospitals. Baseline characteristics and laboratory results were collected and analyzed. Receiver operating characteristic (ROC) curve of NLR and lymphocyte subsets analysis were performed.

resultsThe study enrolled 143 term neonates in the late neonatal period with confirmed SARS-CoV-2 infection, comprising 54 severe cases and 89 non-severe cases, along with 59 age-matched uninfected controls. The NLR was identified as an associated factor for severe SARS-CoV-2 in term neonates in the late neonatal period. Furthermore, the levels of CD4+CD45RA and CD8+CD28+ T cells were significantly reduced in neonates with SARS-CoV-2 compared to healthy neonates, and a significant decrease in CD8+CD28+ T cells was observed in the severe SARS-CoV-2 group compared to the non-severe group.

conclusionsNLR is an associated factor of severe SARS-CoV-2 in term neonates in the late neonatal period. The pathogenicity of severe SARS-CoV-2 infection in term neonates in the late neonatal period may be related to alterations in lymphocyte subsets CLINICAL TRIAL: Not applicable.

Indexed as

COVID-19LymphocytesLymphocyte SubsetsNeutrophilsFemaleHumansInfant, NewbornLymphocyte CountMaleRetrospective StudiesROC CurveSARS-CoV-2Severity of Illness IndexLymphocyte subsetsNeonatesNeutrophil-to-lymphocyte ratioSARS-CoV-2

Identifiers

PMID41749119
PMCPMC13040804

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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.