Evidence map›Paper›PMID 34790206›Full record

ArticleFrontiers in immunology2021

Immune Profiling of Cord Blood From Preterm and Term Infants Reveals Distinct Differences in Pro-Inflammatory Responses.

Jeremy Anderson, Cao Minh Thang, Le Quang Thanh, Vo Thi Trang Dai, Van Thanh Phan, Bui Thi Hong Nhu, Do Ngoc Xuan Trang, Phan Thi Phuong Trinh, Thuong Vu Nguyen, Nguyen Trong Toan and 5 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

36 citing papers in PubMed, 44 citations in OpenAlex.

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  12. Comparison of cytokine responses to group BInfection and immunity · 2025
    Article
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  15. Perturbation of the Preterm Human Immune System in Early Life.medRxiv : the preprint server for health sciences · 2025
    Article
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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

15 authors at 4 institutions in 3 countries.

Jeremy AndersonInfection and Immunity, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Cao Minh ThangDepartment of Microbiology and Immunology, Pasteur Institute of Ho Chi Minh City, Ho Chi Minh, Vietnam.
Le Quang ThanhTu Du Hospital, Ho Chi Minh, Vietnam.
Vo Thi Trang DaiDepartment of Microbiology and Immunology, Pasteur Institute of Ho Chi Minh City, Ho Chi Minh, Vietnam.
Van Thanh PhanDepartment of Microbiology and Immunology, Pasteur Institute of Ho Chi Minh City, Ho Chi Minh, Vietnam.
Bui Thi Hong NhuDepartment of Labour Delivery, Tu Du Hospital, Ho Chi Minh, Vietnam.
Do Ngoc Xuan TrangDepartment of Labour Delivery, Tu Du Hospital, Ho Chi Minh, Vietnam.
Phan Thi Phuong TrinhDepartment of Labour Delivery, Tu Du Hospital, Ho Chi Minh, Vietnam.
Thuong Vu NguyenPasteur Institute of Ho Chi Minh City, Ho Chi Minh, Vietnam.
Nguyen Trong ToanClinical Research Centre, Pasteur Institute of Ho Chi Minh City, Ho Chi Minh, Vietnam.
Christopher M HarpurInfection and Immunity, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Kim MulhollandInfection and Immunity, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Daniel G PellicciInfection and Immunity, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Lien Anh Ha DoInfection and Immunity, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Paul V LicciardiInfection and Immunity, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Institut Pasteur in Ho Chi Minh City · VNMurdoch Children's Research Institute · AUUniversity of Melbourne · AUViet Duc Hospital · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Preterm infants are highly vulnerable to infectious disease. While many factors are likely to contribute to this enhanced susceptibility, the immature nature of the preterm immune system is postulated as one key factor. Methods: In our study, we used high-dimensional flow cytometry and cytokine assays to characterise the immune profiles in 25 preterm (range: 30.4-34.1 weeks gestational age) and 25 term infant (range: 37-40 weeks gestational age) cord blood samples. Results: We found that preterm infants exhibit reduced frequencies of monocytes, CD56 Conclusion: Overall, we identify key differences in pro-inflammatory immune profiles between preterm and term infants. These findings may help to explain why preterm infants are more susceptible to infectious disease during early life and facilitate the development of targeted interventions to protect this highly vulnerable group.

Indexed as

Adaptive ImmunityBiomarkersCordocentesisCytokinesFemaleFetal BloodGestational AgeHumansImmunity, InnateInfant, NewbornInfant, PrematureInflammationInflammation MediatorsIntercellular Signaling Peptides and ProteinsLymphocytesMaleBiomarkersCytokinesInflammation MediatorsIntercellular Signaling Peptides and Proteinsimmune profileinfantinfectioninflammationpreterm

Identifiers

PMID34790206
PMCPMC8591285
OpenAlexW3209600586

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.