Evidence map›Paper›PMID 40076520›Full record

ArticleInternational journal of molecular sciences2025

Malocclusion Worsens Survival Following Sepsis Due to the Disruption of Innate and Acquired Immunity.

Yoshihisa Fujinami, Masafumi Saito, Yuko Ono, Masaya Akashi, Shigeaki Inoue, Joji Kotani

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Yoshihisa FujinamiDepartment of Emergency Medicine, Kakogawa Central City Hospital, Hyogo 675-8611, Japan.ORCID 0000-0002-6521-0418
Masafumi SaitoDepartment of Immunology and Microbiology, National Defense Medical College, Saitama 359-8513, Japan.
Yuko OnoDepartment of Disaster and Emergency and Critical Care Medicine, Graduate School of Medicine, Kobe University, Kobe 650-0047, Japan.
Masaya AkashiDepartment of Oral and Maxillofacial Surgery, Graduate School of Medicine, Kobe University, Kobe 650-0047, Japan.
Shigeaki InoueDepartment of Disaster and Emergency and Critical Care Medicine, Graduate School of Medicine, Kobe University, Kobe 650-0047, Japan.ORCID 0000-0003-3907-8537
Joji KotaniDepartment of Disaster and Emergency and Critical Care Medicine, Graduate School of Medicine, Kobe University, Kobe 650-0047, Japan.

Funding

Japan Society for the Promotion of Science (JSPS) JP22K16634
6 · The paper itself

Abstract

Sepsis is a severe condition with high mortality, in which immune dysfunction plays a critical role. Poor oral health has been linked to frailty, but its impact on sepsis outcomes remains unclear. Therefore, we used a mouse model of malocclusion and sepsis to investigate how tooth loss affects immune responses during sepsis. Adult male C57BL/6 mice were divided into four groups: Control, Malocclusion (Mal), Sepsis (CS), and Malocclusion with Sepsis (Mal + CS). Malocclusion was induced by tooth extraction, and sepsis was induced using cecal slurry injection. We assessed survival rates, immune cell counts, and biochemical markers. The Mal + CS group exhibited significantly lower survival rates and greater weight loss compared to the CS group. The flow cytometry showed reduced neutrophils, monocytes, and T cells in the Mal + CS group. Elevated ALT and AST levels indicated liver damage. No significant differences in bacterial loads were observed, but immune suppression was exacerbated in the Mal + CS group. Malocclusion worsens sepsis outcomes by impairing both innate and adaptive immune responses. These findings emphasize the importance of oral health in improving sepsis prognosis and immune function during critical illnesses.

Indexed as

Adaptive ImmunityImmunity, InnateMalocclusionSepsisAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLNeutrophilsfrailtyimmunological disruptionoral frailtysepsis

Identifiers

PMID40076520
PMCPMC11899844

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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.