Evidence map›Paper›PMID 42464376›Full record

ReviewCell communication and signaling : CCS2026

Platelet homeostasis and heterogeneity in inflammation and sepsis: mechanisms, biological effects, and clinical potential.

Yiyun Pan, Wenling Zhao, Beibei Yu, Ji Zhang, Mengdi Qu, Ruiwen Jiang, Tingye Xu, Dongliang Li, Hao Zhang, Changhong Miao

Abstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2026. 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

10 authors.

Yiyun Pan *Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Wenling Zhao *Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Beibei Yu *Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Ji ZhangDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Mengdi QuDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Ruiwen JiangDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Tingye XuDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Dongliang LiDepartment of Anesthesiology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. ldl@sdu.edu.cn.
Hao ZhangDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. zhang.hao@zs-hospital.sh.cn.
Changhong MiaoDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. miaochanghong_zs@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a life-threatening syndrome resulting from a dysregulated host immune response to infection and is frequently accompanied by coagulation abnormalities and multiple organ dysfunction. As central regulators at the intersection of hemostasis, inflammation, and immunity, platelets play a critical role in the initiation and progression of sepsis. Beyond their traditional function in hemostasis, platelets actively participate in immune modulation, inflammatory amplification, and immunothrombosis. This review systematically summarizes the molecular and cellular mechanisms through which platelets contribute to organ injury in sepsis, with particular emphasis on platelet-immune cell interactions. We discuss how these processes drive the development of acute lung injury, myocardial depression, hepatic and renal dysfunction, and disseminated intravascular coagulation. In addition, we examine the dynamic alterations in platelet phenotype and function during sepsis and their clinical implications. Ultimately, we evaluate the therapeutic potential of antiplatelet strategies, addressing current challenges and future directions for translating platelet-targeted interventions into effective treatments for sepsis.

Indexed as

Blood PlateletsHomeostasisInflammationSepsisAnimalsHumansImmunothrombosisPlatelet–immune cell interactionsPlateletsSepsis

Identifiers

PMID42464376
PMCPMC13656592

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.