Evidence map›Paper›PMID 41316126›Full record

ArticleBMC musculoskeletal disorders2025

Immune cell infiltration and inflammatory response in nucleus pulposus following annular disruption in degenerative disc disease.

Jinmin Lv, Jinbing He, Yichao Ni, Linwei He, Zhuoming Li, Bo Tian, Hao Chen

Abstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2025. 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
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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

7 authors.

Jinmin Lv *Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215123, China.
Jinbing He *Department of Orthopedics, Liyuan Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei, 430060, China.
Yichao Ni *Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215123, China.
Linwei HeSuzhou Medical College, Soochow University, Suzhou, Jiangsu, 215123, China.
Zhuoming LiSuzhou Medical College, Soochow University, Suzhou, Jiangsu, 215123, China.
Bo TianSuzhou Medical College, Soochow University, Suzhou, Jiangsu, 215123, China. 20224233026@stu.suda.edu.cn.
Hao ChenDepartment of Orthopedics, Nanjing Drum Tower Hospital Group Suqian Hospital, Jiangsu, 223800, China. chen609355035@126.com.

Funding

National Natural Science Foundation of China 81873995
6 · The paper itself

Abstract

purposeIntervertebral disc degeneration (IDD) is a common cause of lower back pain. However, the role of annulus fibrosus rupture in altering the immune microenvironment of nucleus pulposus remains unclear. This study elucidated the impact of annulus fibrosus rupture on the immune response within the nucleus pulposus in IDD.

methodsThe study included patients diagnosed with intervertebral disc herniation who underwent surgical treatment at the Orthopedics Department of the Second Hospital of Soochow University from September 2020 to July 2021. Based on the integrity of the annulus fibrosus, patients were categorized into two groups: Annulus Intact (AI) group and Annulus Rupture (AR) group. Nucleus pulposus samples were collected during surgery for analysis. Flow cytometry was used to assess immune cell populations in these samples. Levels of inflammatory factors were measured using RT-PCR and enzyme-linked immunosorbent assay (ELISA).

resultsSamples from patients with annulus rupture showed significantly higher levels of macrophages and T cells compared to those with intact annulus. Gene expression of key inflammatory cytokines, including TNF-α, IL-1β, IL-4, and IL-6, were markedly elevated in the AR group than those in AI group (P < 0.05). The levels of TNF-α and IL-1β detected by ELISA were also significantly increased in AR group (P < 0.05).

conclusionAnnulus fibrosus rupture significantly alters the immune microenvironment of the nucleus pulposus, characterized by increased inflammatory cell infiltration and elevated levels of pro-inflammatory cytokines. This enhanced local inflammatory response may play a crucial role in the pathogenesis and progression of IDD, offering potential targets for immune-modulatory therapies to delay IDD progression.

Indexed as

Annulus FibrosusInflammationIntervertebral Disc DegenerationNucleus PulposusAdultCytokinesFemaleHumansIntervertebral Disc DisplacementMacrophagesMaleMiddle AgedT-LymphocytesCytokinesAnnulus ruptureImmune microenvironmentInflammatory responseIntervertebral disc degeneration

Identifiers

PMID41316126
PMCPMC12664127

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.