Evidence map›Paper›PMID 40858649›Full record

ArticleScientific reports2025

Higher proportion of coagulative necrosis and PD-L1

Jinlong Dai, Lingjing Liu, Junjun Liu, Yuejiao Liu, Runrui Wu, Jin Zhou, Wen Chen

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Jinlong Dai *Chinese PLA Key Laboratory of Tuberculosis, Department of Pathology, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China.
Lingjing Liu *Chinese PLA Key Laboratory of Tuberculosis, Department of Pathology, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China.
Junjun LiuChinese PLA Key Laboratory of Tuberculosis, Department of Pathology, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China.
Yuejiao LiuChinese PLA Key Laboratory of Tuberculosis, Department of Pathology, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China.
Runrui WuChinese PLA Key Laboratory of Tuberculosis, Department of Pathology, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China.
Jin ZhouDepartment of Emergency Medicine, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China. huoshan1975@sina.com.
Wen ChenChinese PLA Key Laboratory of Tuberculosis, Department of Pathology, The 8th Medical Center, Chinese PLA General Hospital, Beijing, 100091, China. dr.chen20160224@foxmail.com.

Funding

The National Natural Science Foundation of China No: 31800814, 32271411
6 · The paper itself

Abstract

Due to its low incidence and non-specific clinical manifestations, early diagnosis of splenic tuberculosis (STB) is extremely challenging. Pathology is the gold standard for disease diagnosis. The spleen's unique structural and functional characteristics may confer distinct pathological features and immune microenvironment in STB. However, no relevant study has been reported to date. Here, we collected seven cases of STB and compared their clinical and pathological characteristics with those of pulmonary tuberculosis (PTB). CT scans revealed that STB primarily manifests as significant enlargement of the spleen, with multiple round-shaped low-density shadows visible within. Compared to the PTB group, the positive rates for molecular detection and acid-fast staining were significantly lower in the STB group, while the proportion of coagulative necrosis was substantially higher. Granulomas, caseous necrosis, abscesses, fibrous proliferation, collagen degeneration, and granulation tissue formation did not show significant differences between the two groups. We further compared infiltrating immune cells and found that the numbers of T cells, CD8

Indexed as

B7-H1 AntigenTuberculosis, SplenicAdultAgedCD8-Positive T-LymphocytesFemaleHumansMacrophagesMaleMiddle AgedNecrosisSpleenTomography, X-Ray ComputedTuberculosis, PulmonaryB7-H1 AntigenCD274 protein, humanCoagulative necrosisImmune suppressionPathological characteristicsSplenic tuberculosis

Identifiers

PMID40858649
PMCPMC12381082

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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.