Evidence map›Paper›PMID 41276845›Full record

ArticleGut pathogens2025

Patients with inflammatory bowel disease exhibit increased susceptibility to HCoV-NL63.

Tingting Ning, Nianchen Liu, Qi Jiang, Nan Zhang, Shengtao Zhu

Abstract read
In one paragraph

Article in Gut pathogens, 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

5 authors.

Tingting Ning *Department of Gastroenterology, Beijing Friendship Hospital, National Clinical Research Center for Digestive Disease, Beijing Digestive Disease Center, State Key Laboratory of Digestive Health, Capital Medical University, Beijing, 100050, No. 95 Yongan Street, Xicheng District, China.
Nianchen Liu *Department of Gastroenterology, Beijing Friendship Hospital, National Clinical Research Center for Digestive Disease, Beijing Digestive Disease Center, State Key Laboratory of Digestive Health, Capital Medical University, Beijing, 100050, No. 95 Yongan Street, Xicheng District, China.
Qi JiangDivision of HIV/AIDS and Sexually Transmitted Virus Vaccines, National Institutes for Food and Drug Control (NIFDC), Beijing, 102600, China.
Nan ZhangDepartment of Gastroenterology, Beijing Friendship Hospital, National Clinical Research Center for Digestive Disease, Beijing Digestive Disease Center, State Key Laboratory of Digestive Health, Capital Medical University, Beijing, 100050, No. 95 Yongan Street, Xicheng District, China. zhangnan_2020@126.com.
Shengtao ZhuDepartment of Gastroenterology, Beijing Friendship Hospital, National Clinical Research Center for Digestive Disease, Beijing Digestive Disease Center, State Key Laboratory of Digestive Health, Capital Medical University, Beijing, 100050, No. 95 Yongan Street, Xicheng District, China. zhushengtao@ccmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunocompromised inflammatory bowel disease (IBD) patients may develop life-threatening pneumonia and bronchiolitis upon HCoV-NL63 infection. However, little is known whether these patients will be more susceptible to HCoV-NL63 infection. We compared the expression of ACE2 in different tissues and cell lines. Besides, the susceptibility of colonic cells to HCoV-NL63 was assessed. We then examined the expression of ACE2 in the colonic mucosa from IBD patients and animal models, and in the inflammatory colonic cells. The susceptibility of inflammatory colonic cells to HCoV-NL63 was detected using a pseudovirus-based system. Pseudovirus based neutralization assay was used to quantify the neutralizing antibodies to HCoV-NL63 in patients with IBD and healthy controls. ACE2 was abundantly expressed in the colonic tissue and cells. And colonic cells were susceptible to pseudotyped HCoV-NL63. The expression of ACE2 was increased in the colonic mucosa from IBD patients and animal models, and in inflammatory colonic cells. Inflammatory colonic cells were more susceptible to pseudotyped HCoV-NL63. Besides, reduced protective neutralizing antibody titers were seen in patients with IBD, especially for male or older IBD patients. These results suggest IBD patients may be particularly susceptible to infection with HCoV-NL63 and thus extra precautions should be taken to prevent them from infection. Further mechanistic studies are needed to support our findings.

Indexed as

ACE2HCoV-NL63IBDNeutralizing antibodySusceptibility

Identifiers

PMID41276845
PMCPMC12683868

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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 OpenQuestion graph.