Evidence map›Paper›PMID 42771994›Full record

ArticleEBioMedicine2026

Age-related changes of FCGR3A

Xiaokai Fang, Fang Li, Yuwen Gao, Yu Zhang, Xingyu Chen, Shan Zhang, Yang Luo, Yuan Zhou, Shangshang Wang, Jingru Tian and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in EBioMedicine, 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

13 authors.

Xiaokai FangJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China; Department of Dermatology, Shanghai Institute of Dermatology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Fang LiJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Yuwen GaoJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Yu ZhangJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Xingyu ChenJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Shan ZhangJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Yang LuoJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Yuan ZhouJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China.
Shangshang WangDepartment of Dermatology, Shanghai Institute of Dermatology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Jingru TianJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China. Electronic address: jingru.tian@pumcderm.cams.cn.
Xiaochun LiuJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China. Electronic address: holmes27@163.com.
Wei LiDepartment of Dermatology, Shanghai Institute of Dermatology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Xu YaoJiangsu Provincial Key Laboratory of Dermatology, Department of Allergy and Rheumatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Institute of Dermatology, Hospital for Skin Diseases, Nanjing, 210042, China. Electronic address: dryao_xu@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing global ageing population has led to a rising prevalence of elderly atopic dermatitis (eAD). Natural killer (NK) cells play an important role in skin homoeostasis; however, their involvement in eAD remains unclear. This study investigates the functional role and mechanisms of NK cells in eAD pathogenesis.

methodsUsing single-cell RNA sequencing (scRNA-seq) complemented by flow cytometry and immunofluorescence, we identified distinct NK cell subsets in eAD lesions. In vivo functional studies were performed in an MC903-induced AD mouse model through NK cell depletion and adoptive transfer experiments. Fibroblast-NK cell-macrophage interactions were further examined using in vitro co-culture systems.

findingsOur results showed that activated NK cells were increased in skin lesions of younger patients with AD. Depletion of NK cell exacerbated skin inflammation in AD mice, whereas adoptive transfer of activated NK cells alleviated it. Notably, patients with eAD exhibited a significant reduction in both NK cell number and function compared to younger patients with AD. scRNA-seq analysis identified three distinct subsets of NK cells in the skin: NK1a (CLNK

interpretationIn conclusion, NK cells, especially the NK2 subset, are associated with AD pathogenesis, with potential implications for elderly patients.

fundingThis work was funded by the National Key R&D Program of China (2022YFC3601800); National Natural Science Foundation of China (82373489, 82504273, 82530099, 82522075, 82330098, 82273542, 82304023, 82404151); CAMS Innovation Fund for Medical Sciences (CIFMS, 2021-I2M-1-059); Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences (2021-RC320-001); Key Project of the Innovation Program of Shanghai Municipal Education Commission (2021-01-07-00-07-E00078).

Indexed as

Atopic dermatitisElderlyFibroblastsMacrophagesNatural killer cells

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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.