Evidence map›Paper›PMID 38232693›Full record

ArticleCell reports. Medicine2024

Fc-fused IL-7 provides broad antiviral effects against respiratory virus infections through IL-17A-producing pulmonary innate-like T cells.

Dong-Il Kwon, Subin Park, Yujin L Jeong, Young-Min Kim, Jeongyong Min, Changhyung Lee, Jung-Ah Choi, Yoon Ha Choi, Hyun-Jung Kong, Youngwon Choi and 12 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

22 authors at 3 institutions in 1 country.

Dong-Il KwonDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Subin ParkDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Yujin L JeongDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Young-Min KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Jeongyong MinDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Changhyung LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Jung-Ah ChoiScience Unit, International Vaccine Institute, Seoul 08826, Republic of Korea.
Yoon Ha ChoiDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Hyun-Jung KongGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea.
Youngwon ChoiGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea.
Seungtae BaekResearch Institute of NeoImmuneTech Co., Ltd., Pohang 37666, Republic of Korea.
Kun-Joo LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Yeon-Woo KangDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Chaerim JeongDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Gihoon YouDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Youngsik OhDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Sun-Kyoung ImResearch Institute of NeoImmuneTech Co., Ltd., Pohang 37666, Republic of Korea.
Manki SongScience Unit, International Vaccine Institute, Seoul 08826, Republic of Korea.
Jong Kyoung KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
Jun ChangGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea.
Donghoon ChoiResearch Institute of NeoImmuneTech Co., Ltd., Pohang 37666, Republic of Korea. Electronic address: dhchoi@neoimmunetech.com.
Seung-Woo LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang 37666, Republic of Korea. Electronic address: sw_lee@postech.ac.kr.
Pohang University of Science and Technology · KREwha Womans University · KRInternational Vaccine Institute · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Repeated pandemics caused by the influenza virus and severe acute respiratory syndrome coronavirus (SARS-CoV) have resulted in serious problems in global public health, emphasizing the need for broad-spectrum antiviral therapeutics against respiratory virus infections. Here, we show the protective effects of long-acting recombinant human interleukin-7 fused with hybrid Fc (rhIL-7-hyFc) against major respiratory viruses, including influenza virus, SARS-CoV-2, and respiratory syncytial virus. Administration of rhIL-7-hyFc in a therapeutic or prophylactic regimen induces substantial antiviral effects. During an influenza A virus (IAV) infection, rhIL-7-hyFc treatment increases pulmonary T cells composed of blood-derived interferon γ (IFNγ)+ conventional T cells and locally expanded IL-17A+ innate-like T cells. Single-cell RNA transcriptomics reveals that rhIL-7-hyFc upregulates antiviral genes in pulmonary T cells and induces clonal expansion of type 17 innate-like T cells. rhIL-7-hyFc-mediated disease prevention is dependent on IL-17A in both IAV- and SARS-CoV-2-infected mice. Collectively, we suggest that rhIL-7-hyFc can be used as a broadly active therapeutic for future respiratory virus pandemic.

Indexed as

Influenza, HumanInterleukin-17AnimalsAntiviral AgentsHumansInterleukin-7MiceSARS-CoV-2T-LymphocytesAntiviral AgentsInterleukin-17Interleukin-7influenza A virusinnate-like T cellsinterleukin-17Ainterleukin-7SARS-CoV-2virus infection

Identifiers

PMID38232693
PMCPMC10829794
OpenAlexW4390921275

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.