Evidence map›Paper›PMID 41425569›Full record

ArticleFrontiers in immunology2025

Proteomics-driven screening of artemisinin-based combination ratios and mechanistic insights into

Liyu Hao, Jianhui Sun, Jianliang Li, Zongyuan Li, Zeyue Yu, Hanhui Huang, Guimin Liu, Zhenru Shen, Hairu Huo, Qili Yuan and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 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

12 authors.

Liyu HaoSchool of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang, China.
Jianhui SunInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Jianliang LiInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Zongyuan LiInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Zeyue YuInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Hanhui HuangInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Guimin LiuInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Zhenru ShenInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Hairu HuoInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Qili YuanInstitute of Traditional Chinese Medicine Health Industry, China Academy of Chinese Medical Sciences, Nanchang, China.
Hongmei LiInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Luqi HuangSchool of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Malaria, a life-threatening mosquito-borne disease caused by Methods: We systematically screened antimalarial compound ratios using murine malaria models and optimized a formula comprising arteannuin B, artemisinic acid, and scopoletin. Through integrated proteomic profiling and western blot validation, we elucidated the immunomodulatory mechanisms underlying the antimalarial efficacy of this combination. Results: Specifically, the formula strengthened host defense by modulating phagocytic activity in splenic macrophages, dendritic cells, and natural killer cells via Fcγ receptor-mediated pathways. Discussion: These findings provide mechanistic insights into artemisinin-associated immune potentiation. Moreover, we have proposed a novel ACT strategy targeting host-parasite interactions, offering a promising approach to circumvent emerging artemisinin resistance in

Indexed as

AntimalarialsArtemisininsMalariaPlasmodium bergheiProteomicsAnimalsDisease Models, AnimalDrug Therapy, CombinationFemaleMacrophagesMiceMice, Inbred C57BLAntimalarialsartemisininArtemisininsartemisininartemisinin-based combination therapydrug resistance reversalFcγ receptor signalingMalaria

Identifiers

PMID41425569
PMCPMC12715000

What OpenQuestion holds

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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.