Evidence map›Paper›PMID 26060601›Full record

ReviewEmerging microbes & infections2015

The role of C5a in acute lung injury induced by highly pathogenic viral infections.

Renxi Wang, He Xiao, Renfeng Guo, Yan Li, Beifen Shen

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Emerging microbes & infections, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 123 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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.

NCT04369820 nacompletednot on this mapstarted 2020, after this paper: background citation

C5a Receptor Expression in Circulating Myeloid Cells in ARDS Secondary to COVID-19

TypeinterventionalSponsorAssistance Publique Hopitaux De MarseilleRan2020 to 2023Enrolled61ConditionsCOVID-19Armsdraw blood
NCT04449588 phase2 / phase3terminatednot on this mapstarted 2020, after this paper: background citation

A Multi-center, Open-label, Randomized Parallel Controlled Evaluation on the Efficacy and Safety of BDB-001 Injection in the Treatment of Progressive Severe COVID-19 in Phase II/III

TypeinterventionalSponsorStaidson (Beijing) Biopharmaceuticals Co., LtdRan2020 to 2024Enrolled369ConditionsCOVID-19 PneumoniaArmsBDB-001 Injection, Conventional treatment
3 · Its place in the literature

Who cites it

123 citing papers in PubMed, 1 synthesis or guideline pooled it, 174 citations in OpenAlex.

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  4. Differential virulence potential of different clades of multidrug-resistantmedRxiv : the preprint server for health sciences · 2026
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63 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 2 countries.

Renxi WangLaboratory of Immunology, Institute of Basic Medical Sciences , Beijing 100850, China.
He XiaoLaboratory of Immunology, Institute of Basic Medical Sciences , Beijing 100850, China.
Renfeng GuoDepartment of Pathology, University of Michigan , Ann Arbor, Michigan 48109, USA ; InflaRx GmbH , Jena 07745, Germany.
Yan LiLaboratory of Immunology, Institute of Basic Medical Sciences , Beijing 100850, China.
Beifen ShenLaboratory of Immunology, Institute of Basic Medical Sciences , Beijing 100850, China.
Institute of Basic Medical Sciences of the Chinese Academy of Medical SciencesUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complement system, an important part of innate immunity, plays a critical role in pathogen clearance. Unregulated complement activation is likely to play a crucial role in the pathogenesis of acute lung injury (ALI) induced by highly pathogenic virus including influenza A viruses H5N1, H7N9, and severe acute respiratory syndrome (SARS) coronavirus. In highly pathogenic virus-induced acute lung diseases, high levels of chemotactic and anaphylatoxic C5a were produced as a result of excessive complement activaiton. Overproduced C5a displays powerful biological activities in activation of phagocytic cells, generation of oxidants, and inflammatory sequelae named "cytokine storm", and so on. Blockade of C5a signaling have been implicated in the treatment of ALI induced by highly pathogenic virus. Herein, we review the literature that links C5a and ALI, and review our understanding of the mechanisms by which C5a affects ALI during highly pathogenic viral infection. In particular, we discuss the potential of the blockade of C5a signaling to treat ALI induced by highly pathogenic viruses.

Indexed as

Acute Lung InjuryAnimalsComplement C5aDisease Models, AnimalHumansReactive Oxygen SpeciesVirus DiseasesVirusesComplement C5aReactive Oxygen Speciesacute lung injuryC5apro-inflammatory cytokines

Identifiers

PMID26060601
PMCPMC4451266
OpenAlexW330731027

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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.