Evidence map›Paper›PMID 32277381›Full record

ArticleMycopathologia2020

Effect of Fonsecaea monophora on the Polarization of THP-1 Cells to Macrophages.

Jinglin Qin, Jing Zhang, Minglan Shi, Liyan Xi, Junmin Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Mycopathologia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. CXCL1 and CXCL2: Key Regulators of Host Defense AgainstJournal of inflammation research · 2025
    Article
  3. Article
  4. Article
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 3 institutions in 1 country.

Jinglin QinDepartment of Dermatology and Venereology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Jing ZhangDepartment of Dermatology and Venereology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Minglan ShiDepartment of Dermatology and Venereology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Liyan XiDepartment of Dermatology and Venereology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Junmin ZhangDepartment of Dermatology and Venereology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China. junminmx@163.com.
Sun Yat-sen Memorial Hospital · CNSun Yat-sen University · CNNanfang Hospital · CN

Funding

National Natural Science Foundation of China 81571970
6 · The paper itself

Abstract

backgroundChromoblastomycosis is a chronic, progressive fungal disease of the skin and subcutaneous tissue caused by a unique group of dematiaceous fungi. Fonsecaea monophora, a new species distinct from Fonsecaea pedrosoi strains, is the main pathogen responsible for chromoblastomycosis in south China. Macrophages can be polarized into two categories: classically activated and alternatively activated.

objectivesLittle is known about the relationship between F. monophora and macrophage polarization. This study aimed to study the effect of F. monophora on the polarization of THP-1 cells to macrophages.

methodsWe established coculture systems of F. monophora and THP-1-derived macrophages in different activation states.

resultsF. monophora enhanced the phagocytosis by macrophages in the initially activated state and weakened the phagocytosis by classically activated macrophages without affecting that by alternatively activated macrophages. Classically activated macrophages had the strongest killing effect on F. monophora, while the initially activated macrophages had the weakest. The pathogen could not be rapidly cleared by any type of macrophage. F. monophora promoted the expression of proinflammatory cytokines and inhibited that of anti-inflammatory cytokines.

conclusionsF. monophora promoted the polarization of THP-1 cells to classically activated macrophages and inhibited that of THP-1 cells to alternatively activated macrophages.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD68 MoleculeCell DifferentiationCoculture TechniquesCytokinesEnzyme-Linked Immunosorbent AssayFlow CytometryFluorescence PolarizationFonsecaeaHumansMacrophagesPhagocytosisReal-Time Polymerase Chain ReactionTHP-1 CellsAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD68 antigen, humanCD68 MoleculeCytokinesChromoblastomycosisFonsecaea monophoraMacrophagesPolarizationTHP-1

Identifiers

PMID32277381
OpenAlexW3015734501

What OpenQuestion holds

Textmetadata
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.