Evidence map›Paper›PMID 36753031›Full record

ArticleFolia microbiologica2023

In vitro and in vivo synergistic effects of hydroxychloroquine and itraconazole on Cryptococcus neoformans.

Xue Wang, Xuemei Long, Songgan Jia, Jiali Zhu, Zhan Zhou, Sarah Ahmed, Yinhui Jiang, Yanping Jiang

Abstract read
PubMed Publisher
In one paragraph

Article in Folia microbiologica, 2023. 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
1.5field-weighted citation impact, top 18% 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, 7 citations in OpenAlex.

  1. A review of the current anti-New microbes and new infections · 2026
    Review
  2. Journal of fungi (Basel, Switzerland) · 2025
    Review
  3. Pathogens (Basel, Switzerland) · 2024
    Review
  4. Medical mycology case reports · 2024
    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

8 authors at 2 institutions in 2 countries.

Xue WangDepartment of Dermatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Xuemei LongDepartment of Dermatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Songgan JiaDepartment of Dermatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Jiali ZhuDepartment of Dermatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Zhan ZhouDepartment of Dermatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Sarah AhmedCentre of Expertise in Mycology of Radboud University Medical Center/Canisius Wilhelmina Hospital, Nijmegen, Netherlands.ORCID http://orcid.org/0000-0003-0155-8113
Yinhui JiangLaboratory of Medical Molecular Biology, Guizhou Medical University, Guiyang, China.
Yanping JiangDepartment of Dermatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China. jiangyanping119@163.com.ORCID http://orcid.org/0000-0003-0668-280X
Guiyang Medical University · CNRadboud University Nijmegen · NL

Funding

Guizhou Medical University Xiaobo J [2022]013Guizhou Medical University [ZK (2021) zhongdian030]National Natural Science Foundation of China 81960368Science and Technology Program of Guizhou Province ZK [2022] General 426
6 · The paper itself

Abstract

Cryptococcus neoformans is an opportunistic fungal pathogen that can cause life-threatening invasive fungal infections. As its prevalence and drug resistance continue to rise, cryptococcosis requires new treatment options. Tapping into the potential antifungal effects of traditional drugs or combination therapy has become one of the options. This study was the first to examine the interaction of hydroxychloroquine (HCQ) and itraconazole (ITR) on Cryptococcus neoformans in vitro and in vivo. Our results showed that HCQ alone and in combination with ITR exhibited antifungal activity against C. neoformans planktonic cells. When HCQ was combined with ITR, the minimal inhibitory concentration (MIC) value of HCQ decreased to 32 μg/mL, and the MIC value of ITR decreased from 0.25 μg/mL to 0.06-0.25 μg/mL. The time-killing curve showed that the combined application of HCQ and ITR significantly shortened the killing time, dynamically defining the antifungal activity. The minimum biofilm clearance concentration (MBEC) of HCQ was only 32 μg/mL, which was significantly lower than the MIC of HCQ for planktonic cells. When combined with ITR, the MBEC of ITR decreased from 128 μg/mL to 2-1 μg/mL, and the MBEC of HCQ decreased from 32 μg/mL to 4 μg/mL, indicating a synergistic antifungal biofilm effect. In comparison to ITR alone, the combination of HCQ and ITR treatment increased the survival of C. neoformans-infected Galleria mellonella larvae and decreased the fungal burden of infected larvae. Mechanistic investigations revealed that HCQ might damage C. neoformans cell membranes, impact the structure of fungal cells, cause extracellular material leakage, and have a potent affinity for attaching to the C. neoformans genomic DNA. In conclusion, HCQ has potential clinical application in the treatment of cryptococcosis.

Indexed as

CryptococcosisCryptococcus neoformansAnimalsAntifungal AgentsHydroxychloroquineItraconazoleMicrobial Sensitivity TestsAntifungal AgentsHydroxychloroquineItraconazoleAntifungal activityCryptococcus neoformansHydroxychloroquineItraconazoleSynergism

Identifiers

PMID36753031
OpenAlexW4319457598

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.