Evidence map›Paper›PMID 26748233›Full record

ArticleThe Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases

Antiretroviral drugs saquinavir and ritonavir reduce inhibitory concentration values of itraconazole against Histoplasma capsulatum strains in vitro.

Raimunda Sâmia Nogueira Brilhante, Érica Pacheco Caetano, Giovanna Barbosa Riello, Glaucia Morgana de Melo Guedes, Débora de Souza Collares Maia Castelo-Branco, Maria Auxiliadora Bezerra Fechine, Jonathas Sales de Oliveira, Zoilo Pires de Camargo, Jacó Ricarte Lima de Mesquita, André Jalles Monteiro and 3 more

Open access · goldAbstract read
In one paragraph

Article in The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  7. Aspartic peptidase ofJournal of enzyme inhibition and medicinal chemistry · 2020
    Article
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  10. Protease inhibitors and azolic antifungals in HIV patients with histoplasmosis: a clinical pharmacokinetics perspective.The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases
    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

13 authors at 3 institutions in 1 country.

Raimunda Sâmia Nogueira BrilhanteSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Postgraduate Program in Medical Sciences, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil. Electronic address: brilhante@ufc.br.
Érica Pacheco CaetanoSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Giovanna Barbosa RielloSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Glaucia Morgana de Melo GuedesSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Débora de Souza Collares Maia Castelo-BrancoSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Postgraduate Program in Medical Sciences, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Maria Auxiliadora Bezerra FechinePostgraduate Program in Medical Sciences, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Jonathas Sales de OliveiraSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Zoilo Pires de CamargoDepartment of Microbiology, Immunology and Parasitology, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.
Jacó Ricarte Lima de MesquitaHospital São José, Fortaleza, CE, Brazil.
André Jalles MonteiroDepartment of Statistics and Applied Mathematics, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Rossana de Aguiar CordeiroSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Postgraduate Program in Medical Sciences, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Marcos Fábio Gadelha RochaSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Postgraduate Program in Veterinary Sciences, Universidade Estadual do Ceará (UECE), Fortaleza, CE, Brazil.
José Júlio Costa SidrimSpecialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Postgraduate Program in Medical Sciences, Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil.
Universidade Federal do Ceará · BRHospital Geral de Fortaleza · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that some drugs that are not routinely used to treat fungal infections have antifungal activity, such as protease inhibitor antiretroviral drugs. This study investigated the in vitro susceptibility of Histoplasma capsulatum var. capsulatum to saquinavir and ritonavir, and its combination with the antifungal itraconazole. The susceptibility assay was performed according to Clinical and Laboratory Standards Institute guidelines. All strains were inhibited by the protease inhibitor antiretroviral drugs. Saquinavir showed minimum inhibitory concentrations ranging from 0.125 to 1μgmL(-1) for both phases, and ritonavir presented minimum inhibitory concentrations ranging from 0.0312 to 4μgmL(-1)and from 0.0625 to 1μgmL(-1) for filamentous and yeast phase, respectively. Concerning the antifungal itraconazole, the minimum inhibitory concentration values ranged from 0.0019 to 0.125μgmL(-1) and from 0.0039 to 0.0312μgmL(-1) for the filamentous and yeast phase, respectively. The combination of saquinavir or ritonavir with itraconazole was synergistic against H. capsulatum, with a significant reduction in the minimum inhibitory concentrations of both drugs against the strains (p<0.05). These data show an important in vitro synergy between protease inhibitors and itraconazole against the fungus H. capsulatum.

Indexed as

Antifungal AgentsDrug SynergismHistoplasmaHIV Protease InhibitorsItraconazoleMicrobial Sensitivity TestsRitonavirSaquinavirAntifungal AgentsHIV Protease InhibitorsItraconazoleRitonavirSaquinavirHistoplasma capsulatumItraconazoleRitonavirSaquinavir

Identifiers

PMID26748233
PMCPMC9427650
OpenAlexW2310121151

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.