Evidence map›Paper›PMID 40183878›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2025

Comparative analysis of two immunosuppression protocols for vulvovaginal candidiasis induction in Wistar rats.

Félix Roman Munieweg, Thais Pinheiro Ribeiro, Jean Ramos Boldori, Nathane Rosa Rodrigues, Nicolle Lauay Carvalho Sanches Hoesel, Ana Luiza Reetz Polleto, Cheila Denise Ottonelli Stopiglia, Sandra Elisa Haas, Cristiane Casagrande Denardin

Abstract readComparative Study
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 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

9 authors.

Félix Roman MuniewegResearch Group GBTOXBIO, Federal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Thais Pinheiro RibeiroResearch Group GBTOXBIO, Federal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Jean Ramos BoldoriResearch Group GBTOXBIO, Federal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Nathane Rosa RodriguesResearch Group GBTOXBIO, Federal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Nicolle Lauay Carvalho Sanches HoeselResearch Group GBTOXBIO, Federal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Ana Luiza Reetz PolletoFederal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Cheila Denise Ottonelli StopigliaFederal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Sandra Elisa HaasFederal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil.
Cristiane Casagrande DenardinResearch Group GBTOXBIO, Federal University of Pampa, Campus Uruguaiana, BR 472, Km 592, Uruguaiana, RS, Brazil. cristianedenardin@unipampa.edu.br.ORCID http://orcid.org/0000-0002-0912-1357

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico CNPq 400869/2019-5Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Universidade Federal do Pampa Inovapampa 2021
6 · The paper itself

Abstract

Vulvovaginal candidiasis (VVC) is a prevalent public health problem worldwide. The frequent recurrences and treatment failures associated with existing therapies highlight the urgent need to explore new potential treatments. However, protocols for inducing vulvovaginal candidiasis in rodents are limited and lack standardization. Most approaches rely on immunosuppression to mimic human conditions. This study aimed to compare two immunosuppression protocols in a vulvovaginal candidiasis infection model using female Wistar rats. The animals were subjected to two immunosuppression: Chemical immunosuppression using cyclophosphamide (IMS) and a chronic unpredictable mild stress model (CUMS). Following the immunosuppression period, the rats were inoculated with C. albicans ATCC10231. After confirming the infection, the animals were treated with a vaginal cream containing clotrimazole (10 mg/g) or a vehicle for 7 days. During this period, behavioral parameters, food consumption, body weight, and vaginal microbial load were evaluated. At the end of treatment, the animals were euthanized, and blood, histological tissue, and microbiological parameters were analyzed. Animals subjected to the CUMS protocol exhibited significant behavioral changes, reduced food consumption, and impaired weight gain. They also displayed hematological and histological alterations, indicating severe immunosuppression and infection. Clotrimazole treatment failed to cure all animals in this group. In contrast, animals in the IMS protocol experienced milder immunosuppression, and clotrimazole treatment successfully cured all treated animals. The IMS method is more suitable for investigating primary vulvovaginal candidiasis infection compared to the CUMS method. The CUMS protocol induced more pronounced changes, such as weight loss and behavioral alterations, which may not accurately reflect primary VVC in humans. The IMS method, however, resulted in a vaginal infection with minimal systemic changes, more closely resembling the condition observed in women with primary VVC.

Indexed as

Candidiasis, VulvovaginalImmunosuppression TherapyImmunosuppressive AgentsAnimalsAntifungal AgentsCandida albicansClotrimazoleCyclophosphamideDisease Models, AnimalFemaleRatsRats, WistarVaginaAntifungal AgentsClotrimazoleCyclophosphamideImmunosuppressive AgentsCandida albicansChronic unpredictable mild stressCyclophosphamideFungal infectionImmunosuppressionVulvovaginal candidiasisWistar rats

Identifiers

PMID40183878
PMCPMC12095724

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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.