Evidence map›Paper›PMID 41169135›Full record

ReviewCurrent pharmaceutical design2026

Novel Targets and Nanotechnology Approaches in Treating Vulvovaginal Candidiasis: Insights into Host-Microbe Interactions and Immunotherapy.

Astha Lalwani, Sudhir Singh, Suparna Parua, Deepika Ahuja, Krishnendu Adhikary, Rajkumar Maiti, Koushik Bhattacharya, Sourajit Kumar Banerjee, Alak Kumar Syamal

Abstract readReview
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In one paragraph

Review in Current pharmaceutical design, 2026. 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.

Astha LalwaniDepartment of Obstetrics and Gynecology, Teerthanker Mahaveer Medical College and Research Centre, Teerthankar Mahaveer University, Moradabad, Uttar Pradesh, India.ORCID 0000-0002-5730-8554
Sudhir SinghDepartment of Microbiology, Teerthanker Mahaveer Medical College and Research Centre, Teerthankar Mahaveer University, Moradabad, Uttar Pradesh, India.ORCID 0009-0007-5090-4592
Suparna ParuaSchool of Paramedics and Allied Health Sciences, Centurion University of Technology and Management, Jatni, Khurda Road, Odisha, Bhubaneswar, India.ORCID 0009-0003-8798-1226
Deepika AhujaSchool of Paramedics and Allied Health Sciences, Centurion University of Technology and Management, Jatni, Khurda Road, Odisha, Bhubaneswar, India.
Krishnendu AdhikaryDepartment of Interdisciplinary Science, Centurion University of Technology and Management, Paralakhemundi, Odisha, Bhubaneswar, India.ORCID 0000-0002-9942-1491
Rajkumar MaitiDepartment of Physiology, Bankura Christian College, Bankura, West Bengal, India.ORCID 0000-0002-6714-408X
Koushik BhattacharyaSchool of Paramedics and Allied Health Sciences, Centurion University of Technology and Management, Jatni, Khurda Road, Odisha, Bhubaneswar, India.ORCID 0000-0003-0153-4357
Sourajit Kumar BanerjeeSchool of Paramedics and Allied Health Sciences, Centurion University of Technology and Management, Vizianagaram, Andhra Pradesh, Bhubaneswar, India.
Alak Kumar SyamalPost Graduate Department of Physiology, Hooghly Mohsin College, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this article is to study recent developments in the management of vulvovaginal candidiasis (VVC) with emphasis on overcoming antifungal resistance and recurrent VVC by examining hostmicrobe interaction, new molecular targets, immunotherapeutic interventions, and nanotechnology-based strategies. This review integrates recent VVC pathogenesis, immune response, and therapeutic development literature with a focus on immunomodulation, vaccine development, and nanotechnology interventions. Literature on immunotherapy and nanoparticle-based drug delivery systems was comprehensively reviewed. Immunotherapeutic concepts, such as cytokine modulation and vaccine therapy candidates, hold promise to substitute or supplement current antifungals. Nanoparticles exhibit efficacy in advancing drug solubility, reaching fungal cells, and minimizing unwanted effects. The synergy between nanotechnology and immunotherapy provides combined advantages over the multiple drawbacks of current therapies. Although novel methodologies have shown strong promise, aspects of safety, clinical relevance, and regulatory issues continue to remain key challenges. Nanotechnology-based host-targeted immunotherapy is most probably going to transform the scenario of VVC treatment, especially in drug-resistant cases. Additional research is needed to elucidate molecular host-fungal interaction mechanisms, validate vaccine efficacy in the clinic, and design standardized, reproducible nanotherapeutic platforms. Personalized regimens of treatment through immunological and microbiome profiling can enhance long-term outcomes in VVC treatment.

Indexed as

Antifungal AgentsCandidiasis, VulvovaginalHost-Pathogen InteractionsImmunotherapyNanotechnologyAnimalsFemaleHumansAntifungal AgentscandidiasisFungal infectionimmunotherapymolecular targetsnanotechnologyvaginal microbiome

Identifiers

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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.