Evidence map›Paper›PMID 42067847›Full record

ArticleBMC oral health2026

Salivary proteomics suggests persistent inflammatory signatures after clinical healing in recurrent aphthous stomatitis: a hypothesis-generating case-control study.

Paola Andrea Camargo-Ayala, Camila Paz Muñoz-Grez, Paulo Victor Mendes Peñafort, Pablo Agustin Vargas, Alan Roger Santos-Silva, Jessica Zúñiga-Hernández, Juliana Nunes Botelho, Jenaro Garcia-Huidobro, Nathalia B Dias, Fabiane M Nachtigall and 4 more

Abstract read
In one paragraph

Article in BMC oral health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

14 authors.

Paola Andrea Camargo-AyalaOral and Maxillofacial Histopathology Laboratory, Department of Stomatology, Faculty of Dentistry, Universidad de Talca, Talca, Chile.ORCID 0000-0002-5066-8370
Camila Paz Muñoz-GrezMolecular and Translational Immunology Laboratory, Department of Clinical Biochemistry and Immunology, Pharmacy Faculty, Universidad de Concepción, Concepción, Chile.ORCID 0000-0003-3058-4273
Paulo Victor Mendes PeñafortDepartment of Oral Diagnosis, Piracicaba Dental School, Universidade Estadual de Campinas, Piracicaba, Brazil.ORCID 0000-0002-7032-5762
Pablo Agustin VargasDepartment of Oral Diagnosis, Piracicaba Dental School, Universidade Estadual de Campinas, Piracicaba, Brazil.ORCID 0000-0003-1840-4911
Alan Roger Santos-SilvaDepartment of Oral Diagnosis, Piracicaba Dental School, Universidade Estadual de Campinas, Piracicaba, Brazil.ORCID 0000-0003-2040-6617
Jessica Zúñiga-HernándezDepartment of Basic Biomedical Sciences, Faculty of Health Sciences, Universidad de Talca, Talca, Chile.ORCID 0000-0003-2930-991X
Juliana Nunes BotelhoDepartment of Pediatric Stomatology, Faculty of Dentistry, Universidad de Talca, Talca, Chile.ORCID 0000-0002-1917-3812
Jenaro Garcia-HuidobroMedical Research Center, Faculty of Medicine, Universidad de Talca, Talca, Chile.ORCID 0000-0001-5599-6800
Nathalia B DiasFacultad de Ingeniería, Instituto de Ciencias Aplicadas, Centro de Investigación e Innovación, Universidad Autónoma de Chile, Huechuraba, Chile.ORCID 0000-0002-5902-634X
Fabiane M NachtigallInstituto de Ciencias Aplicadas, Universidad Autónoma de Chile, Talca, Chile.ORCID 0000-0002-3733-1319
Leonardo S SantosInstituto de Química de Recursos Naturales, Universidad de Talca, Talca, Chile.ORCID 0000-0002-1697-4200
Walter L SiqueiraCollege of Dentistry, University of Saskatchewan, Saskatoon, SK, Canada.ORCID 0000-0003-1921-3658
Estefanía Nova-LampertiMolecular and Translational Immunology Laboratory, Department of Clinical Biochemistry and Immunology, Pharmacy Faculty, Universidad de Concepción, Concepción, Chile.ORCID 0000-0002-7673-0013
César RiveraOral and Maxillofacial Histopathology Laboratory, Department of Stomatology, Faculty of Dentistry, Universidad de Talca, Talca, Chile. cerivera@utalca.cl.ORCID 0000-0002-5491-4233

Funding

Agencia Nacional de Investigación y Desarrollo FONDECYT Iniciación #11180170Agencia Nacional de Investigación y Desarrollo FONDECYT Iniciación #11190607Agencia Nacional de Investigación y Desarrollo FONDECYT Iniciación #11200258Agencia Nacional de Investigación y Desarrollo FONDECYT Regular #1211480Agencia Nacional de Investigación y Desarrollo PhD scholarship #21220448Facultad de Odontología de la Universidad de Talca Fondo de Desarrollo Científico Odontológico (FONDECO-FOUTALCA) #2023-1Red Estatal de Odontología Concurso de Proyectos de Investigación de Alto Nivel en Odontología #REO19-012
6 · The paper itself

Abstract

backgroundRecurrent aphthous stomatitis is a common inflammatory condition of the oral mucosa characterized by painful ulcers that heal spontaneously but recur unpredictably. Although lesions resolve clinically, the biological processes occurring during remission remain poorly understood. This exploratory study investigated whether salivary molecular profiles persist after clinical healing and may be associated with the recurrent nature of the disease.

methodsIn this hypothesis-generating case-control study, saliva samples were collected from patients with recurrent aphthous stomatitis during ulcerative and remission stages and from healthy controls. The salivary pellet was analyzed using discovery-based mass spectrometry proteomics. Complement components and dipeptidyl peptidase-4 (DPP4) were evaluated using immunological assays. Microbial identification was performed using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and quantitative polymerase chain reaction. The functional interaction between bacteria and oral keratinocytes was explored in vitro using a high-dose infection model to probe epithelial responsiveness.

resultsProteomic analysis identified stage-dependent molecular differences across the clinical course of recurrent aphthous stomatitis. Complement-related proteins and Mammaglobin-B (SCGB2A1) were found to be enriched during remission compared with healthy controls, suggesting persistent molecular signatures of epithelial and immune activity after clinical healing. Microbial profiling revealed enrichment of Streptococcus pneumoniae and Clostridium species in disease stages. In a controlled experimental setting, exposure of oral keratinocytes to Streptococcus pneumoniae was associated with increased DPP4 expression and activation of pathways linked to epithelial stress and immune signaling. Collectively, these exploratory findings suggest that remission is characterized by molecular features distinct from the healthy state.

conclusionsThis exploratory proteomic study suggests that persistent molecular features associated with inflammation and epithelial stress can be detected in saliva after clinical healing in recurrent aphthous stomatitis. Complement-related protein enrichment, epithelial stress markers, and microbial associations were observed during remission, pointing to incomplete molecular recovery of the oral mucosa. While causality cannot be inferred, these hypothesis-generating findings offer a basis for future mechanistic studies and suggest that salivary molecular features warrant investigation as potential candidates for monitoring disease activity.

Indexed as

ProteomicsSalivaStomatitis, AphthousAdultCase-Control StudiesFemaleHumansInflammationMaleMiddle AgedRecurrenceSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationWound HealingAphthous stomatitisComplement systemDipeptidyl Peptidase 4Mammaglobin-BStreptococcus pneumoniae

Identifiers

PMID42067847
PMCPMC13251032

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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.