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Gene expression profile of chronic oral graft-versus-host disease.
Pinto, Giselle Rocha; Sarmento, Viviane Almeida; de Carvalho-Filho, Paulo Cirino; Fortuna, Vitor Antonio; Costa, Ryan Dos Santos; Conceição, Rogério Reis; Trindade, Soraya Castro.
Afiliación
  • Pinto GR; Department of Dentistry, Federal University of Bahia (UFBA), Salvador, Bahia, Brazil.
  • Sarmento VA; Department of Dentistry, Federal University of Bahia (UFBA), Salvador, Bahia, Brazil.
  • de Carvalho-Filho PC; Department of Dentistry, School of Medicine and Public Health, Salvador, Bahia, Brazil.
  • Fortuna VA; Health Science Institute, Federal University of Bahia (UFBA), Salvador, Bahia, Brazil.
  • Costa RDS; Health Science Institute, Federal University of Bahia (UFBA), Salvador, Bahia, Brazil.
  • Conceição RR; Health Science Institute, Federal University of Bahia (UFBA), Salvador, Bahia, Brazil.
  • Trindade SC; Health Science Institute, Federal University of Bahia (UFBA), Salvador, Bahia, Brazil.
PLoS One ; 17(4): e0267325, 2022.
Article en En | MEDLINE | ID: mdl-35486633
ABSTRACT
Among the complications observed after allogeneic hematopoietic stem cell transplantation, graft-versus-host disease (GVHD) is the primary cause of post-transplant mortality. The oral cavity is the second most affected organ target in chronic GVHD. Tissue damage results from the upregulation of inflammatory mediators, which play a critical role in the immunopathogenesis of the disease. This case series observational study aims to evaluate the participation of cytokines, chemokines, transcription factors, and heat shock proteins in the pathogenesis of oral GVHD (oGVHD), describing the mRNA expression of 28 genes selected. Peripheral blood mononuclear cells were isolated from six participants with oGVHD and two without GVHD, and relative expression of transcripts with established roles as inflammatory mediators was determined in triplicate using the human RT2 Profiler™ PCR Array. The gene expression levels in the group with oGVHD were mainly up-regulated compared to those without GVHD. PBMC from oGVDH expressed consistently higher IFN-γ, TNF, IL-1ß, CCL2, HSP60 (HSPD1) and HSP90 (HSP90B1). These results can provide a basis for developing new molecular diagnostics and targets therapies for the clinical management of oGVHD.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped Tipo de estudio: Etiology_studies / Observational_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2022 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped Tipo de estudio: Etiology_studies / Observational_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2022 Tipo del documento: Article País de afiliación: Brasil