Role of Extracellular Vesicles in Crohn's Patients on Adalimumab Who Received COVID-19 Vaccination.
Maria De LucaBiagia MusioFrancesco BalestraValentina ArrèRoberto NegroNicoletta DepaloFederica RizziRita MastrogiacomoGiorgia PanzettaRossella DonghiaPasqua Letizia PesoleSergio ColettaEmanuele PiccinnoViviana ScalavinoGrazia SerinoFatima MaqoudFrancesco RussoAntonella OrlandoStefano TodiscoPietro MastrorilliMaria Lucia CurriVito GalloGianluigi GiannelliMaria Principia ScavoPublished in: International journal of molecular sciences (2024)
Crohn's disease (CD) is a type of inflammatory bowel disease (IBD) affecting the gastrointestinal tract that can also cause extra-intestinal complications. Following exposure to the mRNA vaccine BNT162b2 (Pfizer-BioNTech) encoding the SARS-CoV-2 Spike (S) protein, some patients experienced a lack of response to the biological drug Adalimumab and a recrudescence of the disease. In CD patients in progression, resistant to considered biological therapy, an abnormal increase in intestinal permeability was observed, more often with a modulated expression of different proteins such as Aquaporin 8 (AQP8) and in tight junctions (e.g., ZO-1, Claudin1, Claudin2, Occludin), especially during disease flares. The aim of this study is to investigate how the SARS-CoV-2 vaccine could interfere with IBD therapy and contribute to disease exacerbation. We investigated the role of the SARS-CoV-2 Spike protein, transported by extracellular vesicles (EVs), and the impact of various EVs components, namely, exosomes (EXOs) and microvesicles (MVs), in modulating the expression of molecules involved in the exacerbation of CD, which remains unknown.
Keyphrases
- sars cov
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- poor prognosis
- chronic obstructive pulmonary disease
- mesenchymal stem cells
- rheumatoid arthritis
- respiratory syndrome coronavirus
- peritoneal dialysis
- emergency department
- intensive care unit
- patient reported outcomes
- endothelial cells
- risk factors
- juvenile idiopathic arthritis
- long non coding rna
- high resolution
- amino acid
- patient reported
- cell therapy
- replacement therapy
- protein protein
- atomic force microscopy