# Role of Extracellular Vesicles in Crohn’s Patients on Adalimumab Who Received COVID-19 Vaccination

**Authors:** Maria De Luca, Biagia Musio, Francesco Balestra, Valentina Arrè, Roberto Negro, Nicoletta Depalo, Federica Rizzi, Rita Mastrogiacomo, Giorgia Panzetta, Rossella Donghia, Pasqua Letizia Pesole, Sergio Coletta, Emanuele Piccinno, Viviana Scalavino, Grazia Serino, Fatima Maqoud, Francesco Russo, Antonella Orlando, Stefano Todisco, Pietro Mastrorilli, Maria Lucia Curri, Vito Gallo, Gianluigi Giannelli, Maria Principia Scavo

PMC · DOI: 10.3390/ijms25168853 · 2024-08-14

## TL;DR

This study explores how the SARS-CoV-2 vaccine might affect Crohn’s disease treatment and worsen symptoms through extracellular vesicles.

## Contribution

The study investigates the role of extracellular vesicles in vaccine-related disease exacerbation in Crohn’s patients.

## Key findings

- Extracellular vesicles may transport the SARS-CoV-2 Spike protein and influence intestinal permeability.
- Modulated expression of proteins like AQP8 and tight junctions is linked to disease flares in Crohn’s patients.
- Vaccine exposure may interfere with the effectiveness of Adalimumab in some Crohn’s patients.

## Abstract

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.

## Linked entities

- **Proteins:** TJP1 (tight junction protein 1), CLDN7 (claudin 7), CLDN2 (claudin 2), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3)
- **Diseases:** Crohn’s disease (MONDO:0005011), inflammatory bowel disease (MONDO:0005265)

## Full-text entities

- **Genes:** TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, CLDN2 (claudin 2) [NCBI Gene 9075] {aka OAZON, claudin-2}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, AQP8 (aquaporin 8) [NCBI Gene 343] {aka AQP-8}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}
- **Diseases:** CD (MESH:D003424), IBD (MESH:D015212), COVID-19 (MESH:D000086382)
- **Chemicals:** Adalimumab (MESH:D000068879)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11355036/full.md

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Source: https://tomesphere.com/paper/PMC11355036