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<dc:title xml:lang="fr">Rôle du "B-cell activating factor" (BAFF) et des lymphocites B dans la fibrose pulmonaire et cutanée dans la sclérodermie systémique</dc:title>
<dcterms:alternative xml:lang="en">Role of "B-cell activating factor" (BAFF) and B-cells in lung and skin fibrosis in systemic sclerosis</dcterms:alternative>
<dc:subject xml:lang="fr">Sclérodermie</dc:subject>
<dc:subject xml:lang="fr">Fibrose</dc:subject>
<dc:subject xml:lang="fr">BAFF</dc:subject>
<dc:subject xml:lang="fr">Poumon</dc:subject>
<dc:subject xml:lang="fr">Lymphocyte B</dc:subject>
<dc:subject xml:lang="fr">Immunologie</dc:subject>
<dc:subject xml:lang="fr">Autoimmunité</dc:subject>
<dc:subject xml:lang="fr">MicroARN</dc:subject>
<dc:subject xml:lang="en">Systemic sclerosis</dc:subject>
<dc:subject xml:lang="en">Fibrosis</dc:subject>
<dc:subject xml:lang="en">BAFF</dc:subject>
<dc:subject xml:lang="en">Lung</dc:subject>
<dc:subject xml:lang="en">B-cell</dc:subject>
<dc:subject xml:lang="en">Immunology</dc:subject>
<dc:subject xml:lang="en">Auto-immunity</dc:subject>
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<tef:elementdEntree autoriteExterne="029791197" autoriteSource="Sudoc">Lymphocytes B</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">La sclérodermie systémique (ScS) est une maladie autoimmune rare qui se caractérise par une fibrose cutanée et parfois pulmonaire. Nous avons tout d’abord évalué le rôle de BAFF, une cytokine impliquée dans le développement des lymphocytes B (LB), dans la fibrose pulmonaire induite par la bléomycine chez la souris. Nous avons démontré que BAFF était augmenté en réponse à la bléomycine et que les souris BAFF-/- ou traitées par le BAFF-R-Ig sont protégées de la fibrose pulmonaire. Ensuite, nous avons évalué si les LB et BAFF pouvaient moduler la production de collagène par des fibroblastes de peau isolés de patients atteints de ScS. Nous avons démontré que les LB augmentent la production de collagène et de cytokines impliquées dans la fibrose cutanée et l’ajout de BAFF augmente cet effet des LB sur les fibroblastes. Enfin, nous avons étudié la régulation de l’expression de BAFF par les microARNs. Nos résultats montrent que les miR-30a*, d* et e* ciblent directement l’ARNm de BAFF.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Systemic sclerosis (SSc) is a rare autoimmune disease characterized by skin fibrosis and occasionally pulmonary fibrosis. We first assessed the role of BAFF, a cytokine involved in B cell maturation, in bleomycin-induced pulmonary fibrosis in mice. We showed that BAFF was increased in response to bleomycin and that BAFF-/- mice or BAFF-R-Igtreated mice are protected from pulmonary fibrosis. Then, we assessed whether B cells and BAFF could regulate collagen production by skin fibroblasts isolated from SSc patients. We demonstrated that B cells increase collagen production and cytokines involved in skin fibrosis. The addition of BAFF increases the effect of B cells on fibroblasts. Lastly, we studied the regulation of BAFF expression by microRNAs. Our results show that miR-30a*, d* and e* directly target the BAFF mRNA.</dcterms:abstract>
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