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J Neuroimmunol ; 318: 87-96, 2018 05 15.
Artigo em Inglês | MEDLINE | ID: mdl-29526407

RESUMO

Experimental autoimmune encephalomyelitis (EAE) mice were administered with murine anti-CD52 antibody to investigate its therapeutic effect and whether the treatment modulates IL-33 and ST2 expression. EAE severity and central nervous system (CNS) inflammation were reduced following the treatment, which was accompanied by peripheral T and B lymphocyte depletion and reduced production of various cytokines including IL-33, while sST2 was increased. In spinal cords of EAE mice, while the number of IL-33+ cells remained unchanged, the extracellular level of IL-33 protein was significantly reduced in anti-CD52 antibody treated mice compared with controls. Furthermore the number of ST2+ cells in the spinal cord of treated EAE mice was downregulated due to decreased inflammation and immune cell infiltration in the CNS. These results suggest that treatment with anti-CD52 antibody differentially alters expression of IL-33 and ST2, both systemically and within the CNS, which may indicate IL-33/ST2 axis is involved in the action of the antibody in inhibiting EAE.


Assuntos
Alemtuzumab/farmacologia , Antineoplásicos Imunológicos/farmacologia , Antígeno CD52/antagonistas & inibidores , Encefalomielite Autoimune Experimental/imunologia , Proteína 1 Semelhante a Receptor de Interleucina-1/imunologia , Interleucina-33/imunologia , Animais , Encefalomielite Autoimune Experimental/patologia , Feminino , Proteína 1 Semelhante a Receptor de Interleucina-1/efeitos dos fármacos , Interleucina-33/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos C57BL , Medula Espinal/imunologia , Medula Espinal/patologia
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