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ACS Appl Bio Mater ; 4(1): 387-391, 2021 01 18.
Article in English | MEDLINE | ID: mdl-35014289

ABSTRACT

Multiple sclerosis is complex and heterogeneous. Better tools are needed to be able to monitor this disease among individuals, but blood-based biomarkers are often too rare to profile. In this work, we developed antigen-specific biomaterials to replicate the central nervous system niche where multiple sclerosis biomarkers are amplified. We incorporated mouse brain homogenate into a microporous gelatin methacrylate network. Homogenate-containing biomaterials differentially stimulated cells and led to the marked amplification of disease-relevant, antigen-specific B cells. These results demonstrate that biomaterials containing primary tissue homogenate retain antigen specificity and may be a useful tool for decoding human autoimmunity.


Subject(s)
Antigens/metabolism , Biocompatible Materials/chemistry , Brain/metabolism , Animals , Antigens/chemistry , Autoimmunity , B-Lymphocytes/cytology , B-Lymphocytes/immunology , B-Lymphocytes/metabolism , B7-2 Antigen/metabolism , Encephalomyelitis, Autoimmune, Experimental/metabolism , Encephalomyelitis, Autoimmune, Experimental/pathology , Gelatin/chemistry , Mice , Myelin Proteolipid Protein/chemistry , Myelin Proteolipid Protein/immunology , Myelin Proteolipid Protein/metabolism , Peptide Fragments/chemistry , Peptide Fragments/immunology , Peptide Fragments/metabolism , Spleen/cytology , Spleen/metabolism
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