Physical state of the neuroantigen in adjuvant emulsions determines encephalitogenic status in the BALB/c mouse

• Published in: Journal of immunological methods 1996-03, Vol.190 (1), p.133-141
• Main Authors: Määttä, Jorma A., Erälinna, Juha-Pekka, Röyttä, Matias, Salmi, Aimo A., Hinkkanen, Ari E.
• Format: Article
• Language: English
• Subjects: Adjuvant ultrastructure; Adjuvants, Immunologic - chemistry; Animals; BALB/c mouse; Biological and medical sciences; Emulsions; Encephalomyelitis, Autoimmune, Experimental - immunology; Experimental allergic encephalomyelitis resistance; Experimental and animal immunopathology. Animal models; Female; Immunopathology; Medical sciences; Mice; Mice, Inbred BALB C - immunology; Microscopy, Electron; Nerve Tissue Proteins - chemistry; Nerve Tissue Proteins - immunology; Sonication; Spinal Cord - immunology
• ISSN: 0022-1759; 1872-7905
• DOI: 10.1016/0022-1759(95)00273-1

A novel form of adjuvant-neuroantigen formulation was established which was highly encephalitogenic in previously resistant BALB/c mice. The antigen formulation contained mouse whole spinal cord homogenate (MSCH), mycobacteria, and mineral oil, identically to the conventional preparation, but emulsification was completed by sonication instead of extrusion. Sonication of MSCH alone did not render a conventionally prepared emulsion encephalitogenic. The novel adjuvant formulation showed reduced water-oil droplet size, and the neuroantigen was located on the surface of the droplets as well as in the intermicellar space, while in the extruded formulation the material was buried in the droplet interior. Mice inoculated with the sonicated emulsion showed strong brain and spinal cord infiltration of lymphoid cells. The sonicated emulsion was highly encephalitogenic in all six BALB/c substrains tested. The results suggest that availability of the neuroantigen is of critical importance for the development of clinical EAE in the BALB/c mouse.