A Suppression of Cellular Immunity in Patients with Multiple Sclerosis (original) (raw)
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Infection and immunity, 1974
The occurrence of a local production in the central nervous system (CNS) of antibodies against different selected viruses was analyzed by comparison of titers in serum and cerebrospinal fluid samples from groups of 50 patients with multiple sclerosis from Finland, Norway, and Sweden. Measles antibodies were determined in hemagglutination inhibition, hemolysis inhibition, and nucleocapsid complement fixation tests; mumps, parainfluenza virus type 1, and rubella virus antibodies were determined in hemagglutination inhibition tests; and herpes simplex virus type 1 antibodies were determined in passive hemagglutination tests. For reference purposes tests were also made for adenovirus antibodies in penton hemagglutination enhancement tests and poliovirus antibodies in neutralization enhancement tests. Among the 150 multiple sclerosis patients, a local production of antibodies against measles virus was found in the CNS in 57%, against rubella virus in 19%, mumps virus in 15%, herpes simpl...
Scandinavian journal of immunology, 1978
An imprint electroimmunofixation (IEIF) technique was used to study measles, rubella, mumps and herpes simplex virus antibodies in serum and concentrated cerebrospinal fluid (CSF) from ten patients with multiple sclerosis (MS). Electrophoretically restricted virus-specific antibodies were detected in sera or CSF from nine of the ten patients. Comparison of the antibody patterns in matching serum and CSF samples indicated that electrophoretically restricted populations of antibody against one or more of the four viruses were produced locally in the central nervous system of nine patients. No association between the locally produced antibody populations the oligoclonal IgG of the CSF could be demonstrated. The virus-specific antibodies studied thus seem to constitute only a minor fraction of the total IgG of the CSF from MS patients.
Journal of Neuroimmunology, 1987
Thirty consecutive isoelectric point (pI)-discrete IgG fractions were isolated from multiple sclerosis (MS) cerebrospinal fluid (CSF) and used to immune precipitate measles virus (MV) polypeptides. Most basic fractions were enriched in activity against nucleocapsid protein (NP), and to a lesser extent against hemagglutinin (H) protein; intermediate fractions were enriched in activity against H and fusion (F) proteins; and more anodic pl fractions were almost exclusively enriched in activity against the large (L) protein of MV. In MS there are marked differences between CSF and autologous serum in regard to antibody activity to MV. In contrast, there were similar profiles of antibody response to MV proteins in SSPE CSF and serum.
Multiple sclerosis. Current etiological concepts
California Medicine, 1972
An animal model for acute multiple sclerosis (MSa) is experimental allergic encephalomyelitis (EAE). EAE is produced by intradermal injection of a protein component of central nervous system (CNS) myelin. Ultrastructural studies of EAE and of a peripheral nerve analog, experimental allergic neuritis (EAN), have revealed an orderly sequence of cellular events leading to the destruction and removal of myelin with sparing of axons (primary demyelination). Acute MS has not been studied electron microscopically, but the ultrastructural similarities between EAN and a case of acute Landry-Guillain-Barre syndrome, a primary demyelinating disease of the peripheral nervous system, suggest that a similar sequence of events might be found in acute MS. While the pathological findings support a cellmediated or delayed hypersensitivity response, there is also evidence for the pathogenetic role of circulating antibodies. Among such evidence is included the finding that sera from animals with EAE and humans with acute MS rapidly produce a reversible block of complex (polysynaptic) electrical activity when applied to CNS tissue cultures, which suggests a possible mechanism for transient symptoms in Ms. Epidemiological and other studies link MS with a viral cause, although no direct evidence that MS is caused by a virus exists. Viral and immunological mechanisrs are not mutually exclusive in considering pathogenetic possibilities for MS, for it can be postulated that a viral infection of the central nervous system acts as a triggering agent for a series of immune responses, including production of a bioelectric blocking antibody and demyelination mediated by sensitized cells, the combination of which ultimately produces the total clinical picture of MS.
Journal of Neuroimmunology, 1987
Immune complexes isolated from sera of patients with multiple sclerosis (MS) were analyzed for their antigenic content. Immune complexes precipitated with polyethylene glycol were inoculated into rabbits. The antisera raised were shown to react to MS and normal brain antigens by crossed immunoelectrophoresis, ELISA and nitrocellulose transfer. Additionally, these antisera reacted by co-precipitation with the measles nucleocapsid antigen. As persistent viral infection has not been shown to occur in MS, these studies support the possibility that brain antigens within the immune complex share antigenic determinants with a specific viral antigen seen earlier in life by the host.
Clinical and experimental immunology, 1983
Paired samples of serum and concentrated cerebrospinal fluid (CSF) from 20 multiple sclerosis (MS) patients and 10 controls with no central nervous system disease were electrofocused and analysed for IgG and measles and varicella zoster virus IgG antibodies by imprint immunofixation using IgG subclass specific monoclonal antibodies. All but one of the MS patients had intrathecally synthesized bands of oligoclonal IgG in the CSF. In fifteen of the MS patients the oligoclonal IgG bands were restricted to the IgG1 subclass. Intrathecal synthesis of both IgG1 and IgG3 bands was observed in three, and of IgG1, IgG2 and IgG3 bands in one patient. Fourteen and 15 of the MS patients displayed intrathecal synthesis of oligoclonal varicella zoster and measles virus specific IgG1 antibodies, respectively, and no serum or CSF sample contained antibodies of other IgG subclasses to these viruses. Low levels of polyclonal IgG1 antibodies to measles or varicella zoster viruses were detected in seru...