Literature DB >> 20563772

[The macrophage electrophoretic mobility LAD test - a diagnostic method for multiple sclerosis.].

H Meyer-Rienecker1, H L Jenssen, H Köhler, J K Günther.   

Abstract

With the MEM test (Field) one can establish a cellular immune reaction because the sensitized lymphocytes release the macrophage slowing factor (MSF) upon interaction with the appropriate antigen. A macrophage migration inhibition was detected in some neurological diseases with destruction of the parenchyma. The modification MEM-LAD (linoleic acid depression) test made further differentiation possible in the 146 neurological patients and normals. The reduction of macrophage mobility inhibition was 94.7+/-4.7% in multiple sclerosis (MS) cases as compared with that of normals of 55.1+/-3.7% and of other neurological diseases of 47.8+/-7.1%. There were no significant differences due to the course and duration of the disease or to immunosuppressive therapy. The pathogenically important results in relatives of MS patients with values between the MS and normal group (78.5+/-0.7%) in mothers suggested a familial (genetic) disposition. The same value was found in a monozygotic twin of an MS patient. The results in the children studied showed that besides the endogenic metabolic component the aetiopathogenically important exogenic factors can operate early in life. In correlation with the principle of the MEM-LAD test the suppressive action of linoleic acid can result in a further therapeutic concept.

Entities:  

Year:  1976        PMID: 20563772     DOI: 10.1007/BF00313233

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  36 in total

1.  Electrophoretic mobility test for lymphocyte sensitization using tanned sheep erythrocytes.

Authors:  H L Jenssen; B K Shenton
Journal:  Acta Biol Med Ger       Date:  1975

2.  [Use of the macrophage-electrophoretic-mobility test in the diagnosis of tumours of the central nervous system (author's transl)].

Authors:  H Meyer-Rienecker; H L Jenssen; H Köhler; J K Günther
Journal:  Dtsch Med Wochenschr       Date:  1975-03-14       Impact factor: 0.628

3.  Studies on the mechanism of corticosteroid-induced lymphocytolysis.

Authors:  R W Turnell; L H Clarke; A F Burton
Journal:  Cancer Res       Date:  1973-02       Impact factor: 12.701

Review 4.  Fatty acid metabolism in multiple sclerosis.

Authors:  R H Thompson
Journal:  Biochem Soc Symp       Date:  1972

5.  [Aspects of the diagnostic criterions and the classification of the multiple sclerosis (author's transl)].

Authors:  H J Meyer-Rienecker; R M Olischer
Journal:  Fortschr Neurol Psychiatr Grenzgeb       Date:  1974-08

6.  Letter: Diagnostic test for multiple sclerosis.

Authors:  J B Foster; J Mertin; A M Thomson
Journal:  Br Med J       Date:  1974-03-09

7.  Sensitization of blood lymphocytes to possible antigens in neurological disease.

Authors:  E A Caspary; E J Field
Journal:  Eur Neurol       Date:  1970       Impact factor: 1.710

8.  Genetical factors in the aetiology of multiple sclerosis.

Authors:  R J Berry
Journal:  Acta Neurol Scand       Date:  1969       Impact factor: 3.209

9.  Histocompatibility determinants in multiple sclerosis.

Authors:  C Jersild; B Dupont; T Fog; P J Platz; A Svejgaard
Journal:  Transplant Rev       Date:  1975

10.  Letter: Immunosuppression by linoleic acid.

Authors:  D Hughes; E A Caspary; H M Wisniewski
Journal:  Lancet       Date:  1975-09-13       Impact factor: 79.321

View more
  3 in total

1.  [Demonstration of a factor in cerebrospinal fluid with inhibitory activity for electrophoretic cell mobility in multiple sclerosis (author's transl)].

Authors:  H L Jenssen; H J Meyer-Rienecker; H Werner
Journal:  J Neurol       Date:  1976-11-26       Impact factor: 4.849

2.  Erythrocyte-UFA (Eufa) mobility test for multiple sclerosis: implications for pathogenesis and handling of the disease.

Authors:  E J Field; G Joyce; B M Smith
Journal:  J Neurol       Date:  1977-01-13       Impact factor: 4.849

3.  Anomalous lymphocyte-antigen reaction in relatives of multiple sclerosis patients. A study of a possible genetic factor in the disease.

Authors:  E J Field; H J Meyer-Rienecker; B K Shenton; H L Jenssen; H Köhler
Journal:  J Neurol       Date:  1977-09-12       Impact factor: 4.849

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.