Premium
Autologous lymphocyte proliferation in multiple sclerosis and the effect of intravenous ACTH
Author(s) -
Birnbaum Gray,
Kotilinek Linda
Publication year - 1981
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.410090505
Subject(s) - multiple sclerosis , lymphocyte , medicine , immunology , mixed lymphocyte reaction , lymphocyte activation , immune system , t cell
The proliferative reponse of peripheral blood T cells to autologous non–T cells, a reaction called the autologous mixed lympbocyte reaction (MLR), was significantly increased in 17 patients with active multiple sclerosis (MS) compared to age‐ and sex‐matched individuals with other neurological diseases (OND). Following a 10‐day course of intravenous adrenocorticotropic hormone (ACTH) therapy the value were reduced to control levels. No differences were noted between MS patients and controls in their response to alloantigens. The increased autologous MLR in patients with active MS appeared to result from an increased stimulatory capacity of non–T cells rather than from an intrinsically greater T cell proliferative potential. ACTH appeared to induce a change in the populations of circulating non–T cells such that these cells had a decreased stimulatory capacity in both autologous and allogeneic MLR. The disease in stimulatory MLR was, however, significantly greater than the decrease in allogeneic stimulatory capacity, suggesting a functional decrease of specific non–T cellenriched subpopulations. No significant changes in the numbers of myeloperoxidase‐positive (MP+) cells were noted in the blood of MS patients before and after ACTH therapy. Since the autologous MLR results in generation of cells that regulate immune responsiveness, the changes noted provide additional evidence for abnormal immune regulation in MS.