Abstract
Suppressor cell activity (SCA) in patients with insulin-dependent diabetes mellitus (IDDM), has been found depressed at diagnosis and normal in the remission period. To investigate whether poor metabolic control as seen at diagnosis influences SCA, two groups of patients in poor glycaemic control were examined. Group 1 consisted of nine patients with IDDM of 27±4 months, with a mean glucosuria of 84±19 (s.e.m.) g/24 hr. Group 2 comprised eight patients with newly diagnosed IDDM, examined for the first time 4±1 days after diagnosis, when having a mean glucosuria of 43±14 g/24 hr. After 1 week of hospitalization with strict glycaemic control resulting in a massive reduction of the glucosuria (group 1 now showing 0±0 g/24 hr, group 2, 16±5 g/24 hr), the patients were re-examined. SCA was investigated for the third time after approximately 4 weeks (group 1) and after 5 months (group 2), when the patients were outpatients (glucosuria: group 1, 61±20 g/24 hr; group 2, 17±6 g/24 hr). The suppressive effect of lymphocytes was investigated after incubation with concanavalin A followed by inactivation. Suppression was measured as the ability of the lymphocytes to inhibit 3H-thymidine incorporation in concanavalin A-stimulated normal donor lymphocytes. There were no significant differences in SCA between the first (group 1,25±7; group 2, 22±11) and the second (group 1, 22±8; group 2, 15±5) examination. At the third examination, group 1 patients displayed 35±5, and group 2 patients, now being in the remission period, 44±4. Only the third value of group 2 patients was significantly higher than the second value (P<0·01). SCA of healthy controls were 35±3. It is concluded that short-term effects on SCA of improvement of the glycaemic control are unlikely, at least in patients without severe ketoacidosis. On the other hand, late effects on SCA of good metabolic control, after weeks or months, could not be excluded.
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Selected References
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- Bach M. A., Phan-Dinh-Tuy F., Tournier E., Chatenoud L., Bach J. F., Martin C., Degos J. D. Deficit of suppressor T cells in active multiple sclerosis. Lancet. 1980 Dec 6;2(8206):1221–1223. doi: 10.1016/s0140-6736(80)92480-0. [DOI] [PubMed] [Google Scholar]
- Bottazzo G. F., Florin-Christensen A., Doniach D. Islet-cell antibodies in diabetes mellitus with autoimmune polyendocrine deficiencies. Lancet. 1974 Nov 30;2(7892):1279–1283. doi: 10.1016/s0140-6736(74)90140-8. [DOI] [PubMed] [Google Scholar]
- Buschard K., Madsbad S., Rygaard J. Depressed suppressor cell activity in patients with newly diagnosed insulin-dependent diabetes mellitus. Clin Exp Immunol. 1980 Jul;41(1):25–32. [PMC free article] [PubMed] [Google Scholar]
- Buschard K., Rygaard J. Is the diabetogenic effect of streptozotocin in part thymus-dependent? Acta Pathol Microbiol Scand C. 1978 Feb;86(1):23–27. doi: 10.1111/j.1699-0463.1978.tb02552.x. [DOI] [PubMed] [Google Scholar]
- Buschard K., Rygaard J., Lung E. The inability of a diabetogenic virus to induce diabetes mellitus in athymic (nude) mice. Acta Pathol Microbiol Scand C. 1976 Aug;84(4):299–303. doi: 10.1111/j.1699-0463.1976.tb00033.x. [DOI] [PubMed] [Google Scholar]
- Böyum A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g. Scand J Clin Lab Invest Suppl. 1968;97:77–89. [PubMed] [Google Scholar]
- Cahill G. F., Jr, McDevitt H. O. Insulin-dependent diabetes mellitus: the initial lesion. N Engl J Med. 1981 Jun 11;304(24):1454–1465. doi: 10.1056/NEJM198106113042403. [DOI] [PubMed] [Google Scholar]
- Faber O. K., Binder C. C-peptide response to glucagon. A test for the residual beta-cell function in diabetes mellitus. Diabetes. 1977 Jul;26(7):605–610. doi: 10.2337/diab.26.7.605. [DOI] [PubMed] [Google Scholar]
- Heding L. G. Radioimmunological determination of human C-peptide in serum. Diabetologia. 1975 Dec;11(6):541–548. doi: 10.1007/BF01222104. [DOI] [PubMed] [Google Scholar]
- Horowitz S. D., Borcherding W., Bargman G. J. Suppressor T cell function in diabetes mellitus. Lancet. 1977 Dec 17;2(8051):1291–1291. doi: 10.1016/s0140-6736(77)92704-0. [DOI] [PubMed] [Google Scholar]
- Jansen F. K., Müntefering H., Schmidt W. A. Virus induced diabetes and the immune system. I. Suggestion that appearance of diabetes depends on immune reactions. Diabetologia. 1977 Sep;13(5):545–549. doi: 10.1007/BF01234511. [DOI] [PubMed] [Google Scholar]
- Lernmark A., Freedman Z. R., Hofmann C., Rubenstein A. H., Steiner D. F., Jackson R. L., Winter R. J., Traisman H. S. Islet-cell-surface antibodies in juvenile diabetes mellitus. N Engl J Med. 1978 Aug 24;299(8):375–380. doi: 10.1056/NEJM197808242990802. [DOI] [PubMed] [Google Scholar]
- Like A. A., Rossini A. A. Streptozotocin-induced pancreatic insulitis: new model of diabetes mellitus. Science. 1976 Jul 30;193(4251):415–417. doi: 10.1126/science.180605. [DOI] [PubMed] [Google Scholar]
- Madsbad S., Krarup T., Reguer L., Faber O. K., Binder C. Effect of strict blood glucose control on residual B-cell function in insulin-dependent diabetics. Diabetologia. 1981 May;20(5):530–534. doi: 10.1007/BF00252760. [DOI] [PubMed] [Google Scholar]
- Morimoto C., Abe T., Homma M. Altered function of suppressor T lymphocytes in patients with active systemic lupus erythematosus--in vitro immune response to autoantigen. Clin Immunol Immunopathol. 1979 Jun;13(2):161–170. doi: 10.1016/0090-1229(79)90060-6. [DOI] [PubMed] [Google Scholar]
- Nerup J., Andersen O. O., Bendixen G., Egeberg J., Gunnarsson R., Kromann H., Poulsen J. E. Cell-mediated immunity in diabetes mellitus. Proc R Soc Med. 1974 Jun;67(6 Pt 1):506–513. doi: 10.1177/00359157740676P135. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paik S. G., Fleischer N., Shin S. I. Insulin-dependent diabetes mellitus induced by subdiabetogenic doses of streptozotocin: obligatory role of cell-mediated autoimmune processes. Proc Natl Acad Sci U S A. 1980 Oct;77(10):6129–6133. doi: 10.1073/pnas.77.10.6129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reinherz E. L., Schlossman S. F. Current concepts in immunology: Regulation of the immune response--inducer and suppressor T-lymphocyte subsets in human beings. N Engl J Med. 1980 Aug 14;303(7):370–373. doi: 10.1056/NEJM198008143030704. [DOI] [PubMed] [Google Scholar]
- Slater L. M., Murray S. L., Kershnar A., Mosier M. A. Immunological suppressor cell activity in insulin dependent diabetes. J Clin Lab Immunol. 1980 Mar;3(2):105–109. [PubMed] [Google Scholar]
- Strelkauskas A. J., Callery R. T., McDowell J., Borel Y., Schlossman S. F. Direct evidence for loss of human suppressor cells during active autoimmune disease. Proc Natl Acad Sci U S A. 1978 Oct;75(10):5150–5154. doi: 10.1073/pnas.75.10.5150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zilko P. J., Dawkins R. L., Holmes K., Witt C. Genetic control of suppressor lymphocyte function in myasthenia gravis: relationship of impaired suppressor function to HLA-B8/DRW3 and cold reactive lymphocytotoxic antibodies. Clin Immunol Immunopathol. 1979 Oct;14(2):222–230. doi: 10.1016/0090-1229(79)90143-0. [DOI] [PubMed] [Google Scholar]
