Literature DB >> 7039882

Cell number requirements for lymphocyte stimulation in vitro: changes during the course of multiple sclerosis and the effects of immunosuppression.

S C Knight, B Harding, S Burman, J Mertin.   

Abstract

Peripheral blood lymphocytes from 20 patients with clinically definite, relapsing and remitting multiple sclerosis (MS) were studied during their participation in a double-blind trial of immunosuppressive treatment. Proliferative responses occurring with different numbers of cells in culture and on different days of culture in the presence of phytohaemagglutinin (PHA) or with allogeneic cells from lymphoid cell lines (MLC) were assessed. Cells taken from patients before treatment showed similar responses to cells from laboratory personnel. However, when cells were taken from patients in relapse or from untreated patients as the disease progressed, there was an alteration in the pattern of response; higher number of cells were required in culture to produce responses. A change in the responsiveness to PHA or in MLC may therefore accompany the progression of the disease in MS (reflecting clinical relapses and possibly subclinical activity of the disease), perhaps resulting from a simple reduction in the proportion of cells able to respond. After intense immunosuppression followed by long-term maintenance on azathioprine, cells from patients gave similar responses to those found before treatment. Thus long-term immunosuppression prevented the progressive alteration in lymphocyte function. Shifts in the total cell number and time in culture required to allow proliferation with mitogens of cells from untreated MS patients could explain both the 'low' of PHA responses reported and the changes of in vitro 'suppressor' function of these cells.

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Year:  1981        PMID: 7039882      PMCID: PMC1536319     

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  18 in total

1.  Help and suppression by lymphoid cells as a function of cellular concentration.

Authors:  J Farrant; S C Knight
Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

Review 2.  Cellular immunity in multiple sclerosis.

Authors:  S C Knight
Journal:  Br Med Bull       Date:  1977-01       Impact factor: 4.291

3.  Responses of alloantigen-primed lymphocytes in vitro. Quantitative analysis of the relative frequency of reactive lymphocytes in primed populations which respond to allogeneic stimulating cells.

Authors:  R B Corley
Journal:  Eur J Immunol       Date:  1977-02       Impact factor: 5.532

Review 4.  Histocompatibility antigens and their relevance to multiple sclerosis.

Authors:  J R Batchelor
Journal:  Br Med Bull       Date:  1977-01       Impact factor: 4.291

5.  A simple technique for harvesting lymphocytes cultured in Terasaki plates.

Authors:  J O'Brien; S Knight; N A Quick; E H Moore; A S Platt
Journal:  J Immunol Methods       Date:  1979       Impact factor: 2.303

6.  Relative ability to provide help: an explanation for Con A-induced suppression.

Authors:  J Farrant; C Newton
Journal:  Clin Exp Immunol       Date:  1981-09       Impact factor: 4.330

7.  Suppressor cell function in multiple sclerosis.

Authors:  B G Arnason; J Antel
Journal:  Ann Immunol (Paris)       Date:  1978 Feb-Mar

8.  Altered regulation of mitogen responsiveness by suppressor cells in multiple sclerosis.

Authors:  R L Gonzalez; P C Dau; L E Spitler
Journal:  Clin Exp Immunol       Date:  1979-04       Impact factor: 4.330

9.  T suppressor (TG) lymphocytes fluctuate in parallel with changes in the clinical course of patients with multiple sclerosis.

Authors:  J R Huddlestone; M B Oldstone
Journal:  J Immunol       Date:  1979-10       Impact factor: 5.422

10.  Synergistic interaction of macrophages and lymphocytes in antigen-induced transformation of lymphocytes.

Authors:  R C Seeger; J J Oppenheim
Journal:  J Exp Med       Date:  1970-07-01       Impact factor: 14.307

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  6 in total

1.  Peripheral blood and synovial fluid T cells differ in their response to alloantigens and recall antigens presented by dendritic cells.

Authors:  A J Stagg; B Harding; R A Hughes; A Keat; S C Knight
Journal:  Clin Exp Immunol       Date:  1991-04       Impact factor: 4.330

2.  Failure in antigen responses by T cells from patients with common variable immunodeficiency (CVID).

Authors:  A J Stagg; M Funauchi; S C Knight; A D Webster; J Farrant
Journal:  Clin Exp Immunol       Date:  1994-04       Impact factor: 4.330

3.  Lymphocyte responses in juvenile chronic arthritis and Behçet's disease--cell number requirements and effects of glucocorticosteroid therapy.

Authors:  A de Vere-Tyndall; S Knight; S Burman; A M Denman; B M Ansell
Journal:  Clin Exp Immunol       Date:  1982-12       Impact factor: 4.330

4.  Primary human T-cell responses to the major outer membrane protein of Chlamydia trachomatis.

Authors:  A J Stagg; W A Elsley; M A Pickett; M E Ward; S C Knight
Journal:  Immunology       Date:  1993-05       Impact factor: 7.397

5.  Spontaneous and mutagen induced sister chromatid exchange in multiple sclerosis.

Authors:  M S Newton; C M Steel; H J Evans; B Pentland
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

6.  The distribution and functional properties of dendritic cells in patients with seronegative arthritis.

Authors:  A J Stagg; B Harding; R A Hughes; A Keat; S C Knight
Journal:  Clin Exp Immunol       Date:  1991-04       Impact factor: 4.330

  6 in total

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