Literature DB >> 1083579

Suppressor T cells in the pathogenesis of hypogammaglobulinemia associated with a thymoma.

T A Waldmann, S Broder, M Durm, M Blackman, R Krakauer, B Meade.   

Abstract

The nature of the immunological defect in patients with hypogammaglobulinemia associated with a thymoma was investigated using a technique established to study the differentiation of lymphocytes into immunoglobulin synthesizing and secreting cells. Exhaustively washed peripheral blood lymphocytes were cultured for 7 days in RPMI-1640 medium supplemented with fetal calf serum in the presence of the lectin, pokeweed mitogen. The IgG, IgA, and IgM synthesized and secreted into the medium were measured by competitive double antibody radio-immunoassays. Twenty-two normal individuals synthesized 1625 ng of IgG, 1270 ng of IgA, and 4910 ng of IgM per 2 million lymphocytes in culture. In contrast, the three patients with hypogammaglobulinemia and a thymoma synthesized less than 100 ng of each class of immunoglobulin. When lymphocytes from 2 of the 3 patients studied were cocultured with normal lymphocytes and pokeweed mitogen, the synthesis of immunoglobulin by normal lymphocytes was depressed by a factor of 66 to 97%. Co-cultue of purified T cells from the hypogammaglobulinemic patients with normal lymphocytes resulted in an 87% suppression of immunoglobulin synthesis by the normal cells. However, no suppression of immunoglobulin synthesis was observed when preparations of B cells and macrophages depleted of T cells from the hypogammaglobulinemic patients were co-cultured with normal lymphocytes. In addition, in control studies no such suppression of immunoglobulin synthesis was seen when normal cells were co-cultured with lymphocytes from unrelated normals, patients with isolated IgA deficiency, patients with chronic lymphocytic leukemia or patients with the Sezary syndrome, a T cell leukemia nor were they inhibited when incubated with T cells from unrelated normals. These observations suggest that in some patients the hypogammaglobulinemia associated with a thymoma may be caused or perpetuated by an abnormality of regulatory T cells which suppress the maturation of lymphocytes into antibody producing cells.

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Year:  1975        PMID: 1083579

Source DB:  PubMed          Journal:  Trans Assoc Am Physicians        ISSN: 0066-9458


  9 in total

1.  Quantitative measurements of T- and B-cell function in "variable" primary hypogammaglobulinaemia: evidence for a consistent B-cell defect.

Authors:  E G de la Concha; G Oldham; A D Webster; G L Asherson; T A Platts-Mills
Journal:  Clin Exp Immunol       Date:  1977-02       Impact factor: 4.330

2.  A morphologic and immunologic surface marker study of 299 cases of non-Hodgkin lymphomas and related leukemias.

Authors:  R J Lukes; C R Taylor; J W Parker; T L Lincoln; P K Pattengale; B H Tindle
Journal:  Am J Pathol       Date:  1978-02       Impact factor: 4.307

Review 3.  Good's syndrome remains a mystery after 55 years: A systematic review of the scientific evidence.

Authors:  Theodoros Kelesidis; Otto Yang
Journal:  Clin Immunol       Date:  2010-02-10       Impact factor: 3.969

4.  Use of a human plaque-forming cell assay to study peripheral blood bursa-equivalent cell activation and excessive suppressor cell activity in humoral immunodeficiency.

Authors:  H G Herrod; R H Buckley
Journal:  J Clin Invest       Date:  1979-05       Impact factor: 14.808

5.  Disorders of B cells and helper T cells in the pathogenesis of the immunoglobulin deficiency of patients with ataxia telangiectasia.

Authors:  T A Waldmann; S Broder; C K Goldman; K Frost; S J Korsmeyer; M A Medici
Journal:  J Clin Invest       Date:  1983-02       Impact factor: 14.808

6.  Pre-B cell suppression by thymoma patient lymphocytes.

Authors:  A R Hayward; P Paolucci; A D Webster; P Kohler
Journal:  Clin Exp Immunol       Date:  1982-05       Impact factor: 4.330

7.  Thymoma and hypogammaglobulinaemia with and without T suppressor cells.

Authors:  M K Brenner; J G Reittie; H R Chadda; A Pollock; G L Asherson
Journal:  Clin Exp Immunol       Date:  1984-12       Impact factor: 4.330

8.  Two immunologically distinct forms of late-onset hypogammaglobulinaemia.

Authors:  T A Platts-Mills; G C De Gast; A D Webster; G L Asherson; S R Wilkins
Journal:  Clin Exp Immunol       Date:  1981-05       Impact factor: 4.330

Review 9.  Good's Syndrome: Time to Move on From Reviewing the Past.

Authors:  Aunonna Kabir; Reza Alizadehfar; Christos M Tsoukas
Journal:  Front Immunol       Date:  2022-01-12       Impact factor: 7.561

  9 in total

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