Literature DB >> 61346

A suppressor T-cell defect in tropical splenomegaly syndrome.

Y M Fakunle, B M Greenwood.   

Abstract

Serum-IgM is always abnormally high in tropical splenomegaly syndrome. It is postulated that patients with this disease have an abnormal immunoglobulin response to malaria because they lack effective T suppressor cells. This defect may be genetically determined, thus explaining the tribal and familial aggregation of the disease. Hypermacroglobulinaemia is associated with the formation of large amounts of high-molecular-weight immune complexes. These complexes are important in the pathogenesis of the clinical features of the syndrome.

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Year:  1976        PMID: 61346     DOI: 10.1016/s0140-6736(76)90671-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  3 in total

1.  Low molecular weight (7S) IgM and free light chains in the sera of patients with the tropical splenomegaly syndrome.

Authors:  Y M Fakunle; B M Greenwood
Journal:  Clin Exp Immunol       Date:  1977-04       Impact factor: 4.330

2.  Antibody-mediated killing of suppressor T lymphocytes as a possible cause of macroglobulinemia in the tropical splenomegaly syndrome.

Authors:  W F Piessens; S L Hoffman; A A Wadee; P W Piessens; S Ratiwayanto; L Kurniawan; J R Campbell; H A Marwoto; L L Laughlin
Journal:  J Clin Invest       Date:  1985-06       Impact factor: 14.808

3.  Cryoglobulinaemia and circulating immune complexes in tropical splenomegaly syndrome.

Authors:  Y M Fakunle; I I Onyewotu; B M Greenwood; I Mohammed; E J Holborow
Journal:  Clin Exp Immunol       Date:  1978-01       Impact factor: 4.330

  3 in total

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