Abstract
Patients with acquired hypogammaglobulinaemia usually have near normal numbers of B cells and normal T cell function. When hypogammaglobulinaemia occurs in association with thymoma, then B cell numbers have been reported as low, and distinctive T cells are present which inhibit immunoglobulin production by normal cells. It has been suggested that these T cells are responsible for the observed hypogammaglobulinaemia. We report a patient with thymoma and hypogammaglobulinaemia who lacks these distinctive suppressor cells and has normal B cell numbers. It is therefore incorrect to propose a single pathogenic mechanism for hypogammaglobulinaemia in association with thymoma.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 619-624 |
| Number of pages | 6 |
| Journal | Clinical and Experimental Immunology |
| Volume | 58 |
| Issue number | 3 |
| State | Published - 1984 |
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology
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