Expansion of a suppressor T-cell population associated with the hyper-IgM syndrome and generalized lymphadenopathy
- 31 July 1991
- journal article
- case report
- Published by Elsevier in Clinical Immunology and Immunopathology
- Vol. 60 (1) , 118-127
- https://doi.org/10.1016/0090-1229(91)90117-s
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Immunoglobulin deficiency with increased immunoglobulin M in three siblings: effect of long-term immunoglobulin therapyEuropean Journal of Pediatrics, 1988
- X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locusHuman Genetics, 1987
- Primary immunodeficiency diseases: Report of a World Health Organization Scientific GroupClinical Immunology and Immunopathology, 1986
- Evidence for a Defect in Switch T Cells in Patients with Immunodeficiency and Hyperimmunoglobulinemia MNew England Journal of Medicine, 1986
- Hypogammaglobulinemia with hyper-IgM, severe T-cell defect, and abnormal recirculation of OKT4 lymphocytes in a girl with chronic lymphadenopathyClinical Immunology and Immunopathology, 1986
- Hyper IgM immunodeficiency. A primary dysfunction of B lymphocyte isotype switching.Journal of Clinical Investigation, 1983
- Immunologic studies of three family members with the immunodeficiency with hyper-IgM syndromeJournal of Clinical Immunology, 1983
- Hyper Immunoglobulin M Immunodeficiency (Dysgammaglobulinemia)Journal of Clinical Investigation, 1979
- 702 EVIDENCE FOR EXCESSIVE T SUPPRESSOR CELL ACTIVITY IN X-LINKED IMMUNODEFICIENCY WITH HYPER-IgMPediatric Research, 1978
- ROLE OF SUPPRESSOR T CELLS IN PATHOGENESIS OF COMMON VARIABLE HYPOGAMMAGLOBULINÆMIAThe Lancet, 1974