T cell heterogeneity in patients with common variable immunodeficiency as assessed by abnormalities of T cell subpopulations and T cell receptor gene analysis
Open Access
- 1 August 1992
- journal article
- Published by Oxford University Press (OUP) in Clinical and Experimental Immunology
- Vol. 89 (2) , 198-203
- https://doi.org/10.1111/j.1365-2249.1992.tb06932.x
Abstract
T lymphocyte regulation of immunoglobulin production may be abnormal in some patients with common variable immunodeficiency (CVI). Phenotypic analysis of peripheral blood T lymphocytes from nine patients with CVI was conducted to examine whether an abnormal distribution could be detected in a functionally distinct T lymphocyte subpopulation. The percentage of CD8+ lymphocytes proved to be increased in some patients and decreased in others. In comparison with normal controls, many patients with CVI had reduced percentages of lymphocytes expressing both CD4 and CD45RA, a phenotype associate with naive CD4+ cells. There was no significant difference in CD4+ populations bearing CD29 or leucocyte adhesion molecule-1 (LAM-1) antigens. The pattern of gene rearrangement of the T cell antigen receptor (TCR) was studied using peripheral blood lymphocytes from these patients with CVI. Genomic DNA from freshly isolated lymphocytes as well as from selectively propagated CD4+ or CD8+ populations were examined using Southern blot analysis and a probe for the β chain of the TCR. A polyclonal pattern of TCR gene rearrangement, without the appearance of dominant non-germline bands, was demonstrated in all patient samples. These data suggest that the T lymphocytes in patients with CVI have a polyclonal pattern of TCR rearrangement despite an abnormal distribution of T cell subpopulations in some patients.Keywords
This publication has 26 references indexed in Scilit:
- Clinical and immunologic analyses of 103 patients with common variable immunodeficiencyJournal of Clinical Immunology, 1989
- In vitro induction of T cell-dependent B cell differentiation in patients with common varied immunodeficiencyClinical Immunology and Immunopathology, 1988
- Characterization of the suppressor activity in lymphocytes from patients with common variable hypogammaglobulinemia: Evidence for an associated primary B-cell defectClinical Immunology and Immunopathology, 1983
- Three distinct stages of B-cell defects in common varied immunodeficiency.Proceedings of the National Academy of Sciences, 1982
- Abnormalities of regulatory T-cell subpopulations in patients with primary immunoglobulin deficienciesClinical Immunology and Immunopathology, 1982
- Abnormalities of T cell maturation and regulation in human beings with immunodeficiency disorders.Journal of Clinical Investigation, 1981
- Antihelper T cell autoantibody in acquired agammaglobulinemia.Journal of Clinical Investigation, 1981
- Agammaglobulinemia with Arthritis and Celiac Disease Developing after Infectious Mononucleosis: Follow-up Study of a CaseScandinavian Journal of Infectious Diseases, 1977
- Suppression of B-cell differentiation by leukocytes from hypogammaglobulinemic patients.Journal of Clinical Investigation, 1976
- ROLE OF SUPPRESSOR T CELLS IN PATHOGENESIS OF COMMON VARIABLE HYPOGAMMAGLOBULINÆMIAThe Lancet, 1974