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Abnormalities of Immunoregulatory T Cells in Disorders of Immune Function

New England Journal of MedicinePublished 8 November 1979
Ellis L. Reinherz, Arye Rubinstein, Raif S. Geha, Anthony J. Strelkauskas, Fred S. Rosen, Stuart F. Schlossman
Citations213
SJR quartileQ1
SJR score19.08
SNIP13.47

TL;DR

It is concluded that the characterization of T cells may provide insight into the causes of a number of abnormal immune states in man.

Abstract

We studied a five-year-old girl with several autoimmune disorders and a 16-year-old boy with acquired agammaglobulinemia to determine whether aberrations of immunoregulatory T cells could explain some instances of immunodeficiency or autoimmunity. The normal peripheral blood T-cell population, as defined by specific heteroantiserums, is 20 per cent TH2+ and 80 per cent TH2-. Human suppressor cells are TH2+, whereas helper cells are TH2-. In addition, each subset expresses Ia antigens upon activation. Our patient with autoimmune disease had no demonstrable TH2+ cells, and her lymphocytes could not be induced to suppress. Her circulating T cells were of an activated-helper phenotype, i.e., TH2-,Ia+. In contrast, in the boy with agammaglobulinemia, the T-cell population was predominantly of an activated-suppressor phenotype, i.e., TH2+,Ia+. This patient's T cells abrogated both his own and his histoidentical brother's B-cell secretion of immunoglobulins. We conclude that the characterization of T cells may provide insight into the causes of a number of abnormal immune states in man.

Keywords

Immunology and Microbiology