Decreased α/β Heterodimer among CD8 Molecules of Peripheral Blood T Cells in Wiskott–Aldrich Syndrome
pmid: 8906743
Decreased α/β Heterodimer among CD8 Molecules of Peripheral Blood T Cells in Wiskott–Aldrich Syndrome
Cell surface CD8 molecules exist as either alpha/alpha homodimers or alpha/beta heterodimers, and most CD8+ T cells that undergo differentiation in the thymus express alpha/beta heterodimers. CD8 molecules on peripheral blood lymphocytes of patients with Wiskott-Aldrich syndrome (WAS), an X-linked immunodeficiency disease, have now been shown to be composed mostly of alpha/alpha homodimers, while the total number of lymphocytes was maintained. This observation may indicate aberrant differentiation of CD8+ T cells in the thymus of WAS. Decreased CD8alpha/beta heterodimer expression, and the relative increase of CD8+ T cells expressing CD8alpha/alpha homodimer, may explain a part of the defective lymphocyte functions in WAS patients.
Aging, CD3 Complex, Receptors, Antigen, T-Cell, alpha-beta, Immunoglobulins, Infant, CD8-Positive T-Lymphocytes, Flow Cytometry, Wiskott-Aldrich Syndrome, Killer Cells, Natural, Humans, Lymphocyte Count
Aging, CD3 Complex, Receptors, Antigen, T-Cell, alpha-beta, Immunoglobulins, Infant, CD8-Positive T-Lymphocytes, Flow Cytometry, Wiskott-Aldrich Syndrome, Killer Cells, Natural, Humans, Lymphocyte Count
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