Abnormalities of quantities and functions of linker for activations of T cells in severe aplastic anemia

Objective Severe aplastic anemia (SAA) is a rare immune‐regulated disease characterized by severe pancytopenia and bone marrow failure, caused by destruction of hematopoietic cells by the activated T lymphocytes. Linker for activation of T cells (LAT), a transmembrane adaptor protein, plays a key role in T‐cell and mast cell functions. However, it remains unclear how LAT may change in patients with SAA. This study aims at understanding the role of lymphocyte LAT in SAA. Methods The expression of LAT, related signaling molecules, and T‐cell effector molecules was determined by flow cytometry. LAT mRNA was evaluated by quantitative real‐time PCR. Cytokine production by cultured T cells was determined by ELISA. Results Patients with SAA had an increased levels of LAT and both total phosphorylated LAT and of the related molecule (ZAP‐70) in circulating T cells compared with normal controls. In patients with SAA, the expression of LAT was positively associated with the expression of perforin and granzyme B in CD8+ T cells. Inhibition of LAT expression in T cells from patients with SAA decreased the activation of the CD4+ and CD8+ T‐cell subsets. Overexpression of LAT in T cells from normal controls increased the activation of CD4+ and CD8+ T‐cell subsets with increased apoptosis of K562 cells in coculture. Conclusions Our findings demonstrate that dysregulation of LAT expression and activation may contribute to over‐function of T cells, imbalance of Th1/Th2 subsets and thus lead to hematopoiesis failure in SAA. Immunosuppressive therapy dramatically reduced the expression of LAT making it an attractive therapeutic target in SAA.