Abstract
During embryonic development of the mouse, before expressing classical T cell markers, the blast cells colonizing the thymus react with the monoclonal antibody AMT‐13 shown previously to detect interleukin 2 receptors. The proportion of AMT‐13+ cells decreases as gestation time increases. On the other hand, the proportion of Thy‐1+, Lyt‐1+ and Lyt‐2+ cells increases during ontogenesis. On the 19th day of gestation when the thymus architecture is comparable to the adult thymus, the AMT‐13+ cells become localized in the subcapsular area of the cortex. In the adult thymus after cortison treatment the regenerating cells express the AMT‐13 antigen. The AMT‐13 antigen presumably the interleukin 2 receptor is the first marker of the early embryonic thymocytes reported until now that may be related to cellular function.