A small percentage of normal mouse thymus and spleen lymphocytes form rosettes with autologous erythrocytes. The number of these autologous rosettes increases 15-to 20-fold after adult thymectomy and to a lesser degee with aging. Autologous rosette level is also abnormally high in nude (congenitally athymic) mice. The high level of autolo gous rosette-forming celmsfound after adult thymectomy is normalized by injecting ng amounts of purified circulating thymic factor. Autologous rosette-forming cells adhere to nylon, belong to the less dense spleen cells, are in majority steroid-resistant in the thymus. All these properties suggest that autologous rosette-forming cells might belong to immature T-cell (thymic-dependent cell) precursors. Thymic-dependent cell (T-cell) maturation involves several steps from the primitive stem cell to the fully competent peripheral T-cell (1-5). The difficulties in visualizing these different steps come from the absence of morphological criteria available for other blood cell lineages or of markers used to distinguish B-and T-cells.A small percentage of normal mouse lymphoid cells bind autologous erythrocytes, forming rosettes. These autologous rosette-forming cells (A-RFC) are found predominantly in the thymus and at lower percentages in the spleen (6, 7). A-RFC have elicited a great interest because of their potential use as a model of self-recognition (6, 7). We report here that A-RFC level in the spleen is dramatically increased after adult thymectomy and that purified thymic hormone corrects such increase.These data and others, also presented here, suggest that autologous rosette formation may be a selective property of immature T-cells which could eventually be used as a marker of this cell population.MATERIAL AND METHODS Mice. Male and female mice of the CBA-H (histocompatibility type H-2k) or C57BI/6 (H-2b) strains were used in most experiments. In some cases, nude (congenitally athymic) mice were also utilized. When not specified, the mice were 6-8 weeks old. Thymectomies were performed by suction; "thymus-deprived" mice were prepared by thymectomy followed by irradiation (850 rads) and reconstitution by intravenous (i.v.) injection of 15 X 106 syngeneic bone marrow cells.Antitheta Serum (AOS). This was prepared by injecting 107 CBA thymocytes intraperitoneally (i.p.) into AKR mice once weekly for 8 weeks (5).