The capacity o f mice to produce antibody-forming cells (AFC) to sheep erythrocytes and t o low doses of two haptenated proteins increases logarithmically with age in the postnatal period. This increase is prevented by thymectomy. These findings, together with those on the ability o f suckling mice to make high numbers of AFC t o high doses of at least one of the antigens used, indicate that T cells are the limiting cell type in neonatal humoral immune responses. An analysis of variance of the number of AFC in individual spleens as a measure for T cells showed that the data are in agreement with random generation and subsequent proliferation of these cells during ontogenesis. Different antigen reactivities carried by these cells seem t o arise at different times during fetal life.