In a previous report (1), guinea pigs primed with the hapten 2,4-dinitrophenyl (DNP) coupled directly to mycobacteria were shown to possess thymus-derived (T) lymphocytes responsive to DNP on a wide variety of carriers. This system is of interest for several reasons. First, it contrasts with most T-cell responses to hapten-carrier conjugates, which are specific for carrier or for specific conjugate determinants, but not for the same hapten on heterologous carriers (2). Second, it allows the comparison of responses of T lymphocytes to those of thymusindependent, bone-marrow-derived (B) lymphocytes to the same, chemically defined determinant. Finally, it permits the precise analysis of the structure of antigenic determinants recognized by such T cells; since it is necessary that the determinant contain the hapten for T-cell responses to occur, the hapten becomes a marker for the determinant. If the specificity of such T-cell responses could be shown to resemble closely the specificity of B-cell responses to DNP, and of anti-DNP antibody, then a strong argument could be made for the identity of the specific receptors for antigen on T and B lymphocytes; Blymphocyte receptors are generally believed to be immunoglobulin (Ig) in nature (2-4). On the other hand a clear difference in the specificity ofT-lymphocyte responses compared to B-lymphocyte responses might imply that these two types of lymphocytes use entirely different molecules to perform a similar function, namely specific antigen recognition.Previous studies (1) of guinea pigs immunized with DNP-mycobacteria have shown that the in vitro proliferative response of a purified population of guinea pig T lymphocytes to DNP conjugates is independent of the few B cells in the system, and is indeed a T-cell response. The determinant recognized involves both hapten and carrier, since neither alone can stimulate such T cells. The