The human Ia-like antigens were recognized initially as a series of HLA-linked alloantigens primarily represented on B lymphocytes with multiple pregnancy sera (I). Later, they were detected by hetero-antisera raised against the isolated protein from cell membranes (2-4). In addition to their presence on B cells and monocytes, they have been detected on the leukemic blast in eases of acute lymphocytic leukemia, acute myelogenous leukemia, and chronic myelogenous leukemia in blastic crisis (4-6). Recently, these Ia antigens were also shown to be present on the surface of precursor cells responsible for colony formation of both the myeloid monocytic and erythroid series (7-9) and on the surface of nonblood cells such as epidermal Langerhans cells (10).The presence of certain types of Ia antigens on T lymphoeytes has been demonstrated in murine systems, although the exact molecular character remains unclear (11). The presence of Ia antigens on human T cells has not been well documented. The present studies demonstrate the presence of Ia antigens on a small population of normal circulating human T lymphocytes, on T lymphocytes grown in long-term cultures, and on certain leukemic T cells. Evidence also is presented showing that cells responsible for the generation of helper activity during a mixed lymphocyte reaction are contained in this Ia-bearing T-cell population.
Materials and MethodsIsolation of Lymphocytes. Mononuclear cells from the peripheral blood of normal individuals and patients with leukemia and various lymphoproliferative states and tonsillar mononuclear cells were isolated as described previously (12). Spontaneous rosette formation between human lymphocytes and sheep erythrocytes (SRBC) were performed with neuraminidase-treated SRBC (E). The rosette-forming cells (E-RFC) were separated from the nonrosette-forming cells by Ficoll-Hypaque (Pharmacia Fine Chemicals, Div. of Pharmacia Inc., Piscataway, N. J.) gradient centrifugation. The RFC-enriched fraction was purified further by repeated gradients until no significant numbers of cells were observed at the interphase. The E-RFCs were recovered after lysis of SRBC by a Tris-buffered ammonium chloride solution. Tonsillar B cells were obtained by the depletion of E-RFCs from the mononuclear cell preparations.