thymosin and Dysgammaglobulinemia

Topics: B-Lymphocytes; Cells, Cultured; Dysgammaglobulinemia; Humans; Hypoparathyroidism; Immunologic Deficiency Syndromes; Infant, Newborn; Lymphocyte Activation; Male; Rosette Formation; T-Lymphocytes; Thymosin; Thymus Hormones

A 6 1/2-month-old male with severe combined immunodeficiency (SCID) had a low percentage and number of T cells (11%; 241/mm3) and a high percentage and number of B cells (52%; 1187/mm3) and null cells (37%; 868/mm3). In vitro studies were performed to determine if this child's primary defect involved differentiation of both T and B lymphocytes or if failure of B lymphocytes to differentiate into immunoglobulin producing cells was secondary to T lymphocyte abnormalities. Immunoglobulin production by lymphocytes in response to polyclonal mitogens (pokeweed mitogen and foetal calf serum) was measured by pulse-labelling cells with 3H-leucine and then precipitating cytoplasmic and secreted immunoglobulins with polyvalent anti-human immunoglobulin and S. aureus (Cowan strain I) protein A. The patient's lymphocytes did not synthesize immunoglobulins in vitro in response to mitogens. They did not suppress synthesis of immunoglobulins by normal lymphocytes. However, addition of normal purified T cells, which themselves did not synthesize immunoglobulins, enabled the patient's B lymphocytes to become immunoglobulin synthesizing and secreting cells. Gamma, mu, and light chains were secreted. This suggests that the primary abnormality was in the T-cell axis at the level of lymphoid stem cells or prothymocytes and that failure of B lymphocytes to become immunoglobulin-producing cells was secondary to this defect.

Topics: Antibody-Producing Cells; B-Lymphocytes; Cell Differentiation; Cell Division; Dysgammaglobulinemia; Humans; Immunization, Passive; Immunoglobulin G; Immunoglobulins; Immunologic Deficiency Syndromes; In Vitro Techniques; Infant; Leukocyte Count; Male; Mitogens; Monocytes; Receptors, Antigen, B-Cell; T-Lymphocytes; Thymosin