Induction Of Cellular Immunity Research Articles

Tumor-specific transplantation antigen activity of freshly adenovirus-infected cells. Intercurrent immunization against viral tumorigenesis with virus-infected cells.

Newborn hamsters were inoculated with human adenovirus type 12 (Ad12) within 24 hr of birth for tumor induction, and 15 days later, intercurrently immunized with Ad12-infected cells (KB; HeLa; FL; HEK; MoE; HaE). Tumor development was then observed for 75 days thereafter. Tumor formation was prevented at a statistically significant level by immunization with any of the above-mentioned infected cells. The immunization was effective even with abortively infected cells (HaE; MoE) or with cells infected in the presence of 5-fluorodeoxyuridine. The induced immunity was Ad12-specific, since neither cells infected with Ad2, Ad7 or Ad18 nor CV-1 cells infected with SV40 were able to prevent tumor formation. The most plausible explanation to these findings could be that Ad12-specific tumor-specific transplantation antigen is induced on the surface of freshly virus-infected cells and it is responsible for induction of specific cellular immunity. This gives an experimental support to our hypothesis on the mechanism of induction of cellular immunity against virus infections and to the hypothesis proposed by Habel and by Sjogren to explain the immunoresistance against tumor cells induced following viral immunization.

The induction of cellular immunity with soluble murine histocompatibility antigens

Soluble transplantation antigens have been prepared from various lymphoid organs of the mouse strains A and C57BL. These preparations have been partially characterized by gel filtration on Sephadex G-200 and G-100. The distribution of various antigenic activities, such as precipitation with rabbit antisera, inhibition of the cytotoxic reactions of heterologous antisera and of alloantibodies, differed considerably among the chromatographic fractions. The soluble antigen preparations retained their antigenic and immunogenic properties, as demonstrated by their ability to block the cytotoxic reactions of alloantisera and to modify tumor growth in immunized recipients. Immunization of normal recipients with the immunogenic transplantation antigen preparations led to the production of sensitized lymphocytes, capable of destroying allogeneic target cells in vitro. Sensitized lymphocytes appeared in the regional lymph nodes after a single injection of 200–300 μg of the antigen preparation, reaching a peak level between 9 and 12 days. On reimmunization, the cytolytic activity of lymph node cells increased considerably and sensitized lymphocytes also appeared in the spleens of immunized animals.

An in vitro model system for the study of the induction of cellular immunity

An in vitro model system for the study of the induction of cellular immunity

An in vitro model system for the study of the induction of cellular immunity

An in vitro model system for the study of the induction of cellular immunity

Colostral leukocytes.

AbstractLeukocytes of human colostrum were studied for their phagocytic activity and ability to migrate in vitro. Samples were collected from healthy females in the first 2 weeks after delivery. Leukocytes were found with great regularity in concentrations of 2200–4100/mm3. These colostral leukocytes displayed glass adhesiveness, amoeboid movement, and the ability to migrate in capillary tubes. The phagocytic activity of colostral leukocytes against nonencapsulated Cryptococcus neoformans approached the normal values of peripheral blood leukocytes. The colostral leukocytes reacted to specific antigen similar to the donors' peripheral blood leukocytes and correlated with the dermal reactivity of the donor. The finding that these leukocytes are in relatively large numbers and possess phagocytic activity supports the concept that this is a naturally occurring in vivo phenomenon and that these cells may protect the breast against invading microorganisms; also, since these cells demonstrate the presence of cell‐mediated hypersensitivity and are normally ingested by the neonate, they may play a role in the development and/or induction of cellular immunity in the neonate.

Expermental salmonellosis. XI. Induction of cellular immunity and formation of antibody by transfer agent of mouse mononuclear phagocytes.

When mice were injected intraperitoneally with a ribonucleic acid (RNA) preparation extracted from the peritoneal mononuclear phagocytes (termed monocytes) of immunized mice, these macrophages developed cellular immunity and cellular antibodies. The peritoneal monocytes were obtained from normal mice and maintained in tissue culture bottles in a homogeneous cell population. When they were treated in vitro with an immune RNA preparation, they acquired cellular immunity, and cellular antibodies were detectable in such monocytes. These results suggest that the mononuclear phagocytic cell line constitutes a cell line responsible for antibody formation.