Epidermal Langerhans cells can function as stimulatory cells but not as accessory cells in CTL induction.
Open Access
- 1 March 1984
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 132 (3) , 1163-1168
- https://doi.org/10.4049/jimmunol.132.3.1163
Abstract
In this study, we determined whether Langerhans cells (LC) can function as both stimulatory and accessory cells (ACC) in alloreactive and syngeneic modified CTL induction in vitro. LC exhibited potent Ia+ stimulatory function, comparable to spleen cells, in both allo-CTL induction and in TNP-modified CTL induction assays. In contrast to spleen cells, however, when LC were syngeneic to the responders in an Ia+-adherent cell-depleted CTL culture, they could not restore the CTL responses. This was due, in part, to the suppression of CTL induction, presumably via secretion of prostaglandin E by epidermal cells (EC), because addition of indomethacin reversed the suppression. Even in the presence of indomethacin, however, LC were unable to exhibit ACC function. Finally, we tested the possibility that both Ia+ and Ia- cells were required to fulfill ACC functions. However, when spleen cells treated with anti-Ia antibody and complement and EC and indomethacin were added to an Ia+-adherent cell-depleted CTL culture, there was no significant restoration of the CTL response. Thus, LC can clearly act as Ia+ stimulatory cells in CTL induction but cannot serve as ACC in CTL induction, whereas Ia+ spleen cells may subserve both functions. These data suggest a functional heterogeneity of Ia+ antigen-presenting cells in spleen and in epidermis.This publication has 19 references indexed in Scilit:
- Ia Antigens in Mouse Skin Are Predominantly Expressed on Langerhans CellsThe Journal of Immunology, 1979
- CELL-MEDIATED IMMUNE-RESPONSE TO SYNGENEIC UV-INDUCED TUMORS .3. REQUIREMENT FOR AN IA+ MACROPHAGE IN THE INVITRO DIFFERENTIATION OF CYTOTOXIC LYMPHOCYTES-T1979
- A Subpopulation of Adherent Accessory Cells Bearing Both I-A and I-E or C Subregion Antigens Is Required for Antigen-Specific Murine T Lymphocyte ProliferationThe Journal of Immunology, 1978
- "Panning" for lymphocytes: a method for cell selection.Proceedings of the National Academy of Sciences, 1978
- Cellular and genetic control of antibody responses in vitro. III. Immune response gene regulation of accessory cell functionThe Journal of Experimental Medicine, 1978
- CELLULAR AND GENETIC-CONTROL OF ANTIBODY-RESPONSES INVITRO .4. EXPRESSION OF IA ANTIGENS ON ACCESSORY CELLS REQUIRED FOR RESPONSES TO SOLUBLE-ANTIGENS INCLUDING A RESPONSE UNDER IR GENE CONTROL1978
- Accessory cell dependence of lectin‐induced proliferation of mouse T lymphocytesEuropean Journal of Immunology, 1977
- EXPRESSION OF IA ANTIGENS ON IMMUNOCOMPETENT CELLS IN GUINEA-PIG .2. IA ANTIGENS ON MACROPHAGES1977
- Macrophage Requirement for the in Vitro Response to TNP Ficoll: A Thymic Independent AntigenThe Journal of Immunology, 1976
- A Requirement for Two Cell Types for Antibody Formation in vitroScience, 1967