Three bovine serum albumin-specific Lyt-2 + T suppressor (Ts) cell clones from CBA/J mice have been analyzed with regard to expression of L3T4 molecules. All three Ts-cell clones can be stained with monoclonal antibodies (mAb) to L3T4. Tested for the two clones restricted to recognition of E k deter
Specific lysis of Listeria monocytogenes-infected macrophages by class II-restricted L3T4+ T cells
✍ Scribed by Stefan H. E. Kaufmann; Erika Hug; Ulla Väth; Gennaro De Libero
- Book ID
- 102828252
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 973 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
✦ Synopsis
Mice were infected with the intracellular bacterium, Lisferia monocytogenes, and T cell clones from spleens, lymph nodes and peritoneal exudates were established. The capacity of L3T4', Lyt2-T-cell clones to specifically lyse L. monocytogenes-infected macrophages was analyzed. As a source of target cells, bone marrow macrophages (BMMQ,) after 9 days of culture in hydrophobic teflon bags were used. These BMMQ were totally Ia-; however, significant Ia-expression could be induced by interferon-y (IFN-y). IFN-y-stimulated BMMQ,, after priming with live or killed L. monocyfogenes organisms were effectively lysed by the vast majority of L3T4' T cell clones. In the absence of either IFN-y stimulation or antigen priming, no lysis occurred. Cytolysis was demonstrable in a conventional 4-h "Cr-release assay and in an 18-h neutral red uptake assay and was antigen specific and class I1 restricted. Native T cells from L. monocytogenes-infected mice failed to lyse stimulated, L. monocytogenes-primed BMMQ and gained their cytolytic activity after antigenic restimulation in vitro. These data demonstrate that L. monocytogenes-specific L3T4' T cells could lyse MQ, presenting listerial antigens provided that Ia antigen expression had been induced. L3T4' T cell clones produced IFN-Q after restimulation with antigen plus accessory cells in vifro and IFNy secretion could be increased by costimulation with recombinant IL 2. These T cell clones conferred significant protection upon recipient mice which was more pronounced in the liver. The possible relevance of lysis by L3T4' T cells of infected MQ, to protection against and pathogenesis of intracellular bacterial infections is discussed.
📜 SIMILAR VOLUMES
Anti-idiotype antibody therapy of B-cell lymphomas, despite numerous promising experimental and clinical studies, has so far met with limited success. Tailor-made monoclonal antiidiotype antibodies have been injected into a large series of lymphoma patients, with a few impressive complete tumour rem