T-cell activation induced by anti-CD3 × anti-B-cell lymphoma monoclonal antibody is enhanced by pretreatment of lymphoma cells with soluble CD40 ligand

 T cells play a key role in the control of abnormal B cell proliferation. Factors that play a role in inadequate T cell responses include absence of expression of costimulatory and adhesion molecules by the malignant B cells and lack of cytotoxic T cells specific for tumor-associated antigens. A number of approaches have been used to enhance T cell response against malignant B cells. Agents such as soluble CD40 ligand can enhance expression of costimulatory molecules by the malignant B cells and improve their ability to activate T cells. Anti-CD3-based bispecific antibodies can retarget T cells toward the tumor cells irrespective of T cell specificity. We used the V 38C13 murine lymphoma model to assess whether the combination of soluble CD40 ligand and anti-CD3-based bispecific antibody can enhance T cell activation induced by malignant B cells more effectively than either approach alone. Expression of CD80, CD86, and ICAM-1 on lymphoma cells was up-regulated by soluble CD40 ligand. Syngeneic T cells were activated more extensively by lymphoma cells when the lymphoma cells were pre-treated with soluble CD40 ligand. Bispecific-antibody induced T cell activation was more extensive when lymphoma cells pretreated with soluble CD40 ligand were present. The combination of soluble CD40 ligand plus bispecific antibody enhanced the median survival of mice compared to mice treated with bispecific anibody alone. We conclude that pretreatment of tumor cells with agents capable of inducing costimulatory molecule expression, such as soluble CD40 ligand can enhance the ability of malignant B cells to activate T cells. This effect is enhanced by the addition of bispecific antibody. The combination of enhanced expression of costimulatory molecules and retargeting of T cells by bispecific antibody may allow for a more effective T-cell-based immunotherapy. Accepted: 14 October 1997     

Larval release rhythms and tidal exchange in the estuarine mudprawn, Upogebia africana

The mudprawn, Upogebia africana is common in intertidal regions of many South African estuaries. The life cycle is complex, incorporating a marine phase of development during the larval stages. Breeding peaks are in summer and first-stage larvae are released into the plankton at night. Maximum release activity and export to the marine environment follow a semi-lunar cycle synchronized to the time when high water in the estuary is crepuscular. This occurs after peak spring tidal amplitude. Estuarine reinvasion by postlarvae is also nocturnal, and maximum return occurs after neap's when low water at sea occurs around sunset. Rhythmic cycles of larval export and postlarval estuarine reinvasion are therefore asynchronous during the lunar cycle and are best explained by the timing of the change in light intensity relative to high and low water respectively. If maximum activity rhythms of Stage 1 and postlarvae are independent of tidal amplitude, then timing of maximum release and reinvasion during the lunar cycle would alter as the time of sunset shifts between solstices. Much of southern Africa experiences a semi-arid type climate and most estuaries close off from the sea for varying periods owing to sandbar development across tidal inlets. Larvae do not metamorphose if trapped in estuaries and recruitment ceases. Thus, mudprawn populations are directly affected by tidal inlet dynamics. In extreme cases populations become locally extinct if inlets remain closed for extended periods.