Abstract: A non-transitory computer readable medium, a system, and a method for displaying a remote browser isolation (RBI) configuration window are disclosed. In an embodiment, a non-transitory computer readable medium includes instructions to be executed in a computer system, where the instructions when executed in the computer system perform a method comprising displaying an RBI configuration window, displaying an on/off activation feature within the RBI configuration window, and displaying an RBI profile selection menu within the RBI configuration window, where the RBI profile selection menu includes a plurality of spatially grouped sets that include an RBI profile selector, RBI profile identifier text, and selectable RBI protected browsing action icons that indicate to a user whether a corresponding RBI protected browsing action is included in an RBI policy.

Abstract: A non-transitory computer readable medium, a system, and a method for displaying a remote browser isolation (RBI) configuration window are disclosed. In an embodiment, a non-transitory computer readable medium includes instructions to be executed in a computer system, where the instructions when executed in the computer system perform a method comprising displaying an RBI configuration window, displaying an on/off activation feature within the RBI configuration window, and displaying an RBI profile selection menu within the RBI configuration window, where the RBI profile selection menu includes a plurality of spatially grouped sets that include an RBI profile selector, RBI profile identifier text, and selectable RBI protected browsing action icons that indicate to a user whether a corresponding RBI protected browsing action is included in an RBI policy.

Abstract: The invention relates to superantigen mediated expansion of antigen-specific T cells for cancer and infectious agent treatment/prophylaxis. Mice were injected with inactivated B16F10 mouse melanoma cells, followed by injection with a combined SEA/SEB injection or a sham injection on days 3 and 6, followed by day 4 challenge with live melanoma cells. The SEA/SEB recipient mice survived longer post-challenge and had a higher CTLs against tumor cells than did the sham injected mice. SEA/SEB TCR activation has been reported to be independent of antigen specificity of TCRs. This invention provides a method whereby a combination of Staphylococcal enterotoxin superantigens is used to enhance specific immune responses to activating antigens to enhance immune responses against cancers and infectious agents.