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Biomedical subjects

D Blakeley

Publications and source records attributed to D Blakeley.

4 recordsLinked to original sources

A genetically inactivated herpes simplex virus type 2 (HSV-2) vaccine provides effective protection against primary and recurrent HSV-2 disease.

A glycoprotein H (gH)-deleted herpes simplex virus type 2 (HSV-2) was evaluated as a vaccine for the prevention of HSV-induced disease. This virus, which we term a DISC (disabled infectious single cycle) virus, can only complete one replication cycle in normal cells and should thus be safe yet still able to stimulate broad humoral and cell-mediated antiviral immune responses. A gH-deleted HSV-2 virus that has been tested as a vaccine in the guinea pig model of recurrent HSV-2 infection was constructed. Animals vaccinated with DISC HSV-2 showed complete protection against primary HSV-2-induced disease, even when challenged 6 months after vaccination. In addition, the animals were almost completely protected against recurrent disease. Even at low vaccination doses, there was a high degree of protection against primary disease. A reduction in recurrent disease symptoms was also observed following therapeutic vaccination of animals already infected with wild type HSV-2.

Animals↗

Dry instant blood typing plate for bedside use.

A monoclonal antibody-derived, dry blood grouping plate, based upon the simple disaccharide, trehalose, is described that is indefinitely stable at room temperature and was found to have a 99.8% accuracy when tested against a standard semiautomated assay. This plate can be used by personnel with no specific training to check the recorded A,B,O, and Rhesus blood type of potential transfusion recipients in the field and at the bedside. Trehalose-based reagents may be important for bedside testing and in developing countries where refrigeration is unreliable.

Agglutination Tests↗

Migration of fluoresceinated pig lymphocytes in vivo: technical aspects and use in studies of autologous and homologous cell survival for up to three weeks.

Optimum conditions were determined for FITC and RITC labelling of pig blood lymphocytes with bright fluorescence and high viability and for their enumeration during their long survival after infusion in vivo. For at least 9 days, FITZ-labelled autologous lymphocytes and lymphocytes from MHC-identical donors showed no detectable difference in patterns of survival in the blood. After initial equilibration with extra-vascular lymphoid tissues, the fall-off suggested the expected presence of populations with a variety of life-spans, with some autologous labelled lymphocytes surviving beyond 3 weeks. A trace of cytotoxic antibody specific for labelled cells developed in these pigs later and could be boosted by a further FITC-labelled cell infusion.

Animals↗