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S G Simkins

Publications and source records attributed to S G Simkins.

2 recordsLinked to original sources

Immunization with Treponema pallidum outer membrane vesicles induces high-titer complement-dependent treponemicidal activity and aggregation of T. pallidum rare outer membrane proteins (TROMPs).

The purpose of this study was to determine whether immunization with purified outer membrane vesicles (OMV) from Treponema pallidum (T.p. ) could elicit Abs capable of killing this organism. It is well established that the immunization of rabbits or mice with killed T.p. or with recombinant T.p. Ags has failed to generate serum killing activity comparable with that of infection-derived immunity. Because of the small amount of T.p. OMV obtainable, a single mouse was immunized with purified OMV. The mouse anti-OMV serum and infection-derived immune rabbit serum (IRS) were compared by reactivities on two-dimensional T.p. immunoblots and by the T.p. immobilization test, a complement-dependent killing assay. Whereas IRS detected >40 Ags, the anti-OMV serum identified only 6 Ags corresponding to proteins identified previously in the outer membrane. T.p. immobilization testing showed that IRS had a 100% killing titer of 1:44 and a 50% killing titer of 1:662. By comparison, the mouse anti-OMV serum had a significantly greater 100% killing titer of 1:1,408 and a 50% killing titer of 1:16,896. Absorption of the anti-OMV serum to remove Ab against outer membrane-associated lipoproteins did not change the 100% killing titer. Freeze-fracture analysis of T.p. incubated in IRS or anti-OMV serum showed that T.p. rare membrane-spanning outer membrane proteins were aggregated. This is the first demonstration of high-titer killing Abs resulting from immunization with defined T.p. molecules; our study indicates that the targets for these Abs are T. p. rare outer membrane proteins.

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A system employing a minimal defined medium for the selection of tumorigenic cells.

Populations of normal and tumorigenic epithelial cells were plated in normal (serum supplemented) and a minimal defined medium. The ability of cells to grow in the minimal defined medium vs. the normal medium was related to their tumorigenic ability. All of the clones that were capable of growth in the minimal defined medium demonstrated tumorigenic ability. None of the normal clones survived in the minimal defined medium. As expected, some of the tumorigenic clones could not grow in the minimal medium. However, at no time did a clone that grew in the minimal defined medium fail to demonstrate tumorigenic ability. This validated that this system can be an animal-free means for selecting tumorigenic epithelial cells out of a mixed population.

Animals↗