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S Stadtsbaeder

Publications and source records attributed to S Stadtsbaeder.

31 records · Page 2Linked to original sources

In vitro activity of cotrimoxazole on the intracellular multiplication of Toxoplasma gondii.

Cotrimoxazole, from 60 mug/ml, inhibited the replication of Toxoplasma gondii within Hela cells and mouse peritoneal macrophages. The percentage of inhibition reached practically 100% after 18 hours of treatment at 37 degrees C. More prolonged treatment resulted in an eradication of the organisms from the cell monolayers. In contrast, similar doses of spiramycin were quite ineffective against intracellular toxoplasma. The active doses of cotrimoxazole used were not harmful for cell cultures. Cotrimoxazole also destroyed clones (rosaces) of toxoplasma which were formed during the past 18 hours of intracellular replication in the absence of the drug. Trimethoprim was the only effective compound of cotrimoxazole on intracellular parasites; the adjunction of sulfamethoxazole produced a marked synergistic effect. The present findings confirm the great efficiency of cotrimoxazole in the treatment of experimental toxoplasmosis in mice performed previously in this laboratory.

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[L forms].

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Antibodies↗

Respective role of antibodies and immune macrophages during acquired immunity against toxoplasmosis in mice.

Immunity of animals correlated with the destructive ability of their macrophages. Intraperitoneal inoculation of T. gondii led to a very limited infection of macrophages from immune mice. This infection was next rapidly and completely inhibited. Conversely, macrophages from mice immunized with killed toxoplasma were massively invaded and evolved like control cells. Similar results were also obtained with macrophage cultures infected in vitro and followed over a period of 4 days. Even after several washes, immune macrophages still preserved their ability to inhibit intracellular replication of toxoplasma. However, this resistance was not homogenous: in the absence of antibodies, some macrophages supported a parasitic growth whereas some others remained intact. Results have also shown that the engulfment capability of immune macrophages was not modified. The primary role of resistant macrophages in the immune response did not however exclude a participation of humoral factors. Specific antibodies acted on extracellular toxoplasma either by lysing them in the presence of the accessory factor or by slowing their active penetration into the cells. Furthermore, they did not affect the phagocytic activity of macrophages. The in vitro protective role of peritoneal exudate from immune mice seemed similar to that afforded by sera anti-toxoplasma antibodies.

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[Antitoxoplasmic immunity on congenitally athymic nude mice].

Susceptibility to toxoplasmic infection was found to be the same in Nude mice (nu/nu) as in controls. Vaccination with avirlent toxoplasma (Beverley strains) confered an incomplete immunity to Nude mice: in 20 to 40% of cases, mortality was delayed as compared to unvaccinated control. Cellular (activation of macrophages) and humoral (circulating antibodies) immune responses were partially present in Nude mice.

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