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Biomedical subjects

T W Holbrook

Publications and source records attributed to T W Holbrook.

27 records · Page 2Linked to original sources

Stimulation of resistance in mice to sporozoite-induced Plasmodium berghei malaria by injections of avian exoerythrocytic forms.

Mice received a series of injections of formalin-killed merozoites (FKM) of exoerythrocytic stages of Plasmodium fallax prior to challenge with sporozoites of P. berghei. In one study 4 of 16 FKM-immunized mice never exhibited parasitized erythrocytes after 2 challenges of 10(4) P. berghei sporozoites each, while all control animals died with high parasitemias. FKM-immunized mice were as susceptible as control mice to infections initiated with parasitized erythrocytes. In a second study, 14 of 16 mice immunized via the intravenous (i.v.) or combined intramuscular (i.m.) and i.v. routes were immune to an initial challenge with 10(4) sporozoites, but were susceptible to a second challenge. Three injections of FKM via the i.m. or intraperitoneal routes did not elicit a protective response against sporozoite challenge. Sera harvested from FKM-immunized and control mice prior to challenge produced no visible CSP reaction with P. berghei sporozoites, nor was infectivity of sporozoites altered after incubation in sera, showing that SNA was absent. In additional experiments results were less encouraging. An attempt to repeat the result of the second experiment failed. Each of 5 mice which received the same number of FKM by a similar schedule became infected after sporozoite challenge. In an additional study the immunization schedule was increased from 3 to 7 injections of FKM and 40% of FKM-immunized mice resisted challenge. However, mice which had received FKM prior to sporozoite challenge consistently displayed an increased prepatent period compared with control animals. A department from methods of the more successful studies was necessitated in these later studies in which FKM were harvested from cell cultures maintained for longer periods of time.

Animals↗

Comparison of two geographic strains of Leishmania donovani by resistance of mice to superinfection.

Groups of mice were injected with Leishmania donovani strains Et (Burma) or IS (Sudan) and the courses of infection were followed. Between days 20 and 30 after infection by treatment with pentostam. Et- and 1S-recovered mice were challenged by intravenous injection of amastigotes of each strain. Although resistance to superinfection was apparent the L. donovani strains could not be differentiated by this method.

Animals↗

The effect of BCG-vaccine upon experimental visceral leishmaniasis in hamsters.

Stimulation with Bacillus Calmette-Guerin (BCG) vaccine has been reported to enhance resistance of mice against Leishmania donovani infection. Such infection is usually lethal in hamsters, thus providing a more stringent animal model to assess the effect of BCG upon visceral leishmaniasis. Animals receive two IP injections (2-8 X 10(7) BCG) pre or post IC challenge with 4 X 10(6) amastigotes. Controls received BCG alone (with no infection) or were untreated (NT). Pretreated animals exhibited significantly fewer (P less than 0.05) hepatic or splenic amastigotes than NT animals at days 7, 14, and 28 post challenge, but most BCG treated hamsters died earlier than NT. Post treated hamsters showed no significant reduction in parasite burdens, or in median time to death as compared to NT group. Hamsters which received BCG but were not infected appeared healthy during the study. The reason for increased susceptibility of BCG-treated hamsters to disease is not clear, but observed pathologic complications of L. donovani infected hamsters appear to be exacerbated by BCG stimulation.

Animals↗

Non-specific and specific stimulation of resistance against Leishmania donovani in C57BL/6 mice.

Stimulation by intravenous injections of glucan, a beta 1,3 polyglucose, provided a significant degree of resistance in mice against Leishmania donovani. The response of C57BL/6 animals was dose-dependent. A single glucan injection before or after infection induced significant resistance but to a lesser degree than two or three injections. Immunization by injections of formalin-killed promastigotes with glucan via the subcutaneous or intravenous routes provided greater resistance than glucan or dead parasites alone against subsequent infection with viable parasites. Subcutaneous immunization with promastigotes from cultures passaged 10 times in vitro and those from cultures maintained for 25 passages elicited a similar degree of resistance against infection and induced positive skin test responsiveness against leishmanial antigen prior to infection.

Adjuvants, Immunologic↗