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Biomedical subjects

M Kennedy

Publications and source records attributed to M Kennedy.

At least 253 records · Page 14Linked to original sources
PubMed1982

Role of antibody in the protection of mice from arthritis induced by Mycoplasma pulmonis.

C3H and C57Bl10 mice exhibit a differential susceptibility to arthritis induced by Mycoplasma pulmonis. Resistant C57Bl10 mice consistently demonstrated higher complement-fixing antibody titres than susceptible C3H mice throughout the development of the acute arthritis. A strong correlation was demonstrated between the levels of anti-mycoplasma antibody and resistance to acute arthritis in six strains of mice. To test the hypothesis that the difference of arthritis resistance of C3H and C57Bl10 mice was caused by a different susceptibility of their lymphocytes to mitogenic stimulation by M. pulmonis, we investigated the generation of non-specific immunoglobulin in vivo and in vitro. M. pulmonis acted as a polyclonal mitogen, but stimulated approximately equal responses in lymphocytes of both strains.

Animals↗
PubMed1980

Individual-specific (idiotypic) T-B cell interactions regulating the production of anti-2,4,6-trinitrophenyl antibody. I. Generation of suppressor T cells and antibody directed against immunocompetent cells.

It is known from several experimental systems that the production of dominant antibody idiotypes may be regulated by anti-idiotypic mechanisms. Our aim has been to test whether the potential for such control also exists in the more typical heterogeneous antibody responses of inbred mice to the trinitrophenyl (TNP) hapten, where dominant idiotypes are not recognized. CBA mice were hyperimmunized to trinitrophenylated keyhole limpet hemocyanin. Serum or lightly fixed spleen cells from these mice were injected into normal syngeneic "recipients". The serum and spleen cells from these recipients were found to have the power to suppress in vitro anti-TNP antibody responses made by further spleen cells from the donor mice. This suppression was specifically directed against the cells of the individual donor animals suggesting idiotype-related regulation.

Animals↗
PubMed1980

Individual-specific (idiotypic) T-B cell interactions regulating the production of anti-2,4,6-trinitrophenyl antibody. II. Development of idiotype-specific helper and suppressor T cells within mice making an immune response.

The previous report demonstrated that serum and cells from CBA mice immunized with trinitrophenyl (TNP), when injected into normal, syngeneic "recipient" mice, induce the formation of apparently idiotype-specific suppressor cells and serum factors, and that such regulatory elements develop within the serum of the TNP-immunized animals themselves. In this report, it is indicated that regulator cells develop also within the spleens of TNP-keyhole limpet hemocyanin-immunized animals, and may in part be responsible for our earlier observation that T cells from TNP-immune CBA mice stimulate optimal antibody production in culture when paired with B cells from the same individual animal. While some evidence for individual-specific T helper cells was obtained, the poorer response of mismatched T and B cells could be attributed in part to Ly-2.2-bearing suppressor T cells. Overall, the results support the view that idiotype-related regulation is not confined to dominant-idiotype models but is also involved in heterogeneous anti-hapten antibody responses.

Animals↗
PubMed1980

The '18' variant of human placental alkaline phosphatase is identical to the 'D-variant'.

Samples of the rare SD, FD and ID phenotypes of placental alkaline phosphatase were compared by starch gel electrophoresis and by measuring L-leucine inhibition with the numbered phenotypes of Donald and Robson. The 'D-variant' was found to be identical to 'variant 18'. 'Variant 17' was also found to be inhibited by L-leucine to the same extent as 'variant 18'. There was a statistically significant excess of male births with the variant 18 enzyme.

Alkaline Phosphatase↗
PubMed1979

Macrodosage of phenytoin.

Large doses (up to 1200 mg) of phenytoin were required to achieve therapeutic plasma concentrations and to control post-traumatic seizures in a 62-year-old woman. The elimination half-life of phenytoin was calculated to be 3.5 hours. Frequent monitoring of the plasma concentration was essential to optimize the therapeutic control and to avoid systemic toxicity.

Drug Resistance↗
PubMed1979

Injuries in Rugby League football.

All injuries occurring in the top three grades of a New South Wales club were documented over a one-year period (1978). Two hundred and four injuries were recorded and over half of these injuries (51%) occurred in the lower limbs. The injury rate was calculated at one injury per 3.6 man hours of play. There was a significant difference in the type of injury sustained by forwards and backs, the forwards receiving more cuts, bruises and haematomas, and fewer joint injuries. This difference is probably because of the nature of the game played by these subgroups.

Athletic Injuries↗
PubMed1979

Drug metabolism.

Explore the source record for details and available documents.

Acetylation↗
PubMed1979

Plasma quantitation of warfarin and warfarin alcohol by gas chromatography chemical ionization mass spectrometry in patients on warfarin maintenance therapy.

A quantitative method has been developed to measure plasma concentrations of warfarin and warfarin alcohol. The analytical procedure uses deuterated analogues as internal standards, and the technique of selected ion monitoring following gas chromatography methane chemical ionization mass spectrometry of the 4'-methyl ethers of warfarin and warfarin alcohol. Concentrations of warfarin and warfarin alcohol have been measured in plasma samples from 43 patients maintained on chronic warfarin therapy and compared with the 'apparent warfarin' concentration as measured by a fluorometric procedure. The study demonstrated a high degree of correlation between the gas chromatography mass spectrometric derived sum of the individual concentrations of warfarin and warfarin alcohol, and the 'apparent warfarin' concentration determined from a spectrofluorometric assay.

Chromatography, Gas↗