19 research outputs found

    The innate resistance of CBA mice to endogenous murine leukaemia virus infection.

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    The incidence of lymphomata in CBA mice is low and furthermore is unaltered by transplantation at the early blastocyst stage and being born from the lymphoma-prone AKR. The number of C-type murine leukaemia virus particles in CBA derived in this manner and milk-fostered by AKR mice in no way differs from normal CBA. The results suggest that the oncogenic Gross virus does not pass through either the transplacental or transmammary routes, or alternatively that viral replication in the CBA was in some way inhibited. Both possibilities have still to be distinguished

    Évolution de l’utilisation d’animaux de laboratoire en France : aspects quantitatifs et qualitatifs

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    Mahouy Guy. Évolution de l’utilisation d’animaux de laboratoire en France : aspects quantitatifs et qualitatifs. In: Bulletin de l'Académie Vétérinaire de France tome 151 n°4, 1998. p. 441

    French Working Group ‘Primatology’

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    Virus-induced leukaemias in animals and humans

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    Failure to induce autoimmune disease with neonatal bursectomy in chickens

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    To assess the effect of abnormal control of bursa-derived B cell function upon the development of spontaneous autoimmune disease, newly hatched chicks were surgically bursectomized or sham-bursectomized and studied up to 4 months of age. The presence of autoimmune disease was assessed by direct Coombs' test, measurement of antinuclear antibody, total hemoglobin, packed cell volume, plasma bilirubin, red cell survival, and immunofluorescence studies on frozen kidney sections. Despite abnormal immunoglobulin levels detected in bursectomized chickens, no significant differences in terms of autoimmune activity could be demonstrated between the two groups. This suggests that primary B cell control is an unlikely factor in the etiology of autoimmune disease and supports earlier studies which imply that a major factor leading to progressive autoimmune disease is the failure of a normal T cell suppression function. </jats:p
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