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J Stuart

Publications and source records attributed to J Stuart.

222 records · Page 13Linked to original sources

Factors influencing collagen-induced autoimmune ear disease.

In 1981, the authors described a type II collagen-induced autoimmune ear disease (CIAED) model. The purpose of this study was to gather further evidence that this is a sound animal model to use in evaluating inner ear diseases. The temporal bone lesions of CIAED in Lewis and Wistar rats were characterized by the presence of sensorineural hearing loss with mild atrophy of the organ of Corti and spiral ganglion degeneration, vestibular dysfunction with vacuolar degeneration of the crista ampullaris, otospongiosis-like lesions in the tympanic annules, cochlear vasculitis, and eustachian tube disease. Both cellular and humoral immune responses to type II collagen were demonstrated. The induction of ear lesions depends on many factors. In general, animals immunized with antigens in complete Freund's adjuvant showed relatively more severe lesions than animals immunized with antigens in incomplete Freund's adjuvant, but the duration of the immunization seems to be a more important factor in reproducing severe lesions. The strain and the source of the animals are also important factors in autoimmune inner ear diseases, as is the condition of the host animals. Subclinical or clinical mycoplasma infection in the rat markedly reduced the incidence and severity of lesions in type II collagen-induced arthritis. Many researchers did not consider sialoductal adenovirus, widely present among laboratory rats, a lesion-producing factor in rats. Although many factors influence the induction and severity of CIAED, these animal models provide an excellent new avenue of inner ear research.

Animals↗

Type II collagen-induced autoimmune salpingitis in rats.

Autoimmune salpingitis was induced in 17 (85%) of 20 outbred Wistar rats by immunization with bovine type II collagen; three of those also developed eustachian tube chondritis. The lesions were characterized by infiltrations of a large number of mononuclear cells in the mucosa and submucosa, destruction of cartilaginous structure, and deposition of IgG and complement C3. The animals had high titers of anti-type II collagen antibody. Immunohistochemical examination using monoclonal antibody to type II collagen revealed the presence of type II collagen in the eustachian tube cartilage. These observations suggest a causal relationship between autoimmunity to type II collagen and salpingitis in the rat, and this animal model may be useful in defining the pathogenesis of eustachian tube diseases mediated by immunity to type II collagen.

Animals↗

Experimental Staphylococcus aureus brain abscess.

The virulent organism Staphylococcus aureus produced brain abscesses that were quantitatively and qualitatively different from those caused by less virulent organisms. S. aureus abscesses created larger lesions, as earlier ependymitis, delayed progress toward healing, and caused areas of inflammatory escape outside the collagen capsule. Imaging tests revealed similar findings: the abscesses were larger, had more extensive central necrosis, and showed earlier evidence of ependymitis. This virulent organism also demonstrated that white matter is more susceptible than overlying gray matter to destruction by infection. The pattern of spread and other histologic findings suggest that collagen capsule formation has less of an infection "containment" function than was previously thought.

Animals↗

Care after bone marrow transplantation.

Assessments vital to the recovery of patients following bone marrow transplant are detailed in this article, and the protective environment in which they need to be nursed is outlined. Common infections and side effects are highlighted.

Bone Marrow Transplantation↗