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Biomedical subjects

A L Parodi

Publications and source records attributed to A L Parodi.

At least 37 records · Page 2Linked to original sources

The BLV-induced leukemia--lymphosarcoma complex in sheep.

Sheep are highly susceptible to BLV infection and can be infected via several different means (routes). In all inoculated animals, specific anti-BLV antibodies can be demonstrated 1 to 3 months post-inoculation (p.i.). Between 10 and 13 months p.i., a moderate but persistent lymphocytosis (PL) may be detected in about 50% of the infected animals. This hematological disorder may be, but is not necessarily, associated with the development of a lymphosarcoma and can (might) be interpreted as a true lymphoid leukemia. According to findings revealed by immunolabelling and mitogen stimulation of peripheral blood lymphocytes, BLV-induced PL appears to be a B-cell disorder. Induced lymphosarcoma appears in about 40% of infected sheep during the 6 years p.i. It too is of B-lymphocyte lineage. In vitro studies demonstrate that BLV antigen is expressed exclusively in B-lymphocytes. Yet, BLV expression is greatly stimulated in whole lymphocyte culture by the addition of T-cell mitogen. This same phenomenon occurs when the supernatant of stimulated T-lymphocyte cultures is added to isolated BLV-infected B-lymphocytes. This observation supports the hypothesis that, as is the case with other retroviruses such as HIV, BLV is able to use the regular activation machinery of the immune system for its own replication and transmission. It seems, therefore, that the leukemia-lymphoma complex in sheep may serve as an accurate experimental model for the study of the biological properties of retroviruses.

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Natural mode of horizontal transmission of bovine leukemia virus (BLV): the potential role of tabanids (Tabanus spp.).

In order to evaluate the potential role of hematophagous insects in the natural spreading of bovine leukemia virus (BLV) infection in cattle, a 2-year survey was carried out involving sequential serological tests on 3328 cattle in three different areas. A parallel entomological study was run over the same period, using continuous trapping, in order to determine both the density and variations of horsefly (Tabanus spp.) populations in the close vicinity of the herds. After statistical analysis, this space-time study showed that: (1) There is a significant positive geographical correlation between the rate of incidence of BLV infection and the density of the horsefly population. (2) Seasonal variations in the incidence rate exist; the highest rates are generally observed during summer (from July of September), and the lowest during winter, spring and early summer (from November to mid-July). (3) There is a time link between the rate of sero-conversion and the variations in activity of the horsefly population. All these data combined would appear to indicate that tabanids play a considerable role in the spread of BLV under natural conditions.

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Doxorubicin-loaded nanoparticles: increased efficiency in murine hepatic metastases.

Free doxorubicin and doxorubicin associated with polyisohexlycyanoacrylate were tested for their therapeutic efficiency in hepatic metastasis-bearing mice. The metastases originated from the M 5076 reticulum cell sarcoma. Irrespective of the dose and the administration schedule, the reduction of the number of metastases was much larger with the doxorubicin-loaded nanoparticles than with free doxorubicin. This was clearly confirmed by histological examination. Although pharmacological and pharmacokinetic data indicated a strong capture of the nanoparticles by the hepatic issue, the mechanism of nanoparticle therapeutic efficiency remains unclear.

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Relationship between levels of Clostridium difficile toxin A and toxin B and cecal lesions in gnotobiotic mice.

Various Clostridium difficile strains were studied with respect to their pathogenicity in monoassociated mice in relation to levels of toxin A and toxin B in vivo and in vitro. Two strains which were the most potent toxin producers in vitro induced mortality (100%); mice monoassociated with these strains were found to have high levels of both toxins in their ceca and an intense cecal epithelial ulceration together with a severe inflammatory process. No mortality was observed with the other strains. Strains which were moderately toxinogenic in vitro induced inflammation of the cecum but no ulceration, and no toxin A was found. Inflammation intensity was not related to toxin B levels. After 3 weeks, ceca returned to normal in spite of a chronic cytotoxin production. When compared with in vitro results, which showed a good correlation between the levels of the two toxins, toxin A amounts in vivo were found to be lowered relative to toxin B levels. The lack of detectable toxin A levels in animals infected with all but the two most highly toxinogenic strains prevented death. This work points out the importance of investigation of toxin A for the understanding of C. difficile pathogenicity.

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[Histologic study of a bovine lymph node before and after antigenic stimulation. 1. Histology, cytology and histometry].

The effect of antigenic stimulation on a bovine lymph node was studied using conventional histological and cytological techniques. The lesions observed in the bovine lymph node following immunological stimulation are similar to those described in other mammalian species. Histometrical studies showed an increase in the size of the nucleus of lymphoid cells in the stimulated lymph nodes. This probably reflects an activation of the lymphoid cell population. The number of the various cell types in the germinal centers appeared to be positively correlated with the stimulation intensity. The complete identification of the different sub-lines of lymphoid cells requires complementary immunocytochemical and electron-microscopic studies.

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Trichostrongylus colubriformis: effects on villi and crypts along the whole small intestine in infected rabbits.

In control and Trichostrongylus colubriformis-infected rabbits histological samples were taken from the small intestine at 25-cm intervals from the pylorus. Length of villi, surface of glands of Lieberkühn, and number of epithelial cells per unit length were measured with a digitized table. Two zones were so delimited along the parasitized mucosa: in the proximal part of the gut, both shortened villi and dilated crypts were found; in the distal region of the intestine, which was also the area with the lowest density of parasites, dilatation of crypts was associated with an increase in the size of villi. In both regions, the size of enterocytes was unchanged. Correlation coefficients calculated between worm burdens and relative variation in length of villi were significant and negative. Conversely, the same coefficients were significant and positive between worm burdens and surface of crypts. The possibility of local and general actions of Trichostrongylus colubriformis on both villi and crypts is evoked to explain the changes in the two zones. The functional importance of the hypertrophy in the distal region is still to be investigated during a T. colubriformis infection.

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T-B cell cooperation for bovine leukemia virus expression in ovine lymphocytes.

Bovine leukemia virus (BLV) replication in B lymphocytes from experimentally infected sheep depends on three conditions. First, viral production is detected only when the infected animals exhibit blood lymphocytosis. Second, it requires in vitro cultivation but is never observed in vivo. Third, enhancement of virus expression after phytohemaglutinin (PHA) or concavalin A stimulation is observed in lymphocyte cultures for all infected animals, whereas specifically B cell mitogens are inefficient. The PHA effect is linked to the presence of T lymphocytes. In addition, the conditioned medium prepared from PHA-stimulated normal lymphocytes greatly enhances BLV production. Altogether, these results establish that T lymphocytes, through a lymphokine production, are important and may be essential for BLV growth in B lymphocytes.

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[Effects of exposure of spontaneously leukemic mice (AKR mice) to an electric field].

Spontaneously leukemic AKR mice were exposed from 6 weeks age to a 50 kV/m electric field 12 hrs./day. In this study, carrying on 50 exposed and 50 sham-exposed mice, like in the two preceding experiments, the exposed group mortality is lightly retarded, and reaches 100% only 10 weeks after the sham-exposed group. These differences are not however statistically significative.

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T and B peripheral blood lymphocytes in normal and lymphocytotic sheep.

Surface immunoglobulins (SIg), Peanut Agglutinin (PNA), spontaneous erythrocyte rosette (E-rosette) and Helix pomatia (HP) marker were investigated in normal and Bovine leukemia virus (BLV)-infected sheep. In normal sheep, 19.3% +/- 4.9 of peripheral blood lymphocytes (PBL) were SIg+, whereas 58% +/- 5.69 were PNA+, and 19.6 +/- 5.2 were E-rosette forming cells (E-RFC). In BLV-induced lymphocytotic sheep, SIg+ cells in PBL reached 59.4% +/- 15.06. In the same animals, PNA bound to 20.6% +/- 9.69 and E-RFC were 8.7% +/- 4.5. A panning technique was applied with an anti sheep-immunoglobulins coated plates to separate SIg+ (adherent cells = A) and SIg- cells (non-adherent cells = NA). The (A) population was 94-95% SIg+ cells and 2-3% PNA+, while the (NA) population was 0-4% SIg+ and 79-85% PNA+ cells. Thus PNA is a T cell marker in sheep species. HP, a marker for bovine T lymphocytes was also studied. Sheep PBL do not bind to HP. However, after panning separation about 50% of NA cells became HP+.

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Wheat germ agglutinin (WGA): a bovine T lymphocyte marker.

Bovine peripheral blood lymphocytes (PBL) were examined for their ability to bind wheat germ agglutinin (WGA). This lectin labelled 43.8% +/- 11.95 of bovine PBL, whereas peanut agglutinin (PNA), a T cell marker, bound 59.4% +/- 8.67 cells, and surface immunoglobulin (SLG)-bearing cells constituted 24.15% +/- 8.47 of PBL. After panning fractionation of B (Slg+) and T (PNA+) lymphocytes. WGA labelled 89 to 97% of the enriched T cell population (80/87% PNA+; 2-4% Slg+) but only 6 to 8% of the enriched B cell population (85-91% Slg+; 5-7% PNA+).

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Bovine leukemia virus replicates in sheep B lymphocytes under a T cell released factor.

In order to determine which cell supports BLV replication in experimentally infected sheep, peripheral blood lymphocytes (PBL) were separated into purified B and T populations by a panning technique. Our data demonstrate that viral replication takes place only in B lymphocytes. However, PHA, a T cell mitogen, is necessary for BLV replication both in PBL and enriched surface immunoglobulin bearing cells, whereas B cell mitogens have no effect on viral replication. Altogether, these results suggest that BLV activation in enriched B lymphocytes is dependent on the presence of residual T cells, and occurs through a T cell interaction, probably mediated by a soluble factor. This possibility was confirmed by the fact that the conditioned medium from cultures of BLV-free sheep T lymphocytes greatly enhances viral production by infected B lymphocytes. Our data favor the hypothesis that BLV multiplication occurs through the regular activation mechanisms of the immune system.

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Selective tropism of bovine leukemia virus (BLV) for surface immunoglobulin-bearing ovine B lymphocytes.

Bovine leukemia virus (BLV) is experimentally infectious for sheep. Virus production does not occur in the animals, but only after in vitro cultivation of infected lymphocytes in the presence of phytohemagglutinin. Lipopolysaccharide or dextran sulfate 500 had no effect. After panning separation, it was possible to demonstrate that, in peripheral blood lymphocytes, BLV was integrated in the B lymphocytes only and that BLV expression took place in a fraction of this population. The ovine leukemia may constitute a good experimental model for understanding the virus-induced leukemias of the BLV-human T cell leukemia virus group.

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Development of leukemia and lymphosarcoma induced by bovine leukemia virus in sheep: a hematopathological study.

The hematological and neoplastic disorders induced in sheep by experimental bovine leukemia virus (BLV) infection are described. Seventeen of 19 BLV-inoculated sheep developed a marked increase in peripheral blood lymphocytes by 36 months after the intraperitoneal injection of peripheral blood lymphocytes from a BLV-infected cow. This increase correlated with an increase in the number of circulating B lymphocytes as demonstrated by the presence of surface immunoglobulins (SIg) and a high cell proliferative response to lipopolysaccharide and was considered to be a persistent B cell lymphocytosis. Lymphosarcoma developed in five BLV-infected sheep between 19 and 38 months postinoculation and was preceded in four out of five of these cases by an elevation in peripheral blood lymphocytes which began 4 to 26 months before death due to lymphosarcoma. The majority of tumor cells in all lymphosarcoma cases were of the centroblastic type, and in two cases in which the presence of SIg was assayed, the majority of tumor cells were SIg-positive. Thus, BLV-induced lymphosarcoma in sheep seems to be a B lymphocyte-derived tumor.

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Incidence of bovine leukemia virus-specific antibodies in West African cattle.

A sero-epidemiological survey of bovine leukemia virus (BLV) infection in indigenous West African cattle was undertaken using a radioimmunoassay and enzyme-linked immunosorbent assay. A high incidence of anti-BLV antibodies was found in the breeds tested and their crosses, whatever the test used. More extensive studies are needed to establish the prevalence of BLV infection in other parts of Africa; these may provide additional data on the similarities found between human and bovine leukemia viruses.

Africa, Western↗

Hyena disease in cattle: a review.

Hyena disease was first reported in France in 1975 and since then has been recognized in many countries. It is currently regarded as a disorder of skeletal development, mainly localised in the pelvic limbs of young cattle. Some investigators consider that it is a metabolic disease but the authors believe that it may be caused by a virus. Their hypothesis, according to which bovine virus diarrhoea-mucosal disease virus is involved, is based on epidemiological, histopathological and immunological evidence.

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