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Biomedical subjects

G Corthier

Publications and source records attributed to G Corthier.

At least 73 records · Page 4Linked to original sources

Postnatal development of protein absorption in conventional and germ-free mice.

In the jejunal epithelium of adult animals, horseradish peroxidase (HRP) is transported via two functional pathways: a major route involving lysosomal degradation and a minor route allowing transport of the intact protein. The postnatal development of HRP absorption and the influence of conventional microflora were studied in vitro, using jejunal epithelium of conventional and germ-free suckling mice mounted in Ussing chambers. In conventional mice, tritiated peroxidase ([3H]HRP) transport from mucosa to serosa did not change with age except during days 3 and 4, when it increased fivefold. This increase was entirely due to the rise in intact HRP transport and was not related to a decrease in lysosomal cathepsin B and D activities. In germ-free mice, HRP transport developed similarly but decreased by 75% along both pathways. This reduced absorption was associated with lower cathepsin B and D activities. These results strengthen the existence of two transcellular pathways in nonimmunoglobulin protein absorption by the proximal gut with a limiting step situated before the lysosomal system, presumably at the brush-border membrane. Their development is not parallel and does not correlate with gut closure to immunoglobulin transfer.

Animals↗

Modulation of cytotoxin production by Clostridium difficile in the intestinal tracts of gnotobiotic mice inoculated with various human intestinal bacteria.

Gnotobiotic mice died 2 days after inoculation of a cytotoxigenic Clostridium difficile strain. Protection occurred when mice were previously inoculated with a strain of Escherichia coli or Bifidobacterium bifidum. Intestinal cytotoxin production was highly reduced in the surviving mice, whereas the C. difficile population level did not decrease to a great extent.

Adult↗

Production of coproantibodies and immune complexes in piglets infected with rotavirus.

The local immune response of newborn piglets to experimental infection with rotavirus was analyzed by means of coproantibodies, immune complexes, and the detection of rotavirus. Immune complexes appeared in the feces on day 4 after inoculation when the production of rotavirus began to decrease; they reached a peak when no rotavirus could be detected in the feces. The presence of free IgA and IgM antibodies to rotavirus could be demonstrated on day 7 when the immune complexes had already reached a maximum level. An enzyme-linked immunosorbent assay was used for all of the analyses.

Animals↗

Detection of antirotavirus immunoglobulins A, G, and M in swine colostrum, milk, and feces by enzyme-linked immunosorbent assay.

An enzyme-linked immunosorbent assay was developed to allow direct detection of class-specific antirotavirus antibodies. In colostrum and in milk, antirotavirus antibodies were found in the three immunoglobulin classes. Antirotavirus immunoglobulins G and M were predominant in colostrum, whereas antirotavirus immunoglobulin A was predominant in milk and feces.

Animals↗

Measurement of porcine faecal IgA, IgG and IgM levels by a competitive enzyme-linked immunosorbent assay.

The concentrations of IgG, IgA and IgM were compared in faecal material of healthy and diarrhoeic pigs using a competitive enzyme-linked immunosorbent assay (ELISA). The relative concentrations of faecal immunoglobulins (Ig) in healthy piglets and adults were significantly different (P less than 0.01). IgA was the most important Ig in adult faeces while IgM was predominant in piglet faeces. IgG appears to be a relatively rare component. No significant differences could be detected between groups of healthy and diarrhoeic piglets. In adult faeces, significant changes (P less than 0.02 to P less than 0.001) in Ig relative concentrations were observed between diarrhoeic and healthy animals.

Aging↗

[Immunologic abnormalities in pigs with hog cholera virus infection (author's transl)].

The effects of an acute Hog Cholera Virus (HCV) infection upon immune functions of experimentally infected pis were studied. Leukopenia was found to occur in both vaccinated and non-vaccinated infected animals but without any decrease in lymphocyte proportion. Lymphocytes from infected pigs had an altered response to phytohemagglutinin (PHA) as judged by an in vitro tritiated thymidine uptake of PHA-stimulated lymphocyte cultures. The beginning of a secondary humoral immune response to lysozyme appeared to be significantly depressed in HCV diseased animals.

Animals↗

Cellular and humoral immune response in pigs given vaccinal and chronic hog cholera viruses.

Humoral immune response (seroneutralization) and cellular immune response (lymphocyte-stimulation test) were analyzed in pigs inoculated with low virulent strains of hog cholera virus or vaccinated with a live-virus vaccine. Vaccinated animals exhibited an intense neutralizing antibody production, but cellular immune response was not detected. Neutralizing antibodies were not found in infected pigs, but a brief cellular immune response (18 days after inoculation) was observed.

Animals↗

Comparison of the immune response in serum and bucco-pharyngeal secretions following immunization by different routes with a live hog cholera virus vaccine (Thiverval strain).

The influence of vaccination route on local and systemic immune response was studied with hog cholera virus vaccine. Kinetics of antibody synthesis in serum and bucco-pharyngeal secretion was observed. Results show that, whatever the vaccination route (intranasal or intramuscular) a good systemic and local immune response were induced and pigs resisted to a virulent challenge. However the highest local immune response was obtained by intranasal vaccination with large vaccine dosage (10(7) P.F.U./pig). After a virulent challenge performed by intranasal route, no clear anamnestic immune response was detected in bucco-pharyngeal secretions.

Administration, Intranasal↗

[Hog cholera virus: influence of colostral passive antibody on immune response of pig following vaccination with the rabbit adapted Chinese strain (author's transl)].

Using the rabbit adapted chinese strain of Hog cholera, active immunization of piglets having passive colostral antibodies was studied. 65 piglets born from 11 sows were used. Concerning sows, vaccination was performed 5-6 months and 1 month before service (3 sows), 30 days (2 sows) and 60 days (3 sows) after service. Divided in 5 lots, piglets were vaccinated at 4 different periods after birth (15, 30, 60 and 90 days). Hog cholera immunity was determined for each animal by means of kinetic of serum neutralizing antibodies and resistance to virulent challenge performed 5 months after birth. High levels of neutralizing antibodies were observed in serum of each vaccinated sow at the time of farrowing. In piglets having ingested low quantities of colostrum, vaccination induces a good antigenic stimulation characterized by a normal humoral immune response and challenge resistance. But in piglets having ingested a normal quantities of colostrum, colostral passive antibodies have a partial or complete suppressive effect on primary immune response which is characterized by a delay in serum antibodies formation and by a low level at the time of challenge. According the conditions of sows vaccination, differences were observed in the properties of colostral passive antibodies (intensity of suppressive effect on active immune response, in vitro "avidity" for Hog cholera virus, mean value of half-life) present in piglets serum. On practical aspect, vaccination with the chinese strain becomes fully effective in piglets having passive immunity when they are 30-60 days old.

Animals↗

Local immunity in the pig respiratory tract. II. -- Relationship of serum and local antibodies.

Antibody passage from blood to respiratory secretions was studied on pigs. The animals were passively immunized and have a high anti-hog cholera serum antibody titer. With normal animals as with swine influenza animals, no serum antibody could be recovered neither in buccopharyngeal secretions nor in lung washings: it seems that in such conditions no detectable transudation occurs from blood to local secretions. Following intranasal inoculation of swine influenza virus or intramuscular injection of live attenuated hog cholera virus, local antibodies appear, which are considered to be locally produced.

Animals↗