1999
DOI: 10.1111/j.1439-0450.1999.tb01249.x
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Phenotypical Characterization of Peripheral Blood Leucocytes in the Newborn Calf

Abstract: The present study was undertaken to establish reference values for the composition of blood leucocyte populations in neonatal calves by differential leucocyte cnunts and immunophenotyping. Neonatal calves 1 h post parturn @.p.) wcrc found to have a vcry high absolute number of granulocytes whde the number of peripheral blood mononuclear cclls was lower than in calves aged 3-9 weeks. The relative numbers of T cell subpopulations were similar in newborn and older calves, but newborn calves had lower percentages … Show more

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Cited by 11 publications
(8 citation statements)
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“…The percentage of B cells increased with time, most notably from 32 to 60 d of age. Similar age-dependent increases in the proportion of circulating B cells in young calves have been reported (Senogles et al, 1978;Menge, et al, 1999;Nonnecke et al, 1999) and also is typical of the maturing immune system of the calf. The transient, early increase in percentages of CD4 + T cells and cells expressing activation antigens (i.e., MHC class II antigen and IL-2r expression increased on stimulated lymphocytes and monocytes) may be indicative of a state of immune activation.…”
Section: Discussionsupporting
confidence: 77%
“…The percentage of B cells increased with time, most notably from 32 to 60 d of age. Similar age-dependent increases in the proportion of circulating B cells in young calves have been reported (Senogles et al, 1978;Menge, et al, 1999;Nonnecke et al, 1999) and also is typical of the maturing immune system of the calf. The transient, early increase in percentages of CD4 + T cells and cells expressing activation antigens (i.e., MHC class II antigen and IL-2r expression increased on stimulated lymphocytes and monocytes) may be indicative of a state of immune activation.…”
Section: Discussionsupporting
confidence: 77%
“…Immediately after preparation or at the end of the cultivation period, IEL were thoroughly resuspended and transferred to V-shaped microtiter plates (Greiner, Frickenhausen, Germany) for immunolabeling as described previously (22,25). Briefly, the cells were centrifuged (at 137 ϫ g and 4°C for 7 min) and resuspended in 50 l of cell culture medium as a negative control or with supernatants or diluted ascites fluid of hybridoma cell lines.…”
Section: Methodsmentioning
confidence: 99%
“…After stimulation. PBMC were thoroughly resuspended and transferred to V-shaped microtiter plates (Greiner, Frickenhausen, Germany) at the end of the cultivation period and were pelleted by centrifugation (150g at 4°C for 7 min) as described by Menge et al (23). The pellets were resuspended in 50 J.LI of cell culture medium as a negative control or with supernatant of hybridoma cell lines (lL-A 43 for BoCD2, IL-A II for BoCD4, IL-A I05 for BoCD8, IL-A65 for BoCD21.…”
Section: Peripheral Blood Mononuclear Cell (Pbmc)mentioning
confidence: 99%