1976
DOI: 10.1042/cs050012pb
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Enumeration of Immunoglobulin-Bearing Lymphocytes in Whole Peripheral Blood

Abstract: tritiated water as a diffusible indicator. This method requires extensive arterial sampling and time-consuming laboratory procedures for liquid scintillation counting. Besides, it does not provide information on the regional content of ELW. Regional information can be obtained by using gamma emitting tracers. Using the cyclotron produced 1 5 0 labelled water we demonstrated the feasibility of estimating ELW by external counting in the dog. The technique has now been extended to man. It is relatively non-invasi… Show more

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Cited by 5 publications
(6 citation statements)
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“…Determination of the total number of cells localizing in the spleen showed no differences between control and CoF-treated animals (Table 3) in accordance with the results obtained by Pepys et al [28] using transfer of radiolabeled cells after CoF treatment. This suggests that the observed differences in localization in the spleens of CoF-treated animals are mainly due to changes in the relative distribution of T and B cells.…”
Section: Discussionsupporting
confidence: 90%
“…Determination of the total number of cells localizing in the spleen showed no differences between control and CoF-treated animals (Table 3) in accordance with the results obtained by Pepys et al [28] using transfer of radiolabeled cells after CoF treatment. This suggests that the observed differences in localization in the spleens of CoF-treated animals are mainly due to changes in the relative distribution of T and B cells.…”
Section: Discussionsupporting
confidence: 90%
“…Their level was comparable to that found by the Japanese group in their controls [19,20], and higher than that found in normal subjects by other groups [27,28], Serum IgA, mg/100ml < 350 < 350 Fig. 2.…”
Section: Resultssupporting
confidence: 52%
“…Using blood from normal individuals, this method separates the T-cells and the null cells from total mononuclear cells with less than I % B-cell contamination. To ascertain whether the ATG and complement selectively destroyed the T-cells, the total mononuclear cells separated by Ficoll-Hypaque (Bo yum, 1968) were counted and the percentage of T-cells and B-cells was determined (Jondal et al, 1972;Pepys et al, 1976). After removal of the rosette-forming cells, the cell suspension, containing mostly the null cells, was placed on a glass petri dish for 0.5 h at 37°C to remove the adherent cells.…”
Section: Methodsmentioning
confidence: 99%
“…After incubation, the cells were washed and suspended in appropriate medium for myeloid and erythroid cultures. To ascertain whether the ATG and complement selectively destroyed the T-cells, the total mononuclear cells separated by Ficoll-Hypaque (Bo yum, 1968) were counted and the percentage of T-cells and B-cells was determined (Jondal et al, 1972;Pepys et al, 1976). The percentage of these cells were also determined in a duplicate sample of the mononuclear cells after treatment with ATG and complement.…”
Section: Methodsmentioning
confidence: 99%