Search results for: SensiTek Anti-Polyvalent
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Increase of T cells bearing Fc epsilon R-associated antigen in patients with atopic asthma.
Subpopulations of peripheral blood mononuclear cells (PBMC) in patients with atopic asthma and control donors were analyzed by means of flow cytometry. T cells were isolated from PBMC by rosetting with sheep erythrocytes. The proportions of PBMC and T cells bearing receptors for Fc fragment of IgE (Fc epsilon R) were elevated in patients when determined with monoclonal antibody to Fc epsilon R-associated antigen (H107). Significant correlations were observed between the serum-IgE levels and proportions of Fc epsilon R+ T cells (r = .71, P greater than .002). In contrast, no differences were observed between the groups in the proportions of PBMC and T cells bearing receptors for Fc fragment of IgG (Fc8R) when measured with model IgG-immunocomplexes. The proportions of cells reacting with monoclonal anti-IgE (9G2), T11 (E receptor), Leu-2a (suppressor), Leu-3a (helper), Leu-4 (pan-T), Leu-12 (pan-B), and anti-polyvalent immunoglobulin did not differ significantly between the groups. The results indicate that Fc epsilon R+ T cells are increased in patients with atopic asthma, suggesting that these cells may be involved in the regulation and/or synthesis of IgE antibody formation in man.T Matsumoto, H Takahashi, T Miike
2608 related Products with: Increase of T cells bearing Fc epsilon R-associated antigen in patients with atopic asthma.
96 tests0.1ml0.1ml96 assays0.1ml (1mg/ml)50ul0.1ml0.1ml100 ug/vial
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A B-lymphoma cell line that forms rosettes with neuraminidase-treated sheep erythrocytes through monoclonal surface immunoglobulin.
Undifferentiated lymphoma from a 39-year-old female became serially xenotransplantable to preirradiated nude mice. The tumor cells (KT) possessed a monoclonal surface immunoglobulin (SIg mu, kappa) and formed rosettes with neuraminidase-treated sheep erythrocytes (SEn). Precise characterizations of the SEn rosette, however, revealed the following facts: (1) Neuraminidase-untreated or 2-aminoethylisothiuronium bromide (AET) treated sheep erythrocytes were not bound to the KT cells. (2) SEn rosettes on the KT cells did not show a temperature dependency. (3) Neuraminidase-treated erythrocytes from man, horse, mouse, and rabbit were not bound to the KT cells. (4) Preincubation of the KT cells with antipolyvalent immunoglobulin or anti-kappa-chain serum abolished the SEn rosette formation. (5) Trypsinization decreased both SEn rosettes and SIg on the KT cells. (6) SEn rosettes on the KT cells were too loose to be separated from nonrosetting cells by a Percoll gradient centrifugation method. Summarizing these results, the monoclonal SIg on the KT cells recognized sheep erythrocyte antigen(s) that were exposed only after the neuraminidase treatment. Therefore, this was considered to be a case with peculiar B-lymphoma cells that bound SEn through their SIg.Y Tsutsumi, S Suzuki, A Mikata, H Suzuki, K Kageyama, S Watanabe, K Minato, M Shimoyama
2888 related Products with: A B-lymphoma cell line that forms rosettes with neuraminidase-treated sheep erythrocytes through monoclonal surface immunoglobulin.
100.00 ug1 mg1 mg100.00 ug100.00 ug25ug100 plates100ul100ul1 mL100 µg1.5x10(6) cells
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Passive oral immunization with bovine immunoglobulins: enterpathogenic Escherichia coli from infants and bovine anti-E. coli lactoserum assayed in the rabbit ileal loop model.
The effect of immune bovine lactoserum (BLS) antipolyvalent enteropathogenic Escherichia coli on bacterial growth, viability and bacteria-induced fluid accumulation was examined in rabbit ileal loops. Human enteropathogenic E. coli strains 0125:K70 (B15), 0111:K58 (B4) and 055:K59 (B5) (1-3 X 10(9) per inoculum) induced secretion of 4-6 ml fluid per 10 cm loop. This effect was inhibited effectively by BLS (corresponding to 50 mg IgG 1 per loop) while the viability of bacteria counts decreased 2-25 fold compared with bovine serum albumin. E. coli 026:K60 (B6), 0126:K71 (B16) and 0127:K63 (B8) caused moderate secretion (2-3 ml/10 cm loop) that was significantly neutralized by BLS. E. coli 086:K61 (B7) and 0128:K67 (B12) did not give positive loops. The fluid secretion was shown to be dose dependent for E. coli 0125:K70 (B15) over the range from 2.5 X 10(9) to 8 X 10(7) bacteria/loop. The titration of the effect of BLS on fluid secretion caused by the same strain revealed a dose dependent decrease. The best inhibition was obtained with 100 mg BLS/loop, the highest dose tested.R M Zinkernagel, A Colombini