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  • 1
    ISSN: 1569-8041
    Keywords: CD20 ; chimeric IDEC-C2B8 ; lymphoma ; monoclonal antibody ; pharmacokinetics ; feasibility study
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background: In clinical trials in the USA, IDEC-C2B8 (a mouse-humanchimeric anti-CD20 monoclonal antibody) has demonstrated high response rateswith only mild toxic effects in relapsed B-cell lymphoma at a dose of fourweekly 375 mg/m2 infusions. The aim of the present trial wasto determine whether or not this dose is practically applicable to Japanesepatients with relapsed B-cell lymphoma with respect to safety,pharmacokinetics and efficacy. Patients and methods: Patients with relapsed CD20+ B-cell lymphomareceived intravenous infusions of IDEC-C2B8 once a week for four weeks. Atotal of 12 patients (four at 250 mg/m2 and eight at 375mg/m2) were enrolled. Results: All 11 eligible patients treated with either dose leveltolerated IDEC-C2B8 well. Commonly observed adverse drug reactions weregrades 1 or 2 non-hematologic toxicities during the infusion, consistingmostly of flu-like symptoms and skin reactions. All of the observedhematologic toxicities were of grade 3 or less, and transient. A rapid andsustained B-cell decrease in peripheral blood was observed, but noinfectious episodes were encountered. Human anti-mouse and anti-chimericantibodies were not detected. Of the 11 eligible patients (eight withfollicular, two with diffuse large-cell and one with mantle cell lymphoma),two showed a complete response and five showed a partial response, and allof the seven responders had lymphoma with follicular histology. Apharmacokinetic analysis showed that the elimination half-life (T1/2) ofIDEC-C2B8 was 445 ± 361 hours, and that the serum antibody levelsincreased in parallel with the course of infusions, and in most patients wasstill measurable at three months. Conclusions: The dose of four weekly 375 mg/m2 infusionsof IDEC-C2B8 is safe and effective in Japanese patients with relapsed B-celllymphoma. Further studies evaluating IDEC-C2B8 are warranted.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2145
    Keywords: Key words Anther ; Self-incompatibility ; S-locus glycoprotein ; Tapetum-specific promoter ; Transgenic Brassica
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  S-locus glycoprotein (SLG) is known to be one of the proteins related to self-incompatibility in Brassica, and its transcripts are detected in anthers as well as stigmas. However, an SLG protein has not been detected in anthers so far. Because of sporophytic control of the self-incompatibility (SI) phenotype of pollen, an SLG gene is expected to be expressed in the sporophytic tissue of anthers, i.e., the tapetum. Overexpression of an SLG gene in the tapetum would enable us to predict the localization and function of an SLG protein in anthers. In this study, an SLG gene of self-incompatible B. campestris under the control of a tapetum-specific promoter was introduced into self-compatible B. napus. Immunoblot analysis using anti-SLG antiserum detected the exogenous SLG protein in the immature anthers, but not in the mature anthers. Immunoelectron microscopy showed the SLG protein to be localized in the tapetum and in the exine cell wall layer at the stage when the tapetum was degenerating. This result indicates the possible movement of the SLG protein from the tapetum to the pollen surface. A pollination test indicated that the pollen of the transgenic B. napus did not gain the SI phenotype.
    Type of Medium: Electronic Resource
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