Clinical & Experimental Immunology · 1994 · 44 citations · 17 references
PharmacyClinical PharmacokineticsPharmacokineticsClinical ImmunologyImmunology Of Infectious DiseasesMonoclonal AntibodiesAntibody CharacterizationAntibody PharmacokineticsHumoral ImmunityPharmacokinetics Of Monoclonal AntibodiesHollow Fiber BioreactorsImmunoglobulin E (Ige)Intramuscular Injection SafetyIntramuscular Injection Technique
Two human MoAbs, BRAD-3 (an IgG3 anti-D) and BRAD-5 (an IgG1 anti-D), were produced from Epstein-Barr virus (EBV)-transformed B lymphoblastoid cell lines grown in hollow fibre bioreactors. Six Rh D-negative male volunteers were injected intramuscularly with anti-D; two received BRAD-3 (approx. 1500 micrograms, 2600 IU), two were given BRAD-5 (300 micrograms, 2000 IU), and two had polyclonal anti-D immunoglobulin (500 IU, approx. 100 micrograms anti-D). Levels of anti-D in plasma samples taken up to 42 days later were measured by a sensitive AutoAnalyser method. The half life of BRAD-5 (mean 22.2 days) was greater, and that of BRAD-3 (mean 10.2 days) less than that of polyclonal anti-D (mean 15.6 days). The bioavailability (plasma uptake) of the MoAbs (mean 33.9%) was less than that of the polyclonal anti-D (mean 60.3%). BRAD-3 and BRAD-5 may be suitable for use in antenatal and post-natal prophylaxis against Rh D haemolytic disease of the newborn.
17
WHO technical report series 200 (1960).
Michael Pittman · PubMed · 1974 · 1.4K citations
Blood Transfusion in Clinical Medicine
Edgar H. Pierce · JAMA · 1994 · 349 citations