Premium
Freedom from Transmission of Hepatitis‐B of Gamma‐Globulin and Heat‐Inactivated Plasma Protein Fraction Prepared from Contaminated Human Plasma by Fractionation with Solid‐Phase Polyelectrolytes 1
Author(s) -
Harris Robert B.,
Johnson Alan J.,
Semar Martin,
Detente Jacques,
Fields Joseph E.
Publication year - 1979
Publication title -
vox sanguinis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.68
H-Index - 83
eISSN - 1423-0410
pISSN - 0042-9007
DOI - 10.1111/j.1423-0410.1979.tb04413.x
Subject(s) - hbsag , fractionation , chromatography , chemistry , gamma globulin , radioimmunoassay , antibody , globulin , hepatitis b immune globulin , elution , fraction (chemistry) , virology , immunology , biochemistry , medicine , hepatitis b virus , virus
. Plasma contaminated with hepatitis B surface antigen (HBsAg) and shown by others to be infectious when injected in a dilution of 1:1,000,000 in chimpanzees, was fractionated by a solid‐phase polyelectrolyte (PE) procedure for its content of plasma protein fraction (PPF) and δ–globulin (immune serum globulin; ISG). Quantitative Ausria II radioimmunoassays showed that nearly half the HBsAg was bound by the PE and could be eluted at low pH, while the rest was found in the heat‐inactivated PPF. When the ISG was concentrated to 16%, the 13 mg/kg (comparable to a human dose) was injected intramuscularly in 6 chimpanzees, or when the PPF was heated at 60°C for 10 h and injected intravenously in 2 chimpanzees, there was no clinical or laboratory evidence of hepatitis B infection after 12 months, although 1 chimp of 2 who received the same material showed a borderline positive anti‐HBsAg antibody result on one of 52 weekly serum samples. Since the new PE fractionation method is essentially nondenaturing, and simpler than the classical ethanol procedures, it was important to establish the noninfectivity of the final products.