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Biomedical subjects

B W Griffiths

Publications and source records attributed to B W Griffiths.

At least 19 recordsLinked to original sources

The role of isotype and epitope specificity of monoclonal antibody mixtures in immunodiffusion reactions.

Twenty monoclonal antibodies to human alpha-fetoprotein have been characterized in terms of IgG subclass, epitope specificity and immunodiffusion properties. The Ig molecules consisted of six G1, ten G2a and four G2b isotypes. The epitope analysis was conducted by a solid-phase RIA employing 125I-labelled AFP. The RIA analysis resulted in the identification of seven determinants, two of which were specific for one antibody each, while others were specific for two or more antibodies. In Ouchterlony tests with the antibodies, none formed bands of immunoprecipitate when diffused individually against the antigen. Tests with all possible mixtures of pairs of the antibodies (190) resulted in positive immunodiffusion responses with only two mixtures. These each contained antibodies of the 2b isotype and demonstrated distinct epitope specificities. The immunodiffusion of mixtures of three antibodies from a group of 12 that were selected to represent equal numbers of isotypes resulted in 84 positive responses and 136 negative responses, i.e. from a total of 220 mixtures. A striking correlation was noted between positive immunodiffusion tests and composition of antibody isotypes and of epitope specificities of the mixtures. Each mixture was found to contain antibodies of at least one 2b isotype and of different epitope specificities. None of the mixtures that lacked a 2b isotype (56) responded in immunodiffusion tests. Similarly, in instances (46) in which the epitope specificities of the antibodies in the mixture were the same, i.e. duplicated or triplicated, the results were again negative despite the presence of a 2b isotype. The comparison of these studies with similar studies of a smaller group of antibodies to pregnancy-specific beta 1-glycoprotein strongly suggests that the G3 antibody isotype may have an immune precipitation enhancing effect similar to the G2b isotype.

Animals↗

Human serum vitamin B12 assay methods--a review.

The clinical importance of a reliable human serum vitamin B12 assay to aid the diagnosis of pernicious anemia (PA) cannot be overemphasized. Our review of the literature indicates that a reference method for the quantitation of serum vitamin B12 (serum B12) with the required accuracy, precision and rapidity has not been reported to-date. Controversies, debates and criticisms over human serum B12 assays (especially commercial kits) have been common-place. Various methods of quantitation of B12 reviewed in this communication include: microbiological, radioisotopic, high-performance liquid chromatography (HPLC) and the most recent radioimmunoassay (RIA) techniques. This review attempts to provide awareness of the limitations of these methods and establishes the base for eventual development of a B12 reference method in our laboratory.

Binding, Competitive↗

Development and characterization of monoclonal antibodies to pregnancy-specific beta 1-glycoprotein.

Six monoclonal antibodies were developed to pregnancy-specific beta 1-glycoprotein (PS beta 1G). Studies of ascitic fluid antibodies by a double-antibody radioimmunoassay (RIA) included an evaluation of titers, dose-response parameters, and mass action properties. Four of the antibodies demonstrated moderate to high titers ranging from 1/40 000 to greater than 1/120 000, as determined by the specific binding of 125I-labeled PS beta 1G. In inhibition studies utilizing a standard containing known quantities of placental PS beta 1G, two of the antibodies (AR#11 and B#2) were highly sensitive and only slightly lower in this regard than a high affinity polyclonal antiserum. The binding affinities of AR#11 and B#2 monoclonals were greater than 10(9) mol-1 which underline their importance as potential clinical reagents for the RIA of PS beta 1G. The Scatchard plots, for several of the antibodies, were linear and in full agreement with a single order of binding sites predicted for specific monoclonal reagents. Immunodiffusion results provide preliminary evidence that at least three distinct determinants on PS beta 1G are recognized by a number of the monoclonal antibodies. Further studies on the fine specificities of the antibodies by solid-phase RIA, as well as a detailed evaluation of their clinical applications, are in progress.

Animals↗

Comparative studies of Iodo-bead and chloramine-T methods for the radioiodination of human alpha-fetoprotein.

Human alpha-fetoprotein (h-AFP) of iodination grade was radiolabeled with Na125I by chloramine-T (conventional method) and by Iodo-bead (solid-phase method) in our laboratory under standard and varied conditions, such as quantity of h-AFP and volume of the reaction mixture. We have slightly modified the chloramine-T method and developed a protocol for the Iodo-bead method of iodination. Our results show that while the chloramine-T method yields radiolabeled h-AFP of apparently 40% higher specific radioactivity (SR) than those of the Iodo-bead method, the latter appears to be a simpler, more controllable and milder method, giving rise to a more stable population of [125I]h-AFP. This is supported by the results of radioactive counting of [125I]h-AFP collected from a Sephadex G-50 column after radioiodination, storage stability and immunoreactivity with anti-h-AFP.

Chloramines↗

Preparation and calibration of a reference preparation for human serum proteins.

A reference preparation for human serum proteins (RPHSP) has been developed to aid in the standardization of a wide variety of protein analytes commonly tested by immunodiagnostic procedures. The U.S. national RPHSP was used to cross-calibrate our reference serum by single radial immunodiffusion for the analytes alpha 1-acid glycoprotein, alpha 1-antitrypsin, alpha 2-macroglobulin, ceruloplasmin, C3, C4, haptoglobin, transferrin, IgA, IgG, IgM and by Laurell "rocket" assay for albumin. The statistical evaluation of the cross-calibration study indicates high precision of estimates of the specific proteins assigned to the Canadian RPHSP relative to those of the U.S. reference preparation. Protein concentrations were assigned in both WHO international units (when available) and mass units.

Adult↗

Heterogeneity of pregnancy-specific beta 1-glycoprotein following purification from maternal serum and partial characterization of a high-molecular-weight component.

Pregnancy-Specific beta 1-Glycoprotein (PSB1G) has been purified from maternal serum by physico-chemical and immunochemical methods. Marked instability of the protein was noted after partial purification which correlated with hydroxylapatite chromatography of PSB1G. Three molecular heterogeneous forms were demonstrated by gel filtration on Sephacryl S-200 which were designated as PSB1G-I, II and III. Each of the latter purified materials displayed altered immunoelectrophoretic mobility, i.e., altered from beta 1 to gamma mobility. In immunodiffusion experiments PSB1G-I reacted in complete immunological identity with 'native' serum PSB1G whereas PSB1G-II and III reacted in partial identity with each of the latter, suggesting that they are dissociation and/or degradation products of the parent PSB1G. The apparent molecular weights of PSB1G-I, II and III as determined by gel filtration were 280 000, 69 000 and 23 000, respectively, PSB1G-I was selected for structural analysis on the basis of its immunological identity with 'native' antigen. SDS-PAGE studies of PSB1G-I with and without reducing agent strongly suggest that PSB1G-I and 'native' serum antigen are composed of two dissimilar subunits of equal molecular size which are bonded together by non-covalent linkage. One of the subunits appears to represent a single polypeptide chain, whereas the other subunit appears to be composed of two polypeptide chains of unequal size that are linked together by covalent bonds. Investigations are continuing towards confirmation of the proposed structural model of PSB1G-I by an alternate methodology of protein structure analysis.

Blood Protein Electrophoresis↗

Studies on the subunit and polypeptide structure of a polymeric form of pregnancy-specific beta 1-glycoprotein.

The structure of a high-molecular-weight form of Pregnancy-Specific beta 1-Glycoprotein designated PSB1G-I that had been previously isolated from maternal serum was studied by gel chromatography in guanidine hydrochloride dissociating solvent. Evidence was obtained that subunits of identical size (bonded together non-covalently) but of differing polypeptide compositions constitute the PSB1G-I molecule. The subunits of PSB1G-I have been designated alpha and beta subunits. Reduction of PSB1G-I results in an intact alpha chain and two beta chains (beta 1 and beta 2) that are linked in the parent beta subunit by covalent bonds. The collective molecular weights of the alpha, beta 1 and beta 2 chains are equal to 97 800 which is assumed to represent the 'true' molecular weight of 'native' serum PSB1G.

Chemical Phenomena↗

Development of a provisional reference human cord serum standard for alpha-fetoprotein determination.

A lyophilized human cord serum secondary reference standard (988 vials of 1 mL/vial) has been prepared at the Laboratory Centre for Disease Control (L.C.D.C.) in Ottawa to assist in the standardization of AFP determinations. HBSAG-negative lots of cord serum were used to prepare the standard. The moisture content of the freeze-dried material was less than 0.5 percent. AFP mass calibration standards were prepared by direct weighing in duplicate of highly purified freeze-dried material. Two RIA calibration runs were conducted on the reference cord serum employing the WHO First International Standard for AFP (72/225) and L.C.D.C. mass standards. Parallelism of dose response curves within assays was demonstrated between reference cord serum and mass standards and between the latter and the WHO standard. The mean WHO kIU of AFP per vial of reference serum (+/- coefficient of variation) was 63.0 +/- 6.4 and the mean mass of AFP determined as micrograms per vial was 80.7 +/- 7.9. A small-scale (pilot) interlaboratory calibration of the reference cord serum in mass units resulted in heterogeneous AFP estimates which ranged from 54.4 to 80.7 micrograms/vial. Greater uniformity of the latter results was noted following conversion of the mass estimates to WHO international units conversion factors provided by several laboratories.

Fetal Blood↗

The molecular heterogeneity and instability of radioiodinated human chorionic gonadotrophin.

Gel chromatographic studies on radioiodinated HCG have shown that a polymer and fragmented materials are associated with the radiolabelled product which interfere in the RIA of HCG in serum. Scatchard plots of experimental data indicated that the polymer material (fraction I) has two species of antigenic determinants that recognize two species of binding sites on the anti-HCG-beta. The use of purified 125I-HCG (gel chromatographic fraction II) for radioligand improved the reliability of the RIA. It was further demonstrated that a labelled preparation of HCG could be used for RIA tests for periods of five weeks or longer provided that chromatographic purification was carried out immediately prior to the assay.

Binding Sites, Antibody↗