Report on group 1: anti-A. July 1987.
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ABO Blood-Group System↗
Biomedical subjects
J T Hardman
Publications and source records attributed to J T Hardman.
Report on group 2: anti-B and anti-A + B.
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ABO Blood-Group System↗
Fatal intravascular immune hemolysis induced by hydrochlorothiazide.
A patient receiving antihypertensive therapy developed acute intravascular hemolysis and died. Hemolysis was due to an immune process associated with antibody to thiazide. Only two other cases have been reported. Thiazide-induced hemolysis appears to be confined to those patients treated concommitantly with methyldopa.
Anemia, Hemolytic↗
Salivary ABO antibodies and periodontal disease.
The purpose of this study was to determine and to compare the titers of salivary anti-A and anti-B antibodies in two groups of patients with periodontal disease as measured by Russell's Periodontal Index (PI). Forty volunteer subjects, who were new patients assigned to a screening clinic, were selected for the study based on the following criteria: (1) blood group, (2) medical history, (3) age and (4) periodontal condition. One group of patients (N = 20) had a PI of less than 2.0 and the other group of patients (N = 20) had a PI of greater than 4.0. Following screening, a 10-ml sample of unstimulated whole saliva was collected, centrifuged and frozen. Within 30 days the saliva was thawed, titrated and tested for presence of anti-A and anti-B. Saliva agglutinin titers were determined using a variation of previous testing techniques. Statistically significant differences between the two groups were not obtained in the titers of salivary anti-A (U = 192.5; P greater than 0.1) or the titers of salivary anti-B (U = 162.8; P greater than 0.1). All 40 group O patients were found to have anti-A and anti-B in their saliva.
ABO Blood-Group System↗
Characterization of human erythrocyte alloantibodies by IgG subclass and monocyte interaction.
Human blood group antibodies of 11 specificities were examined for ability to mediate interaction with normal blood monocytes, IgG subclass composition, and titer score. Most antibodies were normally non-complement-binding (except anti-JKa) and clinically significant (except anti-Lub). A simple and relatively rapid in-vitro assay for the visualization of sensitized erythrocyte-monocyte interaction is described. Capillary procedures were adapted for IgG subclass composition determinations. Standard serologic tests were used to assess antibody titer score. A relationship appeared to exist between increased antibody titer score and increased interaction of sensitized erythrocytes (RBC) with normal blood monocytes (MNL), insofar as the mean titer score for antibodies that did mediate significant interaction was 52, whereas titer scores for antibodies that did not averaged 25. One or more examples within all antibody specificity, mediated significant RBC-MNL interaction. No relationship was observed between IgG subclass composition and mediation of RBC-MNL interaction except that all antibodies that did mediate interaction contained IgG1 or IgG3. Characteristic patterns of IgG subclass composition were observed for many antibody specificity groups, although too few examples were tested for valid statistical analysis. This study identifies two features of common blood group antibody populations that are instrumental in mediating erythrocyte destruction by monocytes in vitro. Similar information may be of value in predicting the result of erythrocytes transfused to patients with antibodies of unknown clinical significance.
Cell Adhesion↗
Hemolytic disease of the newborn associated with anti-Jk3.
This report documents a mild case of hemolytic disease of the newborn (HDN) associated with anti-Jk3. The Filipino mother had previously had six children none of whom had been affected by HDN. She had been transfused at the time of her second pregnancy. Anti-Jkb and anti-Jk3 were detected in the maternal serum at the time of her seventh delivery. No prenatal serologic tests for blood group antibodies had been performed. The cord blood was found to have a positive direct antiglobulin test and anti-Jkb plus anti-Jk3 were eluted. The infant was treated with phototherapy.
Adult↗
A modified capillary test using 4% ficin.
A capillary technique is described for economical Rh-phenotyping of large numbers of blood samples using diluted antisera and 4% ficin solution. This system is no more time consuming that conventional tube techniques, since enzyme premodification of the cells is not required.
Blood Grouping and Crossmatching↗
Hemagglutination in capillaries: correlation with blood group specificity and IgG subclass.
Two hundred four examples of blood group antibodies, reactive only by the indirect antiglobulin test, were examined by the two-layer albumin capillary (TLAC) technique. Fifty-nine per cent of the examples tested were reactive by this technique. TLAC reactivity appeared to be related to antibody specificity, but a positive association between TLAC reactivity and IgG subclass composition was not confirmed.
Antibody Specificity↗
Incompatibility associated with the bite of a brown recluse spider (Loxosceles reclusa).
Red cell samples from a patient who was suffering from massive hemolysis due to a brown recluse spider (Loxosceles reclusa) bite were found to be reactive by indirect antiglobulin test with most ABO-compatible serum samples. Spider venom, enzymes related to those in spider venom, and antisera to plasma proteins and Rh antigens were used to investigate the unusual reactivity of the patient's cells. IgG was detected on the patient's cells by indirect antiglobulin tests. Cells treated with brown recluse spider venom or phosphatidylcholine phosphatidohydrolase reacted similarly. These findings suggest that sphingomyelinase D, which has been identified in brown recluse spider venom, may be related to the unusual reactivity of the patient's cells. Unexpected reactions were observed when venom-treated cells were tested with Rh antibodies: O negative cells absorbed and eluted anti-D from Rh immune globulin; E negative cells were reactive with a commercial anti-E reagent.
ABO Blood-Group System↗
Range forb lectins.
In this study we tested the seeds of uncultivated plants for lectin activity. Extracts prepared from the seeds of 167 forb species were tested against human red cell samples. Extracts of 54 species agglutinated unmodified or enzyme-modified red cells. In nine species, the hemagglutinating lectin activity could be neutralized by N-acetyl-D-galactosamine, mannose, or glucose.
Hemagglutination Tests↗