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Questions and Answers

What is the main characteristic of the weak D antigen (Du)?

  • It is weakly expressed on the red cell. (correct)
  • It is only expressed in certain populations.
  • It is absent on the red cell.
  • It is strongly expressed on the red cell.
  • What is required to detect the weak D antigen?

  • Indirect antiglobulin test (IAT). (correct)
  • Serum hemagglutination test.
  • Direct coombs test.
  • Monoclonal antibody test.
  • What result would be expected from the indirect antiglobulin test (IAT) for weak D?

  • Positive at room temperature.
  • No result is possible.
  • Positive at immediate spin.
  • Negative at immediate spin. (correct)
  • Why is testing for weak D important in blood donors?

    <p>To identify donors with potential for Rh incompatibility.</p> Signup and view all the answers

    Which of the following statements about weak D antigen is true?

    <p>Testing is essential for some blood donors.</p> Signup and view all the answers

    What is indicated by the presence of anti-A 4+ and anti-B 1+ in a blood test?

    <p>Subgroup AB with A₂B probable presence</p> Signup and view all the answers

    When testing serum against additional A1, A2, and O cells, what result would imply a subgroup of AB blood?

    <p>A1 Cells 1+, B Cells 1+, O Cells 0</p> Signup and view all the answers

    If a patient has negative forward and reverse ABO results, what is the next appropriate step?

    <p>Test serum against additional A1 and A2 cells</p> Signup and view all the answers

    What could a positive autocontrol indicate in ABO typing?

    <p>Presence of an autoantibody or disease</p> Signup and view all the answers

    In the context of blood typing, what does a result of O Cells 0 indicate?

    <p>No reaction to O type antigens</p> Signup and view all the answers

    Study Notes

    Blood Banking & Immunohematology - Notice

    • All rights reserved. No part of this material may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, database, online or otherwise, without prior permission.
    • This material is for personal use only, and reproduction or distribution is not permitted.

    Blood Banking & Immunohematology - 1

    • ABO and Rh blood group systems are discussed.
    • Other blood group systems are also included.
    • Pretransfusion and compatibility testing are covered, including HDFN.

    ABO & H Blood Group Systems

    • The ABO and H blood group systems are the most important.
    • Anti-A and Anti-B are IgM antibodies, and are primarily of the IgG class.
    • ABO antibodies are detectable in infants 3-6 months after birth, but not until 5 years of age.
    • Blood type incompatibility can cause acute hemolysis of RBCs and lead to renal failure/death.
    • The ABO locus is on chromosome 9 (or chromosome 19).
    • A and B genes are dominant or codominant; O is recessive.
    • The O gene is amorphic and does not produce a detectable antigen.

    Landsteiner's Rule (1900-1901)

    • Relationship between ABO antigens and antibodies.
    • Group AB possesses both A and B antigens.
    • Group A possesses A antigens.
    • Group B possesses B antigens.
    • Group O lacks both A and B antigens.
    • Group AB lacks ABO antibodies.
    • Group A possesses anti-B.
    • Group B possesses anti-A.
    • Group O possesses anti-A and anti-B.

    ABO & H Blood Group Systems

    • ABO and H antigens are found in secretions.
    • The H gene is needed to form ABO antigens in RBCs and secretions.
    • H antigen is a precursor for A and B antigens.
    • The amount of H antigen determines ABO blood type: O > A₂ > B > A₂B > A₁ > A₁B.
    • H (FUT1) is a-2-L-fucosyltransferase.
    • Glycosyltransferases add specific sugars to precursor substances to form A, B, and H antigens.

    ABO Discrepancies

    • Discrepancies in red cell and serum/plasma results.
    • Extra positive reaction or weak/missing ABO antibodies.
    • Weaker reactions often indicate a discrepancy.
    • Transfusion is sometimes needed when discrepancies are noted.

    ABO Subgroups (A1 and A2)

    •  80% of group A individuals are A1, 20% are A2.
    • Differentiate A1 with anti-A1 lectin (Dolichos biflorus).
    • Some A2 individuals will have insignificant reactions with anti-A1.

    Bombay (Oh) Phenotype

    • First reported by Bhende in 1952 in Bombay, India.
    • hh genotype (H-null).
    • No production of a-2-L-fucosyltransferase (H-enzyme), no L-fucose, no A, B, or H antigens.
    • Phenotype is as blood group O.
    • RBCs will not react with anti-H lectin (Ulex Europaeus).

    Rh Blood Group System

    •  Rh refers to a specific red blood cell (RBC) antigen (D).
    • Rh-specific antigens reside on proteins.
    • Production of anti-D and other Rh antibodies requires immune stimulation.
    • A primary cause of hemolytic disease of the fetus and newborn (HDFN).
    • Five antigens make up the Rh system (D, C, c, E, e).
    • RH genes are located on chromosome 1.

    Wiener: Rh-Hr Terminology

    • One gene is responsible for defining Rh; r = absence of D antigen.
    •  Presence of C by a' or double prime ("), and E by double prime (").

    Rosenfield and Coworkers: Alphanumeric Terminology

    • Number assigned to each Rh antigen, with a minus sign (-) for absent antigen.
    • Rh1 = D, Rh2 = C, Rh3 = E, Rh4 = c, and Rh5 = e.

    Other (minor) Blood Group Systems

    • Details about the blood group systems were included.

    System with cold antibodies

    • Details about this blood group system were included.

    Lewis (LE)

    •  Details about the structure, interaction, and occurrence of Lewis antigens were provided.

    P antigens

    • Details about P antigens, and their antibodies were provided.

    MNSs

    • Details about the MNS system were given.
    • Details about the antigens M, N, S, s, and U were included.

    Kell System

    • Kell antigens (K, k, Kpa, Kpb) were discussed.
    • Information about the K cell and its antibodies was provided.

    Duffy System

    • Information about Duffy antigens (Fya, Fyb) and their connection to malaria.
    • Information about the occurrence of Duffy antibodies in different populations was given.

    Kidd System

    • Information about Kidd antigens (Jka, Jkb) and their connection to HDN was provided.

    Lutherans

    • Information about Lutheran antigens (Lua, Lub), associated diseases, and frequencies was given.
    • Information about the antibodies associated with the antigens was included

    Enzyme Treatment of Red Blood Cell Antigens

    • Proteolytic enzymes used in the treatment of RBC antigens.

    Clinical Significance of Red Cell Antibodies

    • Significance classification of antibodies related to different conditions and diseases.
    • Different blood group antibodies related to different infections.

    Human Leukocyte Antigens (HLAs)

    • Details about HLA genes and its functions.
    • HLA role in tissue/organ transplant, stem cell transplantation, and platelet matching.
    • Information about incompatibility causes was given.

    Platelet Antigens

    • Platelets have protein antigens.
    • Antibodies that react with platelets may be ABO, HLA, or platelet-specific.
    • Diseases related to platelet conditions were mentioned

    Pretransfusion & Compatibility Testing

    • ABO/Rh antibody screening and crossmatching.

    Antibody Screen

    • Screening cells are used to detect antibodies
    • Group O donors are used because they lack A and B antigens.
    • Unexpected antibodies (other than anti-A and anti-B) are detected using a screening process.
    • An unexpected reaction indicates an atypical/unexpected antibody.

    Red Cell Dosage Phenomenon

    • Heterozygous cells express fewer antigens/quantity compared to homozygous cells.
    • Stronger agglutination occurs when a red cell antigen is expressed from homozygous genes

    Which pair of cells?

    • Questions about cells ideal for blood screening were included.

    Antibody Identification Panel Cells

    • Procedure for identification of specific antibodies present and their class.
    • Antibody panel cells are used for identification when antibody screen is positive.
    • Information about autoantibodies and alloantibodies as well as their reaction conditions was included.

    Elution

    • A method to dissociate antibodies from sensitized cells.
    • Useful in cases of positive DAT due to IgG.
    • Can help identify autoimmune hemolytic anemia.

    Adsorption

    • Removes unwanted antibodies from a serum sample.
    • Helps isolate specific antibodies during testing.
    • Can separate multiple antibodies
    • Enables the identification of underlying alloantibodies.

    Ig Class Identification (inactivation)

    • Dithiothreitol (DTT) and AET to inactive Kell system antigens.
    • ZZAP (dithiothreitol and papain) to remove IgG autoantibodies and destroy RBC antigens.

    Crossmatch

    • A procedure for checking compatibility.
    • Major crossmatch: testing patient plasma with donor cells.
    • Minor crossmatch: testing patient cells with donor plasma.
    • Incompatible reactions/results are noted

    Examples of Incompatible Crossmatches

    • Different reactions that indicate blood incompatibility.

    Types of Graft

    • Autograft, isograft (syngraft), allograft, and xenograft.

    Antiglobulin (Coombs') Test (AHG)

    • Detects IgG or complement proteins attached to RBCs.
    • AHG reagents are monospecific and polyspecific.

    Preparation of Blood Components

    • Various methods and materials used.

    Apheresis

    • Automated blood separation/collection system.
    • Procedure for separating and collecting specific components while returning residual blood to donor.

    Adverse Transfusion Reactions

    • Classifications/types of reactions.
    • Clinical/disease signs related.
    • Causes and comments included

    Acute Immunologic Transfusion Reactions

    • Clinical signs of the reactions and the causes.
    • Comments/additional information.

    Delayed Transfusion Reactions

    • Clinical signs of these reactions and the causes.
    • Comments/additional information.

    Acute Nonimmunologic Transfusion Reactions

    • Clinical signs and possible causes of the reactions.
    • Additional comments.
    • Different possible causes for the nonimmune reactions.

    Determination of feto-maternal hemorrhage

    • Procedure to determine the quantity of fetal-maternal hemorrhage(FMH).

    Overview of ABO compatibility & blood components for transfusion

    • Various ABO types and their compatibility requirements.
    • Important information/requirements for transfusion of different components.

    ABO Group Selection Order for Transfusion of RBCs.

    • Table with selection order of ABO blood types for RBC transfusion for various patient types.

    Antibody Typing

    • Methodology, reagents, and results for typing.

    Frequency of ABO and Rh Antigens

    • Frequency of ABO and Rh antigens in different populations.

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