alloimmunisation to blood group antigens

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    Abdullah Meshi, BMSc (CLSc), MSc(UK).Head of blood bank

    King Fahd central Hospital-Jazan

    [email protected]

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    ` Blood group systems & Immune response to RBC

    antigens.

    ` Clinical significance of RBC alloantibodies.

    ` Current and future methods forAbs identification

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    `What does immunesystem do??

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    ` Primary IR Slow (weeks to months

    Low level of IgM Needed high dose of

    Ag.

    ` Secondary IR Rapid

    Ab titer rising 48 hrs IgG , peaks 6 days

    after injection

    Need smallerAg dose

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    ` T-cell-dependent antibody formation

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    ` Sources of alloimmunisation to RBC antigens:

    Blood transfusion

    pregnancy

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    ` Immunogenicity The ability of an antigen to stimulate an immune

    response or antibody production.

    Most blood group antigens are poor immunogens (

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    Antibodies Detected Number of Patients

    anti-K

    10 (2.8%)anti-E 9 (2.5%)

    anti-c 6 (1.6%)

    anti-Lea 5(1.4%)

    anti-M 4 (1.1%)

    anti-E, c 3 (0.8%)

    anti-Leb 2 (0.5%)

    anti-S 1(0.3%)

    anti-D & anti-C 1(0.3%)

    anti-c, E & K 1(0.3%)

    anti-Lea & Leb 1(0.3%)

    anti-Xga 1(0.3%)

    others 6 (1.6%)

    Total 50 (13.8%)

    Blood group antibodies detected in SCD patients at (KFCH), Jazan (n=362) *

    *Abdullah S. & Meshi A., 2006 (unpublished data)

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    ` Acute Haemolytic transfusion reaction (AHTR) Most blood group antibodies can causeAHTR

    ` Delayed haemolytic transfusion reaction (DHTR) Most blood group antibodies can causeDHTR

    ` Haemolytic disease of the foetus and newborn

    (HDFN) Rh & Kell antibodies.

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    ` Liquid-phase (tube/plate)

    ` Column-agglutination (gel cards)

    ` Solid-phase (microplate coated with RBCs)

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    ` The genesencoding most of the major blood group

    determinants have been cloned & sequenced

    ` Recombinant DNA technology was applied to

    engineer clinically significant blood group antigens

    (e.g. Kell, Duffy, Gerbich).

    ` These recombinant antigens can be used indetecting & identifying Abs in clinical laboratories

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    0

    0.02

    0.04

    0.06

    0.08

    0.1

    0.12

    0.14

    MeanOD(min

    us

    blank)

    sr LAG-K/Kpa/Jsa K300

    FLAG-Kell fusion prote in

    anti-K

    anti-Kpa

    anti-k

    Antigen capture ELISA*

    Meshi A., 2005 (unpublished data)

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    Suspension Bridge

    Bristol, UK (2005)

    THANK YOU