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Untitled - D Ank Unlimited

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Kidd blood group system 432 kinetochore autoantibodies<br />

Ki-67⎯carcinoma of the breast.<br />

not clinically useful. The Ki protein contains an antigenic<br />

determinant that is homologous to the Sv40 large T antigen<br />

nuclear localization signal.<br />

Kidd Blood Group System<br />

Reactions with<br />

Anti- Phenotype Frequency<br />

Phenotype Jk a Jk b Caucasian African American<br />

Jk (a+b–) + 0 28 57<br />

Kj (a+b+) 0 + 49 34<br />

Jk (a–b+) + + 23 9<br />

Jk (a–b–) 0 0 Very rare Very rare<br />

Kidd blood group system<br />

The anti-Jk a antibodies originally detected in the serum of a<br />

woman giving birth to a baby with hemolytic disease of the<br />

newborn (HDN). The anti-Jk b antibodies were discovered<br />

in the serum of a patient following a transfusion reaction.<br />

Although Kidd system antibodies sometimes lead to HDN,<br />

the disease is not usually severe; however, the antibodies<br />

are problematic and cause severe hemolytic transfusion<br />

reactions, especially of the delayed type. These occur<br />

when antibodies developing quickly in a booster response<br />

to antigens on transfused erythrocytes destroy red cells in<br />

the circulation. As shown in the table, four phenotypes are<br />

revealed by the reactions of anti-Jk a and anti-Jk b antibodies.<br />

A dominant inhibitor gene (In[Jk]) may encode a null<br />

phenotype. Jk3 is believed to be present on both Jk(a + ) and<br />

Jk(b + ) red cells. Anti-Jk3 is frequently induced by red blood<br />

cell stimulation.<br />

killed vaccine<br />

An immunizing preparation composed of viral or bacterial<br />

microorganisms that are dead but retain their antigenicity,<br />

making them capable of inducing a protective<br />

immune response with the formation of antibodies and/<br />

or stimulation of cell-mediated immunity. Inactivation is<br />

by irradiation, chemical treatment, or heat. Killed vaccines<br />

do not induce even mild cases of the disease that are<br />

sometimes observed with attenuated (greatly weakened<br />

but still living) vaccines. Although the first killed vaccines<br />

contained intact dead microorganisms, some modern<br />

preparations contain subunits or parts of microorganisms<br />

to be used for immunization. Killed microorganisms<br />

may be combined with toxoids, as in the case of the DPT<br />

(diphtheria–pertussis–tetanus) preparations administered to<br />

children.<br />

killed virus vaccines<br />

Immunogen preparation containing virons deliberately<br />

killed by heat, chemicals, or radiation.<br />

killer activatory receptors (KARs)<br />

Natural killer (NK) cell or cytotoxic T cell surface receptors<br />

that can activate killing by these cell types.<br />

killer cell (K cell)<br />

A large granular lymphocyte bearing Fc receptors on<br />

its surface for immunoglobulin G (IgG), which makes it<br />

capable of mediating antibody-dependent, cell-mediated<br />

cytotoxicity. Complement is not involved in the reaction.<br />

Antibody may attach through its Fab regions to target cell<br />

epitopes and link to the killer cell through attachment of its<br />

Fc region to the Fc receptor of the K cell, thereby facilitating<br />

cytolysis of the target by the killer cell, or an IgG<br />

antibody may first link via its Fc region to the Fc receptor<br />

on the killer cell surface and direct the K cell to its target.<br />

Cytolysis is induced by insertion of perforin polymer in<br />

the target cell membrane in a manner that resembles the<br />

insertion of C9 polymers in a cell membrane in complement-mediated<br />

lysis. Perforin is showered on the target cell<br />

membrane following release from the K cell.<br />

killer cell immunoglobulin-like receptors (ICIRs)<br />

Molecular configurations on NK cells that interact with<br />

MHC class I molecules and transmit either activating or<br />

inhibitory signals to natural killer (NK) cells. NK cell<br />

receptors that bind to MHC class I molecules and transmit<br />

either activating or inhibitory signals to the T cell.<br />

killer inhibitory receptors (KIRs)<br />

Natural killer (NK) cell receptors that recognize self major<br />

histocompatibility complex (MHC) class I molecules and<br />

transmit inhibitory signals that block activation of NK cell<br />

cytolytic processes. These receptors prevent NK cells from<br />

killing normal host cells expressing MHC class I molecules<br />

but allow lysis of virus-infected cells for which MHC class<br />

I expression has been suppressed. The inhibitory receptors<br />

fall into several classes that include immunoglobulin<br />

superfamily members, heterodimers of CD94 and selectin,<br />

and Ly49. These receptors possess cytoplasmic tails bearing<br />

immunoreceptor tyrosine inhibition motifs (ITIMs) that<br />

participate in initiating inhibitory signal pathways.<br />

killer T cell<br />

A T lymphocyte that mediates a lethal effect on a target cell<br />

expressing a foreign antigen bound to major histocompatibility<br />

complex (MHC) molecules on target cell surfaces. A<br />

synonym for a cytotoxic T cell.<br />

kilobase (kb)<br />

One thousand DNA or RNA base pairs.<br />

kinetochore autoantibodies<br />

Autoantibodies specific for the mitotic spindle apparatus;<br />

also known as centromere autoantibodies. They have<br />

been found in the cutaneous form of systemic sclerosis,

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