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Untitled - D Ank Unlimited

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alternative pathway 35 alums<br />

alternative pathway<br />

Activation of complement not by antibody but through<br />

the binding of complement protein C3b to the surface of a<br />

pathogenic microorganism. This innate immune mechanism<br />

amplifies complement activation through the classic<br />

pathway.<br />

alternative pathway C3 convertase<br />

Alternate unstable C3bB complex that splits C3 into C3a<br />

and C3b. Factor P, also known as properdin, stabilizes<br />

C3bB to yield C3bBbP. C3 nephritic factor can also stabilize<br />

C3bB.<br />

alternative splicing<br />

A process whereby the RNA splicing apparatus may handle<br />

primary transcripts of a selected gene at splice acceptor<br />

sites 3′ of different exons leading to mRNA populations<br />

comprising different exon subsets; exons whose splice<br />

acceptor sites are deleted from the mRNA, rendering<br />

their corresponding amino acid sequences lacking in the<br />

resulting protein. Thus, one gene can encode two or more<br />

versions of the same protein.<br />

C3b<br />

C3<br />

C3a<br />

C3<br />

Positive feedback<br />

Cn<br />

C3bBbP<br />

C3b<br />

C3a<br />

+ B<br />

Factor P or<br />

C3 nephritic factor<br />

C3b<br />

C3bBb<br />

C3bB<br />

C3b<br />

Factor B<br />

– Activated complement component<br />

– Enzymic action<br />

Alternative pathway C3 convertase.<br />

B<br />

+ D<br />

C3b<br />

Ba<br />

B<br />

AP convertase<br />

+ P<br />

C3b<br />

P<br />

B<br />

Stabilized<br />

AP convertase<br />

Feedback loop of alternative pathway.<br />

Factor D<br />

+ C3<br />

C3b<br />

P<br />

C3b<br />

n<br />

C3a<br />

alum granuloma<br />

A tissue reaction in the form of a granuloma produced at<br />

the local site of intramuscular or subcutaenous inoculation<br />

of a protein antigen precipitated from solution by an aluminum<br />

salt acting as adjuvant. Slow release of antigen from<br />

the granuloma is considered to facilitate enhanced antibody<br />

synthesis to the antigen.<br />

alum-precipitated antigen<br />

A soluble protein antigen such as a toxoid adsorbed to<br />

aluminum salts during precipitation from solution. The aluminum<br />

salt acts as an adjuvant that facilitates an immune<br />

response to such antigens as diphtheria and tetanus toxoids.<br />

Soluble protein antigen is combined with 1% potassium<br />

aluminum sulfate, and sodium hydroxide is added until<br />

floccules are produced.<br />

alum-precipitated toxoid<br />

Refer to alum-precipitated antigen.<br />

aluminum adjuvant<br />

Aluminum-containing substances that have a powerful<br />

capacity to adsorb and precipitate protein antigens from<br />

solution. The use of these preparations as immunogens<br />

causes depot formation in the tissues at the site of inoculation,<br />

from which the antigen is slowly released, thereby<br />

facilitating greater antibody production than if the antigen<br />

is dissipated and rapidly lost from the body. Substances<br />

used extensively in the past for this purpose include aluminum<br />

hydroxide gel, aluminum sulfate, and ammonium<br />

alum, as well as potassium alum.<br />

aluminum hydroxide gel<br />

Aluminum hydroxide [Al(OH) 3] was widely used in the<br />

past as an immunologic adjuvant by reacting antigen<br />

with 2% hydrated AL(OH) 3 to adsorb and precipitate<br />

the protein antigen from solution. See also aluminum<br />

adjuvant.<br />

alums<br />

Aluminum salts employed to adsorb and precipitate protein<br />

antigens from solution, followed by the use of the precipitated<br />

antigen as an immunogen that forms a depot in animal<br />

tissues. See also aluminum adjuvant.<br />

B<br />

+<br />

A

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