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cobra venom factor (CVF) 181 coelomocyte<br />

vesicles convey receptor–macromolecule complexes from<br />

extracellular to intracellular locations. Clathrin-coated<br />

vesicles convey proteins from one intracellular organelle to<br />

another. Refer also to coated pit.<br />

cobra venom factor (CVF)<br />

A protein in the venom of the Indian cobra, Naja naja. It<br />

is the equivalent of mammalian C3b and thus can activate<br />

the alternative pathway of complement. Mammalian factor<br />

I does not inactivate cobra venom, which leads to the<br />

production of a stable alternative pathway C3 convertase<br />

if CVF is injected intravenously into a mammal. Thus, the<br />

injection of cobra venom factor into mammals has been<br />

used to destroy complement activity for experimental purposes.<br />

A component of cobra venom interacts specifically<br />

with the serum complement system, leading to its continuous<br />

activation. CVF is a structural and functional analog<br />

of complement component C3. It has been employed<br />

to decomplement laboratory animals to investigate the<br />

biological functions of complement. It has been used in<br />

animal experiments involving xenotransplantation to show<br />

that complement is a principal contributor to hyperacute<br />

rejection of a transplanted organ. It has also been used<br />

in antibody conjugates to render monoclonal antibodies<br />

cytotoxic.<br />

Arthur Fernandez Coca.<br />

Coca, Arthur Fernandez (1875–1959)<br />

American allergist and immunologist. He was a major force<br />

in allergy and immunology. He named atopic antibodies<br />

and was a pioneer in the isolation of allergens. He and<br />

Robert A. Cooke classified allergies in humans.<br />

co-capping<br />

If two molecules are associated in a membrane, capping<br />

of one induced by its ligand may lead also to capping<br />

of the associated molecule. Antibodies to membrane<br />

molecule x may induce capping of membrane molecule<br />

y and x if x and y are associated in the membrane. In<br />

this example, the capping of the associated y molecule is<br />

termed co-capping.<br />

Coccidioides immunity<br />

Immunity against Coccidioides immitis depends upon T<br />

lymphocytes. IFN-γ plays an important role in protection<br />

conferred by the recombinant form of this cytokine in<br />

experimental mice. Monocytes have a precise role in limiting<br />

infection before a specific immune response develops.<br />

Spherules and arthroconidia induce the synthesis of TNFα<br />

by human monocytes in vitro. TNFα alone or combined<br />

with IFN-γ promotes killing of spherules by human<br />

monocytes in vitro. TNFα and IL6 levels have been shown<br />

to be elevated in patients with overwhelming infections<br />

by this organism. Antigen overload, specific suppressor T<br />

lymphocyte activity from a circulating humoral suppressor<br />

substance, may sometimes suppress the T lymphocyte A<br />

Coccidioides-specific responses in some patients. A positive<br />

skin test indicates previous infection. Results usually<br />

remain positive for the patient’s lifetime. Of all infected<br />

individuals, 90% develop antibody responses to C. immitis.<br />

Mycelial phase antigens are most often used in serodiagnosis.<br />

Immunoglobulin M (IgM) forms early but disappears<br />

after 6 months, whereas IgG elevated titers may indicate<br />

dissemination.<br />

coccidioidin<br />

A Coccidioides immitis culture extract used in a skin test<br />

for cell-mediated immunity against the microorganism in a<br />

manner analogous to the tuberculin skin test.<br />

coccidiosis immunity<br />

Immunity induced by infection is species- and in some<br />

instances strain-specific, yet immunization with purified<br />

antigens may induce heterologous protection. Immunity is<br />

mediated by T cells and is far more significant to resistance<br />

than the humoral immune response that is also stimulated.<br />

Antibodies act mainly against extracellular parasites to reduce<br />

invasion. CD4 + T cells control primary infections, whereas<br />

CD8 + lymphocytes are more significant in later stages of<br />

infection. There is a vaccine for chickens, but it is expensive.<br />

coding joint<br />

A structure formed when a V gene segment joins imprecisely<br />

to a (D)J gene segment in immunoglobulin or T cell<br />

receptor genes.<br />

codominant<br />

The expression of both alleles of a pair in a heterozygote.<br />

The traits they determine are codominant as in the expression<br />

of blood group A and B epitopes in type AB persons.<br />

codominantly expressed<br />

Gene expression when both alleles at one locus are expressed<br />

in approximately equal amounts in heterzygotes. The highly<br />

polymorphic major histocompatibility complex (MHC)<br />

genes, as well as most other genes, manifest this property.<br />

codon<br />

A three-adjacent nucleotide sequence mRNA that acts as a<br />

coding unit for a specific amino acid during protein synthesis.<br />

The codon controls which amino acid is incorporated<br />

into the protein molecule at a certain position in the polypeptide<br />

chain. Of 64 codons, 61 encode amino acids, and 3<br />

act as termination codons.<br />

coelomate<br />

An animal possessing a body cavity.<br />

coelomocyte<br />

A circulating or fixed ameboid phagocytic leukocyte that<br />

participates in the defense of invertebrate animals that have<br />

coeloms by phagocytosis and encapsulation.<br />

C

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