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kallidin 430 Kawasaki’s disease<br />

Elvin Abraham Kabat.<br />

Elvin A. Kabat (left) of Columbia University and Merrill W. Chase of<br />

Rockefeller University at the 75th Annual Meeting of the American<br />

Association of Immunologists in Las Vegas, Nevada, 1988.<br />

kallidin<br />

Refer to kinins.<br />

kallikrein<br />

An enzyme that splits kininogens to generate bradykinin,<br />

which has an effect on pain receptors and smooth muscle<br />

and exerts a chemotactic effect on neutrophils. Bradykinin<br />

is a nonapeptide that induces vasodilation and increases<br />

capillary permeability. Kallikreins, also known as kininogenases,<br />

are present in both plasma and tissues and also in<br />

glandular secretions such as saliva, pancreatic juice, tears,<br />

and urine, among others. Trypsin, pepsin, proteases of<br />

snake venoms, and bacterial products are also able to hydrolyze<br />

kininogens, but the substrate specificity and potency<br />

of kallikreins are greater. Plasma and tissue kallikreins are<br />

physically and immunologically different. It is not known<br />

whether plasma contains more than one form of kallikrein.<br />

kallikrein inhibitors<br />

Natural inhibitors of kallikreins belong to the group of<br />

natural inhibitors of proteolysis. They also inhibit other<br />

proteolytic enzymes, but each has its own preference for one<br />

protease or another. Apronitin, also known by its registered<br />

name of Trasylol , is particularly active on tissue kallikreins.<br />

kallikrein–kinin system<br />

Vasopressive peptides that control blood pressure through<br />

maintenance of regional blood flow and the excretion of<br />

water and electrolytes. Kallikrein causes the release of<br />

renin and the synthesis of kinins that interact with the<br />

immune system, increase urinary sodium excretion, and act<br />

as powerful vasodilators.<br />

Kaposi’s sarcoma<br />

A malignant neoplasm that may consist of a discrete<br />

intradermal nodule with vascular channels lined by atypical<br />

endothelial cells and extravasated erythrocytes with<br />

deposits of hemosiderin. This vascular tumor, seen largely<br />

in elderly patients of Mediterranean and Jewish heritage,<br />

is now recognized in a more aggressive form as one of the<br />

presentations of AIDS. Whereas classical Kaposi’s sarcoma<br />

is on the lower limbs and is only very slowly progressive,<br />

the more aggressive form seen in AIDS involves discrete<br />

vascular tumors scattered widely over the body. This tumor<br />

is associated with infection by Kaposi’s-sarcoma-associated<br />

herpesvirus (human herpesvirus 8).<br />

κ (kappa)<br />

Designation for one of the two types of immunoglobulin<br />

light chains; the other designation is λ.<br />

κ–λ exclusion<br />

Means whereby the generation of a functional κ light chain<br />

from the Igk locus on one chromosome prevents futher<br />

V(D)J rearrangement at the other Igk allele, and also blocks<br />

V(D)J rearrangement of either Ig1 allele.<br />

κ chain<br />

One of two types of light polypeptide chains present in<br />

immunoglobulin molecules of humans and other species.<br />

κ Light chains are found in approximately 60% of human<br />

immunoglobulin, whereas λ light chains are present in<br />

approximately 40%. A single immunoglobulin molecule<br />

contains either κ or λ light chains, not one of each.<br />

κ light chain deficiency<br />

A rare condition in which point mutations in the Cκ gene<br />

at chromosome 2p11 cause an absence of κ light chains in<br />

the serum and generate B lymphocytes whose surfaces are<br />

bereft of κ light chains.<br />

karyotype<br />

The number and shape of chromosomes within a cell. A<br />

karyotype may be characteristic for a particular species.<br />

Kawasaki’s disease<br />

Mucocutaneous lymph node syndrome that occurs in<br />

children under 5 years of age. The incubation period may<br />

be 1 to 2 weeks. It is an acute febrile disease characterized<br />

by erythema of the conjunctiva and oral cavity, skin rash,<br />

and swollen (especially cervical) lymph nodes. It occurs<br />

mostly in Japan, although some cases have been reported in<br />

the United States. Cardiac lesions such as coronary artery<br />

aneurysms may be found in 70% of the patients. Coronary<br />

arteritis causes death in 1 to 2% of patients. Necrosis and<br />

inflammation of the vessel wall are present. The etiology<br />

is unknown, but it has been suggested to be infection by<br />

a retrovirus. Considered to be an autoimmune disease.<br />

Associated immunoregulatory disorders include T and B<br />

lymphocyte activation, circulating immune complexes, and<br />

autoantibodies cytolytic for endothelial cells activated by<br />

cytokines.

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