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Untitled - D Ank Unlimited

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HCC-1 313 heavy chain diseases<br />

In transgenic mouse-induced hepatomas, it may promote<br />

development of hepatocellular carcinoma.<br />

HCC-1<br />

A β chemokine (CC family) isolated from the hemofiltrates<br />

of chronic renal failure patients. HCC-1 has 46% sequence<br />

identity with MIP-1α and MIP-1β, and 29 to 37% with the<br />

remaining human β chemokines. In contrast to other β<br />

chemokines, HCC-1 is expressed constitutively in normal<br />

spleen, liver, skeletal and heart muscle, gut, and bone marrow.<br />

It reaches significant concentrations (1 to 80 nM) in plasma. It<br />

is expressed by monocytes and hematopoietic progenitor cells.<br />

hCG (human choriogonadotrophic hormone)<br />

A glycoprotein comprised of lactose and hexosamine that<br />

is synthesized by syncytiotrophoblast, fetal kidney, and<br />

liver-selected tumors. It may be measured by radioimmunoassay<br />

or enzyme-linked immunosorbent assay (ELISA).<br />

It is elevated in patients with various types of tumors, such<br />

as carcinoma of the liver, stomach, breast, pancreas, lungs,<br />

kidneys, and renal cortex, and conditions such as lymphoma,<br />

leukemia, melanoma, and seminoma.<br />

HCT<br />

Abbreviation for hematopoietic cell transplant.<br />

HD 50<br />

An uncommon designation for CH 50, the hemolytic complement<br />

activity of a serum sample.<br />

HDN<br />

Hemolytic disease of the newborn.<br />

heaf test<br />

A type of tuberculin test in which an automatic multiple<br />

puncture device with six needles is used to administer the<br />

test material by intradermal inoculation. The multiple needles<br />

advance 2 to 3 mm into the skin. Also called Tine test.<br />

heart–lung transplantation<br />

A procedure that has proven effective for the treatment<br />

of primary respiratory disease with dysfunction of gas<br />

exchange and alveolar mechanics, together with a secondary<br />

elevation in pulmonary vascular resistance, and in<br />

primary high-resistance circulatory disorder associated<br />

with pulmonary vascular disease.<br />

heat-aggregated protein antigen<br />

Partial denaturation of a protein antigen by mild heating.<br />

This diminishes the protein’s solubility, but causes it to<br />

express new epitopes. An example is the greater reactivity<br />

of rheumatoid factor (e.g., IgM anti-IgG autoantibody) with<br />

heat-aggregated γ globulin than with unheated γ globulin.<br />

heat inactivation<br />

Loss of biological activity through heating. Heating a serum<br />

sample at 56°C in a water bath for 30 minutes destroys complement<br />

activity through inactivation of C1, C2, and factor B. By<br />

diminishing the heat to 52°C for 30 minutes, only factor B is<br />

destroyed, whereas C1 and C2 remain intact. This inactivates<br />

the alternative complement pathway but not the classical<br />

pathway. Immunoglobulin G (IgG), IgM, and IgA are resistant<br />

to incubation in a 56°C water bath for 30 minutes, whereas IgE<br />

antibodies are destroyed by this temperature.<br />

heat-labile antibody<br />

An antigen-specific immunoglobulin that loses its ability to<br />

interact with antigen following exposure to heating at 56°C<br />

for 30 minutes.<br />

heat shock protein antibodies<br />

Antibodies of the immunoglobulin M (IgM), IgG, and IgA<br />

classes specific for a 73-kDa chaperonin that belongs to the<br />

hsp70 family present in the sera of approximately 40% of<br />

systemic lupus erythematosus (SLE) patients and in 10 to<br />

20% of individuals with rheumatoid arthritis. Antibodies<br />

specific for the 65-kDa heat shock protein derived from<br />

mycobacteria show specificity for rheumatoid synovium.<br />

RA synovial fluid T cells specific for a 65-kDa mycobacterial<br />

heat shock protein have been reported to be inversely<br />

proportional to the disease duration.<br />

heat shock proteins (HSPs)<br />

A restricted number of highly conserved cellular proteins<br />

that increase during metabolic stress such as exposure to<br />

heat, inflammation, or tumor transformation. Inside cells,<br />

HSPs escort peptides from the proteasome to TAP in the<br />

course of endogenous antigen processing. Stressed cells<br />

may release HSPs as “danger signals” linking Toll-like<br />

receptors. They may facilitate exogenous antigen processing<br />

and cross presentation. Heat shock proteins affect<br />

assembly into protein complexes, proper protein folding,<br />

protein uptake into cellular organelles, and protein sorting.<br />

The main group of HSPs are 70-kDa proteins. Heat<br />

shock (stress) proteins are expressed by many pathogens<br />

and are classified into four families based on molecular<br />

size: HSP90, HSP70, HSP60, and small HSP (

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