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Untitled - D Ank Unlimited

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HLA class II 334 HLA-DO<br />

Human class I histocompatibility antigen (HLA-A 0201) complexed with<br />

a decameric peptide from calreticulin HLA-A 0201. Human recombinant<br />

extracellular fragment expressed in Escherichia coli; peptide synthesis<br />

based on sequence of human calreticulin.<br />

Class I histocompatibility antigen HLA-B*2705 complexed with nonapeptide<br />

arg–arg–ile–thr–leu–lys (theoretical model).<br />

HLA class II<br />

Refer to MHC genes and class II MHC molecules.<br />

HLA class II molecules<br />

The term used to describe MHC class II molecules in humans.<br />

HLA class III<br />

Refer to MHC genes and class III MHC molecules.<br />

HLA-D region<br />

The human major histocompatibility complex (MHC) class II<br />

region comprised of three subregions designated DR, DQ, and<br />

DP. Multiple genetic loci are present in each of these. Each of<br />

the DN (previously DZ) and DO subregions is comprised of<br />

one genetic locus. Each HLA class II molecule is composed<br />

of one α chain and one β chain that constitute a heterodimer.<br />

Genes within each subregion encode the α and β chains of<br />

a particular class II molecule. Class II genes that encode α<br />

chains are designated A, and class II genes that encode β<br />

chains are designated B. A number is used following A or B if<br />

a particular subregion contains two or more A or B genes.<br />

HLA disease association<br />

Certain human leukocyte antigen (HLA) alleles occur in<br />

higher frequencies in individuals with particular diseases<br />

than in the general population. This type of data permits estimation<br />

of the relative risk of developing a disease with every<br />

known HLA allele. For example, a strong association exists<br />

between ankylosing spondylitis, an autoimmune disorder<br />

involving the vertebral joints, and the major histocompatibility<br />

complex (MHC) class I allele HLA-B27. A strong association<br />

exists between products of the polymorphic class II<br />

alleles HLA-DR and -DQ and certain autoimmune diseases,<br />

because MHC class II molecules are of great importance<br />

in the selection and activation of CD4 + T lymphocytes that<br />

regulate the immune responses against protein antigens. For<br />

example, 95% of Caucasians with insulin-dependent (type<br />

I) diabetes mellitus have HLA-DR3 or HLA-DR4 or both.<br />

A strong association of HLA-DR4 with rheumatoid arthritis<br />

also exists. Numerous other examples are the targets of current<br />

investigations, especially in extended studies employing<br />

DNA probes. Calculation of the relative risk (RR) and absolute<br />

risk (AR) can be found elsewhere in this dictionary.<br />

Clip<br />

HLA-DM.<br />

MHC<br />

Class II<br />

HLA-DR<br />

HLA-DM<br />

HLA-DM<br />

Invariant MHC class II molecule that facilitates the loading<br />

of antigenic peptides onto major histocompatibility complex<br />

(MHC) class II molecules in humans. As a result of proteolysis<br />

of the invariant chain, a small fragment called the<br />

class-II-associated invariant chain peptide (CLIP) remains<br />

bound to the MHC class II molecule. CLIP is replaced<br />

by antigenic peptides; however, this does not occur in the<br />

absence of HLA-DM. The HLA-DM molecule present in<br />

endosomal compartments plays some part in removal of<br />

CLIP and in the loading of antigenic peptides. Although<br />

HLA-DM is structurally similar to MHC class II molecules,<br />

it is not polymorphic.<br />

HLA-DO<br />

A negative modulator of HLA-DM-mediated MHC class<br />

II peptide loading. By stably associating with HLA-DM,<br />

the catalytic action of HLA-DM on class II peptide loading<br />

is inhibited. Therefore, HLA-DO affects the peptide

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