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IgM 353 IL4<br />

have recurrent respiratory infections and recurring pyogenic<br />

sinopulmonary infections with Hemophilus influenzae,<br />

Staphylococcus aureus, and Streptococcus pneumoniae.<br />

Some patients manifest features of autoimmune disease,<br />

such as systemic lupus erythematosus (SLE). IgG 2–IgG 4<br />

deficiency is often associated with recurrent infections or<br />

autoimmune disease. IgG 2 deficiency is reflected as recurrent<br />

sinopulmonary infections and nonresponsiveness to<br />

polysaccharide antigens such as those of Pneumococcus. A<br />

few individuals have IgG 3 deficiency and develop recurrent<br />

infections. In IgG 4-deficient patients, recurrent respiratory<br />

infections and autoimmune manifestations also occur. The<br />

diagnosis is established by the demonstration of significantly<br />

lower levels of at least one IgG subclass in the patient compared<br />

with IgG subclass levels in normal age-matched controls.<br />

γ Globulin is the treatment choice. Very infrequently, C<br />

gene segment deletions may lead to IgG subclass deficiency.<br />

IgM<br />

Refer to immunoglobulin M.<br />

IgM, 7S<br />

Monomeric IgM.<br />

IgM deficiency syndrome<br />

An infrequent condition characterized by diminished<br />

activation of complement and decreased B lymphocyte<br />

membrane 5-ecto nucleotidase. Patients manifest heightened<br />

susceptibility to pulmonary infections, septicemia,<br />

and tumors.<br />

IgM index<br />

Reflects total IgM formation in the blood–brain barrier. The<br />

index is elevated in infectious meningoencephalomyelitis<br />

and may also be increased in central nervous system lupus<br />

erythematosus (SLE) and multiple sclerosis (MS).<br />

IgM paraproteinemia<br />

Occasional cases of IgM myeloma occur and are characterized<br />

by infiltration of the bone marrow by plasmacytes,<br />

numerous osteolytic lesions, and occasionally bleeding<br />

diathesis. IgM myeloma is distinct from true Waldenström’s<br />

macroglobulinemia but is rare compared with the IgG and<br />

IgA types. Myelomas associated with the minor classes<br />

of immunoglobulin IgD and IgE occur with even less frequency<br />

than do the IgM myelomas.<br />

IgR<br />

A second class of immunoglobulin protein in Raja kenojei.<br />

IgT<br />

An obsolete term for the T lymphocyte antigen receptor that<br />

was incorrectly considered an immunoglobulin of a special<br />

class. IgT should not be confused with IgG.<br />

IgW<br />

An immunoglobulin isotype of sharks.<br />

IgX<br />

An immunoglobulin isotype of Xenopus.<br />

Ii Antigens<br />

Antigen expression<br />

Phenotype I i<br />

I adult Strong Very weak<br />

I cord Weak Strong<br />

i adult Very weak Strong<br />

IgY<br />

An immunoglobulin isotype of Xenopus.<br />

Ii<br />

Refer to invariant chain.<br />

Ii antigens<br />

Two nonallelic carbohydrate antigens (epitopes) on<br />

the surface membranes of human erythrocytes. They<br />

may also occur on some nonhematopoietic cells. The<br />

i epitope is found on fetal erythrocytes and red cell<br />

blood precursors. The I antigen is formed when aliphatic<br />

galactose-N-acetyl-glucosamine is converted to a complex<br />

branched structure. I represents the mature form<br />

and i the immature form. Mature erythrocytes express<br />

I. Antibodies against i antigen are hemolytic in cases of<br />

infectious mononucleosis.<br />

iIELs<br />

Abbreviation for intestinal intraepithelial lymphocytes.<br />

I-J<br />

An area of the murine I region predicted to encode for<br />

a suppressor cell antigen. Recombinant mouse strains<br />

were used to show that the I-J gene locus maps to a<br />

region between the I-A and I-E loci of the H-2 complex.<br />

Monoclonal antibodies against I-J react with antigen-specific<br />

suppressor T cells that secrete suppressive factors. The<br />

anti-I-J specific antibodies react with an epitope among the<br />

suppressor cell factors. I-J determinant is associated with a<br />

13-kDa protein known as the glycosylation-inhibiting factor<br />

that has suppressive activity.<br />

Ikaros<br />

A transcription factor requisite for all lineages of lymphoid<br />

cells to develop.<br />

IL<br />

Abbreviation for interleukin.<br />

IL1<br />

Abbreviation for interleukin-1.<br />

IL1 Ra<br />

Abbreviation for IL1 receptor antagonist.<br />

IL1 receptor antagonist (IL1ra)<br />

Refer to interleukin-1 receptor antagonist (IL1ra).<br />

IL2<br />

Abbreviation for interleukin-2.<br />

IL2/LAK cells<br />

Interleukin-2 lymphokine-activated killer (LAK) cells.<br />

Natural killer (NK) cells that express only the p70 and not<br />

the p55 receptor for IL2, are incubated with IL2, converting<br />

them into an activated form referred to as LAK cells.<br />

The IL2/LAK combination has been used to treat cancer<br />

patients through adoptive immunotherapy, which has been<br />

successful in inducing transient regression of tumors in<br />

selected cases of melanoma, colorectal carcinoma, non-<br />

Hodgkin lymphoma, and renal cell carcinoma, as well as<br />

regression of metastases in the livers and lungs of some<br />

patients. Transient defective chemotaxis of neutrophils<br />

may be present and patients often develop capillary leak<br />

syndrome, producing pulmonary edema. Patients may also<br />

develop congestive heart failure.<br />

IL2 receptor (CD25)<br />

Refer to interleukin-2 receptor (IL2R).<br />

IL3<br />

Abbreviation for interleukin-3.<br />

IL4<br />

Abbreviation for interleukin-4.<br />

I

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