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Untitled - D Ank Unlimited

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monoclonal immunoglobulin deposition disease (MIDD) 507 monogamous bivalency<br />

Immunize mouse<br />

with antigen<br />

Monoclonal Antibodies<br />

Drug Name Active Ingredient<br />

Avastin Bevacizumab<br />

Campath Alemtuzumab<br />

Cea-Scan Arcitumomab<br />

Erbitux Cetuximab<br />

Hemabate Carboprost tromethamine<br />

Herceptin Trastuzumab<br />

Humira Adalimumab<br />

Lucentis Ranibizumab<br />

Mylotarg Gemtuzumab ozogamicin<br />

Myoscint Imciromab pentetate<br />

Prostascint Capromab pendetide<br />

Raptiva Efalizumab<br />

Remicade Infliximab<br />

Reopro Abciximab<br />

Rituxan Rituximab<br />

Simulect Basiliximab<br />

Soliris Eculizumab<br />

Synagis Palivizumab<br />

Tysabri Natalizumab<br />

Vectibix Panitumumab<br />

Select and culture immortalized<br />

fused spleen/myeloma cells<br />

producing desired antibody<br />

Isolate antibody-producing<br />

spleen cells<br />

Purify antibody from<br />

hybridoma culture medium<br />

Mix spleen cells producing<br />

desired antibody with<br />

myeloma cells and fusing agent<br />

Development of a hybridoma for monoclonal antibody production.<br />

cervix, liver, and bladder, Kaposi’s sarcoma, and angiosarcoma.<br />

Selected infections may also evoke monoclonal<br />

immunoglobulin responses, e.g., viral hepatitis, tuberculosis,<br />

and schistosomiasis. Other conditions that stimulate<br />

this response include thalassemia, autoimmune hemolytic<br />

anemia, autoimmune diseases such as scleroderma and<br />

pemphigus vulgaris, and various other conditions.<br />

monoclonal immunoglobulin deposition disease (MIDD)<br />

A condition in which monotypic light or heavy chains are<br />

deposited in tissues. The deposits may be fibrillar or nonfibrillar.<br />

The AL type of amyloidosis, characterized by light<br />

chains and amyloid P component, represents an example<br />

of fibrillar deposits, whereas light chain or light and heavy<br />

chain diseases represent nonfibrillar deposits. Patients may<br />

develop azotemia, albuminuria, hypogammaglobulinemia,<br />

cardiomyopathy, or nephropathy. Some may develop multiple<br />

myeloma or another plasma cell neoplasm. Another<br />

variety of MIDD is amyloid H, which is composed of V H,<br />

D D, J H, and C H3 domains.<br />

+<br />

monoclonal protein<br />

A protein synthesized by a clone of identical cells derived<br />

from a single cell.<br />

monocyte<br />

Mononuclear phagocytic blood cell derived from promonocytes<br />

in the bone marrow. Following a relatively brief residence<br />

in the blood, i.e., approximately one day, they migrate<br />

into the tissues and serous cavities and are transformed into<br />

macrophages. They are less mature than macrophages, as<br />

suggested by fewer surface receptors, cytoplasmic organelles,<br />

and enzymes than the latter. Monocytes are larger<br />

than polymorphonuclear leukocytes, are actively phagocytic,<br />

and constitute 2 to 10% of the total white blood cell<br />

count in humans. Monocytes in the blood circulation have<br />

diameters of 15 to 25 μm and a grayish-blue cytoplasm that<br />

contains lysosomes with enzymes such as acid phosphatase,<br />

arginase cachetepsin, collagenase, deoxyribonuclease,<br />

lipase, glucosidase, and plasminogen activator. The cell<br />

has a reniform nucleus with delicate lace-like chromatin.<br />

Monocytes have surface receptors such as the Fc receptor<br />

for immunoglobulin G (IgG) and a receptor for CR3. They<br />

are actively phagocytic and play a significant role in antigen<br />

processing. Monocyte numbers are elevated in both benign<br />

and malignant conditions. Certain infections stimulate reactive<br />

types of monocytosis such as in tuberculosis, brucellosis,<br />

HIV-1 infection, and malaria.<br />

monocyte chemoattractant protein (MCP-1)<br />

A prototypic chemokine of the β (CC) family first isolated<br />

as a product of the immediate early gene, JE, induced by<br />

PDGF. Cloning of the human homolog of JE reveals an<br />

encoded protein identical to authentic chemokine MCP-1,<br />

which is believed to be one of the most significant chemokines<br />

in chronic inflammatory diseases controlled by<br />

mononuclear leukocytes. Tissue sources include fibroblasts,<br />

monocytes, macrophages, mouse spleen lymphocytes, and<br />

endothelial cells, among others. Target cells include monocytes,<br />

hematopoietic precursors, T lymphocytes, basophils,<br />

eosinophils, mast cells, NK cells, and dendritic cells.<br />

monocyte chemoattractant protein-2 (MCP-2)<br />

Refer to MCP-2.<br />

monocyte chemoattractant protein-3 (MCP-3)<br />

Refer to MCP-3.<br />

monocyte colony-stimulating factor (M-CSF)<br />

A cytokine that induces the production of monocytes from<br />

bone marrow precursor cells. It is synthesized by T lymphocytes,<br />

macrophages, endothelial cells, and stromal fibroblasts.<br />

monocyte-derived neutrophil chemotactic factor<br />

Refer to interleukin-8 (IL8).<br />

monocyte–phagocytic system<br />

A system of cells that provides nonspecific immunity and<br />

is dependent on the activity of the monocyte–macrophage<br />

lineage cells that are especially prominent in the spleen.<br />

monogamous bivalency<br />

The binding of a bivalent antibody molecule such as IgG<br />

with two identical antigenic determinants or epitopes on<br />

the same antigen molecule, in contrast to each Fab region<br />

of the IgG molecule uniting with an identical antigenic<br />

determinant on two separate antigen molecule. For this<br />

monogamous binding to take place, the epitopes must be<br />

positioned on the surface of the antigen molecule in such<br />

a manner that the binding of one Fab region to an epitope<br />

can position the remaining Fab of the IgG molecule<br />

M

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