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Edelman, Gerald Maurice (1929–) 242 Ehrlich, Paul (1854–1915)<br />

Edelman, Gerald Maurice (1929–)<br />

American investigator and professor at Rockefeller<br />

University who shared a Nobel Prize in 1972 with Porter for<br />

their work on antibody structure. Edelman was the first to<br />

demonstrate that immunoglobulins are composed of light<br />

and heavy polypeptide chains. He also did pioneering work<br />

with the Bence–Jones protein, cell adhesion molecules,<br />

immunoglobulin amino acid sequences, and neurobiology.<br />

edema<br />

Tissue swelling as a result of fluid extravasation from the<br />

intravascular space.<br />

edge artifact<br />

In immunoperoxidase staining of paraffin-embedded tissues,<br />

tissue drying may produce nonspecific coloring at the<br />

periphery which is an artifact.<br />

edible vaccine<br />

A genetically altered food containing microorganisms or<br />

related antigens that may induce active immunity against<br />

infection. A plant constituent altered genetically to express<br />

an antigen of a pathogen that can be ingested as food.<br />

efalizumab<br />

An immunosuppressive agent used to treat plaque psoriasis.<br />

Interacts with CD11a, the α subunit of leukocyte<br />

function antigen-1 (LFA-1), which all leukocytes express,<br />

and diminishes cell surface expression of CD11a. Inhibits<br />

binding of LFA-1 to intercellular adhesion molecule-1<br />

(ICAM-1), inhibiting leukocyte adhesion to other cell types.<br />

LFA-1 and ICAM-1 interaction facilitates the initiation and<br />

maintenance of multiple processes, including T lymphocyte<br />

activation, T lymphocyte adhesion to endothelial cells, and<br />

T lymphocyte migration to sites of inflammation, including<br />

psoriatic skin.<br />

effector B cell<br />

Refer to effector lymphocyte (effector cell).<br />

effector cells<br />

Lymphocytes capable of eliminating pathogens from the<br />

body without further differentiation.<br />

effector function<br />

The nonantigen-binding functions of an antibody molecule<br />

that are mediated by the constant regions of heavy<br />

chains. These include Fc receptor binding, complement<br />

fixation, binding to mast cells, etc. Effector function<br />

generally results in removal of antigen from the body, such<br />

as in phagocytosis or complement-mediated lysis. The<br />

elimination of foreign entities by effector cells through<br />

such mechanisms as cytokine secretion, cytotoxicity, and<br />

antibody production.<br />

effector lymphocyte<br />

A lymphocyte activated through either specific or nonspecific<br />

mechanisms to carry out a certain function in<br />

the immune response. The differentiated descendants of<br />

an activated leukocyte that remove a nonself constituent.<br />

Certain effector cells including plasma cells, Th cells, and<br />

cytotoxic T lymphocytes require less costimulation than<br />

their resting naïve counterparts and express homing and<br />

chemokine receptors that are different, thereby permitting<br />

excess inflammatory sites. NKT and ILK cells may function<br />

as effectors without a need to proliferate. Examples of<br />

effector lymphocytes include the natural killer (NK) cell,<br />

tumor-infiltrating lymphocyte (TIF), lymphokine-activated<br />

killer (LAK) cell, cytotoxic T lymphocyte, helper T lymphocyte,<br />

and suppressor T cell. Most commonly, the term<br />

signifies a T lymphocyte capable of mediating cytotoxicity,<br />

suppression, or helper function.<br />

effector mechanism<br />

The means whereby post innate and adaptive immune<br />

responses destroy and eliminate pathogens from the body.<br />

effector phase<br />

That part of an immune response following recognition and<br />

activation phases during which a foreign antigen such as a<br />

microbe is inactivated or destroyed.<br />

effector response<br />

An event that follows antigen recognition and binding by<br />

antibody, such as complement-mediated lysis.<br />

effector site<br />

An isolated area of the mucosa in which there is differentiation<br />

of lymphocytes activated in a mucosal inductive site<br />

into effector cells capable of effector functions, such as<br />

antibody synthesis.<br />

effector stage (hypersensitivity)<br />

Refer to elicitation.<br />

effector T cell<br />

Refer to effector lymphocyte (effector cell).<br />

efferent lymphatic vessel<br />

The channel through which lymph and lymphocytes exit a<br />

lymph node in transit to the blood.<br />

efficacy (vaccine)<br />

Capacity of a vaccine to effectively induce protective<br />

immunity against a disease represented by the percentage<br />

of vaccinated subjects who develop immunity against<br />

the pathogenic microorganism. Frequently evaluated<br />

by post-vaccination seroconversion. Referred to also as<br />

coverage.<br />

Paul Ehrlich.<br />

Ehrlich, Paul (1854–1915)<br />

Born in Silesia, Germany; graduated from the University<br />

of Leipzig as a doctor of medicine. His scientific work<br />

included three areas of investigation. He first became<br />

interested in stains for tissues and cells and perfected<br />

some of the best ones to demonstrate the tubercle bacillus

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