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tumor-associated antigens 720 tumor immunotherapy<br />

Class I<br />

Class II<br />

Class III<br />

Normal<br />

cells<br />

TAA<br />

Neoplastic<br />

cells<br />

tumor-associated antigens<br />

Epitopes of selected tumor cells that are also found on<br />

certain types of normal cells. They may be protein or<br />

carbohydrate molecules expressed in abnormal concentration,<br />

location, or time in a tumor cell compared with<br />

expression in a healthy differentiated cell in the tissue of<br />

origin. Normal cellular genes that have become dysregulated<br />

encode tumor-associated antigens. Examples include<br />

normal cellular proteins, differentiation antigens, tissue<br />

type-specific antigens, embryonic antigens, and idiotypic<br />

antigens. Certain antigens designated CA-125, CA-19-9, and<br />

CA195, among others may be linked to certain tumors such<br />

as lymphomas, carcinomas, sarcomas, and melanomas, but<br />

the immune response to these tumor-associated antigens<br />

is not sufficient to mount a successful cellular or humoral<br />

immune response against the neoplasm. Three classes of<br />

tumor-associated antigens have been described. Class 1<br />

antigens are very specific for a certain neoplasm and absent<br />

from normal cells. Class 2 antigens are found on related<br />

neoplasms from separate individuals. Class 3 antigens are<br />

Macrophage<br />

Helper<br />

T cell<br />

TAA<br />

TAA<br />

TAA<br />

Mast cell<br />

Tc cell<br />

Related<br />

neoplastic cells<br />

TNF-α<br />

TNF-β<br />

TAA<br />

TAA<br />

Tumor-associated antigens (TAAs) among normal and neoplastic cells.<br />

found on malignant and normal cells but show increased<br />

expression in neoplastic cells. Assays of clinical value will<br />

probably be developed for class 2 antigens, as they are<br />

associated with multiple neoplasms and are rarely found in<br />

normal individuals.<br />

tumor enhancement<br />

The successful establishment and prolonged survival<br />

(conversely, the delayed rejection) of a tumor allograft,<br />

especially in mice, as a consequence of contact with specific<br />

antibody.<br />

tumor hypoxia<br />

Diminished oxygen pressure that develops in parts of a<br />

tumor that has outgrown its blood supply. Sensitivity to<br />

radiation and chemotherapy become less effective as tumor<br />

cells undergo hypoxia.<br />

tumor imaging<br />

An experimental and clinical technique employed to localize<br />

neoplastic lesions using a labeled antibody or its fragment.<br />

Tumor imaging is based on the presence of an antigen<br />

expressed only on a tumor cell or exhibits a significant<br />

difference in amount and/or distribution between tumor and<br />

normal tissues.<br />

tumor immunity<br />

A number of experimentally induced tumors in mice<br />

express numerous specific transplantation antigens that<br />

can induce an immune response leading to the destruction<br />

of neoplastic cells in vivo. Lymphocytes play a critical<br />

role in the immunological destruction of many antigenic<br />

tumors. Both cell-mediated and antibody-mediated immune<br />

responses to human neoplasms have been identified and<br />

their targets characterized in an effort to develop clinically<br />

useful immunotherapy.<br />

tumor immunotherapy<br />

Immunological surveillance, first proposed by Paul<br />

Ehrlich 100 years ago, is believed to be a protective<br />

mechanism against the development of neoplasias in intact<br />

healthy subjects. Significant suppression of the immune<br />

system from any cause may favor tumor development.<br />

Contemporary attempts at therapeutic modification of the<br />

immune response include the use of immune response<br />

Tumor cell<br />

Tumor necrosis factor (TNF)-mediated immune reaction.<br />

Tumor cell lysis

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