Use of in vitro assay techniques to measure parameters related t

Drug – bio-affecting and body treating compositions – Lymphokine

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424101, 435 4, 435 29, 435 7, 436811, A61K 3514, A61K 3900, C12Q 102

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active

046108785

ABSTRACT:
Described herein are methods for quantifying in vitro various parameters related to the use of transfer factor (e.g., dialyzable leukocyte extract containing transfer factor) in the therapeutic and/or prophylactic treatment of patients having antigen-selective defects in cell mediated immunity, so as to standardize such parameters, predict or estimate therefrom the effectiveness of such treatment in vivo, determine optimum dosages and/or administrative regimens therefor and monitor the progress of patients receiving such treatment.
In one embodiment of the invention, the quantification of the various parameters is based upon in vitro assays which measure mediators of cellular immunity produced and released by appropriate leukocytes (e.g., those of the patient before treatment, those of potential donors, those of target cells, those of the patient after treatment with transfer factor, and the like) sensitized to a specific antigen. In another embodiment of the invention the in vitro assays employed are those which provide a measure of tumor-antigen specific cytotoxicity mediated by T cells, i.e., a measure of the increase in activity or number of cytotoxic T cells specific for tumor antigens.

REFERENCES:
patent: 3988115 (1976-10-01), Modabber
patent: 4124701 (1978-11-01), Bach et al.
patent: 4284412 (1981-08-01), Hansen et al.
Natelson et al--Clinical Immunochemistry (1978) (article by Fudenberg), pp. 228, 232, 233, 237-238, 241 and 248.
Wilson et al--Lymphokines, vol. 4 (1981), pp. 107-173.
Bach--Immunology (1982), pp. 376-378 (Pub. John Wiley).

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