Abstract
The effect of drugs upon the primary and the secondary antibody response to diphtheria toxoid in mice was studied using an experimental system previously described. Triethylenethiophosphoramide (thio-TEPA), chloramphenicol, 6-mercaptopurine, 8-azaguanine, and versenate were found to inhibit, partially or completely,"priming" for the secondary response. Thio-TEPA, chloramphenicol, and 6-mercaptopurine, in doses exceeding those effective in inhibiting priming, did not cause alteration of the secondary response when given only during the secondary response. However, when chloramphenicol and amethopterin were given for 5 days prior to and at least 5 days after the second antigen injection, slight suppression of peak secondary titers occurred. Therefore, drug dosages effective in suppressing priming had less effect on the secondary response. It thus appears that there is a real difference between "priming" and the induction of antibody synthesis.
Keywords
ACTINOMYCIN
ANTIBODY FORMATION
ANTINEOPLASTIC AGENTS
ANTIPROTOZOAL AGENTS
AZAGUANINE
CHLORAMPHENICOL
CHLORPROMAZINE
COLCHICINE
EDTA
EXPERIMENTAL LAB STUDY
HYDROCORTISONE
IMMUNIZATION
MERCAPTOPURINE
METHOTREXATE
MICE
PHARMACOLOGY
QUINOLINES
THIO-TEPA
MeSH Terms
Animals
Antibody Formation
Antineoplastic Agents
Antiprotozoal Agents
Azaguanine
Chloramphenicol
Chlorpromazine
Colchicine
Dactinomycin
Edetic Acid
Hydrocortisone
Immunization
Mercaptopurine
Methotrexate
Mice
Pharmacology
Quinolines
Research
Thiotepa
Vaccination
Chemicals
Antineoplastic Agents
Antiprotozoal Agents
Quinolines
Dactinomycin
Chloramphenicol
Thiotepa
Edetic Acid
Mercaptopurine
Azaguanine
Colchicine
Chlorpromazine
Hydrocortisone
Methotrexate
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
BUTLER W T
COONS A H
References (10)
10 references, click to expand
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