Popliteal lymph node assay as a tool to predict drug-induced GvH-like reactions.

Details

Serval ID
serval:BIB_54853A0C9E33
Type
Article: article from journal or magazin.
Collection
Publications
Title
Popliteal lymph node assay as a tool to predict drug-induced GvH-like reactions.
Journal
Developments In Biological Standardization
Author(s)
Descotes J., Verdier F., Brouland J.P., Patriarca C.
ISSN
0301-5149 (Print)
ISSN-L
0301-5149
Publication state
Published
Issued date
1992
Peer-reviewed
Oui
Volume
77
Pages
111-114
Language
english
Notes
Publication types: Journal ArticlePublication Status: ppublish
Abstract
The popliteal lymph node (PLN) assay was proposed to study a panel of drug-induced clinical manifestations, e.g. lupus syndrome, serum sickness-like disease, lymphadenopathy, scleroderma-like reaction, the mechanism of which was suggested as being similar to a graft-versus-host (GvH) reaction, hence the term GvH-like reaction. This assay can readily be performed in either the mouse or rat. The commonest endpoint is PLN weight, but cellularity and lymphocyte-phenotype analysis can also be determined. Experiments so far show that most drugs and chemicals known to induce such complications in man can be detected by the PLN assay and false-positive responses are extremely few. Interestingly, preliminary results indicate that cimetidine, an immuno-enhancing agent, can increase the response to phenytoin, a positive reference compound in the PLN assay. Thus, in addition to predicting those drugs with the capacity to induce GvH-like reactions and investigating the mechanism involved, the PLN assay may also prove useful in the pre-clinical assessment of immunomodulating agents.
Keywords
Animals, Drug Evaluation, Preclinical/methods, Drug Interactions, Graft vs Host Reaction, Humans, Immunologic Techniques, Immunophenotyping, Inflammation/chemically induced, Knee, Lymph Nodes/drug effects, Lymph Nodes/pathology, Mice, Predictive Value of Tests, Rats, Toxicology/methods
Pubmed
Web of science
Create date
13/10/2015 9:52
Last modification date
20/08/2019 15:09
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