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PMID: 6798568 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Decrease in macrophage antigen catabolism caused by ammonia and chloroquine is associated with inhibition of antigen presentation to T cells.

Ziegler HK, Unanue ER

Abstract

This paper describes the effects of two lysosomotropic compounds, ammonia and chloroquine, on the interaction of mononuclear phagocytes with immune T cells. The uptake and ingestion of Listeria monocytogenes by macrophages were not affected by the drugs; however, the macrophage catabolism of 125I-labeled Listeria was reduced in a dose-dependent way. The macrophage presentation of Listeria to T cells, an I-region-dependent phenomenon, was also inhibited. The degree of inhibition of catabolism paralleled that of antigen presentation. The inhibition of antigen presentation took place if the macrophages were treated before and during Listeria uptake; minimal inhibition took place if the macrophages were treated 30 min after Listeria ingestion, at which time a significant amount of bacteria was already catabolized. Our previous studies had shown that the macrophage-associated antigen recognized by T cells became apparent 30-60 min after uptake of Listeria. We conclude that ammonia and chloroquine affected an intracellular handling step required for the expression of the immunogen relevant for T-cell recognition.

MeSH Terms
Ammonium Chloride/pharmacology Animals Antigens, Surface/immunology Chloroquine/pharmacology Immunity, Cellular/drug effects Listeria monocytogenes/immunology Macrophages/drug effects,immunology Mice T-Lymphocytes/drug effects,immunology
Chemicals
Antigens, Surface Ammonium Chloride Chloroquine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ziegler H K
Unanue E R
References (27)
27 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1982-01-00
Pages
175-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC345685
Subset
IM
Grants
NIAID NIH HHS · AI 14732 · United States
NIAID NIH HHS · AI 17259 · United States
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