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PMID: 15494519 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Duration of infection and antigen display have minimal influence on the kinetics of the CD4+ T cell response to Listeria monocytogenes infection.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 173 ·No. 9 ·2004-11-01 ·Pages 5679-87

Corbin GA, Harty JT

Abstract

The T cell response to infection consists of clonal expansion of effector cells, followed by contraction to memory levels. It was previously thought that the duration of infection determines the magnitude and kinetics of the T cell response. However, recent analysis revealed that transition between the expansion and contraction phases of the Ag-specific CD8+ T cell response is not affected by experimental manipulation in the duration of infection or Ag display. We studied whether the duration of infection and Ag display influenced the kinetics of the Ag-specific CD4+ T cell response to Listeria monocytogenes (LM) infection. We found that truncating infection and Ag display with antibiotic treatment as early as 24 h postinfection had minimal impact on the expansion or contraction of CD4+ T cells; however, the magnitudes of the Ag-specific CD4+ and CD8+ T cell responses were differentially affected by the timing of antibiotic treatment. Treatment of LM-infected mice with antibiotics at 24 h postinfection did not prevent generation of detectable CD4+ and CD8+ memory T cells at 28 days after infection, vigorous secondary expansion of these memory T cells, or protection against a subsequent LM challenge. These results demonstrate that events within the first few days of infection stimulate CD4+ and CD8+ T cell responses that are capable of carrying out the full program of expansion and contraction to functional memory, independently of prolonged infection or Ag display.

MeSH Terms
Ampicillin/administration & dosage Animals Antigens, Bacterial/immunology,metabolism Bacterial Toxins/immunology,metabolism CD4-Positive T-Lymphocytes/immunology,metabolism,microbiology CD8-Positive T-Lymphocytes/immunology,metabolism,microbiology Cell Line Epitopes, T-Lymphocyte/immunology,metabolism Female Heat-Shock Proteins/immunology,metabolism Hemolysin Proteins Histocompatibility Antigens Class I/immunology,metabolism Immunization, Secondary Immunologic Memory Kinetics Listeria monocytogenes/drug effects,growth & development,immunology Listeriosis/drug therapy,immunology,microbiology Male Mice Mice, Inbred C57BL Peptide Fragments/immunology,metabolism
Chemicals
Antigens, Bacterial Bacterial Toxins Epitopes, T-Lymphocyte Heat-Shock Proteins Hemolysin Proteins Histocompatibility Antigens Class I Peptide Fragments Ampicillin hlyA protein, Listeria monocytogenes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Corbin Gail A
Department of Microbiology, University of Iowa, Iowa City, IA 52242, USA.
Harty John T
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2004-11-01
Pages
5679-87
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI42767 · United States
NIAID NIH HHS · AI46653 · United States
NIAID NIH HHS · AI50073 · United States
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