Inducible costimulator protein controls the protective T cell response against Listeria monocytogenes
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Inducible costimulator protein controls the protective T cell response against Listeria monocytogenes. / Mittrücker, Hans-Willi; Kursar, Mischo; Köhler, Anne; Yanagihara, Donna; Yoshinaga, Steven K; Kaufmann, Stefan H E.
in: J IMMUNOL, Jahrgang 169, Nr. 10, 15.11.2002, S. 5813-7.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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T1 - Inducible costimulator protein controls the protective T cell response against Listeria monocytogenes
AU - Mittrücker, Hans-Willi
AU - Kursar, Mischo
AU - Köhler, Anne
AU - Yanagihara, Donna
AU - Yoshinaga, Steven K
AU - Kaufmann, Stefan H E
PY - 2002/11/15
Y1 - 2002/11/15
N2 - The inducible costimulator protein (ICOS) was recently identified as a costimulatory molecule for T cells. Here we analyze the role of ICOS for the acquired immune response of mice against the intracellular bacterium Listeria monocytogenes. During oral L. monocytogenes infection, low levels of ICOS expression were detected by extracellular and intracellular Ab staining of Listeria-specific CD4(+) and CD8(+) T cells. Blocking of ICOS signaling with a soluble ICOS-Ig fusion protein markedly impaired the Listeria-specific T cell responses. Compared with control mice, the ICOS-Ig treated mice generated significantly reduced numbers of Listeria-specific CD8(+) T cells in spleen and liver, as determined by tetramer and intracellular cytokine staining. In contrast, the specific CD8(+) T cell response in the intestinal mucosa did not appear to be impaired by the ICOS-Ig treatment. Analysis of the CD4(+) T cell response revealed that ICOS-Ig treatment also affected the specific CD4(+) T cell response. When restimulated with listerial Ag in vitro, reduced numbers of CD4(+) T cells from infected and ICOS-Ig-treated mice responded with IFN-gamma production. The impaired acquired immune response in ICOS-Ig treated mice was accompanied by their increased susceptibility to L. monocytogenes infection. ICOS-Ig treatment drastically enhanced bacterial titers, and a large fraction of mice succumbed to the otherwise sublethal dose of infection. Thus, ICOS costimulation is crucial for protective immunity against the intracellular bacterium L. monocytogenes.
AB - The inducible costimulator protein (ICOS) was recently identified as a costimulatory molecule for T cells. Here we analyze the role of ICOS for the acquired immune response of mice against the intracellular bacterium Listeria monocytogenes. During oral L. monocytogenes infection, low levels of ICOS expression were detected by extracellular and intracellular Ab staining of Listeria-specific CD4(+) and CD8(+) T cells. Blocking of ICOS signaling with a soluble ICOS-Ig fusion protein markedly impaired the Listeria-specific T cell responses. Compared with control mice, the ICOS-Ig treated mice generated significantly reduced numbers of Listeria-specific CD8(+) T cells in spleen and liver, as determined by tetramer and intracellular cytokine staining. In contrast, the specific CD8(+) T cell response in the intestinal mucosa did not appear to be impaired by the ICOS-Ig treatment. Analysis of the CD4(+) T cell response revealed that ICOS-Ig treatment also affected the specific CD4(+) T cell response. When restimulated with listerial Ag in vitro, reduced numbers of CD4(+) T cells from infected and ICOS-Ig-treated mice responded with IFN-gamma production. The impaired acquired immune response in ICOS-Ig treated mice was accompanied by their increased susceptibility to L. monocytogenes infection. ICOS-Ig treatment drastically enhanced bacterial titers, and a large fraction of mice succumbed to the otherwise sublethal dose of infection. Thus, ICOS costimulation is crucial for protective immunity against the intracellular bacterium L. monocytogenes.
KW - Administration, Oral
KW - Animals
KW - Antibodies, Blocking
KW - Antibodies, Monoclonal
KW - Antigens, Differentiation, T-Lymphocyte
KW - CD4-CD8 Ratio
KW - CD4-Positive T-Lymphocytes
KW - CD8-Positive T-Lymphocytes
KW - Disease Susceptibility
KW - Epitopes, T-Lymphocyte
KW - Humans
KW - Inducible T-Cell Co-Stimulator Protein
KW - Injections, Intravenous
KW - Injections, Subcutaneous
KW - Interferon-gamma
KW - Listeria monocytogenes
KW - Listeriosis
KW - Lymphocyte Activation
KW - Lymphocyte Depletion
KW - Mice
KW - Mice, Inbred BALB C
KW - Rats
KW - Rats, Inbred Strains
KW - Recombinant Fusion Proteins
KW - Signal Transduction
KW - T-Lymphocyte Subsets
M3 - SCORING: Journal article
C2 - 12421962
VL - 169
SP - 5813
EP - 5817
JO - J IMMUNOL
JF - J IMMUNOL
SN - 0022-1767
IS - 10
ER -