Antiviral immune responses in Itk-deficient mice.

M F Bachmann, D R Littman, X C Liao
Author Information
  1. M F Bachmann: Department of Pathology, University of Zurich, Switzerland.

Abstract

Mice lacking Itk, a T-cell-specific protein tyrosine kinase, have reduced numbers of T cells and reduced responses to allogeneic major histocompatibility molecules. This study analyzed antiviral immune responses in mice deficient for Itk. Primary cytotoxic T-lymphocyte (CTL) responses were analyzed after infection with lymphocytic choriomeningitis virus (LCMV), vaccinia virus (VV), and vesicular stomatitis virus (VSV). Ex vivo CTL activity was consistently reduced by a factor of two to six for the different viruses. CTL responses after restimulation in vitro were similarly reduced unless exogenous cytokines were added. In the presence of interleukin-2 or concanavalin A supernatant, Itk-deficient and control mice responded similarly. Interestingly, while LCMV was completely eliminated by day 8 in both Itk-deficient and control mice, VV cleared from itk-/- mice with delayed kinetics. Antibody responses were evaluated after VSV infection. Both the T-cell-independent neutralizing immunoglobulin M (IgM) and the T-cell-dependent IgG responses were similar in Itk-deficient and control mice. Taken together, the results show that CTL responses are reduced in the absence of Itk whereas antiviral B-cell responses are not affected.

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MeSH Term

Animals
Antibodies, Viral
Antibody Formation
B-Lymphocytes
Cytokines
Cytotoxicity, Immunologic
Enzyme-Linked Immunosorbent Assay
Immunoglobulin G
Immunoglobulin M
Lymphocyte Activation
Lymphocytic choriomeningitis virus
Major Histocompatibility Complex
Mice
Mice, Knockout
Protein-Tyrosine Kinases
T-Lymphocytes
T-Lymphocytes, Cytotoxic
Time Factors
Vaccinia virus
Vesicular stomatitis Indiana virus

Chemicals

Antibodies, Viral
Cytokines
Immunoglobulin G
Immunoglobulin M
Protein-Tyrosine Kinases
emt protein-tyrosine kinase

Word Cloud

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