We describe a murine cDNA, designated Early T lymphocyte activation 1 (ETA-1) which is abundantly expressed after activation of T cells. Eta-1 encodes a highly acidic secreted product having structural features of proteins that bind to cellular adhesion receptors. The Eta-1 gene maps to a locus on murine chromosome 5 termed Ric that confers resistance to infection by Rickettsia tsutsugamushi (RT), an obligate intracellular bacterium that is the etiological agent for human scrub typhus. With one exception, inbred mouse strains that expressed the Eta-1a allele were resistant to RT infection (RicR), and inbred strains expressing the Eta-1b allele were susceptible (RicS). These findings suggest that Eta-1 is the gene inferred from previous studies of the Ric locus (5). Genetic resistance to RT infection is associated with a strong Eta-1 response in vivo and inhibition of early bacterial replication. Eta-1 gene expression appears to be part of a surprisingly rapid T cell-dependent response to bacterial infection that may precede classical forms of T cell-dependent immunity.
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1 July 1989
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July 01 1989
Structural and functional studies of the early T lymphocyte activation 1 (Eta-1) gene. Definition of a novel T cell-dependent response associated with genetic resistance to bacterial infection.
R Patarca,
R Patarca
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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G J Freeman,
G J Freeman
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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R P Singh,
R P Singh
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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F Y Wei,
F Y Wei
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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T Durfee,
T Durfee
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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F Blattner,
F Blattner
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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D C Regnier,
D C Regnier
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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C A Kozak,
C A Kozak
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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B A Mock,
B A Mock
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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H C Morse, 3rd
H C Morse, 3rd
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
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R Patarca
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
G J Freeman
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
R P Singh
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
F Y Wei
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
T Durfee
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
F Blattner
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
D C Regnier
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
C A Kozak
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
B A Mock
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
H C Morse, 3rd
Laboratory of Immunopathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1989) 170 (1): 145–161.
Citation
R Patarca, G J Freeman, R P Singh, F Y Wei, T Durfee, F Blattner, D C Regnier, C A Kozak, B A Mock, H C Morse; Structural and functional studies of the early T lymphocyte activation 1 (Eta-1) gene. Definition of a novel T cell-dependent response associated with genetic resistance to bacterial infection.. J Exp Med 1 July 1989; 170 (1): 145–161. doi: https://doi.org/10.1084/jem.170.1.145
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