Inflammatory impact of IFN-ƴ in CD8+ T cell-mediated lung injury is mediated by both Stat1-dependent and -independent pathways

Chilakamarti V. Ramana*, Matthew P. Deberge, Aseem Kumar, Christopher S. Alia, Joan E. Durbin, Richard I. Enelow

*Corresponding author for this work

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Influenza infection results in considerable pulmonary pathology, a significant component of which is mediated by CD8+ T cell effector functions. To isolate the specific contribution of CD8+ T cells to lung immunopathology, we utilized a nonviral murine model in which alveolar epithelial cells express an influenza antigen and injury is initiated by adoptive transfer of influenza-specific CD8+ T cells. We report that IFN-ƴ production by adoptively transferred influenzaspecific CD8+ T cells is a significant contributor to acute lung injury following influenza antigen recognition, in isolation from its impact on viral clearance. CD8+ T cell production of IFN-ƴ enhanced lung epithelial cell expression of chemokines and the subsequent recruitment of inflammatory cells into the airways. Surprisingly, Stat1 deficiency in the adoptive-transfer recipients exacerbated the lung injury that was mediated by the transferred influenza-specific CD8+ T cells but was still dependent on IFN-ƴ production by these cells. Loss of Stat1 resulted in sustained activation of Stat3 signaling, dysregulated chemokine expression, and increased infiltration of the airways by inflammatory cells. Taken together, these data identify important roles for IFN-ƴ signaling and Stat1-independent IFN-ƴ signaling in regulating CD8+ T cell-mediated acute lung injury. This is the first study to demonstrate an anti-inflammatory effect of Stat1 on CD8+ T cell-mediated lung immunopathology without the complication of differences in viral load.

Original languageEnglish (US)
Pages (from-to)L650-L657
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume308
Issue number7
DOIs
StatePublished - Jan 1 2015

Fingerprint

Lung Injury
T-Lymphocytes
Human Influenza
Lung
Adoptive Transfer
Acute Lung Injury
Chemokines
Alveolar Epithelial Cells
Antigens
Viral Load
Anti-Inflammatory Agents
Epithelial Cells
Pathology
Wounds and Injuries
Infection

Keywords

  • Acute lung injury
  • CD8 T cell
  • Immunopathology
  • Interferon-ƴ
  • Stat1

ASJC Scopus subject areas

  • Physiology
  • Pulmonary and Respiratory Medicine
  • Physiology (medical)
  • Cell Biology

Cite this

Ramana, Chilakamarti V. ; Deberge, Matthew P. ; Kumar, Aseem ; Alia, Christopher S. ; Durbin, Joan E. ; Enelow, Richard I. / Inflammatory impact of IFN-ƴ in CD8+ T cell-mediated lung injury is mediated by both Stat1-dependent and -independent pathways. In: American Journal of Physiology - Lung Cellular and Molecular Physiology. 2015 ; Vol. 308, No. 7. pp. L650-L657.
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Inflammatory impact of IFN-ƴ in CD8+ T cell-mediated lung injury is mediated by both Stat1-dependent and -independent pathways. / Ramana, Chilakamarti V.; Deberge, Matthew P.; Kumar, Aseem; Alia, Christopher S.; Durbin, Joan E.; Enelow, Richard I.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 308, No. 7, 01.01.2015, p. L650-L657.

Research output: Contribution to journalArticle

TY - JOUR

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AU - Ramana, Chilakamarti V.

AU - Deberge, Matthew P.

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AB - Influenza infection results in considerable pulmonary pathology, a significant component of which is mediated by CD8+ T cell effector functions. To isolate the specific contribution of CD8+ T cells to lung immunopathology, we utilized a nonviral murine model in which alveolar epithelial cells express an influenza antigen and injury is initiated by adoptive transfer of influenza-specific CD8+ T cells. We report that IFN-ƴ production by adoptively transferred influenzaspecific CD8+ T cells is a significant contributor to acute lung injury following influenza antigen recognition, in isolation from its impact on viral clearance. CD8+ T cell production of IFN-ƴ enhanced lung epithelial cell expression of chemokines and the subsequent recruitment of inflammatory cells into the airways. Surprisingly, Stat1 deficiency in the adoptive-transfer recipients exacerbated the lung injury that was mediated by the transferred influenza-specific CD8+ T cells but was still dependent on IFN-ƴ production by these cells. Loss of Stat1 resulted in sustained activation of Stat3 signaling, dysregulated chemokine expression, and increased infiltration of the airways by inflammatory cells. Taken together, these data identify important roles for IFN-ƴ signaling and Stat1-independent IFN-ƴ signaling in regulating CD8+ T cell-mediated acute lung injury. This is the first study to demonstrate an anti-inflammatory effect of Stat1 on CD8+ T cell-mediated lung immunopathology without the complication of differences in viral load.

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