[PDF][PDF] Innate immune activation and CD4+ T cell priming during respiratory fungal infection

A Rivera, G Ro, HL Van Epps, T Simpson, I Leiner… - Immunity, 2006 - cell.com
A Rivera, G Ro, HL Van Epps, T Simpson, I Leiner, DB Sant'Angelo, EG Pamer
Immunity, 2006cell.com
Aspergillus fumigatus is a mold that causes a spectrum of diseases, including lethal lung
infections in immunocompromised humans and allergic asthma in atopic individuals. T
helper 1 (Th1) CD4+ T cells protect against invasive A. fumigatus infections whereas Th2
CD4+ T cells exacerbate asthma upon inhalation of A. fumigatus spores. Herein, we
demonstrate that A. fumigatus-specific T cells were rapidly primed in lymph nodes draining
the lung and fully differentiated into interferon-γ (IFN-γ)-producing Th1 CD4+ T cells upon …
Summary
Aspergillus fumigatus is a mold that causes a spectrum of diseases, including lethal lung infections in immunocompromised humans and allergic asthma in atopic individuals. T helper 1 (Th1) CD4+ T cells protect against invasive A. fumigatus infections whereas Th2 CD4+ T cells exacerbate asthma upon inhalation of A. fumigatus spores. Herein, we demonstrate that A. fumigatus-specific T cells were rapidly primed in lymph nodes draining the lung and fully differentiated into interferon-γ (IFN-γ)-producing Th1 CD4+ T cells upon arrival in the airways. T-bet induction in A. fumigatus-specific CD4+ T cells was enhanced by MyD88-mediated signals in draining lymph nodes, but T cell proliferation, trafficking, and Th1 differentiation in the airways were Toll-like receptor (TLR) and MyD88 independent. Our studies demonstrate that CD4+ T cell differentiation during respiratory fungal infection occurs incrementally, with TLR-mediated signals in the lymph node enhancing the potential for IFN-γ production whereas MyD88-independent signals promote Th1 differentiation in the lung.
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