[PDF][PDF] Virus-specific CD8+ T cells in primary and secondary influenza pneumonia

KJ Flynn, GT Belz, JD Altman, R Ahmed, DL Woodland… - Immunity, 1998 - cell.com
KJ Flynn, GT Belz, JD Altman, R Ahmed, DL Woodland, PC Doherty
Immunity, 1998cell.com
Virus-specific CD8+ effector T cells (eCTL) are enriched in the lungs of mice with primary
influenza pneumonia, though later detection of memory T cells (mCTL) in the mediastinal
lymph nodes (MLN) or spleen by peptide-based staining protocols is at the limits of flow
cytometric analysis. Respiratory challenge with an H3N2 virus months after H1N1 priming
induces a massive recall response, which reduces virus titers 2–3 days earlier than in nave
controls. Influenza-specific mCTL produce interferon-γ within 6 hr, but still take 4–5 days to …
Abstract
Virus-specific CD8+ effector T cells (eCTL) are enriched in the lungs of mice with primary influenza pneumonia, though later detection of memory T cells (mCTL) in the mediastinal lymph nodes (MLN) or spleen by peptide-based staining protocols is at the limits of flow cytometric analysis. Respiratory challenge with an H3N2 virus months after H1N1 priming induces a massive recall response, which reduces virus titers 2–3 days earlier than in nave controls. Influenza-specific mCTL produce interferon-γ within 6 hr, but still take 4–5 days to localize to the infected respiratory tract. The delay reflects that the recall response develops first in the MLN, which contains relatively few mCTL. The response to a subdominant epitope is less obvious after secondary challenge.
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