“…Siglec‐F, CD169, and CD206, are present at higher levels on murine resident AMs while monocyte‐derived AMs express higher levels of Ly6C 30,33,34 and the death receptor Fas 30,33 . During infection, e.g.,, with murid herpesvirus 4 (MuHV‐4) in BALB/c mice 35 or influenza in C57/BL6 mice, 36 resident AMs are rapidly depleted after infection, potentially providing a new niche for recruited monocyte‐derived Mϕs. Machiels and colleagues 35 showed that at day 8 after MuHV‐4 infection, a large number of monocytes from BM arrived in the alveolar space, and eventually replaced resident AMs, remaining in this niche for weeks.…”