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. 2016 Nov 5;499:397–398. doi: 10.1016/j.virol.2016.10.018

Corrigendum to ‘Phagocytic cells contribute to the antibody-mediated elimination of pulmonary-infected SARS coronavirus’ [Virology (2014) 157–168]

Fumihiko Yasui a, Michinori Kohara a,, Masahiro Kitabatake b, Tetsu Nishiwaki c, Hideki Fujii d,h, Chise Tateno e, Misako Yoneda f, Kouichi Morita g, Kouji Matsushima c, Shigeo Koyasu d,i, Chieko Kai f
PMCID: PMC7127455  PMID: 27825473

The authors regret that the Fig. 1 that was published is incorrect. The corrected Fig. 1 is given below.

Fig. 1.

Fig. 1

CD4+ T cells play an important role in the control of SARS-CoV infection. (A–C) aged BALB/c mice (n=4–7/time point), young BALB/c mice (n=5–10/time point), and young SCID mice (n=4–8/time point) were infected intranasally with 1×105 TCID50 of SARS-CoV Vietnam strain. (A) Virus titers in the lung (TCID50/g lung tissue) of aged BALB/c mice (closed circles), young BALB/c mice (gray circles), or young SCID mice (open squares) sacrificed at 2, 4, 6, 9, or 21 dpi (except for 20 dpi in young BALB/c mice). p<0.05, ⁎⁎p<0.01 (compared with young BALB/c mice and SCID mice at the respective time point). N.D.: not detected. (B) Representative lung sections (hematoxylin and eosin staining; section thickness 4 μm) from aged BALB/c mice at 9 dpi (a and c) and 21 dpi (b and d) and from young SCID mice at 9 dpi (e and g) and 21 dpi (f and h). For all micrographs, original magnification is 200×. (C) Detection of virus-infected cells in the lungs at 2, 9, or 21 dpi (SARS-CoV nucleocapsid protein [brown staining]; original magnification, 400×). (D) Temporal change of pulmonary virus titer in the following: aged BALB/c mice (green); untreated SCID mice (blue); SCID mice transplanted with splenocytes from naïve BALB/c mice (yellow); or SCID mice transplanted with splenocytes from sensitized BALB/c mice (red). Splenocytes (4×107 cells) were administered intravenously to each recipient SCID mouse 1 day before infection. Data are presented as mean±S.D. (n=4/time point). p<0.05 (compared with naïve splenocyte-transplanted SCID mice at 2 dpi or with other groups at 4 dpi). (E) Representative lung sections (hematoxylin and eosin staining; section thickness 4 μm) from each group in (D) at 9 dpi. SPL, splenocyte. For all micrographs, original magnification is 200×. (F) Flow cytometry analysis of CD4 and CD8 expression on lymphocytes isolated from spleen 1 day after administration of the indicated mAb. (G) Virus titers in the lung of untreated (white), CD8+ cell-depleted (light gray), CD4+ cell-depleted (dark gray), or CD4+ and CD8+ cell-depleted BALB/c mice (black) at 6 and 9 dpi. The limit of detection was <1×103 TCID50/g lung. Data are presented as mean±S.D. (n=3–7/time point).

The authors would like to apologise for any inconvenience caused..


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