Literature DB >> 28046116

Correction: Interleukin-7, but Not Thymic Stromal Lymphopoietin, Plays a Key Role in the T Cell Response to Influenza A Virus.

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Abstract

[This corrects the article DOI: 10.1371/journal.pone.0050199.].

Entities:  

Year:  2017        PMID: 28046116      PMCID: PMC5207491          DOI: 10.1371/journal.pone.0169498

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Fig 4 is incorrectly replaced with Supplemental S4 Fig. The publisher apologizes for the error.
Fig 4

Cell-intrinsic requirement for IL-7Rα, but not TSLPR, signaling in CD8 T cell response to Influenza A.

Lethally irradiated CD45.1 BoyJ mice were reconstituted with (A) 9:1 IL-7Rα449F:BoyJ or (B) 1:1 TSLPR-/-:BoyJ bone-marrow and allowed to recover for 6–8 weeks. Mice were infected with 5HAU of PR8 and the T cell response was analyzed at day 9 post-infection. CD8 T cells were stained for CD45.1 and CD45.2 to identify WT or mutant derived cells. Each population was analyzed for the percent of total CD8 T cells that recognize the NP366–374 tetramer. Data shown is from one representative experiment of two experiments, n = 3–7. *p<0.05 by Student’s t-test.

Please see the correct Fig 4 here.

Cell-intrinsic requirement for IL-7Rα, but not TSLPR, signaling in CD8 T cell response to Influenza A.

Lethally irradiated CD45.1 BoyJ mice were reconstituted with (A) 9:1 IL-7Rα449F:BoyJ or (B) 1:1 TSLPR-/-:BoyJ bone-marrow and allowed to recover for 6–8 weeks. Mice were infected with 5HAU of PR8 and the T cell response was analyzed at day 9 post-infection. CD8 T cells were stained for CD45.1 and CD45.2 to identify WT or mutant derived cells. Each population was analyzed for the percent of total CD8 T cells that recognize the NP366–374 tetramer. Data shown is from one representative experiment of two experiments, n = 3–7. *p<0.05 by Student’s t-test. Supplemental S4 Fig has several errors. The Supplemental S4 Fig lacks changes made during production including the percent of subsets in various flow gates in Panels A and B. Furthermore, the x-axes’ labels titled “NP311-324” should read “NP311-325” in panels A and B. The publisher apologizes for the error. Please see the correct Supplemental S4 Fig here.

Cell-intrinsic requirement for IL-7Rα, but not TSLPR, signaling in CD4 T cell response to Influenza A.

Lethally irradiated CD45.1 BoyJ mice were reconstituted with (A) 9:1 IL-7Rα449F:BoyJ or (B) 1:1 TSLPR-/-:BoyJ bone-marrow and allowed to recover for 6–8 weeks. Mice were infected with 5HAU of PR8 and the CD4 T cell response was analyzed at day 9 post-infection. CD4 T cells were stained for CD45.1 and CD45.2 to identify WT or mutant derived cells. Each population was analyzed for the percent of CD4 T cells that recognize the NP311–325 tetramer. Irrelevant tetramer staining on CD4 T cells is shown below NP311–325 staining in each panel. Data shown is from one representative experiment of two experiments, n = 3–7. *p<0.05 by Student’s t-test. (EPS) Click here for additional data file.
  1 in total

1.  Interleukin-7, but not thymic stromal lymphopoietin, plays a key role in the T cell response to influenza A virus.

Authors:  Adam W Plumb; Daniel T Patton; Jung Hee Seo; Emma-Kate Loveday; François Jean; Steven F Ziegler; Ninan Abraham
Journal:  PLoS One       Date:  2012-11-26       Impact factor: 3.240

  1 in total

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