Skip to main content

CORRECTION article

Front. Immunol., 01 June 2022
Sec. Inflammation
Volume 13 - 2022 | https://doi.org/10.3389/fimmu.2022.926032

Corrigendum: CCR2 Is Dispensable for Disease Resolution but Required for the Restoration of Leukocyte Homeostasis Upon Experimental Malaria-Associated Acute Respiratory Distress Syndrome

This article is a correction to:

  1. CCR2 Is Dispensable for Disease Resolution but Required for the Restoration of Leukocyte Homeostasis Upon Experimental Malaria-Associated Acute Respiratory Distress Syndrome

    1. Read original article
Emilie PollenusEmilie Pollenus1Thao-Thy PhamThao-Thy Pham1Leen VandermostenLeen Vandermosten1Queeny RobaloQueeny Robalo1Hendrik PossemiersHendrik Possemiers1Sofie KnoopsSofie Knoops1Ghislain OpdenakkerGhislain Opdenakker2Philippe E. Van den Steen*Philippe E. Van den Steen1*
  • 1Laboratory of Immunoparasitology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, University of Leuven, Leuven, Belgium
  • 2Laboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, University of Leuven, Leuven, Belgium

A Corrigendum on
CCR2 Is Dispensable for Disease Resolution but Required for the Restoration of Leukocyte Homeostasis Upon Experimental Malaria-Associated Acute Respiratory Distress Syndrome

By Pollenus E, Pham T-T, Vandermosten L, Robalo Q, Possemiers H, Knoops S, Opdenakker G and Van den Steen PE (2021) Front. Immunol. 11:628643. doi: 10.3389/fimmu.2020.628643

“Queeny Robalo” was not included as an author in the published article. The corrected Author contributions statement appears below.

Author Contributions

EP, T-TP, LV, QR, HP and SK performed the experiments. EP and QR analyzed the data. PVdS, EP and GO conceived the study. EP and PVdS wrote the first drafts of the manuscript. EP, T-TP, LV, HP, SK, GO and PVdS critically read and edited the manuscript. All authors contributed to the article, read the article and approved the final version.

Furthermore, one picture of the lungs in Figure 1F in the published article was inadvertently duplicated and mislabeled as “ART+CQ d15” instead of “ART+CQ d14”. The corrected Figure 1 appears below.

FIGURE 1
www.frontiersin.org

Figure 1 A mouse model to study the resolution of malaria-associated acute respiratory distress syndrome (MA-ARDS) after antimalarial treatment. C57BL/6 mice were infected with PbNK65. Mice were injected daily from 8 until 12 days p.i. with 10 mg/kg ART + 30 mg/kg CQ (ART+CQ). (A) Schematic representation of the timing of infection and antimalarial treatments in the mouse model. (B) Parasitemia was determined using Giemsa-stained blood smears. (C) The clinical score was monitored daily starting at 6 days p.i. (D) The change in body weight was calculated compared to day 0 p.i. starting at 6 days p.i. (B, D) Compilation of two experiments. Data are means ± SEM. n=8 for uninfected controls (CON), n=8–16 for the infected untreated group (UT), n=7–21 for the infected ART+CQ-treated group. (E) The protein concentration in the BALF was determined as a measure of alveolar edema. Compilation of two experiments. Each symbol represents data of an individual mouse. n=8 for CON on day 0, UT at 8 and 9 days p.i and ART+CQ at 9 days p.i., n=6 for ART+CQ at 12 days p.i., n=7 for ART+CQ at 15 days p.i. (F) Representative pictures of the left lung.

The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: malaria, inflammation, resolution, monocytes, immunology, parasitology, eosinophils

Citation: Pollenus E, Pham T-T, Vandermosten L, Robalo Q, Possemiers H, Knoops S, Opdenakker G and Van den Steen PE (2022) Corrigendum: CCR2 Is Dispensable for Disease Resolution but Required for the Restoration of Leukocyte Homeostasis Upon Experimental Malaria-Associated Acute Respiratory Distress Syndrome. Front. Immunol. 13:926032. doi: 10.3389/fimmu.2022.926032

Received: 22 April 2022; Accepted: 16 May 2022;
Published: 01 June 2022.

Edited and reviewed by:

Janos G. Filep, Université de Montréal, Canada

Copyright © 2022 Pollenus, Pham, Vandermosten, Robalo, Possemiers, Knoops, Opdenakker and Van den Steen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Philippe E. Van den Steen, Philippe.vandensteen@kuleuven.be

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.