CORRECTION article

Front. Immunol., 21 March 2025

Sec. Vaccines and Molecular Therapeutics

Volume 16 - 2025 | https://doi.org/10.3389/fimmu.2025.1593193

Corrigendum: Enhancing AAV-microdystrophin gene therapy after repeat dosing by blocking phagocytosis

Rita SpathisRita Spathis1Deeva Robles KuriplachDeeva Robles Kuriplach1Sabrina NarvesenSabrina Narvesen1Matthew EybsMatthew Eybs1Karen HuangKaren Huang1Steven TorresSteven Torres1Madison KingMadison King1Elizabeth BagleyElizabeth Bagley1Pia ElustondoPia Elustondo2Michael W. LawlorMichael W. Lawlor3Kanneboyina NagarajuKanneboyina Nagaraju1Melissa Morales*Melissa Morales1*
  • 1Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, Binghamton, NY, United States
  • 2AGADA Biosciences, Halifax, NS, Canada
  • 3Department of Pathology & Laboratory Medicine, Medical College of Wisconsin and Diverge Translational Science Laboratory, Milwaukee, WI, United States

A Corrigendum on
Enhancing AAV-microdystrophin gene therapy after repeat dosing by blocking phagocytosis

by Spathis R, Kuriplach DR, Narvesen S, Eybs M, Huang K, Torres S, King M, Bagley E, Elustondo P, Lawlor MW, Nagaraju K and Morales M (2025) Front. Immunol. 16:1527840. doi: 10.3389/fimmu.2025.1527840

In the published article, there was an error in the Funding statement. The funder “Duchenne UK” was erroneously excluded. The correct Funding statement appears below.

“The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The authors would like to thank the Parent Project Muscular Dystrophy (PPMD) and Duchenne UK for funding this work.”

The authors apologize for this error 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: AAV9, mdx, Duchenne muscular dystrophy, DMD, gene therapy, immune response, TLR, complement

Citation: Spathis R, Kuriplach DR, Narvesen S, Eybs M, Huang K, Torres S, King M, Bagley E, Elustondo P, Lawlor MW, Nagaraju K and Morales M (2025) Corrigendum: Enhancing AAV-microdystrophin gene therapy after repeat dosing by blocking phagocytosis. Front. Immunol. 16:1593193. doi: 10.3389/fimmu.2025.1593193

Received: 13 March 2025; Accepted: 14 March 2025;
Published: 21 March 2025.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2025 Spathis, Kuriplach, Narvesen, Eybs, Huang, Torres, King, Bagley, Elustondo, Lawlor, Nagaraju and Morales. 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: Melissa Morales, bW1vcmFsZXNAYmluZ2hhbXRvbi5lZHU=

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.

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