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CORRECTION article
Front. Immunol. , 14 January 2025
Sec. Primary Immunodeficiencies
Volume 15 - 2024 | https://doi.org/10.3389/fimmu.2024.1544964
This article is a correction to:
Heterogeneous phenotype of a Chinese Familial WHIM Syndrome with CXCR4 V340fs Gain-of-function Mutation
A Corrigendum on
Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation
By Huang Y, Li L, Chen R, Yu L, Zhao S, Jia Y, Dou Y, Zhang Z, An Y, Tang X, Zhao X and Zhou L (2024) Front. Immunol. 15:1460990. doi: 10.3389/fimmu.2024.1460990
In the published article, there was an error. A typo was made.
A correction has been made to Abstract, Results, Paragraph 1. This sentence previously stated:
“We provide and in-depth analysis of their clinical, genetic, immunological and treatment characteristic, noting that these patients exhibited an atypical clinical phenotype when compared to reported CXCR4R334X patients.”
The corrected sentence appears below:
“We provide an in-depth analysis of their clinical, genetic, immunological and treatment characteristic, noting that these patients exhibited an atypical clinical phenotype when compared to reported CXCR4R334X patients.”
1. In the published article, there was an error. A typo was made.
A correction has been made to Introduction, Paragraph 2. This sentence previously stated:
“Thirty-seven distinct CXCR4 variants have been identified, whice including eight nonsense variants, twenty-seven frameshift variants, and two missense variants.”
The corrected sentence appears below:
Thirty-seven distinct CXCR4 variants have been identified, which including eight nonsense variants, twenty-seven frameshift variants, and two missense variants.”
2. In the published article, there was an error. Omission of important information.
A correction has been made to Results, Clinical manifestations of the family with WHIM syndrome, Paragraph 3. This sentence previously stated:
“At the age of, P2 was hospitalized due to edema, and subsequent tests showed proteinuria, hyperlipidemia, and hypoproteinemia, leading to a diagnosis of nephrotic syndrome.”
The corrected sentence appears below:
“At the age of 4, P2 was hospitalized due to edema, and subsequent tests showed proteinuria, hyperlipidemia, and hypoproteinemia, leading to a diagnosis of nephrotic syndrome.”
3. In the published article, there was an error. A typo was made.
A correction has been made to Results, Decreased surface CXCR4 expression on CD8+T cells and B cells from patients, Paragraph 1. This sentence previously stated:
“Interestingly, P1-P4 exhibited relatively higher levels of CXCR4 lexpression, particularly in pediatric patients P1 and P2 (Supplementary Figure SA).”
The corrected sentence appears below:
“Interestingly, P1-P4 exhibited relatively higher levels of CXCR4 expression, particularly in pediatric patients P1 and P2 (Supplementary Figure SA).”
4. In the published article, there was an error. A typo was made.
A correction has been made to Discussion, Paragraph 4. This sentence previously stated:
“n our cohort, all four patients exhibited varying degrees of impaired CXCR4 internalization; pediatric patients showed reduced internalization, while adult patients demonstrated no internalization.”
The corrected sentence appears below:
“In our cohort, all four patients exhibited varying degrees of impaired CXCR4 internalization; pediatric patients showed reduced internalization, while adult patients demonstrated no internalization.”
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.
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: CXCR4 variant, gain-of-function, inborn error of immunity, WHIM syndrome, heterogeneous phenotype
Citation: Huang Y, Li L, Chen R, Yu L, Zhao S, Jia Y, Dou Y, Zhang Z, An Y, Tang X, Zhao X and Zhou L (2025) Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation. Front. Immunol. 15:1544964. doi: 10.3389/fimmu.2024.1544964
Received: 13 December 2024; Accepted: 16 December 2024;
Published: 14 January 2025.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2025 Huang, Li, Chen, Yu, Zhao, Jia, Dou, Zhang, An, Tang, Zhao and Zhou. 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: Lina Zhou, cmFjaGVsemhvdTg4QHFxLmNvbQ==; Xiaodong Zhao, emhhb3hkNTMwQGFsaXl1bi5jb20=
†These authors have contributed equally to this work and share first authorship
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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