Evidence map›Paper›PMID 27170596›Full record

ArticleBlood2016

Abnormalities of follicular helper T-cell number and function in Wiskott-Aldrich syndrome.

Xuan Zhang, Rongxin Dai, Wenyan Li, Hongyi Zhao, Yongjie Zhang, Lina Zhou, Hongqiang Du, Guangjin Luo, Junfeng Wu, Linlin Niu and 6 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Significant decreased CXCR3Frontiers in immunology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 3 countries.

Xuan ZhangMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Rongxin DaiMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Wenyan LiMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Hongyi ZhaoMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Yongjie ZhangMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Lina ZhouMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Hongqiang DuMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Guangjin LuoMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Junfeng WuMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and Division of Immunology, Children's Hospital of Chongqing Medical University, Chongqing, China; and.
Linlin NiuMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Yunfei AnMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and Division of Immunology, Children's Hospital of Chongqing Medical University, Chongqing, China; and.
Zhiyong ZhangMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and Division of Immunology, Children's Hospital of Chongqing Medical University, Chongqing, China; and.
Yuan DingMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and Division of Immunology, Children's Hospital of Chongqing Medical University, Chongqing, China; and.
Wenxia SongDepartment of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD.
Chaohong LiuMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and.
Xiaodong ZhaoMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, and Division of Immunology, Children's Hospital of Chongqing Medical University, Chongqing, China; and.
Institute of Infection and Immunity · CAMinistry of Education of the People's Republic of China · CNChongqing Medical University · CNChildren's Hospital of Chongqing Medical University · CNUniversity of Maryland, College Park · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wiskott-Aldrich syndrome protein (WASp) is a hematopoietic-specific regulator of actin nucleation. Wiskott-Aldrich syndrome (WAS) patients show immunodeficiencies, most of which have been attributed to defective T-cell functions. T follicular helper (Tfh) cells are the major CD4(+) T-cell subset with specialized B-cell helper capabilities. Aberrant Tfh cells activities are involved in immunopathologies such as autoimmunity, immunodeficiencies, and lymphomas. We found that in WAS patients, the number of circulating Tfh cells was significantly reduced due to reduced proliferation and increased apoptosis, and Tfh cells were Th2 and Th17 polarized. The expression of inducible costimulator (ICOS) in circulating Tfh cells was higher in WAS patients than in controls. BCL6 expression was decreased in total CD4(+) T and Tfh cells of WAS patients. Mirroring the results in patients, the frequency of Tfh cells in WAS knockout (KO) mice was decreased, as was the frequency of BCL6(+) Tfh cells, but the frequency of ICOS(+) Tfh cells was increased. Using WAS chimera mice, we found that the number of ICOS(+) Tfh cells was decreased in WAS chimera mice, indicating that the increase in ICOS(+) Tfh cells in WAS KO mice was cell extrinsic. The data from in vivo CD4(+) naive T-cell adoptive transfer mice as well as in vitro coculture of naive B and Tfh cells showed that the defective function of WASp-deficient Tfh cells was T-cell intrinsic. Consistent findings in both WAS patients and WAS KO mice suggested an essential role for WASp in the development and memory response of Tfh cells and that WASp deficiency causes a deficient differentiation defect in Tfh cells by downregulating the transcription level of BCL6.

Indexed as

AnimalsB-LymphocytesCase-Control StudiesCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedGerminal CenterHumansInducible T-Cell Co-Stimulator ProteinInterleukin-21InterleukinsLymph NodesMiceMice, KnockoutPositive Regulatory Domain I-Binding Factor 1Receptors, CXCR5CXCR5 protein, humanICOS protein, humanInducible T-Cell Co-Stimulator ProteinInterleukin-21InterleukinsPositive Regulatory Domain I-Binding Factor 1PRDM1 protein, humanReceptors, CXCR5Repressor ProteinsWas protein, mouseWiskott-Aldrich Syndrome Protein

Identifiers

PMID27170596
PMCPMC4929975
OpenAlexW2392037591

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.