SOSTDC1-producing follicular helper T cells promote regulatory follicular T cell differentiation

Science ◽  
2020 ◽  
Vol 369 (6506) ◽  
pp. 984-988 ◽  
Author(s):  
Xin Wu ◽  
Yun Wang ◽  
Rui Huang ◽  
Qujing Gai ◽  
Haofei Liu ◽  
...  

Germinal center (GC) responses potentiate the generation of follicular regulatory T (TFR) cells. However, the molecular cues driving TFR cell formation remain unknown. Here, we show that sclerostin domain-containing protein 1 (SOSTDC1), secreted by a subpopulation of follicular helper T (TFH) cells and T–B cell border–enriched fibroblastic reticular cells, is developmentally required for TFR cell generation. Fate tracking and transcriptome assessment in reporter mice establishes SOSTDC1-expressing TFH cells as a distinct T cell population that develops after SOSTDC1– TFH cells and loses the ability to help B cells for antibody production. Notably, Sostdc1 ablation in TFH cells results in substantially reduced TFR cell numbers and consequently elevated GC responses. Mechanistically, SOSTDC1 blocks the WNT–β-catenin axis and facilitates TFR cell differentiation.

Immunity ◽  
2010 ◽  
Vol 33 (2) ◽  
pp. 241-253 ◽  
Author(s):  
Elissa K. Deenick ◽  
Anna Chan ◽  
Cindy S. Ma ◽  
Dominique Gatto ◽  
Pamela L. Schwartzberg ◽  
...  

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Sungjun Park ◽  
Seungwon Lee ◽  
Choong-Gu Lee ◽  
Guk Yeol Park ◽  
Hyebeen Hong ◽  
...  

Immunity ◽  
2013 ◽  
Vol 38 (4) ◽  
pp. 655-668 ◽  
Author(s):  
Katharina U. Vogel ◽  
Stephanie L. Edelmann ◽  
Katharina M. Jeltsch ◽  
Arianna Bertossi ◽  
Klaus Heger ◽  
...  

Immunity ◽  
2016 ◽  
Vol 45 (3) ◽  
pp. 540-554 ◽  
Author(s):  
Hu Zeng ◽  
Sivan Cohen ◽  
Cliff Guy ◽  
Sharad Shrestha ◽  
Geoffrey Neale ◽  
...  

2017 ◽  
Vol 180 ◽  
pp. 60-62 ◽  
Author(s):  
Jolanda Gerosa ◽  
Vassilios Lougaris ◽  
Manuela Baronio ◽  
Alessandro Plebani ◽  
Maria Pia Cicalese ◽  
...  

2012 ◽  
Vol 188 (8) ◽  
pp. 3734-3744 ◽  
Author(s):  
Mark A. Kroenke ◽  
Danelle Eto ◽  
Michela Locci ◽  
Michael Cho ◽  
Terence Davidson ◽  
...  

2021 ◽  
Vol 17 (1) ◽  
pp. e1009249
Author(s):  
Hemant Jaiswal ◽  
Thomas Ciucci ◽  
Hongshan Wang ◽  
Wanhu Tang ◽  
Estefania Claudio ◽  
...  

Bcl-3 is an atypical member of the IκB family that acts in the nucleus to modulate transcription of many NF-κB targets in a highly context-dependent manner. Accordingly, complete Bcl-3-/- mice have diverse defects in both innate and adaptive immune responses; however, direct effects of Bcl-3 action in individual immune cell types have not been clearly defined. Here, we document a cell-autonomous role for Bcl-3 in CD8+ T cell differentiation during the response to lymphocytic choriomeningitis virus infection. Single-cell RNA-seq and flow cytometric analysis of virus-specific Bcl3-/- CD8+ T cells revealed that differentiation was skewed towards terminal effector cells at the expense of memory precursor effector cells (MPECs). Accordingly, Bcl3-/- CD8+ T cells exhibited reduced memory cell formation and a defective recall response. Conversely, Bcl-3-overexpression in transgenic CD8+ T cells enhanced MPEC formation but reduced effector cell differentiation. Together, our results establish Bcl-3 as an autonomous determinant of memory/terminal effector cell balance during CD8+ T cell differentiation in response to acute viral infection. Our results provide proof-of-principle for targeting Bcl-3 pharmacologically to optimize adaptive immune responses to infectious agents, cancer cells, vaccines and other stimuli that induce CD8+ T cell differentiation.


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