scholarly journals Moving target: shifting the focus to pulmonary sarcoidosis as an autoimmune spectrum disorder

2019 ◽  
Vol 54 (1) ◽  
pp. 1802153 ◽  
Author(s):  
Ylva Kaiser ◽  
Anders Eklund ◽  
Johan Grunewald

Despite more than a century of research, the causative agent(s) in sarcoidosis, a heterogeneous granulomatous disorder mainly affecting the lungs, remain(s) elusive. Following identification of genetic factors underlying different clinical phenotypes, increased understanding of CD4+ T-cell immunology, which is believed to be central to sarcoid pathogenesis, as well as the role of B-cells and other cells bridging innate and adaptive immunity, contributes to novel insights into the mechanistic pathways influencing disease resolution or chronicity. Hopefully, new perspectives and state-of-the-art technology will help to shed light on the still-elusive enigma of sarcoid aetiology. This perspective article highlights a number of recent advances in the search for antigenic targets in sarcoidosis, as well as the main arguments for sarcoidosis as a spectrum of autoimmune conditions, either as a result of an external (microbial) trigger and/or due to defective control mechanisms regulating the balance between T-cell activation and inhibition.

Cells ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 834
Author(s):  
Frederike A. Hartl ◽  
Jatuporn Ngoenkam ◽  
Esmeralda Beck-Garcia ◽  
Liz Cerqueira ◽  
Piyamaporn Wipa ◽  
...  

The T cell antigen receptor (TCR) is expressed on T cells, which orchestrate adaptive immune responses. It is composed of the ligand-binding clonotypic TCRαβ heterodimer and the non-covalently bound invariant signal-transducing CD3 complex. Among the CD3 subunits, the CD3ε cytoplasmic tail contains binding motifs for the Src family kinase, Lck, and the adaptor protein, Nck. Lck binds to a receptor kinase (RK) motif and Nck binds to a proline-rich sequence (PRS). Both motifs only become accessible upon ligand binding to the TCR and facilitate the recruitment of Lck and Nck independently of phosphorylation of the TCR. Mutations in each of these motifs cause defects in TCR signaling and T cell activation. Here, we investigated the role of Nck in proximal TCR signaling by silencing both Nck isoforms, Nck1 and Nck2. In the absence of Nck, TCR phosphorylation, ZAP70 recruitment, and ZAP70 phosphorylation was impaired. Mechanistically, this is explained by loss of Lck recruitment to the stimulated TCR in cells lacking Nck. Hence, our data uncover a previously unknown cooperative interaction between Lck and Nck to promote optimal TCR signaling.


Cytokine ◽  
2008 ◽  
Vol 42 (3) ◽  
pp. 289-292 ◽  
Author(s):  
T.A. Hill ◽  
S. Lightman ◽  
P. Pantelidis ◽  
A. Abdallah ◽  
P. Spagnolo ◽  
...  

1992 ◽  
Vol 13 (12) ◽  
pp. 477-481 ◽  
Author(s):  
Denis Alexander ◽  
Masahiro Shiroo ◽  
Anne Robinson ◽  
Mark Biffen ◽  
Emer Shivnan

1984 ◽  
pp. 17-22
Author(s):  
P. Erb ◽  
G. Ramila ◽  
A. Stern ◽  
I. Sklenar

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