scholarly journals Inducible Tertiary Lymphoid Structures: Promise and Challenges for Translating a New Class of Immunotherapy

2021 ◽  
Vol 12 ◽  
Author(s):  
Shota Aoyama ◽  
Ryosuke Nakagawa ◽  
James J. Mulé ◽  
Adam W. Mailloux

Tertiary lymphoid structures (TLS) are ectopically formed aggregates of organized lymphocytes and antigen-presenting cells that occur in solid tissues as part of a chronic inflammation response. Sharing structural and functional characteristics with conventional secondary lymphoid organs (SLO) including discrete T cell zones, B cell zones, marginal zones with antigen presenting cells, reticular stromal networks, and high endothelial venues (HEV), TLS are prominent centers of antigen presentation and adaptive immune activation within the periphery. TLS share many signaling axes and leukocyte recruitment schemes with SLO regarding their formation and function. In cancer, their presence confers positive prognostic value across a wide spectrum of indications, spurring interest in their artificial induction as either a new form of immunotherapy, or as a means to augment other cell or immunotherapies. Here, we review approaches for inducible (iTLS) that utilize chemokines, inflammatory factors, or cellular analogues vital to TLS formation and that often mirror conventional SLO organogenesis. This review also addresses biomaterials that have been or might be suitable for iTLS, and discusses remaining challenges facing iTLS manufacturing approaches for clinical translation.

2015 ◽  
Vol 3 (3) ◽  
pp. 424-441 ◽  
Author(s):  
H. M. Rostam ◽  
S. Singh ◽  
N. E. Vrana ◽  
M. R. Alexander ◽  
A. M. Ghaemmaghami

The impact of biomaterial surface topography and chemistry on antigen presenting cells’ phenotype and function.


2008 ◽  
Vol 125 (1-2) ◽  
pp. 18-30 ◽  
Author(s):  
Chutitorn Ketloy ◽  
Anneke Engering ◽  
Utaiwan Srichairatanakul ◽  
Amporn Limsalakpetch ◽  
Kosol Yongvanitchit ◽  
...  

Blood ◽  
2005 ◽  
Vol 105 (6) ◽  
pp. 2421-2427 ◽  
Author(s):  
Laura Piccio ◽  
William Vermi ◽  
Kent S. Boles ◽  
Anja Fuchs ◽  
Carey A. Strader ◽  
...  

AbstractSignal-regulatory proteins (SIRPs) are transmembrane glycoproteins belonging to the immunoglobulin (Ig) superfamily that are expressed in the immune and central nervous systems. SIRPα binds CD47 and inhibits the function of macrophages, dendritic cells, and granulocytes, whereas SIRPβ1 is an orphan receptor that activates the same cell types. A recently identified third member of the SIRP family, SIRPβ2, is as yet uncharacterized in terms of expression, specificity, and function. Here, we show that SIRPβ2 is expressed on T cells and activated natural killer (NK) cells and, like SIRPα, binds CD47, mediating cell-cell adhesion. Consequently, engagement of SIRPβ2 on T cells by CD47 on antigen-presenting cells results in enhanced antigen-specific T-cell proliferation.


1989 ◽  
Vol 92 (2) ◽  
pp. 190-195 ◽  
Author(s):  
Ole Baadsgaard ◽  
Aditya K. Gupta ◽  
R. Stanley Taylor ◽  
Charles N. Ellis ◽  
John J. Voorhees ◽  
...  

2007 ◽  
Vol 16 (8) ◽  
pp. 661-670 ◽  
Author(s):  
Joanna Listopad ◽  
Khusru Asadullah ◽  
Claudia Sievers ◽  
Thomas Ritter ◽  
Christian Meisel ◽  
...  

SLEEP ◽  
2007 ◽  
Vol 30 (4) ◽  
pp. 401-411 ◽  
Author(s):  
Stoyan Dimitrov ◽  
Tanja Lange ◽  
Klaus Nohroudi ◽  
Jan Born

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