The who's who of T-cell differentiation: Human memory T-cell subsets

2013 ◽  
Vol 43 (11) ◽  
pp. 2797-2809 ◽  
Author(s):  
Yolanda D. Mahnke ◽  
Tess M. Brodie ◽  
Federica Sallusto ◽  
Mario Roederer ◽  
Enrico Lugli
2006 ◽  
Vol 176 (7) ◽  
pp. 4051-4058 ◽  
Author(s):  
Jagdeep S. Obhrai ◽  
Martin H. Oberbarnscheidt ◽  
Timothy W. Hand ◽  
Lonnette Diggs ◽  
Geetha Chalasani ◽  
...  

BIO-PROTOCOL ◽  
2014 ◽  
Vol 4 (13) ◽  
Author(s):  
Myoungjoo Kim ◽  
Weiming Ouyang ◽  
Will Liao ◽  
Michael Zhang ◽  
Ming Li

2017 ◽  
Vol 199 (12) ◽  
pp. 4091-4102 ◽  
Author(s):  
Nina Chi Sabins ◽  
Olesya Chornoguz ◽  
Karen Leander ◽  
Fred Kaplan ◽  
Richard Carter ◽  
...  

Blood ◽  
2002 ◽  
Vol 100 (13) ◽  
pp. 4550-4556 ◽  
Author(s):  
Frederique Ponchel ◽  
Ann W. Morgan ◽  
Sarah J. Bingham ◽  
Mark Quinn ◽  
Maya Buch ◽  
...  

Rheumatoid arthritis (RA) is a chronic, inflammatory disease of the synovium of uncertain pathogenesis. A number of phenotypic and functional T-cell defects have been described in RA, including abnormal clonal expansions and suppressed proliferative responses, which suggest a defect in T-cell differentiation. Here, we show that RA patients possess fewer naive CD4+ T cells than healthy controls. Furthermore, a smaller proportion of these cells contains a T-cell receptor excision circle (TREC). Patients with RA also have unusual populations of T cells. These include immature cells characterized as CD45RBbrightCD45RA+CD62L− by flow cytometry and a large population that coexpresses CD45RA and CD45RO. These cells are hyperresponsive to mitogen and TCR stimulation when compared to naive cells. Additionally, an unusual putative central memory subset expressing CD62L, but not CD45RA, appears in RA patients at the expense of more typical cells. Levels of C-reactive protein correlate inversely with the TREC content of naive T cells and positively with the sizes of naive and immature atypical T-cell subsets. These data suggest that inflammation drives proliferation of naive T cells in RA and encourages their differentiation into atypical, hyperresponsive progeny. TREC content of individual naive and atypical T-cell subsets suggests an ontogeny consistent with this hypothesis. These studies provide further evidence of a T-cell differentiation defect in RA, which could explain some of the well-characterized immunologic features of the disease.


2002 ◽  
Vol 4 (5) ◽  
pp. 555-558 ◽  
Author(s):  
Qing Ge ◽  
Hui Hu ◽  
Herman N. Eisen ◽  
Jianzhu Chen

Cell Reports ◽  
2019 ◽  
Vol 28 (8) ◽  
pp. 2169-2181.e4 ◽  
Author(s):  
John D. Gagnon ◽  
Robin Kageyama ◽  
Hesham M. Shehata ◽  
Marlys S. Fassett ◽  
Darryl J. Mar ◽  
...  

Cell ◽  
2009 ◽  
Vol 138 (3) ◽  
pp. 606.e1-606.e2 ◽  
Author(s):  
Matthew E. Pipkin ◽  
Anjana Rao

2002 ◽  
Vol 2 (4) ◽  
pp. 251-262 ◽  
Author(s):  
Susan M. Kaech ◽  
E. John Wherry ◽  
Rafi Ahmed

PLoS ONE ◽  
2010 ◽  
Vol 5 (10) ◽  
pp. e13740 ◽  
Author(s):  
Julie Leignadier ◽  
Nathalie Labrecque

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