#70 I. Norepinephrine concentration and T-cell dependent antibody production: Effect of elevated norepinephrine

2005 ◽  
Vol 19 (4) ◽  
pp. e36
Author(s):  
Sarah L. Kennedy ◽  
Molly Nickerson ◽  
Craig Sharkey ◽  
John D. Johnson ◽  
Monika Fleshner
2005 ◽  
Vol 19 (4) ◽  
pp. e37
Author(s):  
Sarah L. Kennedy ◽  
Craig Sharkey ◽  
Molly Nickerson ◽  
John D. Johnson ◽  
Monika Fleshner

1978 ◽  
Vol 8 (5) ◽  
pp. 360-370 ◽  
Author(s):  
A. Basten ◽  
J. F. A. P. Miller ◽  
R. Loblay ◽  
P. Johnson ◽  
Jennifer Gamble ◽  
...  

1998 ◽  
Vol 6 (3-4) ◽  
pp. 215-222 ◽  
Author(s):  
Jon D. Laman ◽  
Mark De Boer ◽  
Bert A. 'T Hart

The interactions of CD40 and CD40L have been known for some time to critically regulate B-cell responses with respect to proliferation, isotype switching, antibody production, and memory formation. More recent findings demonstrated that CD40 can be expressed on several other antigen-presenting cell (APC) types such as macrophages, dendritic cells, and fibroblasts. This expression of CD40 regulates T-cell-APC interaction and is centrally involved in a wide array of inflammatory events. Here, currently available data are reviewed demonstrating that CD40- CD40L interactions are operational in two chronic inflammatory clinical conditions, namely, multiple sclerosis and atherosclerosis. The functional correlates of these interactions are discussed in the light of recent other findings, shedding light on the multiple effects of CD40- CD40L interactions.


2010 ◽  
Vol 54 (11) ◽  
pp. 691-701 ◽  
Author(s):  
Kentaro Aritomi ◽  
Taku Kuwabara ◽  
Yuriko Tanaka ◽  
Hideki Nakano ◽  
Takuwa Yasuda ◽  
...  

2013 ◽  
Vol 191 (4) ◽  
pp. 1666-1676 ◽  
Author(s):  
Shijuan Grace Zeng ◽  
Yasmeen G. Ghnewa ◽  
Vincent P. O’Reilly ◽  
Victoria G. Lyons ◽  
Ann Atzberger ◽  
...  

2000 ◽  
Vol 164 (4) ◽  
pp. 1734-1740 ◽  
Author(s):  
Suzanne C. Morris ◽  
William C. Gause ◽  
Fred D. Finkelman

2001 ◽  
Vol 193 (12) ◽  
pp. 1373-1382 ◽  
Author(s):  
Chang H. Kim ◽  
Lusijah S. Rott ◽  
Ian Clark-Lewis ◽  
Daniel J. Campbell ◽  
Lijun Wu ◽  
...  

The T helper (Th) cell pool is composed of specialized cells with heterogeneous effector functions. Apart from Th1 and 2 cells, CXCR5+ T cells have been suggested to be another type of effector T cell specialized for B cell help. We show here that CXCR5+ T cells are heterogeneous, and we identify subsets of CXCR5+ CD4 T cells that differ in function and microenvironmental localization in secondary lymphoid tissues. CD57+CXCR5 T cells, hereafter termed germinal center Th (GC-Th) cells, are localized only in GCs, lack CCR7, and are highly responsive to the follicular chemokine B lymphocyte chemoattractant but not to the T cell zone EBI1-ligand chemokine. Importantly, GC-Th cells are much more efficient than CD57−CXCR5+ T cells or CXCR5− T cells in inducing antibody production from B cells. Consistent with their function, GC-Th cells produce elevated levels of interleukin 10 upon stimulation which, with other cytokines and costimulatory molecules, may help confer their B cell helper activity. Our results demonstrate that CXCR5+ T cells are functionally heterogeneous and that the GC-Th cells, a small subset of CXCR5+ T cells, are the key helpers for B cell differentiation and antibody production in lymphoid tissues.


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