Analysis of T-cell activation after bronchial allergen challenge in patients with atopic asthma☆☆☆★★★

1998 ◽  
Vol 101 (5) ◽  
pp. 699-708 ◽  
Author(s):  
Maria L. Lara-Marquez ◽  
Aaron Deykin ◽  
Stephen Krinzman ◽  
James Listman ◽  
Elliot Israel ◽  
...  
Blood ◽  
2006 ◽  
Vol 107 (6) ◽  
pp. 2400-2408 ◽  
Author(s):  
Hui Xu ◽  
Mark S. Williams ◽  
Lisa M. Spain

AbstractThe membrane-spanning 4A (MS4A) family of proteins includes CD20, FcϵRIβ, and HTm4, whose genes are grouped in a chromosomal location that is associated with increased susceptibility to allergy and atopic asthma. One family member, Chandra/MS4a4B, was reported to be expressed in T helper 1 (Th1) T cells but not Th2 T cells. In the present study, Ms4a4b was isolated in a screen of genes differentially expressed during thymocyte development. MS4a4B was detected in immature CD4-CD8-CD44+CD25- thymocytes, turned off during further stages of thymocyte development and reexpressed in mature single-positive thymocytes. MS4a4B expression was found in naive CD8+ and CD4+ peripheral T cells and natural killer (NK) cells but not in B cells. MS4a4B is expressed at the cell surface with its C-terminus located in the cytoplasm. When expressed in a T-cell hybridoma by retroviral vector, MS4a4B protein constitutively associated with lipid raft microdomains, whereas in primary T cells endogenous MS4a4B protein became enriched in rafts after T-cell activation. Overexpression of MS4a4B in primary CD4+ T-cell blasts enhanced T-cell receptor (TCR)-induced Th1 cytokine production. These results suggest that MS4a4B expression is tightly regulated during T-cell development and that MS4a4B expression promotes Th1 function and/or differentiation. (Blood. 2006;107:2400-2408)


Immunology ◽  
2002 ◽  
Vol 105 (4) ◽  
pp. 499-508 ◽  
Author(s):  
Theo A. Out ◽  
Shan-Ze Wang ◽  
Karin Rudolph ◽  
David E. Bice

2021 ◽  
Vol 12 ◽  
Author(s):  
Jutamas Suwanpradid ◽  
Min Jin Lee ◽  
Peter Hoang ◽  
Jeffery Kwock ◽  
Lauren P. Floyd ◽  
...  

Crosstalk between T cells, dendritic cells, and macrophages in temporal leukocyte clusters within barrier tissues provides a new concept for T cell activation in the skin. Activated T cells from these leukocyte clusters play critical roles in the efferent phase of allergic contact hypersensitivity (CHS). However, the cytokines driving maintenance and survival of pathogenic T cells during and following CHS remain mostly unknown. Upon epicutaneous allergen challenge, we here report that macrophages produce IL-27 which then induces IL-15 production from epidermal keratinocytes and dermal myeloid cells within leukocyte clusters. In agreement with the known role of IL-15 as a T cell survival factor and growth cytokine, this signaling axis enhances BCL2 and survival of skin T cells. Genetic depletion or pharmacological blockade of IL-27 in CHS mice leads to abrogated epidermal IL-15 production resulting in a decrease in BCL2 expression in T cells and a decline in dermal CD8+ T cells and T cell cluster numbers. These findings suggest that the IL-27 pathway is an important cytokine for regulating cutaneous T cell immunity.


1998 ◽  
Vol 43 ◽  
pp. 10-10
Author(s):  
Jiu-Y Wang ◽  
Su-F Hwang ◽  
C K Shieh ◽  
Chung-B Yuang ◽  
Huan-Y Lei ◽  
...  

2006 ◽  
Vol 203 (12) ◽  
pp. 2649-2660 ◽  
Author(s):  
Deborah H. Strickland ◽  
Philip A. Stumbles ◽  
Graeme R. Zosky ◽  
Lily S. Subrata ◽  
Jenny A. Thomas ◽  
...  

An important feature of atopic asthma is the T cell–driven late phase reaction involving transient bronchoconstriction followed by development of airways hyperresponsiveness (AHR). Using a unique rat asthma model we recently showed that the onset and duration of the aeroallergen-induced airway mucosal T cell activation response in sensitized rats is determined by the kinetics of functional maturation of resident airway mucosal dendritic cells (AMDCs) mediated by cognate interactions with CD4+ T helper memory cells. The study below extends these investigations to chronic aeroallergen exposure. We demonstrate that prevention of ensuing cycles of T cell activation and resultant AHR during chronic exposure of sensitized rats to allergen aerosols is mediated by CD4+CD25+Foxp3+LAG3+ CTLA+CD45RC+ T cells which appear in the airway mucosa and regional lymph nodes within 24 h of initiation of exposure, and inhibit subsequent Th-mediated upregulation of AMDC functions. These cells exhibit potent regulatory T (T reg) cell activity in both in vivo and ex vivo assay systems. The maintenance of protective T reg activity is absolutely dependent on continuing allergen stimulation, as interruption of exposure leads to waning of T reg activity and reemergence of sensitivity to aeroallergen exposure manifesting as AMDC/T cell upregulation and resurgence of T helper 2 cytokine expression, airways eosinophilia, and AHR.


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