Proteinase activated receptor (PAR)-2 protects against colitis in mice. Evidence for direct modulation of lamina propria T lymphocytes

2001 ◽  
Vol 120 (5) ◽  
pp. A135-A135
Author(s):  
S FIORUCCI ◽  
A MENCARELLI ◽  
B PALAZZETTI ◽  
E DISTRUTTI ◽  
J WALLACE ◽  
...  
2001 ◽  
Vol 120 (5) ◽  
pp. A135
Author(s):  
Stefano Fiorucci ◽  
Andrea Mencarelli ◽  
Barbara Palazzetti ◽  
Eleonora Distrutti ◽  
John L. Wallace ◽  
...  

1991 ◽  
Vol 101 (6) ◽  
pp. 1529-1536 ◽  
Author(s):  
Liang Qiao ◽  
Guido Schürmann ◽  
Michael Betzler ◽  
Stefan C. Meuer
Keyword(s):  

2000 ◽  
Vol 118 (4) ◽  
pp. A357
Author(s):  
Joerg C. Hoffmann ◽  
Sven Henschke ◽  
Karsten Peters ◽  
Birgit Herrmann ◽  
Martin Zeitz
Keyword(s):  

2000 ◽  
Vol 118 (4) ◽  
pp. A357
Author(s):  
Joerg C. Hoffmann ◽  
Karsten Peters ◽  
Sven Henschke ◽  
Martin Zeitz ◽  
Juergen Westermann
Keyword(s):  

Gut ◽  
1998 ◽  
Vol 43 (5) ◽  
pp. 620-628 ◽  
Author(s):  
G Monteleone ◽  
T Parrello ◽  
F Luzza ◽  
F Pallone

Background/Aim—Interleukin (IL) 12 is involved in the mucosal response during intestinal inflammation but its role is not fully understood. The response of human lamina propria T lymphocytes (T-LPL) to IL-12 in terms of interferon γ (IFN-γ) release and proliferation was investigated, exploring whether IL-15 and IL-7 cooperate with IL-12. The role of accessory molecules (CD2 and CD28) was also investigated.Methods—Unstimulated and phytohaemagglutinin preactivated T-LPL cultures were incubated with or without the initial addition of cytokines, anti-CD2 or anti-CD28 antibodies. IFN-γ mRNA was detected by reverse transcriptase polymerase chain reaction, and protein secretion was measured by enzyme linked immunosorbent assay (ELISA).Results—IFN-γ mRNA was induced in T-LPLs by IL-12 and IL-15 but not IL-7, whereas IFN-γ was measured only in IL-12 stimulated T-LPL cultures. IL-12 induced IFN-γ release was not abrogated by neutralising anti-IL-2 antibody or by cyclosporin A. IL-12 synergised with either anti-CD2 or anti-CD28 antibodies in inducing IFN-γ synthesis. In preactivated T-LPLs, IL-7 enhanced IFN-γ release induced by both IL-12 and anti-CD2, whereas IL-15 potentiated only IL-12 induced IFN-γ synthesis. IL-12 did not induce proliferation of either unstimulated or preactivated T-LPLs and it did not enhance the CD2/CD28 stimulated T-LPL proliferative response. No transcript for IL-12 receptor β1 subunit was detected in freshly isolated and activated T-LPLs whereas the β2subunit mRNA was consistently found in T-LPL samples.Conclusions—IL-12 induces human T-LPLs to produce and release IFN-γ, and IL-15 and IL-7 cooperate with IL-12 in expanding the IFN-γ mucosal response.


1991 ◽  
Vol 10 (3-4) ◽  
pp. 218-225 ◽  
Author(s):  
Liang Qiao ◽  
Guido Schürmann ◽  
Michael Betzler ◽  
Stefan C. Meuer

2003 ◽  
Vol 40 (4) ◽  
pp. 395-404 ◽  
Author(s):  
J. Sarradell ◽  
M. Andrada ◽  
A. S. Ramírez ◽  
A. Fernández ◽  
J. C. Gómez-Villamandos ◽  
...  

Porcine enzootic pneumonia (PEN), caused by Mycoplasma hyopneumoniae (Mh), has been described in pigs in all geographic areas. The disease is characterized by high morbidity and low mortality rates in intensive swine production systems. A morphologic and immunohistochemical study was done to determine the cellular populations present in lung parenchyma of infected pigs, with special attention to the bronchus-associated lymphoid tissue (BALT). Polyclonal and monoclonal antibodies were used for the detection of antigens of Mh, T lymphocytes (CD3+, CD4+, and CD8+), IgG+ or IgA+ lymphocytes, and cells containing lysozyme, S-100 protein, major histocompatibility complex class II antigen or myeloid-histiocyte antigen. Findings in lung tissues associated with Mh infection were catarrhal bronchointerstitial pneumonia, with infiltration of inflammatory cells in the lamina propria of bronchi and bronchioles and alveolar septa. Hyperplasia of mononuclear cells in the BALT areas was the most significant histologic change. The BALT showed a high morphologic and cellular organization. Macrophages and B lymphocytes were the main cellular components of germinal centers. T lymphocytes were primarily located in perifollicular areas of the BALT, lamina propria and within the airway epithelium, and plasma cells containing IgG or IgA at the periphery of the BALT, in the lamina propria of bronchi and bronchioles, in alveolar septa, and around bronchial submucosal glands. The hyperplastic BALT in PEN cases consisted of macrophages, dendritic cells, T and B lymphocytes, and IgG+ and IgA+ plasma cells. CD4+ cells predominated over CD8+ cells. Local humoral immunity appears to play an important role in the infection.


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