T and B Lymphocyte Populations in Human Normal Lymph Node, Regional Tumour Lymph Node and Inflammatory Lymph Node

1976 ◽  
Vol 52 (1-4) ◽  
pp. 277-290 ◽  
Author(s):  
O. Eremin ◽  
D. Plumb ◽  
R.R.A. Coombs
2013 ◽  
Vol 2013 ◽  
pp. 1-15 ◽  
Author(s):  
Leoni Villano Bonamin ◽  
Cesar Sato ◽  
Ruggero Zalla Neto ◽  
Graziela Morante ◽  
Thayná Neves Cardoso ◽  
...  

The present study analyzed the immune modulation mechanisms of thymulin 5CH in a granuloma experimental model. Male adult Balb/c mice were inoculated with BCG into the footpad to induce granuloma, which was quantitatively evaluated. The phenotypic characterization of phagocyte, T- and B-lymphocyte populations in the peritoneum, and local lymph node was done by flow cytometry. During all experimental periods, thymulin 5CH and vehicle (control) were givenad libitumto mice, diluted into the drinking water (1.6×10−17 M). After 7 days from inoculation, thymulin-treated mice presented reduction in the number of epithelioid cytokeratine-positive cells (P=0.0001) in the lesion, in relation to young phagocytes. After 21 days, the differentiation of B1 peritoneal stem cells into phagocytes reached the peak, being higher in thymulin-treated mice (P=0.0001). Simultaneously, the score of infected phagocytes in the lesion decreased (P=0.001), and the number of B1-derived phagocytes, CD4+ and CD8+ T lymphocytes in the local lymph node increased in relation to control (P=0.0001). No difference was seen on the CD25+ Treg cells. The results show that thymulin 5CH treatment is able to improve the granuloma inflammatory process and the infection remission, by modulating local and systemic phagocyte differentiation.


2004 ◽  
Vol 122 (4) ◽  
pp. 588-595 ◽  
Author(s):  
Weina Chen ◽  
Sheryl L. Asplund ◽  
Robert W. McKenna ◽  
Steven H. Kroft

1986 ◽  
Vol 93 (1) ◽  
pp. 147-169 ◽  
Author(s):  
Dan Holmberg ◽  
Antonio A. Freitas ◽  
Denis Portnoiu ◽  
Frederic Jacquemart ◽  
Stratis Avrameas ◽  
...  

1988 ◽  
Vol 16 (4) ◽  
pp. 143-145 ◽  
Author(s):  
LUCAS L. COLOMBO ◽  
MARÍA DEL C. LÓPEZ ◽  
JORGE HERKOVITS ◽  
MARÍA E. ROUX

Blood ◽  
2012 ◽  
Vol 119 (4) ◽  
pp. 978-989 ◽  
Author(s):  
Chung Park ◽  
Il-Young Hwang ◽  
Rajesh K. Sinha ◽  
Olena Kamenyeva ◽  
Michael D. Davis ◽  
...  

Abstract B lymphocyte recirculation through lymph nodes (LNs) requires crossing endothelial barriers and chemoattractant-triggered cell migration. Here we show how LN anatomy and chemoattractant receptor signaling organize B lymphocyte LN trafficking. Blood-borne B cells predominately used CCR7 signaling to adhere to high endothelial venules (HEVs). New B cell emigrants slowly transited the HEV perivenule space, and thereafter localized nearby, avoiding the follicle. Eventually, the newly arrived B cells entered the basal portion of the follicle gradually populating it. In contrast, newly arriving activated B cells rapidly crossed HEVs and migrated toward the lymph node follicle. During their LN residency, recirculating B cells reacquired their sphingosine-1 phospate receptor 1 (S1P1) receptors and markedly attenuated their sensitivity to chemokines. Eventually, the B cells exited the LN follicle by entering the cortical lymphatics or returning to the paracortical cords. Upon entering the lymph, the B cells lost their polarity, down-regulated their S1P1 receptors, and subsequently strongly up-regulated their sensitivity to chemokines. These results are summarized in a model of homeostatic trafficking of B cells through LNs.


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