Autologous Melanoma Vaccine Induces Antitumor and Self-Reactive Immune Responses That Affect Patient Survival and Depend on MHC Class II Expression on Vaccine Cells

2010 ◽  
Vol 2010 ◽  
pp. 347-348
Author(s):  
T.J. Eberlein
2009 ◽  
Vol 15 (15) ◽  
pp. 4968-4977 ◽  
Author(s):  
Michal Lotem ◽  
Arthur Machlenkin ◽  
Tamar Hamburger ◽  
Aviram Nissan ◽  
Luna Kadouri ◽  
...  

2002 ◽  
Vol 70 (7) ◽  
pp. 3874-3880 ◽  
Author(s):  
Sandrine Henri ◽  
Joan Curtis ◽  
Hubertus Hochrein ◽  
David Vremec ◽  
Ken Shortman ◽  
...  

ABSTRACT Dendritic cells (DCs) are professional antigen-presenting cells which initiate and regulate T-cell immune responses. Here we show that murine splenic DCs can be ranked on the basis of their ability to phagocytose and harbor the obligately intracellular parasite Leishmania major. CD4+ CD8− DCs are the most permissive host cells for L. major amastigotes, followed by CD4− CD8− DCs; CD4− CD8+ cells are the least permissive. However, the least susceptible CD4− CD8+ DC subset was the best interleukin-12 producer in response to infection. Infection did not induce in any DC subset production of the proinflammatory cytokine gamma interferon and nitric oxide associated with the induction of Th1 responses. The number of parasites phagocytosed by DCs was low, no more than 3 organisms per cell, compared to more than 10 organisms per macrophage. In infected DCs, the parasites are located in a parasitophorous vacuole containing both major histocompatibility complex (MHC) class II and lysosome-associated membrane protein 1 molecules, similar to their location in the infected macrophage. The parasite-driven redistribution of MHC class II to this compartment indicates that infected DCs should be able to present parasite antigen.


2010 ◽  
Vol 184 (10) ◽  
pp. 5654-5662 ◽  
Author(s):  
Yolanda C. Nesbeth ◽  
Diana G. Martinez ◽  
Seiko Toraya ◽  
Uciane K. Scarlett ◽  
Juan R. Cubillos-Ruiz ◽  
...  

2012 ◽  
Vol 94 (10S) ◽  
pp. 131
Author(s):  
J. G. OʼLeary ◽  
H. Kaneku ◽  
B. M. Susskind ◽  
L. W. Jennings ◽  
G. B. Klintmalm ◽  
...  

2011 ◽  
Vol 12 (5) ◽  
pp. 416-424 ◽  
Author(s):  
Xingguang Liu ◽  
Zhenzhen Zhan ◽  
Dong Li ◽  
Li Xu ◽  
Feng Ma ◽  
...  

1997 ◽  
Vol 352 (1359) ◽  
pp. 1327-1330 ◽  
Author(s):  
Brigitte Müller ◽  
Avrion Mitchison

It has long been known that certain MHC class II genes can dominantly suppress immune responses and so increase susceptibility to parasite infections, but the mechanism has been unclear. Recent work has revealed one way in which this form of suppression may operate through gating by MHC class II molecules of the back–signal from activated T cells into macrophages. The two known suppressive genes of the mouse are expressed in macrophages more extensively than are other class II genes. This is asscociated with suppresion of IL–4 production resulting, we infer, from overproduction in the macrophages of IL–12, the counter–cytokine to IL–4. The lack of IL–4 may itself be immunosuppressive, even for Th2 responses, and excess IL–12 can overinduce the antiproliferative cytokine IFN–gamma. Although this mechanism requires further substantiation, we believe that it offers a reasonable answer to an old conundrum.


2000 ◽  
Vol 69 (10) ◽  
pp. 2137-2143 ◽  
Author(s):  
Roslyn B. Mannon ◽  
Carolyn Doyle ◽  
Robert Griffiths ◽  
Matilde Bustos ◽  
Jeffrey L. Platt ◽  
...  

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