Dissociation of macrophage cytolysis and ability to transfer anti-listeria resistance by Concanavalin A-stimulated spleen cells

1992 ◽  
Vol 13 (1) ◽  
pp. 25-35
Author(s):  
Jon T. Roll ◽  
Mary Haak-Frendscho ◽  
James F. Brown ◽  
Charles J. Czuprynski
Keyword(s):  
1982 ◽  
Vol 693 (2) ◽  
pp. 315-319 ◽  
Author(s):  
C. Henrik ◽  
J. Wolff ◽  
Karl E.O. Åkerman
Keyword(s):  

1975 ◽  
Vol 18 (1) ◽  
pp. 41-48 ◽  
Author(s):  
Françoise Delamette ◽  
Nadine Hardt ◽  
Jacques Panijel

1973 ◽  
Vol 137 (3) ◽  
pp. 649-659 ◽  
Author(s):  
Robert R. Rich ◽  
Carl W. Pierce

A population of thymus-derived lymphocytes has been identified that, upon activation by the nonspecific plant mitogen concanavalin A, suppresses the development of plaque-forming cell responses in fresh or 48-h antigen-stimulated cultures of mouse spleen cells. Suppressor cells can inhibit both primary and secondary IgM and IgG responses in vitro. X-irradiation before activation of peripheral thymus-derived cells by concanavalin A abrogates generation of suppressor cells. After a 48 h activation period, however, the function of concanavalin A-activated suppressor cells is radioresistant. As yet uncertain is whether these suppressor cells are a population of cells distinct from thymus-derived "helper" cells. In certain important regards, the cells mediating these two opposing functions share similar characteristics; the effect observed may be determined by the circumstances of activation or the numbers of activated cells, and may consequently represent different functions of a single thymus-derived regulator cell population.


1982 ◽  
Vol 156 (3) ◽  
pp. 918-923 ◽  
Author(s):  
M S Sy ◽  
S H Lee ◽  
M Tsurufuji ◽  
K L Rock ◽  
B Benacerraf ◽  
...  

Treatment of responder cells with monoclonal anti-Ly-1,2 antibodies plus complement in vitro completely eliminated their ability to generate azobenzenearsonate (ABA)-specific cytolytic T lymphocytes (CTL). However, addition of the concanavalin A-stimulated supernatants of rat spleen cells (Con A-Sup) can fully reconstitute the response. Therefore, Lyt-1,2-bearing T cells are required for the generation of ABA-specific CTL, and such requirement can be replaced by factors present in the Con A- sup. Suppressor T cells (Ts), when adoptively transferred into naive recipients, will inhibit the in vivo priming of CTL. This inhibition can also be reversed by in vitro addition of Con A-Sup. furthermore, mice serving as donors of Ts also show profound unresponsiveness when primed and restimulated in vitro. In contrast to the Ts-mediated inhibition, in vitro addition of Con A-Sup was unable to abolish the unresponsiveness observed in these cultures. Thus, we identified two unresponsive states in a hapten-specific killing system that differ in their ability to be reconstituted by Con A-Sup.


Immunobiology ◽  
1984 ◽  
Vol 166 (3) ◽  
pp. 219-227 ◽  
Author(s):  
F. Marcucci ◽  
Beate Klein ◽  
P. Altevogt ◽  
S. Landolfo ◽  
H. Kirchner

1981 ◽  
Vol 153 (3) ◽  
pp. 732-737 ◽  
Author(s):  
C E Taylor ◽  
W Y Weiser ◽  
F B Bang

Genetically resistant G3H mice routinely yielded macrophages that were resistant when grown in 90% horse serum. These mice also routinely yielded macrophages that were susceptible to the same virus, MHV (PRI), in vitro after the mice had been treated with three intraperitoneal doses, of hydrocortisone. Dexamethasone and prednisolone when similarly administered also increased the susceptibility of C3H macrophages taken from the treated animal, but progesterone and testosterone did not. In addition, spleen cells from mice treated with cortisone made the resistant C3H macrophages 100 times more susceptible in vitro. Increased in vitro susceptibility induced in this way by hydrocortisone was reversed by exposure to supernatant fluid removed from cultures of concanavalin A-treated spleen cells.


1983 ◽  
Vol 11 (4) ◽  
pp. 233-237
Author(s):  
Calbert A. Laing ◽  
Curla S. Walters

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