scholarly journals SPONTANEOUS RELEASE OF T-CELL RECEPTORS FOR ALLOANTIGENS

1974 ◽  
Vol 140 (3) ◽  
pp. 603-618 ◽  
Author(s):  
Hansruedy Ramseier

In vitro cultivation of murine spleen cells resulted in a spontaneous release of receptors for alloantigens. This was revealed by the capacity of cell-free culture supernates to recognize alloantigens as measured in the PAR assay. Qualitatively, recognition responses obtained with these supernates reproduced faithfully those found with the corresponding cells. Large amounts of receptors were released by untreated spleen cells and by spleen cells treated with a rabbit antimouse immunoglobulin serum and complement, smaller amounts were released by bone marrow cells, and native thymus cells released none. Spleen cells from nude mice and spleen cells from normal mice treated with anti-θ serum and complement showed no release of receptors. It was concluded that receptors active in the PAR test were of T-cell origin. Release of T-cell receptors was found to be discontinuous and proceeded in waves. The amount of released receptors depended on the number of cells cultivated. Release occurred at 37°C but not at 4°C. Interaction with antigen, however, was temperature-independent. In contrast to T-cell receptors, a release of H-2 antigens could not be detected with the culture conditions employed.

1985 ◽  
Vol 161 (5) ◽  
pp. 953-971 ◽  
Author(s):  
M Brunswick ◽  
P Lake

The role of gamma interferon (IFN-gamma) in T cell-replacing factor (TRF) activity for antigen-specific plaque-forming cell (PFC) responses in vitro was studied using antibodies to murine IFN-gamma (Mu IFN-gamma). TRF activity was present in supernatants (Sn) of Con A- or mixed leukocyte reaction-stimulated murine spleen cells as well as in an IL-2-rich fraction of phytohemagglutinin-stimulated human peripheral blood lymphocyte Sn and in the Sn of the Gibbon T lymphoma MLA-144. The human TRF was highly active with cells from nu/nu mice and normal mice but not with cells from animals with the xid immunologic defect, similar to the activity of murine TRF. Antibodies to IFN-gamma consisted of hyper-immune rabbit antisera, IFN-gamma affinity-purified rabbit immunoglobulin and an interspecies hybridoma specific for Mu IFN-gamma. The results show that the activities of all preparations of TRF are markedly diminished or abrogated by antibody to Mu IFN-gamma but not by antibodies to human IFN-gamma (Hu IFN-gamma), nor by normal rabbit sera or purified rabbit Ig. The degree of inhibition was dose dependent and was quantitatively reversed by the addition to the cultures of recombinant-derived Mu IFN-gamma (Mu rIFN-gamma) but not Hu rIFN-gamma. This reversal was fully antigen specific and thus not attributable to polyclonal B cell activation by IFN-gamma, which is inactive alone in the TRF assay. Kinetic analysis shows that IFN-gamma must act by 24-48 h to produce PFC responses at 4 d. Together, the data demonstrate that IFN-gamma is a necessary mediator for TRF effects and that IFN-gamma is induced by TRF from T-depleted murine spleen cells in sufficient quantity to support large antibody responses. The source of this IFN-gamma may be the potent natural killer cells that are induced in cultures stimulated with TRF.


2017 ◽  
Vol 35 (12) ◽  
pp. 1188-1195 ◽  
Author(s):  
Thomas M Schmitt ◽  
David H Aggen ◽  
Kumiko Ishida-Tsubota ◽  
Sebastian Ochsenreither ◽  
David M Kranz ◽  
...  

2000 ◽  
Vol 236 (1-2) ◽  
pp. 147-165 ◽  
Author(s):  
Alain C Tissot ◽  
Frédéric Pecorari ◽  
Andreas Plückthun

1977 ◽  
Vol 146 (1) ◽  
pp. 49-58 ◽  
Author(s):  
H N Claman ◽  
S D Miller ◽  
M S Sy

Genetic restrictions in generation and expression of hapten-specific suppressor cells for contact sensitivity were found. Dinitrophenol- (DNP) or trinitrophenol-modified mouse spleen cells (SC) induced suppressors in donors able to transfer suppression to normal recipients. When allogeneic DNP-SC were injected into BALB/c mice, cells were generated which were suppressive only in the allogeneic strain providing the DNP-SC. In contrast, when DNP-BALB/c-SC were injected into BALB/c mice, suppressors were generated which were active both in BALB/c and in allogeneic mice (e.g., CBA). This apparent absence of syngeneic major histocompability complex restriction may be explained by cross reactive T-cell receptors which are VH gene products.


Immunology ◽  
2001 ◽  
Vol 104 (1) ◽  
pp. 19-27 ◽  
Author(s):  
Peter S. Evans ◽  
Patrick J. Enders ◽  
Cheng Yin ◽  
Tracy J. Ruckwardt ◽  
Marek Malkovsky ◽  
...  

2021 ◽  
Vol 4 ◽  
pp. 100087 ◽  
Author(s):  
Sanjaykumar V. Boddul ◽  
Ravi Kumar Sharma ◽  
Anatoly Dubnovitsky ◽  
Bruno Raposo ◽  
Christina Gerstner ◽  
...  

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