Kinetics of development of the inhibitory activity of mixed lymphocyte culture supernatants on macrophage migration: Effect of presensitization

1974 ◽  
Vol 12 (2) ◽  
pp. 247-251 ◽  
Author(s):  
N. Thomson ◽  
A. Dimitriu ◽  
M. Dy ◽  
J. Hamburger
1994 ◽  
Vol 40 ◽  
pp. 82
Author(s):  
D. Gonzalez ◽  
S. Echegaray ◽  
A. Rodriguez

1977 ◽  
Vol 146 (2) ◽  
pp. 571-578 ◽  
Author(s):  
M E Dorf ◽  
J H Stimpfling

The ability of various B10 congenic resistant strains to respond to the alloantigen H-2.2 was tested. High and low antibody-producing strains were distinguished by their anti-H-2.2 hemagglutinating respones. However, these strains do not differ in their ability to respond to these antigenic differences in the mixed lymphocyte culture. The humoral response to the H-2.2 alloantigen was shown to be controlled by two interacting genes localized within the H-2 complex. Thus, F1 hybrids prepared between parental low responder strains could yield high level immune responses. In addition, strains bearing recombinant H-2 haplotypes were used to map the two distinct genes controlling the immune response. The alleles at each locus were shown to be highly polymorphic as evidenced by the asymmetric complementation patterns observed. The restricted interactions of specific alleles was termed coupled complementation. The significance of the results in the terms of mechanisms of Ir gene control are discussed.


1968 ◽  
Vol 108 (1) ◽  
pp. 41-48 ◽  
Author(s):  
Margaret Robson Wright ◽  
J. P. Arbuthnott ◽  
I. R. W. Lominski

1. The effect of a number of aromatic polysulphonic acids on the kinetics of haemolysis of rabbit erythrocyte suspensions by crude staphylococcal α-toxin was studied at pH8·6 and 6·8. 2. All of the inhibitory compounds caused an increase in the prelytic lag time (τ) of the sigmoid haemolysis curves, an increase in the time to reach 50% haemolysis (t½) and a decrease in the maximum rate of haemolysis (Rmax.). The most inhibitory compounds caused a 50% decrease in Rmax. at concentrations between 0·1 and 0·2mm. 3. The effect of pH varied considerably: compounds (I) and (II) were almost equally inhibitory at both pH values, compounds (IV) and (IX) were more inhibitory at pH6·8 than at pH8·6, and compounds (VII), (VIII), (X), (XI) and (XII) were more inhibitory at pH8·6. 4. Increased time of premixing α-toxin with compound (I) caused increased inhibition. 5. An attempt was made, where possible, to relate the inhibitory activity to the structure of the test compound.


2002 ◽  
Vol 34 (2) ◽  
pp. 471-473 ◽  
Author(s):  
A Morgun ◽  
N Shulzhenko ◽  
I.D.C.G Silva ◽  
G.F Rampim ◽  
A.P Chinellato ◽  
...  

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