Osmiophilic cytoplasmic inclusions in the lymph node post-capillary venules of the guinea pig

1981 ◽  
Vol 178 (3) ◽  
pp. 237-240 ◽  
Author(s):  
Chr Kittas ◽  
L. Henry ◽  
C. Papadimitriou ◽  
N. X. Papacharalampous
1991 ◽  
Vol 1 (1) ◽  
pp. 30-43 ◽  
Author(s):  
D. A. Basketter ◽  
E. W. Scholes ◽  
I. Kimber ◽  
P. A. Botham ◽  
J. Hilton ◽  
...  

1977 ◽  
Vol 145 (5) ◽  
pp. 1405-1410 ◽  
Author(s):  
C C Whitacre ◽  
P Y Paterson

Supernates derived from incubated lymph node cells of Lewis rats sensitized to guinea pig spinal cord-Freund's adjuvant transfer experimental allergic encephalomyelitis (EAE) to syngeneic recipients. EAE supernatant transfer activity (EAE-STA) is not demonstrable in supernates derived from LNC of control donors not sensitized to nervous tissue. After addition of brain antigen to active supernates, EAE-STA is not longer demonstrable.


1986 ◽  
Vol 126 (3) ◽  
pp. 160-162 ◽  
Author(s):  
A. De Pasquale ◽  
G. Biagini ◽  
S. Pileri ◽  
M. Franchini ◽  
V. Bottanelli ◽  
...  

1978 ◽  
Vol 22 (5) ◽  
pp. 595-601 ◽  
Author(s):  
Amnon Altman ◽  
Herbert J. Rapp

1958 ◽  
Vol 107 (1) ◽  
pp. 109-124 ◽  
Author(s):  
S. B. Salvin ◽  

Guinea pigs were injected in the footpads with either purified diphtheria toxoid or recrystallized egg albumin in Freund adjuvant without mycobacteria. Each guinea pig was then skin-tested only once with the specific antigen and bled for antibody determination. After injection of the sensitizing antigen, a latent period occurred during which neither sensitivity nor circulating antibody could be detected. A period of delayed sensitivity followed wherein circulating antibody could not be discerned and which could be transferred by lymph node cells. Ultimately, the Arthus type sensitivity developed, accompanied by circulating antibody. The duration and severity of reactions to homologous antigens during the last 2 phases varied with the antigen and with the dose. An increase in the sensitizing dose decreased the duration of the delayed type of allergy, a decrease in the dose prolonged the delayed type. Inclusion of mycobacterium in the sensitizing inoculum tended to introduce delayed sensitivity earlier and delay the onset of Arthus type sensitivity. When specific precipitate in antibody excess was included with the toxoid in the sensitizing dose, the onset of the Arthus phase was hastened. When lymph nodes from a large number of sensitized donors were removed during the latter part of the latent period, recipients of the cells showed a delayed type sensitivity.


1994 ◽  
Vol 23 (2) ◽  
pp. 179-187
Author(s):  
D. A. EDWARDS ◽  
T. M. SORANNO ◽  
M. A. AMORUSO ◽  
R. V. HOUSE ◽  
A. C. TUMMEY ◽  
...  

1977 ◽  
Vol 146 (3) ◽  
pp. 766-778 ◽  
Author(s):  
C A Prange ◽  
J Fiedler ◽  
D E Nitecki ◽  
C J Bellone

Shared idiotypy between B- and T-cell receptors specific for the antigen L-tyrosine-p-azophenyltrimethylammonium [tyr(TMA)] was studied in an antigen-binding assay using idiotypic antisera. These idiotypic reagents were prepared by inoculation of rabbits with purified anti-tyr(TMA) antibody raised in strain 13 guinea pigs. The antisera blocked 78-83% of the antigen-binding T cells (T-ABC) and 50-55% of the antigen-binding B cells (B-ABC) from tyr(TMA)-immune strain 13 and outbred lymph node cells (LNC). An excess of normal guinea pig Ig in the ABC assay did not affect the ability of the idiotypic antisera to block T- and B-ABC. Nylon wool-passed tyr(TMA)-immune LNC were trypsin treated resulting in a 75% loss of T-ABC. The trypsin-treated population was then cultured for 16 h which resulted in a return of T-ABC to 92% of pretrypsin values. 77% of these regenerated T-ABC could be blocked with idiotypic antisera. Specificity of the idiotypic antisera was tested in L-tyrosine-p-azobenzenearsonate-immune guinea pig LNC. Neither T- nor B-ABC were blocked in this heterologous system. Further blocking experiments were performed to characterize the nature of the T-ABC receptor. A variety of anti-Ig reagents, some of which block B-ABC, do not inhibit T-ABC suggesting that variable regions on T cells are not linked to Ig Constant regions.


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