scholarly journals The Recognition of Four Red Cell Antigen-Antibody Systems in the Rabbit

1955 ◽  
Vol 53 (4) ◽  
pp. 398-407 ◽  
Author(s):  
D. H. Heard

SummaryFour red cell antigen-antibody systems in the rabbit are described.Three of these systems, Z, Y and W, appear to be inherited as an allelomorphic series. The fourth is inherited independently.Some of the serological properties which allow these sera to be recognized are described and attention is drawn to a property of rabbit red cells, manifested by a variation in their susceptibility to agglutination by homologous antisera, which can complicate the separation of a mixture of antibodies in one serum.

1980 ◽  
Vol 8 (2) ◽  
pp. 115-119 ◽  
Author(s):  
B. H. Webster

Haemolytic transfusion reactions can be defined as the occurrence after transfusion of measurably increased destruction of red cells, of donor or recipient, by alloantibodies. They may be acute (occurring within 24 hours of transfusion) or delayed (when signs of red cell destruction do not occur until 4 to 10 days after transfusion). The severest signs and symptoms of acute reactions follow intravascular red cell lysis and progress to anaemia, fever, haemoglobinuria and jaundice. The subjective responses of pain, restlessness, nausea, skin flushing, dyspnoea and shock are mediated by cleavage products of complement (C3a, C5a) activated by red cell antigen-antibody reaction. The bleeding and renal failure complications that follow are multi-factoral in aetiology but also stem from the activation of intravascular clotting and from the vasomotor disturbances following histamine and kinin release.


Vox Sanguinis ◽  
1971 ◽  
Vol 20 (6) ◽  
pp. 542-554
Author(s):  
A.J. Bowdler ◽  
R.W. Bull ◽  
R. Slating ◽  
S.N. Swisher

Vox Sanguinis ◽  
1971 ◽  
Vol 20 (6) ◽  
pp. 542-554 ◽  
Author(s):  
A. J. Bowdler ◽  
R. W. Bull ◽  
R. Slating ◽  
S. N. Swisher

Blood ◽  
1962 ◽  
Vol 20 (2) ◽  
pp. 214-232 ◽  
Author(s):  
NICOLAS COSTEA ◽  
ROBERT SCHWARTZ ◽  
MATTHEW CONSTANTOULAKIS ◽  
WILLIAM DAMESHEK

Abstract Red cell sensitization by either agglutinating or incomplete antibodies was detected with an I131 labeled rabbit antihuman globulin serum (RAG). Nonspecific absorption of RAG by red cells was reduced to a minimum by the addition of 6 per cent bovine albumin. The reactions between RAG and the sensitized erythrocytes were typical of antigen-antibody reactions and the sensitivity of the test was found to be greater than the standard Coombs test. Quantitative studies of the degree of erythrocyte sensitization by isoimmune or autoimmune antibodies were possible with this technic.


2005 ◽  
Vol 129 (2) ◽  
pp. 190-193 ◽  
Author(s):  
Melanie Osby ◽  
Ira A. Shulman

Abstract Context.—The transfusion of donor red blood cell units (RBCs) that lack certain red cell antigens (such as C, E, and K) when the corresponding antigens are absent from the recipient's red cells has been shown to reduce the risk of red cell alloimmunization in sickle cell disease patients. However, data are limited regarding the extent to which transfusion services routinely perform red cell antigen phenotype testing of nonalloimmunized sickle cell disease patients, and then use that information to select donor RBCs lacking 1 or more of the red cell antigens that the patient's red cells do not express. Objective.—To determine the extent to which transfusion services routinely perform red cell antigen phenotype testing of nonalloimmunized sickle cell disease patients, and then use that information to select donor RBCs lacking 1 or more of the red cell antigens that the patient's red cells do not express. Design.—An educational subsection of a College of American Pathologists Proficiency Testing Survey (J-C 2003) assessed transfusion service practices regarding performance of red cell antigen phenotype testing of nonalloimmunized sickle cell disease patients and how transfusion services use this information for the selection of donor RBCs. The data analysis of the survey included 1182 North American laboratories. Results.—Data from 1182 laboratories were included in the survey analysis, of which the majority (n = 743) reported that they did not routinely perform phenotype testing of sickle cell disease patients for antigens other than ABO and D. The other 439 laboratories reported that they did routinely perform phenotype testing of sickle cell disease patients for antigens in addition to ABO and D. The majority of these 439 laboratories (three fourths; n = 330) reported that they used these patient data for prophylactic matching with donor RBCs when sickle cell disease patients required transfusion. When phenotype-matched donor RBCs were used, the antigens most commonly matched (85% of the time) were C, E, and K. Conclusions.—The majority of North American hospital transfusion service laboratories do not determine the red cell antigen phenotype of nonalloimmunized sickle cell disease patients beyond ABO and D. Those laboratories that do determine the red cell phenotype of nonalloimmunized sickle cell disease patients beyond ABO and D most commonly match for C, E, and K antigens when phenotype-matched donor RBCs are used.


Transfusion ◽  
1990 ◽  
Vol 30 (2) ◽  
pp. 109-113 ◽  
Author(s):  
Y Lapierre ◽  
D Rigal ◽  
J Adam ◽  
D Josef ◽  
F Meyer ◽  
...  

1972 ◽  
Vol 12 (8) ◽  
pp. 933-947 ◽  
Author(s):  
Bruce J. Oberhardt ◽  
Irving F. Miller

1955 ◽  
Vol 53 (4) ◽  
pp. 408-419 ◽  
Author(s):  
D. H. Heard

Summary and Conclusions1. Rabbit cells show a marked variation in agglutination when reacting with apparently homologous iso-antisera.2. This phenomenon has been investigated in two ways:(a) Samples of apparently homologous antisera have been absorbed with (i) strongly agglutinating cells, (ii) poorly agglutinating cells. It was found that strongly agglutinating cells absorbed the antibody completely and rapidly from the serum, whilst poorly agglutinating cells, though they absorbed it completely, did so much more slowly. Also, when a serum which had been absorbed with poorly agglutinating cells until these no longer reacted with it was titrated against strongly agglutinating cells, these were still strongly agglutinated. This showed a source of serious error when investigating new sera by absorption techniques and when using weak antisera for grouping purposes.(b) Poorly agglutinating cells were injected into rabbits, and the antisera so obtained were examined against strongly agglutinating cells and against the poorly agglutinating cell used as the antigen. The antibody response was poor; two out of eight rabbits developed an antibody, and strongly agglutinating cells reacted more strongly with these antisera than the poorly agglutinating cells which had been used as the antigen.3. Three hypotheses for this variation in agglutination have been put forward and discussed:(a) That the variation is due to cross reactions between numbers of closely related antigen-antibody systems. The results of the investigations 2 (a) and 2(b) suggest that this is unlikely.(b) That the disposition of antigen sites on the surface of the red cell is a factor determining the agglutinability of the cell. It is considered that this might play a subsidiary role in the phenomenon as it is shown in the rabbit.(c) That rabbit red cell agglutinability is mainly determined by the number of antigen sites on the cell available to the antibody. The experimental results can be explained on this hypothesis, and it is suggested that this may be the main factor accounting for the behaviour of rabbit red cells. It is pointed out that supporting evidence for this is afforded by measurements with radio iodinated antisera.


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