Changes in serum level and affinity for concanavalin A of human α1-proteinase inhibitor in severe burn patients: relationship to natural killer cell activity

1989 ◽  
Vol 990 (2) ◽  
pp. 122-127 ◽  
Author(s):  
Pierre-Jean Lejeune ◽  
Bernard Mallet ◽  
Catherine Farnarier ◽  
Solange Kaplanski
1992 ◽  
Vol 29 (1) ◽  
pp. 53-59 ◽  
Author(s):  
G. Rappocciolo ◽  
J. S. Allan ◽  
J. W. Eichberg ◽  
T. C. Chanh

Three different species of nonhuman primates (baboons [ Papio hamadryas], rhesus monkeys [ Macaca mulatta], and African green monkeys [ Cercopithecus aethiops]) were evaluated for their natural killer cell activity, and for the ability of their peripheral blood mononuclear cells to proliferate in response to known mitogens (concanavalin A, phytohemagglutinin, and pokeweed mitogen) and to react with a panel of mouse monocional antibodies directed against human leukocyte surface antigens. Rhesus monkeys displayed the highest natural killer cell cytotoxic activity (185.7 ± 33 lytic units) compared with those of baboons (83.8 ± 19 lytic units) and of African green monkeys from West Africa (39.08 ± 8 lytic units) and from the Caribbean basin (37.9 ± 9 lytic units). No correlation was observed between the natural killer cell cytotoxic activity and the percentage of CD 16′ natural killer cells among the three species studied. High spontaneous proliferative capacity was observed in African green monkeys obtained from West Africa compared with those of the other species studied. Although no significant differences were noted in T and B cell mitogen-induced in vitro proliferation, baboon mononuclear cells were less responsive to concanavalin A (stimulation index of 16 ± 3 [ x ± standard error of mean]) than to phytohemagglutinin (stimulation index of 47 ± 12). However, rhesus and African green monkey cells proliferated more efficiently in response to concanavalin A. Unlike in human beings where the ratio between helper-inducer (CD4 +) and cytotoxic-suppressor (CD8 +) T-lymphocytes is generally > 1, the CD4 +/ CD8 + ratios in baboons and rhesus and African green monkeys were 0.58, 0.69, and 0.35, respectively. Basic information on normal immune functions in these primates is important because of their increased use as experimental animal models for the study of human diseases such as acquired immunodeficiency syndrome (AIDS).


Animals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 861
Author(s):  
Justin R. Perrault ◽  
Milton Levin ◽  
Cody R. Mott ◽  
Caitlin M. Bovery ◽  
Michael J. Bresette ◽  
...  

Chelonid alphaherpesviruses 5 and 6 (ChHV5 and ChHV6) are viruses that affect wild sea turtle populations. ChHV5 is associated with the neoplastic disease fibropapillomatosis (FP), which affects green turtles (Chelonia mydas) in panzootic proportions. ChHV6 infection is associated with lung-eye-trachea disease (LETD), which has only been observed in maricultured sea turtles, although antibodies to ChHV6 have been detected in free-ranging turtles. To better understand herpesvirus prevalence and host immunity in various green turtle foraging aggregations in Florida, USA, our objectives were to compare measures of innate and adaptive immune function in relation to (1) FP tumor presence and severity, and (2) ChHV5 and ChHV6 infection status. Free-ranging, juvenile green turtles (N = 45) were captured and examined for external FP tumors in Florida’s Big Bend, Indian River Lagoon, and Lake Worth Lagoon. Blood samples were collected upon capture and analyzed for ChHV5 and ChHV6 DNA, antibodies to ChHV5 and ChHV6, in vitro lymphocyte proliferation using a T-cell mitogen (concanavalin A), and natural killer cell activity. Despite an overall high FP prevalence (56%), ChHV5 DNA was only observed in one individual, whereas 20% of turtles tested positive for antibodies to ChHV5. ChHV6 DNA was not observed in any animals and only one turtle tested positive for ChHV6 antibodies. T-cell proliferation was not significantly related to FP presence, tumor burden, or ChHV5 seroprevalence; however, lymphocyte proliferation in response to concanavalin A was decreased in turtles with severe FP (N = 3). Lastly, green turtles with FP (N = 9) had significantly lower natural killer cell activity compared to FP-free turtles (N = 5). These results increase our understanding of immune system effects related to FP and provide evidence that immunosuppression occurs after the onset of FP disease.


1996 ◽  
Vol 67 (1) ◽  
pp. 67-70 ◽  
Author(s):  
Marcus Wenner ◽  
Noriyuki Kawamura ◽  
Hitoshi Miyazawa ◽  
Yukihiro Ago ◽  
Toshio Ishikawa ◽  
...  

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