scholarly journals Reducing the Incidence of Graft Contamination during Allogeneic Marrow Harvest

2019 ◽  
Vol 25 (3) ◽  
pp. S200-S201
Author(s):  
Elizabeth Harvey ◽  
Dean Merkel ◽  
Sunil Abhyankar ◽  
Leyla Shune
Keyword(s):  
Blood ◽  
1992 ◽  
Vol 80 (5) ◽  
pp. 1358-1364 ◽  
Author(s):  
M Boeckh ◽  
RA Bowden ◽  
JM Goodrich ◽  
M Pettinger ◽  
JD Meyers

Abstract Detection of cytomegalovirus (CMV) antigenemia was compared with shell vial centrifugation cultures for rapid detection of CMV infection. In a prospective study, 59 CMV seropositive patients were monitored weekly during the first 100 days after allogeneic marrow transplantation for virus excretion from urine, throat, and blood and for antigenemia by direct staining of peripheral leukocytes using an antibody pool directed against pp 65. Antigenemia was present in 21 of 22 patients with culture-proven CMV infection and in 3 of 37 without culture-proven CMV infection (sensitivity 95%, specificity 91%). The median time of onset of antigenemia and shell vial cultures was day 47 and 55 after transplant, respectively (P = .0006). Among patients who developed CMV disease without preceding cultures, antigenemia was detected in all patients with CMV pneumonia (N = 6) and in two of three patients with gastrointestinal disease by a median of 10 and 7 days, respectively, before the onset of disease (P = .0002). Levels of antigenemia were significantly higher in patients with disease or viremia than in patients with excretion from urine or throat (P less than .05). Whether the antigenemia assay is more sensitive than rapid culture methods to focus antiviral prophylaxis in marrow transplant patients must be determined in controlled studies.


Blood ◽  
1985 ◽  
Vol 65 (4) ◽  
pp. 789-794 ◽  
Author(s):  
EN Dessypris ◽  
S Redline ◽  
JW Harris ◽  
SB Krantz

Abstract The pathogenesis of diphenylhydantoin-induced pure red cell aplasia was investigated in the case of a 32-year-old man who developed pure red cell aplasia while he was under treatment with diphenylhydantoin. The patient's serum IgG purified from serum drawn at the time of diagnosis suppressed normal allogeneic marrow colony-forming (CFU-E) and burst- forming (BFU-E) and autologous blood BFU-E growth in vitro only in the presence of diphenylhydantoin. This IgG-diphenylhydantoin complex had no effect on CFU-GM growth in vitro. Normal IgG or patient's IgG purified from serum drawn after the remission of red cell aplasia had no effect on erythroid colony formation in vitro in the presence of diphenylhydantoin. The IgG-diphenylhydantoin complex exerted no direct cytotoxic effect on normal marrow erythroblasts, CFU-E, and BFU-E, nor did it interfere with the action of erythropoietin on marrow erythroblasts. These studies suggest that diphenylhydantoin-induced red cell aplasia is immunologically mediated through an IgG inhibitor, which requires the presence of the drug to suppress erythroid colony formation in vitro. This inhibitor seems to exert its effect on erythroid progenitors at or beyond the stage of differentiation of CFU- E, but not on erythroblasts.


1992 ◽  
Vol 54 (6) ◽  
pp. 1002-1007 ◽  
Author(s):  
ANTHONY P. SCHWARER ◽  
J. MICHAEL B. HUGHES ◽  
BEATRICE TROTMAN-DICKENSON ◽  
THOMAS KRAUSZ ◽  
JOHN M. GOLDMAN

1991 ◽  
Vol 79 (1) ◽  
pp. 122-123
Author(s):  
M. Cottler-Fox ◽  
E. Himoe ◽  
J. K. Blancato ◽  
H. J. Deeg

1981 ◽  
Vol 57 (1) ◽  
pp. 219-228 ◽  
Author(s):  
Walter Pierpaoli ◽  
Georges Jean-Marie Maestroni ◽  
Edgar Sache

1994 ◽  
Vol 57 (8) ◽  
pp. 1266-1268 ◽  
Author(s):  
Shinji Nakao ◽  
Masaki Yamaguchi ◽  
Hideyuki Takamatsu ◽  
Shintaro Shiobara ◽  
Tamotsu Matsuda

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