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1 lood count [CBC]), and 102 controls (healthy blood donors).
2 ftment after a second transfer from the same blood donor.
3 atched unrelated donor or 6/6 unrelated cord blood donor.
4 ified the 25P13 antibody from an independent blood donor.
5 ls in communities and 721 (13.0%, 12.1-13.9) blood donors.
6 patitis C virus epitope in a random group of blood donors.
7 d Kingdom and Vietnam and from 26 healthy US blood donors.
8 identify 16 invariant TCRs shared among many blood donors.
9 V RNA-negative plasma and PBMCs from healthy blood donors.
10 Controls comprised healthy blood donors.
11 n a control group of 41 age- and sex-matched blood donors.
12 rroborating with those obtained from healthy blood donors.
13 anti-PEG antibodies in a quarter of healthy blood donors.
14 f antibody responses in 370 WNV-seropositive blood donors.
15 patients with IBD and 112 healthy unrelated blood donors.
16 ith CD, 25 patients with UC and 45 controls, blood donors.
17 widespread in the English population and in blood donors.
18 rica were firstly identified amongst Chinese blood donors.
19 to be damaging and not found among 185 local blood donors.
20 e unequivocal identification of Vel-negative blood donors.
21 tients with osteomyelitis and in 299 matched blood donors.
22 ich were coinfected with HCV, and 54 healthy blood donors.
23 nfected or HIV-1/HCV coinfected patients, or blood donors.
24 recently infected vs more remotely infected blood donors.
25 ors and discrepancies between facilities and blood donors.
26 by blood centers to improve safety for young blood donors.
27 ymorphism (SNP) profile of healthy AA and EA blood donors.
28 d with only 3 of 44 (6.8%) healthy volunteer blood donors.
29 rols were derived from 1280 northern English blood donors.
30 be assessed by follow-up studies of viremic blood donors.
31 lidation, we analyzed plasma samples from 79 blood donors.
32 ng and molecular surveillance of HIV-1 among blood donors.
33 ro generated monocyte-derived DCs of healthy blood donors.
34 ute zoster and in 9% of healthy asymptomatic blood donors.
35 ith neurologic symptoms and 44% of voluntary blood donors.
36 screening of plasma samples from individual blood donors.
37 exposure to the virus in many indeterminate blood donors.
38 es 1, 2, and 5 in samples from South African blood donors.
39 arable controls, but greater than in healthy blood donors.
40 to WNV and to identify potentially infected blood donors.
41 blood mononuclear cells (PBMCs) from healthy blood donors.
42 er among tissue donors than among first-time blood donors.
43 d 5 with arthritis), and sera from 20 normal blood donors.
44 ined by testing 999 specimens from volunteer blood donors.
45 a VWF was studied in a series of 541 healthy blood donors.
46 mong 583 MSM and 583 age-matched repeat male blood donors.
47 e novo TSA developed against 150/244 (61.5%) blood donors.
48 nsity score matching with a series of female blood donors.
49 smatched unrelated, haploidentical, and cord blood donors.
50 emaining components and serum specimens from blood donors.
51 CRC patients was compared with 5270 healthy blood donors.
52 was detected in peripheral blood of healthy blood donors.
53 and hepatitis C seroprevalence trends among blood donors.
54 loped for race differentiation of peripheral blood donors.
55 munities and 5559 (81.4%, 80.4-82.3) of 6832 blood donors.
57 ence interval [95% CI], 0.0025 to 0.007) for blood donors, 0.86 (95% CI, 0.02 to 0.71) for VA patient
58 nd May 3, 2016, 20 757 of the 38 035 invited blood donors (10 843 [58%] men, 9914 [51%] women) partic
59 ietic-cell transplant from an unrelated cord-blood donor (140 patients), an HLA-matched unrelated don
60 disease (n = 106) and 2 control groups (198 blood donors, 151 patients with Crohn's disease) were an
62 selected comparative group of United Kingdom blood donors (2.5 x 10(5) versus 2.9 x 10(6) IU/ml; P =
64 tients with early RA, 2 (2.7%) of 73 healthy blood donors, 2 (2.1%) of 94 individuals with osteoarthr
66 as 20%-significantly higher than that of 177 blood donors (5.1%; P=.001; OR, 4.67; 95% CI, 1.91-11.65
67 HV-8 seroprevalence was 2.8% (29/1023) among blood donors, 7.1% (96/1350) among transfusion recipient
68 years or older) and active (age 17-69 years) blood donors, adjusted seroprevalences were 1.4% (95% CI
70 ive kidney transplant recipients and healthy blood donors after stimulation of peripheral blood monon
71 ELISpot frequencies from healthy HPV-exposed blood donors against HLA-A*0201-binding peptides were un
74 gmatic, randomised trial, we recruited whole blood donors aged 18 years or older from 25 centres acro
75 , pragmatic, randomised trial that recruited blood donors aged 18 years or older from 25 static donor
76 asles seroprevalence survey of 508 Minnesota blood donors aged 20-39 years was conducted; 91% had ser
77 to infection, from a single sample of 1,936 blood donors aged 20-70 years in mainland France in June
78 initially asymptomatic T cruzi-seropositive blood donors, although disease was mild at diagnosis.
79 efficacy, we conducted a linked analysis of blood donor and component data with patients who receive
81 ggregated IgG (H-IgG) (control) in 15 normal blood donors and 16 RA patients not receiving immunosupp
82 nses against clinically relevant TAAs in 114 blood donors and 44 women during their first pregnancy.
84 on of HLA antibodies in plasma of implicated blood donors and a combination of the granulocyte agglut
85 Arg296 was found in 6 other primates, > 250 blood donors and A(pae) family relatives without the A(p
86 ssed SARS-CoV-2 seroprevalence among retired blood donors and combined it with national COVID-19 surv
88 tested serum and plasma samples from healthy blood donors and from patients with blood cultures posit
91 il-specific antibodies in the plasma of both blood donors and recipients have been implicated in the
93 newly generated viral genome sequences from blood donors and recipients, we assess the dynamics of d
94 dengue RNA detection period in asymptomatic blood donors and relationships between donor viremia and
95 ositive (30 with HTLV-I and 55 with HTLV-II) blood donors and their stable (>or=6 months) heterosexua
96 antly elevated in ICU patients compared with blood donors and were the highest in septic patients.
98 region located in SMIM1 intron 2 in Swedish blood donors, and observed a strong correlation between
99 , determinants and importance of low iron in blood donors, and on the efforts to reduce or prevent ir
100 ed from naive T cells, purified from healthy blood donors, and reactivated in the presence of IL-1bet
101 celiac disease patients' sera versus normal blood donors, and their conformational features were eva
107 performed a large, cross-sectional study of blood donors at 6 US blood centers during 2006-2007.
108 ge-scale genotyping for HNA-3a/b to identify blood donors at risk to have HNA-3a-specific antibodies
110 ion of genetic and epidemiological data from blood donor banks may be useful to anticipate epidemic s
111 establishing a 100% voluntary nonremunerated blood donor base and implementing component therapy.
113 tained intermittently from healthy HLA-typed blood donors between 1999 and 2012, we were able to demo
114 lar, and WHO reports using the search terms "blood donor", "blood donation","blood safety", "blood ba
116 lood donor spleen inoculum compared with the blood donor brain inoculum, suggesting lower titres of i
117 ear cells were isolated from 27 non-selected blood donor buffy coats, and ILCs were sorted by FACS.
118 ntenatal clinic groups, 1.99% (1.86-2.12) in blood donors, but 6.9% (6.1-7.5) in other general popula
119 HTLV-2 are prevalent at low levels among US blood donors, but recent data on their prevalence is lac
121 positive and 328 HTLV-II-seropositive former blood donors, by use of real-time polymerase chain react
122 ted through large-scale routine screening of blood donors can complement molecular surveillance studi
124 ate that a significant percentage of healthy blood donors carry Chlamydia pneumoniae in their blood.
125 atic advances in blood banking in the 1970s, blood donor centers began supplying hospitals with indiv
127 gically suppressed patients or to 13 healthy blood donors, circulating CD141 (BDCA-3)(+) and CD1c (BD
130 with newly diagnosed type 1 diabetes and 50 blood donor control subjects, together with the WHO refe
131 derived from data on 200 RA patients and 98 blood donor controls, in which positivity for >/=9 ACPAs
132 nts with chronic HCV infection or uninfected blood donors (controls); NK cells and monocytes were iso
135 evised guidance that recommended a change in blood donor deferral of men who have sex with men (MSM)
139 5 produced from multiple cell lines) and one blood donor-derived anti-D Ig were obtained by HPLC and
140 ailable self-Ag and the genetics of the cord blood donor dictate the levels of central tolerance and
142 pitation studies in macrophages from control blood donors (donor) and patients with either FPN1 p.A77
143 the French West Indies and 72 controls were blood donors during the same period, chikungunya infecti
144 ppressive activity ex vivo as 54% of healthy blood donors examined had fully suppressive Tregs sponta
145 reported that approximately 5-10% of normal blood donors express abnormally high or low levels of A
148 tests of "minipools" of 16 samples to screen blood donors for West Nile virus RNA began in July 2003.
149 ), extracted from the plasma of thousands of blood donors, for removing HLA antibodies (Abs) in highl
150 ed, HCV antibody-positive (HCV+), allogeneic blood donors from 1991 to 2002 and 10,259 HCV antibody-n
151 e level of antibody reactivity among healthy blood donors from 2 widely separated regions of the Unit
152 ropositive, and 799 HTLV-seronegative former blood donors from 5 U.S. blood centers for a median of 1
161 ught to affirm that T. cruzi-seropositive US blood donors have persistent infection with demonstrable
162 ients (UGT1A1*28 homozygous) and 249 healthy blood donors (HBD) were genotyped for UGT1A (UGT1A1*28,
165 comparing CCR5Delta32 distribution among US blood donors identified through a comprehensive blood su
166 Nile virus (WNV) infection, acutely viremic blood donors, identified by nucleic acid amplification t
168 active, 18- to 45-year-old, male, first-time blood donors in 6 US locations were tested for emtricita
175 h malaria parasites are commonly detected in blood donors in malaria-endemic areas, transfusion-trans
177 data were compared with those of first-time blood donors in order to generate estimated incidence ra
178 ucing the antibody negative window period in blood donors in resource limited settings where nucleic
179 less frequent (2 of 14 patients [14.2%]) in blood donors in whom WNV infection was identified by WNV
181 d increase in overall mortality among former blood donors, including significantly increased mortalit
182 ort for the first time an asymptomatic human blood donor infected with B. clarridgeiae, as documented
183 The detection of hepatitis B virus (HBV) in blood donors is achieved by screening for hepatitis B su
184 iated mutations (DRMs) among treatment-naive blood donors is critical for monitoring viral evolution
185 re on how to find, recruit and maintain rare blood donors is not overwhelming, there are quite a few
186 ections in the English population (including blood donors) is unknown, but is probably widespread, an
188 vian Donations and Transfusions) database of blood donors linked with other nationwide health data re
189 globulin G (IgG) and IgM among 10,569 French blood donors living in mainland France and three oversea
193 the assay, serum samples were assembled from blood donors (n = 372), acute hepatitis E patients (n =
196 in two animal facilities and age/sex-matched blood donors (n = 63) as controls were tested for IgG an
197 udy, HIV patients (n = 457) and HIV-negative blood donors (n = 79) presenting to an HIV clinic in Gha
199 1E-heterozygous than TACI-sufficient Swedish blood donors never immunized with pneumococcal antigens.
201 3.1% among personnel compared to 3.2% among blood donors; none were positive for IgM anti-HEV or HEV
203 HLA transfusion-specific antibodies (TSA) to blood donors of transfusions given posttransplant and ex
205 es sampled from four self-limited cases, one blood donor, one fatal adult case, and one newborn with
206 assessed whether HIV incidence in first-time blood donors or associated transfusion risk increased.
209 rates were not elevated compared to those of blood donors (OR, 2.0; 95% CI, 0.10 to 122.9; P = 0.50).
210 was low, 4.0% (2/50), and similar to that of blood donors (P = 0.46; odds ratio [OR], 1.4; confidence
211 (HCV) infection due to large numbers of paid blood donors (PBD), injection drug users (IDU), and sexu
214 ymized samples were representative of the US blood donor population (n = 5000), healthy UK donors (n
217 H1N1 influenza viremia (via RNA testing) in blood donor populations using multiple sensitive detecti
219 ificant research has focused individually on blood donors, product preparation and storage, and optim
220 undant evidence that leukocyte antibodies in blood donor products are somehow involved in transfusion
223 ope mismatches and pretransplant, peripheral blood, donor-reactive IFN-gamma ELISPOT assay results co
225 nly 52.4% of SARS-CoV-2 seropositive retired blood donors reported having been sick since the start o
227 healthy middle-aged and eight healthy older blood donors representing an average age difference of a
228 dependence on recruiting and retaining young blood donors requires a committed approach to donor safe
229 itch regions of memory B cells from European blood donors revealed frequent templated inserts origina
231 E1 and/or NS5B sequences from 411 volunteer blood donors sampled in 17 provinces and municipalities
233 ctivity to 15 other viruses tested or to 420 blood donor samples from the WNV pre-epidemic season.
236 ing of blood from non-outbreak areas until a blood donor screening test becomes available have been i
237 es included antenatal care clinic screening, blood donor screening, HIV/STI bio-behavioural surveys,
241 mice that were pretreated with C57BL/6 (B.6) blood (donor-specific transfusion, DST) and nondepleting
242 onger incubation times were observed for the blood donor spleen inoculum compared with the blood dono
243 Randomized, nonblinded clinical trial of blood donors stratified by ferritin level, sex, and age
244 ut none of the 30 serum samples from healthy blood donors, suggesting its potential application as an
245 t with 30 control serum samples from healthy blood donors, suggesting their potential application for
246 EV between the at-risk group and age-matched blood donors suggests low transmission risk with univers
247 specific responses in 15 of 30 indeterminate blood donors tested, compared with none in controls (p=0
248 xposed individuals, but none of the European blood donors tested, have high levels of LAIR1-containin
250 conclusion, MBL prevalence is much higher in blood donors than previously reported, and although unco
251 raries was obtained from 12 HUE cases and 26 blood donors; the remaining HUE cases were sequenced as
252 d myeloid DC (mDC) from cord blood and adult blood donors to evaluate whether immunological immaturit
254 strategies include matching RBC antigens of blood donors to those of transfusion recipients or provi
255 cytes (CTLs) generated from EBV-seropositive blood donors to treat patients with EBV-positive posttra
256 revention diagnostic criteria and 50 healthy blood donors, using a microarray with a cutoff fold diff
257 ed in 55 patients with CFS/ME and 75 healthy blood donors, using quantitative polymerase chain reacti
259 m four populations with various risks, i.e., blood donors, Veterans Administration (VA) patients, you
261 al after receipt of a transplant from a cord-blood donor was at least as favorable as that after rece
262 C virus (HCV) antibodies (anti-HCV) among US blood donors was 0.36%, but contemporary data on the pre
263 on of healthy United States Caucasian random blood donors was in Hardy-Weinberg equilibrium and CCR5D
269 generated in vitro from the same individual blood donors were exposed to 5 different pathogens, and
270 he TNFRII 196 M/R polymorphism, 79 volunteer blood donors were genotyped at this locus, by polymerase
272 ed from differentiating erythroid cells from blood donors were performed to determine the transcripti
274 nonuclear cells (PBMCs) from 35 WNV-infected blood donors were screened for virus-specific T cell res
275 lood mononuclear cells from 44 healthy human blood donors were tested for reactivity against HLA-matc
278 from HBsAg-seropositive patients and healthy blood donors were used to determine clinical sensitivity
280 Prospective samples were collected from 1004 blood donors who called their donation center within 3 d
281 and class II genes in 231 Chinese voluntary blood donors who had cleared HCV infection spontaneously
282 ood mononuclear cells (PBMC) of seropositive blood donors who had spontaneously or therapeutically cl
283 hese autoantibodies and rheumatoid factor in blood donors who later developed rheumatoid arthritis.
284 lopment and persistence were investigated in blood donors who made WNV RNA-positive (viremic) donatio
285 ence T-cell activation in seven of the eight blood donors who responded strongly to wild-type P99beta
287 by ELISA in plasma samples from asymptomatic blood donors who were reactive for RNA from DENV (n = 71
288 ment and retainment of future generations of blood donors will be needed, and care will be necessary
289 between convalescents and uninfected healthy blood donors with a predominantly CD4+ T cell response.
293 pective cohort study among initially healthy blood donors with an index T cruzi-seropositive donation
294 ion of macrophages from patients and healthy blood donors with genetic variants in NLRP3 and CARD8 an
295 nd general health in non-anemic repeat adult blood donors with iron deficiency (ferritin <= 50 ug/L).
296 of ferritin and hemoglobin levels in repeat blood donors with low iron stores, yet had no effect on
299 bout a 20% decrease in reactions among young blood donors, with the greatest benefit observed among t