scholarly journals Preparation and Pathogen Inactivation of Double Dose Buffy Coat Platelet Products using the INTERCEPT Blood System

Author(s):  
Mohammad R. Abedi ◽  
Ann-Charlotte Doverud
Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 2886-2886
Author(s):  
John D. Roback ◽  
Herve Isola ◽  
Lily Lin ◽  
Jean-Pierre Cazenave

Abstract Background: While many severely immunocompromised patients require cytomegalovirus (CMV)-safe blood components, the standard approach of providing CMV-seronegative and/or leukoreduced components is still associated with breakthrough cases of CMV transmission. The INTERCEPT Blood System™ is a pathogen-inactivation methodology for platelets and plasma which may be a superior approach for providing CMV-safe transfusions. In this study, we compared the efficacy of INTERCEPT with leukoreduction for inactivating and/or removing infectious CMV experimentally introduced at high levels into platelet components. Methods: Pooled buffy-coat platelet concentrates (n=6) were prepared from volunteer whole blood donations at a blood center using standard methods. A high titer stock (>108 pfu/mL) containing both cell-associated and cell-free human CMV (AD169) was then spiked into each unit. After collection of pre-treatment samples, the CMV-spiked components were divided into 2 bags of equal volumes (2.5–6.0 ×1011 platelets in ∼350 mL of 35% plasma and 65% InterSol™). One platelet unit was treated with INTERCEPT using methods in routine daily use at the blood center; the other unit was leukoreduced by filtration using commercial leukofilters (e.g., Asahi PLX5). Post-treatment samples were then collected. Total DNA prepared from each sample was subjected to nested PCR amplification. Plasma samples were added to confluent MRC5 monolayers, and the cultures were examined daily over the course of 6 weeks for the appearance of viral cytopathic effect. Results: Prior to viral spiking, all 6 pooled BC platelet components were CMV-seronegative and had no detectable CMV by either nested PCR or viral culture. After spiking with CMV, all units had readily detectable CMV DNA by PCR; 5 of the 6 units showed replication-competent virus as determined by CMV culture. INTERCEPT uniformly eliminated amplification of the 2,039 bp fragment of CMV UL93 open reading frame, while CMV DNA could be amplified from some filtered units. Using viral culture as a sensitive indicator of replication-competent CMV, INTERCEPT completely prevented CMV replication in all samples. In contrast, each of the 5 components that displayed infectious CMV after spiking still had detectable replication-competent virus after leukoreduction. Discussion: We found that INTERCEPT treatment could completely inactivate CMV in platelet components treated under standard blood center conditions even when CMV was inoculated into the components at artificially high viral loads (final concentration ∼ 106 pfu/mL). In contrast, leukoreduction was ineffective under these conditions since all inoculated units demonstrated replicating CMV after filtration. These data are consistent with PCR results showing that INTERCEPT also eliminated amplifiable CMV DNA from the platelet components. Thus, INTERCEPT treatment greatly reduces, if not eliminates, the risks of CMV transmission by transfusion, suggesting that INTERCEPT-treated platelets may be optimally CMV safe as compared to leukoreduced units.


2002 ◽  
pp. 313-323
Author(s):  
K. Janetzko ◽  
L. Corash ◽  
L. Lin ◽  
J. Flament ◽  
H. Klüter

Transfusion ◽  
2018 ◽  
Vol 58 (10) ◽  
pp. 2395-2406 ◽  
Author(s):  
Debora Bertaggia Calderara ◽  
David Crettaz ◽  
Alessandro Aliotta ◽  
Stefano Barelli ◽  
Jean-Daniel Tissot ◽  
...  

2003 ◽  
Vol 6 (6) ◽  
pp. 742
Author(s):  
R García de Villaescusa Collazo ◽  
J Barallobre ◽  
U Staginnus

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 2278-2278
Author(s):  
Laurence Corash

Abstract Abstract 2278 Introduction: Pathogen inactivation (PI) of platelet components (PC) with amotosalen and UVA light (INTERCEPT Blood System™, Cerus Europe BV, Amersfoort, Netherlands) has been implemented in routine use in > 100 European blood centers. Active hemovigilance (HV) data were utilized to characterize the adverse event (AE) profile in a broad spectrum of patients with specific focus on respiratory safety. Methods: Two, non-overlapping, HV programs which monitored the response to all transfusion of PC for 24 hours after each transfusion in routine were used to compute the frequencies of allergic reactions, transfusion-associated cardiac overload (TACO), transfusion-related acute lung injury (TRALI), and signs and symptoms of respiratory distress. Data from the Agence National de Securité du Médicament et des Produits de Santé (ANSM, Paris, France) were used to compare the safety of conventional (C) and PI PC for allergic AE, TACO, and TRALI for all patients in France. Data from the Cerus HV program were used to estimate the frequencies of all respiratory signs and symptoms including TRALI and TACO in multiple clinical centers outside of France. In both programs, AE clinical severity was classified as: Grade 1 =non-severe no clinical intervention, Grade 2 = severe requiring intervention, Grade 3 = imminently life threatening, and Grade 4 = death. The relationship of the AE to PC transfusion was classified as: 0 = excluded, 1 = possible, 2 = probable, and 3 = certain. TRALI and TACO were defined using established criteria (Toy et al Blood 119:1757, 2011) in which TRALI and TACO differed only by the presence of left atrial hypertension, or fluid overload, or congestive heart failure. AE of all severity grades and any level of imputed relation were included. Results: Starting in 2009, ANSM specifically identified data for PI-PC and C- PC (Table 1). Using ANSM annual HV reports, data were reviewed for 776,401 C-PC and 66,843 PI-PC transfused. From 2009 to 2011 the use of platelet additive solution (PAS) to decrease the plasma protein content of PC increased from 47.8% to 86.1% of transfused PC, and the proportion of whole blood derived pooled buffy coat PC increased from 28.1% to 48.6%. In parallel with these changes, the frequency of allergic reactions, TACO, and TRALI declined from 2009 to 2011(Table 1). The frequency of TACO and TRALI per 104 PC transfused reported by ANSM was compared for C-PC and PI-PC (Table 2). The frequencies of TRALI and TACO declined from 2009 to 2011 for conventional PC and were very low for PI-PC, although smaller numbers of PI-PC were transfused. A second active HV program (Cerus HV) used a protocol similar to the ANSM protocol specifically to monitor allergic AE and all respiratory AE of all grades, including both signs and symptoms, in 4,067 patients transfused with 19,175 PC in 22 clinical centers (Table 3). In contrast to the ANSM program that included all patients in France, the Cerus HV program was predominantly populated by repeatedly transfused hematology-oncology patients. The number of respiratory AE imputed to PC transfusion was increased compared to the ANSM HV program due to reporting of all respiratory signs and symptoms as AE, but no TRALI or TACO were imputed to transfusion of PI-PC. Conclusions: Two non-overlapping active HV programs were sensitive for detection of allergic and respiratory AE including TRALI and TACO. The increased use of PAS and pooled whole derived PC paralleled a decreased frequency of AE imputed to PC transfusion. Consistent with previous observations (Corash et al Blood 117:1014, 2011) transfusion of PI-PC was not associated with an increased frequency of TRALI or TACO. Disclosures: Corash: Cerus Corporation: Employment, Equity Ownership.


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