Pathogen inactivation of double-dose buffy-coat platelet concentrates photochemically treated with amotosalen and UVA light: preservation ofin vitrofunction

Vox Sanguinis ◽  
2014 ◽  
Vol 108 (4) ◽  
pp. 340-349 ◽  
Author(s):  
P. Sandgren ◽  
B. Diedrich
Transfusion ◽  
2018 ◽  
Vol 58 (10) ◽  
pp. 2395-2406 ◽  
Author(s):  
Debora Bertaggia Calderara ◽  
David Crettaz ◽  
Alessandro Aliotta ◽  
Stefano Barelli ◽  
Jean-Daniel Tissot ◽  
...  

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.


2011 ◽  
Vol 68 (6) ◽  
pp. 489-494 ◽  
Author(s):  
Zoran Stanojkovic ◽  
Ana Antic ◽  
Miodrag Stojanovic

Background/Aim. Pathogen inactivation in blood and blood products is one of the major means to achieve a zero risk blood supply and improve transfusion safety. Riboflavin (vitamin B2) activated by ultraviolet (UV) light, produces active oxygen which damages cell membrane and prevents replication of the carrier of diseases (viruses, bacteria, protozoa) in all blood products. The aim of this study was to establish the influence of the process of pathogens photoinactivation using riboflavin and UV rays on the biochemical and functional characteristics of platelet concentrates prepared from ?buffy coat?. Methods. The examination included 80 platelet concentrates prepared from ?buffy coat?, which was separated from whole blood donated by voluntary blood donors around 6 hours from the moment of collection. Concentrates were pooled, filtered and separated unton two groups: one consisted of 10 control units and the other of 10 examined units (pooled platelet concentrates). Examined units of the platelets were treated by riboflavin (35 mL) and UV rays (6.24 J/mL, 265-370 nm) on Mirasol aparature (Caridian BCT Biotechnologies, USA) in approximate duration of 6 min. A total of 35 mL of saline solution was added to the control units. The samples for examining were taken from the control and examined units initially (K0, I0), after the addition of saline (K1) and riboflavin (I1), after illumination (I2), first day of storage (K3, I3) and the fifth day of storage (K4, I4). The following parameters were measured: platelet count and platelet yield, residual erythrocyte and leukocyte count, pH, pO2, pCO2 and bacterial contamination. Results. All the measured parameters showed a statistically significant decrease comparing to K0 and I0; all the results of the first day of platelet storage showed statistically significant decrease comparing to K1 and I1, and all the results of the fifth day of platelet storage (K4, I4) showed a statistically significant decrease comparing to K1 and K3 and to I1 and I3. There was no the mentioned difference in the measured parameters between K4 and I4 (the end of storage - the fifth day). All the platelet units were sterile till the seventh day, when the investigation ended. Conclusion. Platelet concentrates inactivated by riboflavin and UV rays (Mirasol PRT sistem, Caridian BCT, USA) keep all the characteristics assessed by the Guide to the preparation, use and quality assurance of blood components (Council of Europe), during the whole storage period (five days). The obtained data were correlated with existing up to date literature and demonstrated that Mirasol treated platelets were safe and could be incorporated effectively in the routine blood bank and transfusion setting.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 941-941 ◽  
Author(s):  
Laurence Corash ◽  
Fabrice Cognasse ◽  
Jean-Claude Osselaer ◽  
Natalie Messe ◽  
Olivier Garraud

Abstract Background. Platelets (plt) prepared for transfusion contain multiple molecules that modulate immune function, mediate acute transfusion reactions, induce immune responses, and affect hemostasis. These cytokines/chemokines are secreted differentially from plt during storage (Transfusion2006;46:1184), and may be affected by processing, including pathogen inactivation. Aims. The INTERCEPT Blood System (IBS) for platelets utilizes amotosalen-HCl (S-59) with ultraviolet A (UVA) light to inactivate a broad spectrum of pathogens and leukocytes. This study was designed to evaluate the effects of photochemical treatment on in vitro release of immune modulation molecules after processing during 7 days (d) of storage. Methods. Platelet concentrates (n = 10) collected by aphaeresis (CPA) with process leuko-reduction (< 106) containing 8.15x1011 ± 0.8 platelets were suspended in 35% donor plasma and 65% platelet additive solution (Intersol, Baxter, France) and divided into two equal components. One served as an untreated control (C) and the other was prepared with 150 uM amotosalen and a 3 J/cm2 UVA photochemical treatment (PCT) and stored at 22°C with shaking for 7 days. Platelet concentration (106/uL), pH and levels of immune modulation factors were measured: CD62p(ng/mL), PDGF-AB(ng/mL), IL8(pg/mL), sCD40L(pg/mL), IL1β(pg/mL) and TNFα(pg/mL). The concentration of each factor was determined by specific enzyme linked immunosorbent assays in plt and supernatant (s) fractions isolated from stored PCT and C plt components. Mean values ± SD were calculated and compared by paired t-test. Results. Platelet content, pH and cytokine/chemokine content and release from CPA prepared with photochemical treatment were not statistically different (p > 0.05) from C during 7 d of storage (Table). From d1 to d7, the pH of PCT and C units decreased similarly, but remained within acceptable ranges. No detectable IL1β and TNFα were observed in PCT or C CPA. During platelet storage CD62p, PDGF-AB, IL8, and sCD40L increased similarly in supernatants of PCT and C units. The increase in supernatant levels correlated with a decrease of these cytokines in plt. Platelets in PCT and C retained measurable levels of CD62, IL8, sCD40L and PDGF-AB though 7 d. Levels of sCD40L demonstrated marked variation. Conclusions. Cytokines increased moderately in the supernatants of CPA and decreased in platelets during storage. After 7 d C and PCT platelets in CPA retained detectable levels of cytokines. PCT had no differential influence on release of immune modulation molecules in vitro over 7 d of storage. Day O O 5 5 7 7 Product C PCT C PCT C PCT pH 7.1 ±.1 7.1 ±.1 6.9 ±.1 6.8 ±.1 6.9 ±.1 6.8 ±.1 Plt ct 1.29 ±.3 1.30 ±.2 1.30 ±.3 1.19 ±.2 1.27 ±.2 1.18 ±.2 CD62p-s 89 ± 21 87 ± 17 110 ± 23 115 ± 27 117 ± 22 119 ± 25 CD62p-plt 149 ± 33 151 ± 33 141 ± 23 141 ± 25 139 ± 25 139 ± 26 PDGF-s 14.5 ± 3.5 13.6 ± 3.5 17.7 ± 2.4 15.8 ± 1.5 18.0 ± 2.1 17.5 ± 1.8 PDGF-plt 28.3 ± 3.5 30.3 ± 3.1 25.2 ± 3.6 24.9 ± 2.5 23.2 ± 4.0 23.3 ± 3.3 IL8-s 107 ± 17 108 ± 14 136 ± 42 116 ± 9 123 ± 20 120 ± 22 IL8-plt 135 ± 29 134 ± 28 110 ± 11 117 ± 12 103 ± 17 119 ± 32 CD40L-s 51 ± 86 66 ± 94 172 ± 157 237 ± 214 188 ± 198 201 ± 167 CD40L-plt 990 ± 805 1098 ± 747 485 ± 373 474 ± 331 346 ± 293 314 ± 282


Transfusion ◽  
2019 ◽  
Vol 60 (2) ◽  
pp. 367-377
Author(s):  
Freyr Jóhannsson ◽  
Níels Á. Árnason ◽  
Ragna Landrö ◽  
Sveinn Guðmundsson ◽  
Ólafur E. Sigurjonsson ◽  
...  

Transfusion ◽  
2018 ◽  
Vol 58 (11) ◽  
pp. 2657-2668 ◽  
Author(s):  
Stephan Meinke ◽  
Agneta Wikman ◽  
Gunilla Gryfelt ◽  
Kjell Hultenby ◽  
Michael Uhlin ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document