Metabolomics study of platelet concentrates photochemically treated with amotosalen and UVA light for pathogen inactivation

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


2001 ◽  
Vol 20 (10) ◽  
pp. 533-550 ◽  
Author(s):  
V Ciaravino ◽  
T McCullough ◽  
A D Dayan

The pathogen inactivation process developed by Cerus and Baxter Healthcare Corporations uses the psoralen, S-59 (amotosalen) in an ex vivo photochemical treatment (PCT) process to inactivate viruses, bacteria, protozoans, and leukocytes in platelet concentrates and plasma. Studies were performed by intravenous infusion of S-59 PCT formulations-compound adsorption device (CAD) treatment and with non-UVA illuminated S-59, using doses that were multiples of potential clinical exposures. The studies comprised full pharmacokinetic, single and repeated-dose (up to 13 weeks duration) toxicity, safety pharmacology (CNS, renal, and cardiovascular), reproductive toxicity, genotoxicity, carcinogenicity testing in the p53- mouse, vein irritation, and phototoxicity. No specific target organ toxicity (clinical or histopathological), reproductive toxicity, or carcinogenicity was observed. S-59 and/or PCT formulations demonstrated CNS, ECG, and phototoxicity only at supraclinical doses. Based on the extremely large safety margins (>30,000 fold expected clinical exposures), the CNS and ECG observations are not considered to have any toxicological relevance. Additionally, after a complete assessment, mutagenicity and phototoxicity results are not considered relevant for the proposed use of INTERCEPT platelets. Thus, the results of an extensive series of in vitro and in vivo studies have not demonstrated any toxicologically relevant effects of platelet concentrates prepared by the INTERCEPT system.


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.


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