ISSN: 2469-2778 HTIJ

Hematology & Transfusion International Journal
Research Article
Volume 1 Issue 3 - 2015
Evaluation of Anti-A and Anti-B Alloisogglutinin Titer in Group O Plateletpheresis Donors
Bazigou F1, Lempesopoulos K1, Kavallierou L1*, Cheropoulou A2, Mouratidou M1, Baliaga S2, Koutsogianni K1 and Pagonis S1
1Blood Transfusion Service Amalia Fleming Hospital, Greece
2Blood Transfusion Service Sismanoglio Hospital, General Hospital of Attiki Sismanoglio - Amalia Fleming, Greece
Received: June 24, 2015 | Published: October 24, 2015
*Corresponding author: Lilian Kavallierou, Biopathologist, 20 Koudouriotou str, 15126 Melissia, Athens, Greece, Tel: 210-6139870; Email:
Citation: Bazigou F, Lempesopoulos K, Kavallierou L, Cheropoulou A, Mouratidou M, et al. (2014) Evaluation of Anti-A and Anti-B Alloisogglutinin Titer in Group O Plateletpheresis Donors. Hematology & Transfusion International Journal 1(3): 00017. DOI: 10.15406/htij.2015.01.00017


Platelet (PLT) transfusions need to take into account the issues that arise due to significant amounts of ABO antigen being present on the platelets surface and anti-ABO alloisogglutinins being present in the donor’s plasma. Although relatively rare, acute intravascular haemolytic transfusion reactions (AHTRs) have been caused by passive transfer of anti-A and anti–B antibodies, present in apheresis platelets (APs) of group O donors, across a minor ABO incompatibility (group A, B and AB recipients). To date, improving safety of group O PLT transfusions has focused either on establishing a safe level of alloisogglutinin titer or on reducing the volume of incompatible plasma administered. In this current study we evaluated anti-A and anti-B titers in 70 plasma samples from group O APs donors. Sixty (60) were male donors and ten (10) were female donors. Their age ranged from 20 to 58 years old (mean age: 39.8±1.1). The determination of anti-A and anti-B antibodies, was performed using the method of direct agglutination, specifying IgM antibodies (Gel reagent, Ortho BioVue System). Our results showed that, anti-A titers ranged from 2 to 1024 (mean titer: 64), while anti-B titers ranged from 2 to 256 (mean titer: 32). Anti-A titers were significantly higher than anti-B (p <0.01). The critical value of “high-titer” for anti-A and anti-B antibodies, based on our method and internationally accepted criteria, was defined to be at least 64. The frequency of group O APs donors, with “high-titer” anti-A and anti-B was relatively high, 55.8% and 47.2% respectively. There was no statistically significant difference between the donors, when they were divided into two age groups: over/under 40 years (p> 0.857 and p> 0.861). In conclusion, the risk of haemolysis from ABO-incompatible PLT components, due to passive transfused anti-A and / or anti-B alloisogglutinins, is small but present. Transfusion Service Personnel and Clinicians should be aware of the potential risk and they should always be alert and vigilant when it comes to ABO-incompatible platelet transfusions.

Keywords: Plateletpheresis donors; Platelet transfusion; Alloisogglutinins


DAT: Direct Antiglobulin Test; PPLTs: Post Storage, Pooled Plt Concentrates; HTRs: Haemolytic Reactions; FDA: Food and Drug Administration; CAP: College of American Pathologists; TRALI: Transfusion-Related-Acute-Lung-Injury; PAS: Platelet Additive Solution


Clinicians and Blood Service Personnel are well acquainted and experienced with RBC transfusions and practice using well established policies and strategies. To date, pre-transfusion compatibility tests performed, in Blood Banks, are still based on the interaction between antigen and antibody and subsequent agglutination of red blood cells. Tests that identify the antibody indicate the probable specificity of the antibody, but whether an antibody will destroy red blood cells bearing the corresponding antigen depends on various conditions. Thus, the concept of compatibility encompasses much more than cross matching [1]. Particularly, when it comes to PLT transfusion therapy we are dealing with issues arising from the fact that PLTs contain both significant amounts of ABO antigen on their surface, as well as anti-ABO alloisogglutinins in the donor’s plasma. Although relatively rare, intravascular AHTRs have been caused by ABO antibodies after the transfusion of APs, across a minor ABO incompatibility. Additional adverse effects from ABO-incompatible plasma in PLT components include haemoglobinaemia, jaundice, progressive anaemia, spontaneous coagulation, positive Direct Antiglobulin Test (DAT) and increased osmotic fragility of the patient’s red blood cells [2]. Improving safety of group O PLTs has focused on defining a safe level of antibody titer or by reducing the volume of incompatible plasma administrated. Levels of A and B antibodies appear to be influenced mainly by environmental factors and anti-A and anti-B molecules may be IgM, IgG or IgA. Some sera contain all three classes while non-stimulated individuals are predominantly IgM. Changes in the characteristics of anti-A or anti-B occur as a result of further immunization with pregnancy or by incompatible transfusions. They are serologically detectable through increases in titers, agglutinin avidity and haemolytic activity and have greater activity at 37ºC. Sera from group O people contain two separable antibodies, anti-A and anti-B and a cross reacting antibody called anti-A,B (mostly IgG) [3]. From another point of view the risk of “high-titer” units is considered low with group O, post storage, pooled PLT concentrates (PPLTs). Moreover, the majority of laboratories internationally do not include a method to limit the risk of haemolysis when PLTs containing ABO-incompatible plasma must be transfused [4,5]. On the other hand, various studies report that a potential risk does exist when ABO-incompatible PLT units, containing “high-titer” anti-A and anti-B antibodies, are transfused. The risk is even greater when group O PLT components are transfused out-of group. Titers such as 128-250 are considered critical, [6-9] but not all agree [10-12]. It is necessary to establish a “golden standard” method for the determination of antibody titers in order to be able to differentiate accurately between “high-titer” donors from the other donors. In this current study we tested samples from group O plateletpheresis donors to determine anti-A and anti-B titers by direct agglutination gel method, specifying IgM antibodies.


  1. To evaluate anti-A and anti-B titers in the plasma of group O APs donors
  2. To define a critical value of “high-titer” based on our methodology
  3. To increase the awareness of medical staff on the potential risk of ABO-incompatible PLT transfusions

Materials and Methods

We collected plasma samples (EDTA) from 70 prospective group O APs donors obtained from our Blood Bank Service. 60 were male donors and 10 female donors. Donors ranged between 20 and 58 years of age (mean age: 39.8±1.1). All plasma samples were stored at 2o-8oC and tested, within 3 days from collection, for alloisogglutinin titer. Samples were tested, in parallel, for anti-A and anti-B antibodies by direct agglutination using the manual gel method. Prior to initiating plasma dilutions a screening test was performed, to exclude the presence of any unexpected blood group antibodies using the 0.8% Surgiscreen (Ortho Biovue System). Serial twofold dilutions of plasma were prepared in 0.9% saline using a calibrated pipette. Specifically, 10 μl of 3% commercially prepared A1 and B RBCs (Ortho Biovue System) and 40 μl of neat or diluted plasma were added to buffered gel cards (Reverse Diluent Cassette, Ortho Biovue System), and within half an hour, centrifuged (3400 rpm) for 5 min using the Ortho Biovue System centrifuge. Results were read and recorded immediately after centrifugation. The highest dilution causing agglutination was assumed to represent IgM antibody titers. The result were interpreted as the reciprocal of the highest dilution at which macroscopic agglutination (1+) was observed. Thus, anti-A and anti-B titers were determined and, according to international citations for our methodology, “high-titers” were defined as at least 64. The borderline value necessary for a titer to be characterized as high, depends on the serological method used and it can be adjusted to reflect the protocol of each Blood Bank Service [6-16].

Statistical analysis

 The descriptive statistics method was used for the analysis of the results (anti-A/B titers, age). Due to the small number of females (10/70-14.3%) in the donor population, gender correlations were not attempted. Titers were compared for significance using Pearson’s correlation coefficient on the SPSS statistics computer programme.


A total of 70 samples from group O APs donors were tested for anti-A and anti-B antibody titers. The donors were 20 to 58 years old (mean age: 39.8±1.1). Men were prevalent (60/70-85.7%) in the donor population, females were the minority (10/70-14.3%). The screening test for unexpected blood group antibodies was negative for all samples. Anti-A titers ranged from 2 to 1024 (mean titer: 64), Anti-B titers ranged from 2 to 256 (mean titer: 32). Anti-A titers were significantly higher than anti-B (p<0.01). Based on what is most commonly cited [5,17-24] the critical value for “high-titer” anti-A/B antibodies, for our method (direct agglutinin (IgM) by gel), was defined to be at least 64. The prevalence of group O APs donors with “high-titer” anti-A and anti-B, in our study is relatively high, 55.8% and 47.2% respectively. Table 1 shows the results of anti-A and anti-B titers by direct agglutination (IgM) using the manual gel method. The above results are also demonstrated in Figure 1 and Figure 2 as the relative percentage in the form of histograms. There was no significant difference between donors when they were divided into two age groups: over and under 40 years (p>0.857 and p>0.861), (Table 1 & Figure 1 & 2).

IgM Titers

No of Samples

No of Samples





































Table 1: Anti-A and anti-B titers in O group plateletapheresis donors.

Figure 1: Anti-A1 titers in O group plateletapheresis donors.
Figure 2: Anti-B titers in O group plateletapheresis donors.


PLT transfusions are indicated for the prevention and treatment of hemorrhage in patients with thrombocytopenia or PLT function defects. PLTs may also be administered prophylactically to the thrombocytopenic patient with certain risk factors before undergoing an invasive procedure [22,25]. PLTs express ABO antigens on their surface and PLT components are usually suspended in the original donor plasma [26]. It has been recently reported [27] that a group O PLT donor would have no A or B antigen expression on his or her platelets but anti-A, anti-B and anti-A,B alloisogglutinins in the plasma that, if present in “high-titer”, have the potential to haemolyse the red cells of a non-group O recipient (minor ABO-incompatibility). In ABO “major-incompatibility” PLT transfusions (e.g. O recipient receives A, B or AB PLT product) anti-A/anti-B in the recipient may reduce PLT increment [28]. Approximately 10-40% of patients today in the United States (US) receive plasma incompatible PLT transfusions, but haemolytic reactions (HTRs) remain a rare event [7,29]. These reactions are likely rare due to the dilution of the incompatible ABO antibodies in the recipients plasma volume and/or the neutralization of the anti-A or anti-B antibodies by the recipients soluble or endothelial based A and B antigens [30]. The true incidence of HTRs associated with PLT transfusions is unknown. Estimates range widely from 1:2000-1:46147 [31], but reports of significant haemolysis following such transfusions are well established in the literature [32-34]. Unfortunately, fatal haemolytic episodes have been observed, as in the case of an A Rh D (+) patient transfused with a dry-platelet unit from a group O AP donor [35]. The hemovigilance System in England (SHOT 2006, 2008) has reported that PLTs account for 20% (9/44) of acute HTRs overall [36], and 33% (3/9) of HTRs in children [37]. One particular case concerns a child who received a PLT transfusion from her mother with a fatal outcome [38]. In the US, the frequency of published HTRs due to PLTs, containing ABO-incompatible plasma, is low (25 cases during a 30 year period). However, 6 deaths reported to the US Food and Drug Administration (FDA), in a 10 year retrospective study, were attributed to the use of PLTs with ABO-incompatible plasma. The College of American Pathologists (CAP) Transfusion Medicine Proficiency Testing Survey revealed that 83% of North American lab­oratories have a policy to prevent HTRs from ABO-minor mismatched PLT transfusions [39]. The AABB Standards require that the transfusion service shall have a policy concerning transfusion of components containing significant amounts of incompatible ABO antibodies or unexpected red cell antibodies without providing a definition of what value constitutes a “high-titer” antibody [40]. In one small study, 82% of patients receiving incompatible PLTs developed a positive DAT while none of the patients receiving type identical PLTs developed positivity [41]. Acute HTRs occur typically with transfusion of high titer anti-A to A1 recipients [39]. This problem has been particularly apparent in small children receiving SDPs which contain large volumes of incompatible plasma due to their relatively smaller blood volume [42]. Josephson CD et al. [17] confirms the high prevalence of “high-titer” anti-A or anti-A, B in group O APs donors. Furthermore, Kiefel V [18] notes that usually PLT concentrates from group O donors were implicated in severe HTRs. While most reported cases of HTRs due to incompatible plasma involve group O donors, a recent case report identified a group A, AP donor with a “high-titer” anti-B which caused an HTR in two different group B recipients [13]. The first patient experienced severe back and flank pain with hypertension and chest pain within the first 15 minutes of platelet transfusion while the second patient had a syncopal episode after completing the platelet transfusion. The post-transfusion DATs were both positive and evaluates from both recipients contained anti-B. Further investigation of the donor demonstrated an anti-B titer of 16384 [13]. Thus, clinicians should be aware of the risk of HTR when transfusing large volumes of incompatible ABO PLTs (particularly group O PLT components and particularly to children) to out-of-group recipients. On the other hand, transfusion of only ABO-compatible PLTs is not always feasible due to the limited availability at a time of urgent need, the limited shelf-life of PLTs (5 days), and the fact that group O PLT donors outnumber the other donors. In addition, patients who have developed refractory thrombocytopenia may need HLA-compatible PLTs. Not infrequently, it is difficult to identify donors who are both HLA-compatible and ABO-compatible. Because these patients often require multiple PLT transfusions, some PLT donations collected will be HLA-compatible but not ABO-compatible [20]. Strategies to reduce the risk of PLT associated HTRs include screening donor plasma for “high-titer” antibodies, volume reduction – substitution, washed PLTs and setting a maximum volume of incompatible plasma to be transfused to a patient in a defined period of time. Various methods of determining titers include tube saline agglutination with or without indirect antiglobulin testing, micro-column agglutination, automated microplate technology and in vitro haemolysis assays. Critical titers, depending on the method used, include the following: greater than 1:16 for in vitro haemolysis assays, greater than 1:64 to 1:100 for immunoglobulin IgM, and greater than 1:256 to 1:400 for IgG [21]. However, there is a lack of agreement as to what titer is clinically relevant and whether IgM or IgG antibody is more significant [17,31,39]. In Greece, the policy regarding the use of ABO-incompatible PLTs is determined by the medical director of each transfusion facility. It is generally agreed that children, neonates and regularly transfused patients should receive only ABO-compatible PLT components. This proposal is not only adopted by the Hellenic Coordinating Haemovigilance Centre (SKAE) but it is also recom­mended as follows: male-only plasma transfusion implementation for preventing transfusion-related-acute-lung-injury (TRALI) and ABO-compatible PLT transfusions for preventing HTRs [43,44]. Until today, 2 cases of HTRS from ABO-incompatible PLT transfusions have been reported to the SKAE. One of the cases was attributed to the transfusion of group O SDPs to a group A recipient [43,44]. The guidelines for the Blood Transfusion Services in the United Kingdom [23] state that “each Blood Establishment should have a testing and issuing policy to avoid the use of “high-titer” anti-A and/or anti-B in instances where a significant adverse clinical reaction is likely”. It is recommended that a saline agglutination test should give a negative result of a dilution of 1:128 or an equivalent dilution by other techniques. All components (RBCs, PLTs and FFP) of all ABO groups, which are found to be negative for “high-titer”, anti A, B are labeled as “NEG: HT''. This includes pooled PLTs if all constituent donations are negative. Currently procedures now identify approximately 10% of all donations as “high-titer''. The specification for neonatal components include the requirement for donations to be high-titer anti A, B negative [23]. All components labeled as “suitable for neonatal use'' are therefore negative for high-titer anti A, B. After adopting this national uniform approach only eight cases of possible haemolysis in the UK reported to SHOT during an eight year period [45]. Quillen et al. [9] has proposed a critical titer of 250 by gel, which classified 25% of group O PLTs as high-titer. Quillen et al. [9] note that since starting a universal screening, they have not had a single haemolytic transfusion reaction to a PLT product, and they note that they had an incidence of 1 in 2460 prior to implementing universal screening. In another equivalent review, Cooling et al. [5] propose a critical titer of 128-200 by gel. Of course, other factors in addition to the anti-A and anti-B titer are believed to contribute to the associated risk of haemolysis. Studies have shown that documented HTRs have occurred from plasma incompatible PLT transfusions with antibody titers considered to be low (<64) [46-47]. As such, Fauzie et al. [47] reported two HTRs, one of the HTRs occurred in a patient who received 390 ml of group O APs with an anti-A titer of only 32 and severe back pain was the only transfusion symptom reported by this patient. In contrast, the other patient had cyanosis, dyspnea and haemoglobinurea after receiving 598 ml of group O APs with an anti-A titer of 256/512 (IgM/IgG). Another variable is the amount of volume of incompatible plasma transfused. This varies according to the PLT product transfused. Each random-donor PLT unit contains at least 5.5 x 1010 PLTs and contains 50 to 60 ml of donor plasma [48]. Therefore, a typical dose of 5 pooled random PLT units contain at least 2.8 x 1011 PLTs and 250 to 300 ml of plasma. Similarly, an AP product contains 2.5 x 1011 PLTs or more and 200 to 400 ml of plasma. If that single AP donor has a high antibody titer, then subsequent haemolysis may be a concern. However, the pooling of multiple random-donor PLT units should dilute out any antibodies present in the plasma of a single “high-titer'' random donor. Therefore, pooled random donor PLT products generally carry a lower risk of haemolysis [49].

In the above study, analysis of the common characteristics of adults with HTRs, after PLT transfusions pinpoints

  1. Patients repeatedly transfused with incompatible PLT products over days or weeks, and
  2. Those receiving multiple PLT transfusions in a short period of time [49].

Children and neonates are theoretically at a higher risk of hemolysis due to a smaller blood volume [50]. Specifically, premature infants and neonatal patients that require PLT transfusions may develop circulatory overload when administered a 50 ml unit of PLT concentrate. The above study also evaluated the influence of centrifugation and resuspension (steps used to reduce the volume of stored PLT concentrates) on PLT properties by in vitro methods and by determining post-transfusion increments in neonatal patients. PLT morphology, mean PLT volume, hypotonic stress response, synergistic aggregation, and PLT factor 3 activities were not affected by the processing steps. The centrifugation and resuspension steps did not cause an enhanced discharge of lactate dehydrogenase from PLTs. These results indicate that the volume of stored PLT concentrates can be reduced in a manner which maintains PLT properties [49]. Others, tried to determine the best procedure for concentrating PLTs in a smaller volume after storage, they studied PLT loss after concentration at various centrifugation g forces for various times.

Their results showed that

  1. Minimizing the amount of incompatible plasma transfused can result in PLT loss and increase the number of PLTs transfused as much as 50% and
  2. Numbers and viability of PLTs stored up to 5 days in 50 ml plasma and then concentrated in 10 ml plasma after centrifugation at 1500 X g for 7 minutes, 2000 X g for 10 minutes or 5000 X g for 6 minutes should be clinically acceptable [51].

Additionally, plasma reduction requires trained personnel, specialized equipment and time. Controversially, Cid J et al. [27] remarks that PLT manipulation results in activation after centrifugation. Romphruk AV et al. [20] demonstrated that volume reducing group O APs followed by resuspension in group AB plasma reduced the anti-A and anti-B titers to <8 thereby creating a universal donor. Karafin MS et al. [31] managed to lower the risk of HTRs in adults, by limiting the volume of transfused plasma incompatible apheresis products to 600 cc in a 24 hour period. It has been recently shown that PLTs stored in platelet additive solution (PAS) are effective and reduce adverse events associated with PLT transfusion [52-54]. As PAS effectively reduces the plasma from a PLT product, it may also reduce the incidence of haemolysis due to incompatible plasma. It is not yet known whether PAS PLTs will be a cost-effective strategy for the reduction of HTRs. The vital question, as expressed in the study of Daniel-Johnson J et al. [19] is when an AP donor can be considered “safe”. The decision to screen all PLT donors regardless of historical information was based on the concern that some donors may develop higher-titers over time, with pregnancies, immunizations, or ingestion of live bacteria such as those in certain yogurt products and pro-biotic formulations. Also, some donors who were classified as below the cut-off on one donation were classified as “high-titer” on subsequent donations. In order to increase the awareness of medical staff regarding the potential risk of HTRs, when ABO-incompatible PLT products are transfused, the following key messages and recommendations are stated below. These emerge from the previously cited studies [9,13,18,23,31,42]. The risk of HTRs from ABO-incompatible PLT transfusions is due to passive high-titer anti-A and/or anti-B from the donor's plasma. HTRs are typically attributed to transfusions of high-titer anti-A to A1 recipients. Infants and small children may be at greater risk. Incompatible SDPs represent greater risk than random PLTs, if ABO antibody titers are high. Titers change overtime so, a single screening of a donor is not safe. Transfusions of ABO-identical PLTs are preferred if possible. HLA/HPA compatibility is preferred over ABO compatibility when HLA class-I and HPA antibodies exist. Incompatible ABO-PLT transfusions to neonates/children are to be avoided. Transfusing group O PLTs to non group O recipients should be avoided. Use of group A PLTs for group B patients and vice versa is preferred. All PLT units (especially group O SDPs) need to be screened for a cut-off dilution (e.g. saline agglutination negative dilution of 1:128). Units need to be labeled accordingly. PLT components with high-titers anti-A/B must be transfused to ABO-identical recipients or group O recipients. If there is a significant concern about infusing incompatible plasma, volume-reduced, volume substituted, washed PLTs or additive solution PLTs may be considered. Do not transfuse to a patient more than 600 ml of incompatible plasma per day. Clinicians must be aware of the risk of HTRs from ABO-incompatible PLT transfusions, they must observe patients and report accordingly


The risk of haemolysis, from ABO-incompatible PLT components transfusions, due to passively transfused anti-A and/or anti-B alloisogglutinins is small but present. Transfusion Service Personnel and Clinicians should be aware of the potential risk and they need to always be alert and vigilant. The critical value for “high-titer” anti-A/B antibodies, per our method, was defined to be at least 64. Data from our study show that group O AP donors have significantly high-titers of anti-A and anti-B antibodies, 55.8% and 47.2% respectively. Lack of standardization of performing titers and lack of international consensus on what constitutes a critical titer is still an issue.


  1. Malomgre W, Neumeister B (2009) Recent and future trends in blood group typing. Anal Bioanal Chem 393(5): 1443-1451.
  2. Klein HG, Anstee DJ (2005) Mollison's blood transfusion in clinical medicine. (11th edn), Red cell incompatibility in vivo (Chapter 10), Blackwell Publishing, Oxford, UK, pp. 406-454.  
  3. Daniels G (2002) Human blood groups. (2nd edn), Blackwell Publishing, Oxford, UK.
  4. Mazda T, Yabe R, NaThalang O, Thammavong T, Tadokoro K (2007) Differences in ABO antibody among blood donors: a comparison between past and present Japanese, Laotian and Thai populations. Immunohematology 23(1): 38-41.
  5. Cooling LL, Downs TA, Butch SH, Davenport RD (2008) Anti-A and anti- B titers in pooled platelets are comparable to apheresis platelets. Transfusion 48(10): 2106-2113.
  6.  Dunbar NM, Ornstein DL, Dumont LJ (2012) ABO incompatible platelets: risks versus benefit. Curr Opin Hematol 19(6): 475-479.
  7.  Josephson CD, Castillejo MI, Grima K, Hillyer CD (2010) ABO-mismatched platelet transfusions: strategies to mitigate patient exposure to naturally occurring hemolytic antibodies. Transfus Apher Sci 42(1): 83-88.
  8.  Shehata N, Tinmouth A, Naglie G, Freedman J, Wilson K (2009) ABO identical versus non identical platelet transfusion: a systematic review. Transfusion 49(11): 2442-2453.
  9.  Quillen K, Sheldon SL, Daniel-Johnson JA, Lee-Stroka AH, Flegel WA (2011) A practical strategy to reduce the risk of passive hemolysis by screening plateletpheresis donors for high-titer ABO antibodies. Transfusion 51(1): 92-96.
  10. de França ND, Poli MC, Ramos PG, Borsoi CS, Colella R (2011) Titers of ABO antibodies in group O blood donors. Rev Bras Hematol Hemoter 33(4): 259-262.
  11.  Kumlien G, Wilpert J, Säfwenberg J, Tydén G (2007) Comparing the tube and gel techniques for ABO antibody titration, as performed in three European centers. Transplantation 84 (12 Suppl): S17-S19.
  12.  Tanabe K (2007) Interinstitutional variation in the measurement of anti- A/B antibodies: the Japanese ABO-Incompatible Transplantation Committee Survey. Transplantation 84 (12 Suppl): S13-S16.
  13.  Johnson DJ, Leitman S, Klein H, Alter H, Stroka AL, Scheinberg P, et al. (2009) Probiotic-associated high- titer anti-B in a group A platelet donor as a cause of severe hemolytic transfusion reactions. Transfusion 49(9): 1845-1849.
  14. Rieben R, Buchs JP, Flückiger E, Nydegger UE (1991) Antibodies to histo-blood group substances A and B: agglutination titers, Ig class, and IgG subclasses in healthy persons of different age categories. Transfusion 31(7): 607-615.
  15.  Reisner RK, Gauthier CM, Williamson KR, Moore SB (1993) Comparison of patient ABO/Rh/K typing by a column agglutination system and conventional tube methods. Transfusion 33: Suppl 18S.
  16. Pothiwala M, Musa G, Siwa C (1993) Concordance of column agglutination technique to routine tube technique. Transfusion 33(9): Suppl 18S.
  17. Josephson CD, Mullis NC, Van Demark C, Hillyer CD (2004) Significant numbers of apheresis-derived group O platelet units have “high titer” anti-A/A,B: implications for transfusion policy. Transfusion 44(6): 805-808.
  18. Kiefel V (2008) Reactions induced by platelet Transfusions. Transfus Med Hemother 35(5): 354-358.
  19. Sadani DT, Urbaniak SJ, Bruce M, Tighe JE (2006) Repeat ABO-incompatible platelet transfusions leading to hemolytic transfusion reaction. Transfus Med 16(5): 375-379.
  20. Romphruk AV, Cheunta S, Pakoate L, Kumpeera P, Sripara P, et al. (2012) Preparation of single donor platelet with low antibody titers for all patients Transfusion and Apheresis Science 46(2): 125-128.
  21. Pietersz RNI, Engelfriet CP, Reesink HW (2005) International Forum. Transfusion of apheresis platelets and ABO groups. Vox Sang 88(3): 207-221.
  22. Hellenic Haematology Association (2010) Blood Transfusion and Apheresis Section. Guidelines for the Blood and Platelet Transfusion p. 27-38.
  23. Joint UKBTS/NIBSC Professional Advisory Committee (2005) Guidelines for the Blood Transfusion Services in the United Kingdom (7th edn), TSO, Norwich, UK.
  24. Crookston MC (1980) Blood group antigens acquired from the plasma. In: SandIer SG, et al. (Eds), lmmunobiology of the Erythrocyte. AR. Liss, New York, USA, p. 99.
  25. (2003)Guidelines for the use of platelet transfusions. Br J Haematol 122(1): 10-23.
  26. Dunstan RA, Simpson MB, Knowls RW, Rosse WF (1985) The origin of ABH antigens on human platelets. Blood 65(3): 615-619.
  27. Cid J, Harm SK, Yazer MH (2013) Platelet Transfusion- the Art and Science of Compromise. Transfus Med Hemother 40(3): 160-171.
  28. Aster RH (1965) Effect of anticoagulant and ABO incompatibility on recovery of transfused human platelets. Blood 26(6): 732-743.
  29.  McLeod BC, Sassetti RJ, Weens JH, Vaithianathan T (1982) Haemolytic transfusion reaction due to ABO incompatible plasma in a platelet concentrate. Scand J Haematol 28(3): 193-196.
  30. Garratty G (1998) Problems associated with passively transfused blood group alloantibodies. Am J Clin Pathol 109(6): 769-777.
  31. Karafin MS, Blagg L, Tobian AA, King KE, Ness PM, Savage WJ (2012) ABO antibody titers are not predictive of hemolytic reactions due to plasma-incompatible platelet transfusions. Transfusion 52(10): 2087-2093.
  32. Mc Manigal S, Sims KL (1999) Intravascular hemolysis secondary to ABO incompatible platelet products. Am J Clin Pathol 111(2): 202-206.
  33. Gresens C, Gloster E, Wang L, Dimaio T (2003) Acute hemolysis in a group A trauma patients who received a group O plateletapheresis unit. Transfusion 43(suppl): 111A.
  34. Sapatnekar S, Sharma G, Downes KA, Wiersma S, Mc Grath C, et al. (2005) Acute hemolytic transfusion in a pediatric patient following transfusion of apheresis platelets. J Clin Apheresis 20(4): 225-229.
  35. Valbonesi M, De Luigi MC, Lercari G, Florio G, Bruni R, et al (2000) Acute intravascular hemolysis in two patients transfused with dry-platelet units obtained from the same ABO incompatible donor. Int J Artif Organs 23(9): 642-646.
  36. Stainsby D, Jones H, Asher D, Atterbury C, Boncinelli A, et al. (2006) Serious hazards of transfusion: a decade of hemovigilance in the UK. Transf Med Rev 20(4): 273-282.
  37. Stainsby D, Jones H, Wells AW, Gibson B, Cohen H, et al. (2008) Adverse outcomes of blood transfusion in children: analysis of UK reports to the serious hazards of transfusion scheme 1996-2005. Brit J Haematol 141(1): 73-79.
  38. Pierce RN, Reich LM, Mayer K (1985) Hemolysis following platelet transfusions from ABO-incompatible donors. Transfusion 25(1): 60-62.
  39. Fung MK, Downes KA, Shulman IA (2007) Transfusion of platelets containing ABO-incompatible plasma: a survey of 3156 North American laboratories. Arch Pathol Lab Med 131(6): 909-916.
  40. Price T (2009) Standards for blood Banks and Transfusion Services. (26th edn), AABB, Bethesda, USA.
  41. Shanwell A, Ringden O, Wiechel B, Rumin S, Akerblom O (1991) A study of the effect of ABO incompatible plasma in platelet concentrated transfused to bone marrow transplant recipients. Vox Sang 60(1): 23-27.
  42. Win N (2011) High titre Anti-A/B testing donors within NHS Blood and Transplant (NHSBT) INF 178/1.1 Effective: 10/08/11.
  43. Summary Report of Coordinating Haemovigilance Centre SKAE, Hellenic Centre of Diseases Control and Prevention KEELPNO (2008) Epidemiological Surveillance of Transfusion Transmitted Infections (1996-2007), Surveillance of adverse reactions and adverse events associated with blood transfusion (1997-2007), Surveillance of adverse reactions and adverse events during or after donation (2003-2007). p. 1-40.
  44. Summary Report of Coordinating Haemovigilance Centre SKAE, Hellenic Centre of Diseases Control and Prevention KEELPNO (2012) Epidemiological Surveillance of Transfusion Transmitted Infections (1996-2011), Surveillance of adverse reactions and adverse events associated with blood transfusion (1997-2011), Surveillance of adverse reactions and adverse events during or after donation (2003-2011). p. 17-22.
  45. Guidelines for the use of platelet transfusions. (2003)Br J Haematol 122(1): 10-23.
  46. Conway LT, Scott EP (1984) Acute hemolytic transfusion reaction due to ABO incompatible plasma in a plateletpheresis concentrate. Transfusion 24(5): 413-414.
  47. Fauzie D, Shirey RS, Thoman S, Bensen-Kennedy D, King KE (2004) The risk of hemolytic transfusion reactions due to passively-acquired ABO antibodies: a retrospective study of non-group O adult recipients of group O plateletpheresis transfusions. Transfusion 44 (Suppl): 36A.
  48. Silva MA (2004) Standards for Blood Banks and transfusion Services. (23rd edn), AABB Press, Bethesda MD, USA.
  49. Holland L (2006) Role of ABO and Rh Type in platelet trasfusion. Lab Medicine 37(12): 758-760.
  50. Moroff G, Friedman, Robkin-Kline L, Gautier G, Luban NL (1984) Reduction of the volume of stored platelet concentrates for the use in neonatal patients. Transfusion 24(2): 144-146.
  51. Simon TL, Sierra ER (1984) Concentration of platelet units into small volumes. Transfusion 24(2): 173-175.
  52. de Wildt-Eggen J, Nauta S, Schrijver JG, van Marwijk Kooy M, Bins M, van Prooijen HC (2000) Reactions and platelet increments after transfusion of platelet concentrates in plasma or an additive solution: a prospective, randomized study. Transfusion 40(4): 398-403.
  53. Azuma H, Hirayama J, Akino M, Miura R, Kiyama Y, et al. (2009) Reduction in adverse reactions to platelets by removal of plasma supernatant and resuspension in a new additive solution (M-sol). Transfusion 49(2): 214-218.
  54. Kerkhoffs JL, Einkenboom JC, Schipperus MS, van Wordragen-Vlaswinkel RJ, Brand R, et al. (2006) A multicenter randomized study of the efficacy of transfusion with platelets stored in platelet additive solution II versus plasma. Blood 108: 3210-3215.
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