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Blood Adv. 2017 October 24; 1(23): 1977–1982.
Published online 2017 October 11. doi:  10.1182/bloodadvances.2017008805
PMCID: PMC5728284

Potential impact of complement regulator deficiencies on hemolytic reactions due to minor ABO-mismatched transfusions

Key Points

  • An in vitro model shows that hemolysis could be due to the presence of a subclinical PNH clone causing a negative C3b/d DAT.
  • Changes to decay-accelerating factor and membrane inhibitor of reactive lysis may lead to overt hemolysis after minor mismatched transfusions.

Abstract

Minor ABO-mismatched transfusions are a common occurrence, although infrequent transfusion reactions occur. We sought to investigate the regulation of complement C3 activation induced by anti-A. In vitro complement C3 activation was observed with 10 of 30 group O samples and correlated with immunoglobulin M (IgM) anti-A titers. We developed an in vitro paroxysmal nocturnal hemoglobinuria (PNH) model of hemolysis in which group A1 red blood cells (RBCs) were chemically treated with 2-aminoethylisothiouronium (AET) to alter regulators of complement C3 activation. Intravascular hemolysis was simulated by incubating an IgG nonhemolytic group O plasma (titer = 32) with A1 RBCs. IgG was detected on the RBCs, but hemolysis was observed with AET-treated RBCs only. When treated and untreated RBCs were tested together (1:4), we determined that the failure to observe C3b/d deposition on RBCs was due to the complete hemolysis of the AET-treated minor RBC population. A group O patient with a 9% CD59-deficient PNH clone was sensitized with an IgM anti-I. Hemolysis, with a weak positive direct antiglobulin test (DAT) resulting from C3b/d, was observed after incubation with fresh AB serum. Flow cytometry showed an 86% reduction of the PNH clone. Our work indicates that the transfusion of minor ABO-mismatched plasma could cause hemolysis with a negative DAT C3b/d. We propose that the presence of a PNH clone is 1 possible cause of unexplained anemia for recipients of ABO-mismatched product. This work suggests that other acquired or inherited defects of decay-accelerating factor and membrane inhibitor of reactive lysis could be responsible for infrequent but clinically important hemolysis after ABO-mismatched transfusions.

Visual Abstract

figure advances008805absf1

Introduction

Minor ABO-mismatched transfusions in United States are an accepted clinical practice.1 Minor ABO mismatches occur when the donor has an ABO isoagglutinin against ABO antigens expressed on the recipient’s red blood cells (RBCs). A summary of recent studies indicate that ~13% of platelet transfusions are minor ABO-mismatched.2 This practice leads to the transfusion of 270 mL of plasma containing ABO isoagglutinins in apheresis platelet products transfused to ABO-incompatible recipients. Changes to hemoglobin levels are associated with minor ABO-mismatched platelet transfusions,3 and clinically significant acute intravascular hemolysis secondary to the transfusion of donor isoagglutinins have been reported despite the use of low titered products.4-6 Hemolysis related to minor ABO-mismatched platelet transfusions has been found to be associated with unfavorable outcomes.7 Such incompatible transfusions are transfused to some surgical patients.8,9 Moreover, alterations to the molecules that regulate complement deposition on RBCs, decay-accelerating factor (DAF, CD55) and membrane inhibitor of reactive lysis (MIRL, CD59), are known to be risk factors for hemolysis. Paroxysmal nocturnal hemoglobinuria (PNH) cells are devoid of surface molecules, DAF, and MIRL, and minor ABO-mismatched transfusions cause hemolytic reactions.10 Several myelopathies are known to be associated with the presence of subclinical PNH.11 Subclinical PNH is a condition in which a subject has a minor clone of PNH cells and has no clinical or laboratory evidence of hemolysis.11 DAF and MIRL express antigens of the Cromer and CD59 blood group systems, respectively, with Cromer Inab representing a null phenotype.12,13 DAF regulates the activity of C3 convertase and MIRL inhibits the formation of membrane attack complex.14 Other disease-related deficiencies in the expression of these molecules could cause increased susceptibility of RBCs to complement-mediated intravascular hemolysis.15

Mitigation strategies to avoid hemolytic reactions are being adopted, including the use of low-titer ABO platelet products and volume reduction to prevent significant hemolysis in the transfusion of minor ABO-mismatched platelet products.16-18 Avoiding high ABO isoagglutinin titers (eg, ≥100) most directly addresses the risk of RBC hemolysis. However, underlying patient-inherited immune factors could lead to transfusion-associated hemolysis, including complement receptor–dependent monocyte/macrophage-mediated phagocytosis or unregulated complement-mediated intravascular hemolysis.19

We sought to explore the effect on the direct antiglobulin test (DAT) and hemolysis associated with deficiencies in the complement regulating surface molecules DAF and MIRL. We developed a PNH-like clonality model to evaluate complement-mediated ABO isoagglutinin-dependent hemolysis.

Methods

Preparation of MIRL-deficient RBCs

Group A1 RBCs and anti-A obtained from group O blood donors were used in the study. For removal of MIRL, 200 µL 6% solution 2-aminoethylisothiouronium (AET; Sigma Aldrich, MO), brought to pH 8.0 using 5N sodium hydroxide was incubated with 200 µL of saline washed packed RBCs for 20 minutes at 37°C water bath. After incubation, cells were saline washed 3 times at 700g for 3 minutes.

Removal of MIRL from the surface of treated RBCs was evaluated by flow cytometry (FACSCalibur, BD Biosciences, CA) using fluorescein isothiocyanate anti-human CD55 (Clone IA10, BD Biosciences) and phycoerythrin (PE) anti-human CD59 (Clone p282 [H19], BD Biosciences) along with appropriate isotype controls. Untreated and unstained group A1 RBCs were used to gate the cells.

Anti-A evaluation of plasma samples

Initially, 30 healthy group O donor plasma samples were evaluated for direct (immunoglobulin M [IgM]) and indirect (IgG) anti-A and were titered by doubling dilution in phosphate-buffered saline (PBS)/6% bovine serum albumin (BSA) using buffered or IgG gel agglutination cards (Ortho Clinical Diagnostics, Pompano Beach, FL), respectively. A standardized grading system was used to score hemagglutination.20

Complement activation of anti–A-sensitized RBCs

To evaluate the ability of anti-A to activate complement, 400 µL of 1:100 diluted group O plasma in PBS/0.2% BSA was combined with 100 µL of 5% group A1 RBCs in PBS/0.2% BSA for 30 minutes at 37°C. A 100-µL aliquot was washed and evaluated for IgG sensitization using a murine monoclonal anti-IgG (γ-clone, Immucor, Norcross, GA). The remaining anti–A-sensitized RBCs were washed and resuspended in 200 µL of fresh AB serum for 60 minutes at 37°C. After incubation, the reaction mix was centrifuged and visually inspected for hemolysis and a red cell pellet. RBCs were washed 4 times with 0.85% saline and evaluated for C3 activation using a murine monoclonal anti-human C3b/d blend (γ-clone, Immucor). Complete hemolysis was assumed when there was no red cell pellet after incubation at 37°C.

Correlation analysis

A correlation analysis was performed between IgM or IgG anti-A titers and complement activation. Pearson’s correlation coefficient (r) was calculated with a 2-tailed P < .05 considered as the cutoff score for significance.

Anti–A-dependent complement C3 activation studies

A single sample with an IgM titer of 16 and an IgG titer of 32 that did not activate complement was selected to evaluate complement activation using untreated RBCs and AET-treated RBCs.

Mixed red cell population studies

An in vitro study was designed using a mixed red cell format meant to mimic the in vivo clinical setting of ABO-mismatched apheresis platelets transfusion to a recipient with a minor population of DAF- and/or MIRL-deficient RBCs. The ratio of anti-A plasma to RBCs was based roughly on the transfusion of 300 mL of plasma from a platelet apheresis product to a recipient with a blood volume of 5000 mL. Thus, IgG sensitization with 400 μL of a 1:100 dilution of plasma mixed with 100 μL of 5% RBCs would approximate the in vivo situation for a recipient with a 45% hematocrit. Two red cell populations were tested: (1) 100% untreated A1 RBCs and (2) 80% untreated A1 RBCs combined with 20% AET-treated RBCs.

Results

Characterization of DAF- and MIRL-deficient RBCs

Flow cytometry showed that MIRL-deficient RBCs were produced. The treated RBCs had overlapping profiles that corresponded to their isotype-specific antibody controls (Figure 1).

Figure 1.
Flow cytometric evaluation of MIRL. The graphs represent fluorescence counts on the y-axis vs channel PE (MIRL) on the x-axis. (A) Untreated group A1 RBCs expressing MIRL, (B) AET-treated group A1 RBCs lost MIRL and have an overlapping profile with the ...

Evaluation of anti-A plasma samples

Thirty blood donor samples were evaluated for their direct (IgM) and indirect (IgG) anti-A titer and the ability to activate complement C3b with group A1 (untreated) RBCs. All plasma samples had direct agglutinating IgM anti-A titers ≤64 and 4 of 30 had IgG titers <100. Of the 30 samples, 10 activated complement as determined by C3b/d deposition using an indirect antiglobulin test with fresh AB serum as a source of complement. Two of the 4 samples with IgG titers <100 failed to activate complement (Table 1). One of the 2 samples with a titer <100 that did not activate complement was chosen for the in vitro experiments (described in “Methods”).

Table 1.
Anti-A characteristics of 30 group O blood donors

Correlation analysis

A positive correlation was observed between IgM titers and complement activation (r = 0.727, P < .0001). There was no correlation observed between IgG titers and complement activation (r = 0.001, P > .05).

Anti–A-dependent complement C3 activation studies

Untreated and AET-treated RBCs were evaluated for anti–A-associated complement C3 activation. No hemolysis was observed with untreated cells, whereas hemolysis was observed with AET-treated RBCs (Table 2). Further, no C3b/d deposition was observed with the untreated cells, which was consistent with the initial evaluation of the lack of complement activation (Table 1). In contrast, microscopic C3b/d deposition was observed for the AET-treated RBCs because few RBCs remained intact to evaluate C3b/d deposition (Table 2).

Table 2.
Anti-A sensitization and complement activation

In vitro mixed RBC population studies

The mixed cell populations were evaluated for anti-A sensitization and complement C3 activation. There was no hemolysis after incubation with AB serum when 20% AET-treated RBCs sensitized with AB plasma were tested; complement C3b/d was not detected on the RBCs. Hemolysis was observed when 20% AET-treated RBCs were incubated with AB serum after sensitization with group O plasma. The remaining RBCs evaluated for complement activation had no evidence of C3b/d deposition, consistent with the remaining untreated RBCs (Table 3).

Table 3.
Mixed-cell complement lysis: simulation study

Evaluation of a patient with PNH

A patient with PNH showing normal CD55 expression and a 9% CD59 deficiency was evaluated using our model. This sample was group O therefore, a low titer (32) IgM anti-I was used at a dilution of 1:4 to sensitize the patient’s RBCs. Afterward, the sensitized red cells were incubated in fresh AB serum. The sample showed an 86% reduction of the CD59-deficient clone (Figure 2), and weak complement C3 activation was observed (Table 3).

Figure 2.
Antibody-mediated lysis of PNH clone. The graphs represent MIRL-positive cells on the y-axis in a PE channel. The x-axis represents a blank fluorescein isothiocyanate channel. A group O RBC sample with a clone of patient PNH RBCs was used for the study. ...

Discussion

We confirmed that DAF and MIRL are important regulators of complement activation on RBCs; removing DAF and MIRL increases RBC susceptibility to complement dysregulation and hemolysis. The effects of chemical treatment on the red cell membranes related to susceptibility to hemolysis are unknown. Treatment with these chemicals did not cause RBCs to lyse on storage nor when incubated with fresh AB serum at a normal physiologic pH, contrary to other treatments.21 Moreover, published studies have shown that AET treatment mimics PNH biochemically, serologically, and by electron microscopy.22-25 We expanded on the current knowledge about the regulation of complement activation by demonstrating low or absent MIRL antigen expression with or without DAF predispose RBCs to hemolysis. Our study showed that a low titer anti-A isoagglutinin, which normally failed to activate complement in vitro with healthy RBCs, can potentially cause significant hemolysis resulting from RBC-related factors. We found a significant positive correlation between the IgM class of anti-A titers and in vitro complement activation and hemolysis. Specifically, we showed that DAF- and/or MIRL-deficient cells result in significant complement activation and hemolysis with a noncomplement-activating anti-A. The in vitro model was supported by using a confirmed PNH sample under similar experimental conditions.

The implication for the clinical setting is that intravascular hemolysis of a minor population of RBCs could go undetected in a DAT. We propose 1 hypothesis to explain DAT-negative hemolysis: an unrecognized (subclinical) PNH clonal disorder. And although PNH is generally uncommon, the frequency of a PNH clone among the various recipient populations is not known. Undiagnosed PNH clones have been observed with a frequency of 15% in DAT-negative hemolytic anemia and 53% in bone marrow failure.26,27 In a previous incidental report, a patient was found to have PNH after a minor ABO-mismatched whole blood transfusion.10 Moreover, DAF expression can vary widely, and in the absence of DAF, MIRL prevents hemolysis to some degree but does not prevent complement C3 activation.12 Complement C3 activation has clinical implications for extravascular hemolysis because it causes increased macrophage-mediated phagocytosis.28

Hemolysis following ABO-mismatched platelet transfusions is uncommon, with a clinical incidence of ~0.01%.16,29 However, it is becoming increasingly clear that persistent hemolysis may be clinically relevant in terms of organ failure, thrombosis, and mortality. Free hemoglobin is deleterious because it can cause multiple organ damage.30 This observation is particularly important because studies have reported association of ABO-mismatched red cell and platelet transfusions with increased morbidity and mortality.31-33 An international survey of red cell transfusions reported that 54% of group O blood is transfused to non–group O recipients.34 Furthermore, patients given multiple ABO nonidentical transfusions of platelets routinely develop IgG-positive direct antiglobulin tests and require increased red cell transfusion needs suggesting low-grade hemolysis.7,33

As for the reported incidence of hemolysis in platelet transfusion, transfusing out-of-group platelets is common because transfusing ABO-matched platelets is not practical for every patient. The incidence and factors predisposing patients to hemolysis from ABO-incompatible platelet transfusions are unknown. Thus, institutions are adopting mitigation strategies to reduce ABO-associated hemolysis for minor ABO-mismatched transfusions of platelet components. Screening donors for a predefined high titered anti-A/anti-B likely reduces the incidence, but to date, there is no consensus on immunoglobulin class or what level constitutes a critical titer.6,35-37 Volume reduction or replacing the plasma with saline may mitigate such minor ABO-mismatched hemolysis but compromise platelet integrity and function.38

Our work suggests that it is prudent to investigate a clinically significant drop in hemoglobin for minor ABO-mismatched recipients of minor ABO-mismatched products who may have a hematologic myelopathy. The transfusion of low antibody titer platelet products is intended to mitigate significant hemolysis. However, our study with a low-titer anti-A indicates that in spite of safe titers of ABO isoagglutinins in platelet product, hemolysis can potentially occur because of patient-related factors. Further, we do not know if small volumes of high(er) titer ABO antibodies in red cell products can cause incidental clinically significant hemolysis. Our study provides 1 potential disease state to evaluate when hemolytic reactions are associated with minor ABO-mismatched transfusions: subclinical PNH. Evaluation of other potential causes of DAF12,13 and MIRL dysregulation15 could be explored because alterations to these molecules may be the root cause of intravascular hemolysis.

Acknowledgments

The authors thank Brian R. Curtis for providing the paroxysmal nocturnal hemoglobinuria sample for analysis.

This work was funded by a research grant to G.A.D. from the Commonwealth Transfusion Foundation (formerly the Virginia Blood Foundation).

Authorship

Contribution: P.P. performed the experiments, analyzed the data, and wrote the manuscript; W.Q.A. edited the manuscript and contributed to the content of the introduction and discussion; J.L.G. contributed to the content of the discussion; G.A.D. conceived the study, developed the model, analyzed the data, and confirmed the final version of the manuscript; and all authors reviewed the final version of the manuscript.

Conflict-of-interest disclosure: The authors declare no competing financial interests.

Correspondence: Gregory A. Denomme, BloodCenter of Wisconsin, 638 N 18th St, PO Box 2178, Milwaukee, WI 53201-2178; e-mail: ude.wcb@emmoned.yrogerg.

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