Hemolysis, free hemoglobin toxicity, and scavenger protein therapeutics

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Abstract

During hemolysis, erythrophagocytes dispose damaged red blood cells. This prevents the extracellular release of hemoglobin, detoxifies heme, and recycles iron in a linked metabolic pathway. Complementary to this process, haptoglobin and hemopexin scavenge and shuttle the red blood cell toxins hemoglobin and heme to cellular clearance. Pathological hemolysis outpaces macrophage capacity and scavenger synthesis across a diversity of diseases. This imbalance leads to hemoglobin-driven disease progression. To meet a void in treatment options, scavenger protein-based therapeutics are in clinical development.

Introduction

An efficient clearance system comprising macrophages and scavenger proteins maintains homeostasis within the red blood cell (RBC) compartment,¹ by capturing aged and damaged RBCs, shuttling heme-iron to erythropoiesis, and preventing the adverse effects of cell-free hemoglobin (Hb) and heme. Several diseases are characterized by the excessive turnover of RBCs (ie, hemolysis), either as the primary etiology in genetic hemoglobinopathies, membranopathies, and enzyme defects, or as an acquired characteristic associated with blood transfusions, infections, autoimmune diseases, and mechanical stresses.^2,3 RBC lysis in hemolytic anemia may occur not only in circulating peripheral blood, the spleen, or liver, but also within closed compartments after vascular rupture and hematoma formation. Aberrant functioning of RBC membranes in all these conditions results in exposure of the body’s internal milieu to harmful erythrocyte contents, including Hb, arginase,⁴ urate,⁵ and RBC-derived microparticles.^{6, 7, 8} The largest body of evidence exists on the toxicities of cell-free Hb and heme, on which we focus in this review. The capacity of the RBC-Hb-heme clearance system defines the threshold at which hemolysis deviates from a physiological normal RBC turnover process into a disease amplifier. This article delineates the pathophysiological processes induced by cell-free Hb and heme. It further discusses toxicity control by macrophages, haptoglobin, and hemopexin and potential exploitation of these protective features for the development of novel therapeutics.

Pathophysiology of cell-free Hb toxicity

Progression of Hb-induced disease entails persistent RBC rupture, shifting of the dynamic equilibrium of Hb from tetramerization to dimerization, followed by translocation of small Hb dimers (32 kDa) across tissue barriers, such as the vascular endothelium, renal glomeruli, and the ependymal epithelium separating the ventricular cerebral spinal fluid (CSF) space from the brain parenchyma. The pathophysiological outcome of this cascade is the toxic accumulation of Hb and its by-products close to functionally critical parenchymal tissue. Ultimately, the detrimental effects of hemolysis can be traced back to Hb-catalyzed oxidative reactions and heme-ligation of cellular signaling molecules. This concept has been most extensively studied in the vasculature, kidneys, immune system, and subarachnoidal compartments.

Translocation of cell-free Hb from blood across endothelial barriers causes accumulation within interstitial spaces that surround vascular smooth muscle cells.⁹ Subsequent reactions between endothelium-derived nitric oxide (NO) and Hb cause vasoconstriction, aberrant hemodynamics,^10,11 and chronic manifestations of endothelial dysfunction.^9,12 Dioxygenation of oxy-Hb (HbFe(II)O₂) initiates a sequence of NO-consumptive reactions progressing to (HbFe(III)NO⁺) and (HbFe(II)NO), which indicates that low quantities of interstitial Hb may cause substantial loss of autacoid-mediated vascular tone regulation.^13,14

In blood, the majority of cell-free Hb remains in the reduced Fe(II)O₂ state, capable of reactions with NO.¹⁵ However, in conditions with enhanced oxidative stress, Hb reactions initiated by autoxidation and endogenous peroxides can lead to higher heme iron oxidation states (Fe(III), Fe(IV), Fe(IV)=O₂), redox cycling, and generation of Hb degradation and crosslinking products with cytotoxic and inflammatory activities.^{16, 17, 18} Furthermore, HbFe(III) oxidation destabilizes the heme-globin association,¹⁹ favoring heme partitioning into lipid compartments, such as cell membranes and lipoproteins. In these compartments, heme initiates peroxidative chain reactions that contribute to hemolysis-induced cytotoxicity and tissue injury and the generation of proinflammatory by-products.^{20, 21, 22, 23, 24} These reactions cumulatively leave traceable oxidative biomarker signatures in animals²⁵ and humans,^{26, 27, 28} which provide information regarding the extent and duration of cell-free Hb exposure.

Cell-free Hb from high-intensity hemolysis is primarily eliminated from blood by renal clearance. Therefore, the kidney is the most heavily exposed organ during intravascular hemolysis. Postfiltration, the progressive acidification of the urine accelerates Hb-oxidation, globin structural destabilization, and heme release.²² This explains why most observations related to oxidation-driven Hb toxicity have been reported in the context of hemoglobinuria-induced kidney injury.^{29, 30, 31} In addition, because of direct exposure to RBC toxins, vascular pathophysiology is a hallmark of intermittent and chronic intravascular hemolysis. In genetic hemolytic anemias that demonstrate intravascular hemolysis, a common feature of disease progression is pulmonary hypertension caused by NO depletion and hemolysis-induced thrombosis.^{32, 33, 34, 35}

Heme has also been identified as a driver of hemolysis-induced immune deregulation and as a disruptor of functional cell structures, including the proteasome³⁶ and the cytoskeleton.^37,38 The binding of heme to toll-like receptor 4 (TLR4) induces inflammatory NF-kB signaling in sickle cell anemia (SCA) murine models.^39,40 The resulting exposure of P-selectin, which is a key mediator of multicellular adhesive interactions in SCA, suggests a plausible mechanistic framework for the initiation and propagation of vaso-occlusive crisis (VOC) and acute chest syndrome.^{39, 40, 41, 42} Conversely, the various detrimental effects of hemolysis on immune cells lead to hyposplenism, a state of acquired immunodeficiency that enhances the susceptibility to infections in patients with SCA and other hemolytic anemia. These immunosuppressive effects of heme progress via Hmox1,⁴³ and activation of the transcription factor NRF2,^44,45 which represses inflammatory cytokine responses of macrophages.^44,45 Furthermore, activated heme-Nrf2 signaling in myeloid progenitors causes dysregulation of myeloid differentiation trajectories.⁴⁶ This subsequently results in depletion of dendritic cells and reduces antigen presentation capacity and CD4 T-cell priming in murine SCA. Heme-induced distortion of the actin-cytoskeletal dynamics impairs phagocytosis and leukocyte migration and enhances susceptibility to gram-negative sepsis in mice.³⁷ A summary of cell-free Hb driven toxicity pathways is shown in Figure 1.

Figure 1.

Toxicity pathways driven by hemolysis. From a biochemical perspective, hemolysis drives toxicity by Hb oxidation, which generates free heme, and by a sequence of consumptive NO reactions (top panels). The bottom panels symbolize the main targets of hemolysis-driven disease in the immune system, blood vessels, and kidneys. After intravascular hemolysis, cell-free tetrameric Hb dissociates into dimers. Hb dimers can translocate across tissue barriers, leading to toxic exposures of functionally critical compartments, such as vascular smooth muscle cells of arteries or renal glomeruli, leading to vasoconstriction and renal injury. Another toxicity pathway progresses via Hb oxidation, free heme generation, and heme-ligation of TLR4 on endothelial cells and leukocytes, leading to adhesion pathway activation. Finally, Hb and heme exposure of the immune system causes phagocyte dysfunction, suppression of inflammation, and impaired antigen presentation.

Hierarchical defense by erythrophagocytes, haptoglobin, and hemopexin

Protection against hemolytic stress is primarily achieved by metabolism of hemolytic toxins via engulfment and controlled phagolysosomal degradation of RBCs by specialized macrophages with high antioxidant and iron-recycling capacity (erythrophagocytes).^44,47,48 Under physiological conditions, heme-mediated activation of the transcription factor SPI-C drives splenic differentiation of monocyte-derived red pulp macrophages.^49,50 These homeostatic erythrophagocytes recognize aged and damaged RBCs and are largely responsible for the physiological turnover of erythrocyte metabolites. Enhanced capacity for clearance of damaged RBCs in hemolytic anemia requires recruitment of circulating monocytes to the liver, where CSF1, heme-activated NRF2, and HMOX1 regulate their differentiation into on-demand erythrophagocytes.^{44,51, 52, 53} A similar transcription factor network that functions via NRF2 and ATF1 promotes the differentiation of tissue-localized erythrophagocytes within the hematoma microenvironment.^54,55 Heme signaling profoundly impairs the antigen presentation capacity and innate immune functions of erythrophagocytes. This process is accompanied by the downregulation of major histocompatibility complex class 2 expression and suppressed NF-κB activation subsequent to TLR4 or CD40 ligation.^44,46,56 Although this immunoregulatory function of heme can cause immunodeficiency in hemolytic anemia, it likely evolved as a protective mechanism against harmful inflammation and development of autoimmunity during wound healing.

On-demand erythrophagocytes can sustain multiples of physiological RBC turnover and thereby avert cell-free Hb toxicity.⁵¹ However, saturation of the total erythrophagocytic capacity in stressed compartments, or hemolytic mechanisms evading recognition by erythrophagocytes, can lead to RBC degradation and release of cell-free Hb into extracellular spaces. This defines a physiological need for a different defense system targeting cell-free Hb and heme by the high-affinity scavenger proteins haptoglobin and hemopexin.

Haptoglobin binds dimers of HbFe(II)O₂ and HbFe(III) in a stable protein complex.⁵⁷ It exists in humans as a polymorphic protein with genetically determined dimeric or multimeric assemblies of Hb-binding subunits (haptoglobin β chains).⁵⁸ Even the smallest possible configuration of an Hb-haptoglobin complex has a molecular weight of >100 kDa, which far exceeds size restrictions of translocation pathways that permit extravasation of cell-free Hb in the kidney and vasculature.^30,59,60 This simple “size-exclusion mechanism” of haptoglobin is highly effective at protecting the kidney and vascular NO homeostasis against disruption by cell-free Hb.⁹ Furthermore, haptoglobin binding stabilizes the structural integrity of bound Hb dimers and enforces the closed R-state configuration of the heme pocket, thus preventing the release of heme, even under conditions when the heme iron is oxidized.^16,21,57,61 The potent detoxification capacity of haptoglobin against all established modes of Hb toxicity is attributable to these unique structural features, in conjunction with the complex’s capacity to stabilize globin-based ferryl-radicals that are generated in reactions of Hb-haptoglobin complexes with endogenous peroxides.^62,63 However, the destructive lysosomal clearance of the complexes via the macrophage CD163 scavenger receptor pathway results in the consumption, and often complete depletion of plasma haptoglobin in patients with hemolytic anemia.⁶⁴ Therefore, despite ongoing synthesis of haptoglobin by the liver, the overall protective capacity of the haptoglobin scavenger system is limited in conditions with a high rate of cell-free Hb generation.^26,64

Heme lies downstream in the hemolytic toxin release cascade. Spontaneous or oxidant-driven formation of ferric Hb (Fe(III)) weakens the noncovalent bond between globin and heme, thus enabling the transfer of heme to lipophilic compartments, which is followed by radical chain reactions, oxidative injury, inflammation, and immune dysfunction.^20,39,65 Hemopexin irreversibly captures this highly reactive heme in a biochemically inert hexacoordinated complex that is cleared by endocytosis after binding to CD91 on macrophages and hepatocytes.⁶⁶ Because only a small fraction of cell-free Hb is oxidized in most hemolytic conditions, the selectivity of hemopexin for oxidation-generated free heme explains the gradual depletion of hemopexin compared with that of haptoglobin during development of hemolytic anemia.^21,26,67 A summary of protective mechanisms is shown in Figure 2.

Figure 2.

Protective mechanisms against hemolysis-driven disease. Protection mechanisms against Hb and heme toxicity adopt a hierarchical organization to match a diversity of hemolytic scenario. Macrophage recruitment to the liver augments erythrophagocytic capacity (level 1). Haptoglobin captures cell-free Hb dimers in an irreversible complex, stabilizing the heme-pocket structure and preventing tissue-barrier translocation in blood vessels and kidneys by its size-exclusion mechanism (level 2). Ultimately, hemopexin selectively captures free heme released from HbFe(III), blocking oxidative reactions, TLR4 ligation, and heme partitioning into lipophilic compartments (level 3).

Therapeutic potential of haptoglobin and hemopexin

Targeting specific diseases and medical interventions that feature extensive hemolysis offers unique therapeutic niches for haptoglobin and hemopexin. Here, we summarize the potential indications that are most described in the literature to date.

Hemolysis is a primary feature of SCA.⁶⁸ Sickle erythrocytes are highly unstable and are excessively consumed by erythrophagocytosis in the liver and spleen or by intravascular hemolysis, which is estimated to account for one-third of RBC destruction.⁶⁹ The release of Hb and arginase diminishes NO bioavailability, promoting vasculopathy and recurrent VOC.^12,68 Autoxidation of HbFe(II)O₂ to HbFe(III) enhances heme transfer to lipids,^{26,70, 71, 72} neutrophils, macrophages, and the vascular endothelium,³⁹ triggering inflammation⁷³ and cell adhesion pathways⁷⁴ that are important contributors to VOC. Murine models of SCA provide proof of concept that haptoglobin and hemopexin prevent, and in part reverse, Hb- and heme-induced vascular stasis.^75,76 Because haptoglobin consumption is very rapid during brisk hemolysis characteristic of human SCA, haptoglobin replacement therapy may be challenging.^26,67 Consequently, hemopexin dosing is currently under investigation in a multicenter phase 1 clinical safety, tolerability, and pharmacokinetic trial being conducted in patients with SCA (https://clinicaltrials.gov/ct2/show/NCT04285827). Dose finding and pivotal efficacy studies with clinical endpoints will reveal if there is a role for hemopexin as a prevention or treatment for VOC.

RBC damage and hemolysis are common sequelae of extracorporeal circulation. The generation of high plasma cell-free Hb correlates with the incidence of acute kidney injury and adverse outcome after on-pump cardiac surgery,^{77, 78, 79} and in critically ill patients on extracorporeal membrane oxygenation.⁸⁰ The assessment of Hb clearance rates,^80,81 endogenous plasma haptoglobin concentrations,⁸⁰ exogenously administered haptoglobin,⁸² and in-line Hb capture systems⁸³ suggests considerable therapeutic potential. Against this hypothesis, another small study found that acute kidney injury in cardiopulmonary bypass patients was not associated with the level of plasma Hb.⁸⁴ Consequently, rigorous efforts based on large prospective clinical studies to determine patient populations that could benefit most from scavenger protein-based therapeutics are essential to establish measurable endpoints for effectiveness.

RBC storage for transfusion is associated with donor-dependent changes that may compromise the quality of individual blood bags.^{85, 86, 87} After transfusion, this may lead to significant erythrophagocytosis, hemolysis-induced and NO-mediated adverse vascular effects, including posttransfusion vasoconstriction in animals⁶ and impaired blood flow in humans.⁸⁸ Furthermore, renal effects, and iron accumulation in animals^{89, 90, 91} and humans,⁹² are critical observations following transfusion. Hb toxin scavenger proteins may thus be useful in clinical scenarios involving massive transfusion (>10 units of packed RBCs in 24 hours).⁹³ The preclinical proof of concept for haptoglobin and hemopexin administration in poor-quality, high-volume RBC transfusion has been assessed in several species, and the findings suggest potentially substantive effectiveness.^{29,91,94, 95, 96} However, similar to clinical device-associated hemolysis, clinical situations in transfusion medicine that would benefit from treatment need to be identified based on patient risk for poor outcome, owing to Hb and heme exposure.

Prevention and treatment of secondary brain injury in patients with aneurysmal subarachnoid hemorrhage (aSAH) represent another opportunity for scavenger protein-based therapeutics outside the classical hemolysis field. In patients with aSAH, the decomposition of the blood clot generates cell-free Hb in the CSF and concurrence of cerebral vasospasm, ischemia, and secondary brain injury with high CSF-Hb has been described in approximately one-third of patients with aSAH.^13,97 Preclinical evidence demonstrated that CSF-Hb causes cerebral vasospasm and potentially toxic neuronal exposures.^13,97,98 Beneficial downstream effects of intracerebroventricular haptoglobin administration have been modeled in sheep and mice.^13,98

Conclusions

The entire body of work, beginning from the studies conducted by Jayle et al,⁹⁹ Smithies et al,^100,101 and Bunn et al^102,103 to the first protein-ligand complex crystal structures of haptoglobin-Hb⁵⁷ and hemopexin-heme,¹⁰⁴ has facilitated an in-depth proof of concept for refinement of indications for the use of scavenger proteins that can be tested in randomized controlled trials. An extensive summary of the potential therapeutic roles of haptoglobin and hemopexin was published in this journal in 2013.¹ Since then, a substantial volume of research evidence has reinforced the concepts of Hb-driven disease mechanisms and encouraged therapeutic development. The European Commission and Food and Drug Administration designated hemopexin as an orphan drug (CSL889, CSL Behring), for potential use in SCA in 2020, and haptoglobin as an orphan drug (CSL888, CSL Behring), for treatment of subarachnoid hemorrhage in 2021. Clinical trials are currently in initial phases to advance plasma-derived hemopexin into dose-finding and pivotal efficacy trials. In addition, a large multicenter clinical study that aims to define targetable concentrations of cell-free Hb in CSF of patients with aSAH (www.clinicaltrials.gov/ct2/show/NCT04998370) is underway. Although current treatment strategies involving haptoglobin and hemopexin use human plasma-derived proteins, recombinant platforms are being exploited to conceptualize next-generation scavengers. These proteins will be structurally homogenous and contain specific functional subunits to prolong plasma half-life, provide dual Hb and heme-binding specificities, and enhance bioavailability in specific compartments.^60,105,106 These approaches will improve drug formulation, delivery, and tissue distribution.

Conflict-of-interest disclosure: D.J.S. is inventor of patents related to the use of haptoglobin. F.V. and D.J.S. received research grants from CSL Behring. P.W.B. declares no competing financial interests.