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Decay-accelerating factor

Decay-accelerating factor (DAF), also known as CD55, is a glycosylphosphatidylinositol (GPI)-anchored membrane glycoprotein that functions as a primary regulator of the complement system by accelerating the decay of C3 and C5 convertases in both the classical and alternative pathways, thereby preventing the formation of the membrane attack complex and protecting host cells from autologous complement-mediated lysis.^[1]^[2] Discovered in 1969 by E.M. Hoffmann, who isolated it from human erythrocytes as a heat-stable factor inhibiting complement activity, DAF is encoded by the CD55 gene on chromosome 1q32 and exists in both membrane-bound and soluble forms.^[3]^[1] Structurally, DAF consists of four complement control protein (CCP) modules, also known as short consensus repeats (SCRs), each approximately 60 amino acids long, connected by short linkers and suspended above the cell membrane by a serine/threonine/proline-rich region and a GPI anchor.^[2]^[1] The protein's molecular weight ranges from 50 to 100 kDa due to alternative splicing, extensive O-glycosylation in the stalk region, and a single N-linked glycan at asparagine 61 between CCPs 1 and 2, though this glycosylation is not essential for its regulatory function.^[2] CCPs 2 and 3 are primarily responsible for binding and dissociating the classical pathway C3 convertase (C4b2a), while CCPs 2, 3, and 4 mediate activity against the alternative pathway convertase (C3bBb); key residues such as the hydrophobic leucine-phenylalanine pair (L147F148) in CCP3 and the positively charged lysine cluster (KKK125–127) between CCPs 2 and 3 are critical for these interactions.^[2] DAF is broadly expressed on the surface of most human cells, including erythrocytes, leukocytes, endothelial and epithelial cells, as well as in soluble forms in plasma, urine, saliva, tears, and synovial fluid, ensuring widespread protection against inadvertent complement activation.^[1] Beyond complement regulation, DAF modulates innate and adaptive immunity by suppressing T-cell and natural killer (NK) cell activity through interactions with integrins and serves as a ligand for the adhesion G protein-coupled receptor CD97, influencing cell migration and signaling.^[1] It also acts as a receptor for pathogens, notably facilitating invasion by Plasmodium falciparum in malaria, where CD55-null erythrocytes show resistance to infection.^[1] In disease contexts, DAF deficiency underlies conditions like paroxysmal nocturnal hemoglobinuria (PNH), characterized by GPI-anchor defects leading to increased complement-mediated hemolysis, and complement hyperactivation-associated protein-losing enteropathy (CHAPLE), resulting in gastrointestinal symptoms and thrombosis due to unchecked complement activity; CHAPLE is treated with pozelimab (Veopoz), approved by the FDA in 2023 as the first specific therapy.^[1]^[4] Conversely, DAF is frequently overexpressed in various malignancies, including colorectal, breast, ovarian, and lung cancers, promoting tumor immune evasion and progression, which has positioned it as a potential therapeutic target for complement-enhancing anticancer strategies.^[1] Additionally, DAF contributes to autoimmune disorders such as multiple sclerosis and rheumatoid arthritis via CD55-CD97 interactions that exacerbate inflammation.^[1]

Molecular structure

Protein domains

The decay-accelerating factor (DAF), also known as CD55, is a glycoprotein composed of 381 amino acids in its precursor form, including an N-terminal signal peptide of 34 amino acids that directs translocation to the endoplasmic reticulum and a C-terminal glycosylphosphatidylinositol (GPI) signal sequence of approximately 28 amino acids that facilitates membrane anchoring.^[3] The mature extracellular domain spans 319 amino acids, comprising four complement control protein (CCP) domains, also termed short consensus repeats (SCR), followed by a serine/threonine-rich stalk region rich in O-linked glycosylation sites.^[3]^[5] Each of the four CCP domains (CCP1–CCP4) consists of approximately 60 amino acids and exhibits a conserved modular architecture typical of the regulators of complement activation (RCA) family.^[2] These domains feature two intramolecular disulfide bonds formed by four conserved cysteine residues, which stabilize a compact β-barrel-like fold comprising up to eight antiparallel β-strands arranged in a hydrophobic core, often anchored by a conserved tryptophan residue.^[6]^[7] The β-sheet structure creates concave and convex faces, with the concave face implicated in ligand interactions, while flexible loops and turns account for about half of each domain's residues, contributing to functional adaptability.^[7] The CCP domains play distinct yet cooperative roles in DAF's complement regulatory function, primarily by binding to C3b and C4b fragments to accelerate the decay of C3 and C5 convertases. CCP2 and CCP3 form the core binding site for C3b and C4b, with CCP2 containing a positively charged region (residues 125–127) essential for alternative pathway regulation and CCP3 featuring a hydrophobic pocket (residues 147–148) critical for decay acceleration in both classical and alternative pathways.^[2]^[8] CCP1 primarily contributes to structural stabilization and positioning of the binding site, while CCP4 enhances activity specifically in the alternative pathway by supporting the dissociation of Bb from C3bBb convertases, requiring all three CCP2–CCP4 for full efficacy.^[2]^[9] Structural studies, including nuclear magnetic resonance (NMR) spectroscopy of the CCP2–CCP3 fragment and X-ray crystallography of DAF in complex with echovirus 7, reveal an extended, rod-like arrangement of the domains with significant inter-domain flexibility at linker regions, allowing hinge-like adjustments (tilt angles of 35–39°) to accommodate ligand binding without rigid inter-module contacts.^[7]^[5] This flexibility, evidenced by residual dipolar couplings in NMR data, enables the concave faces of adjacent CCPs to align optimally for multivalent interactions with convertase surfaces, underscoring the modular design's role in efficient complement inhibition.^[7]

Anchoring and modifications

The decay-accelerating factor (DAF), also known as CD55, is anchored to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor, which lacks a transmembrane domain and allows flexible lateral movement within the lipid bilayer. The GPI anchor consists of a phosphatidylinositol lipid moiety linked through a conserved glycan core—comprising a glucosamine, three mannoses, and a phosphoethanolamine bridge—to the C-terminal serine residue of the mature protein following proteolytic cleavage of the C-terminal signal sequence.^[10]^[11] This ethanolamine-linked structure integrates DAF into the outer leaflet of the plasma membrane, facilitating its role in surface protection without intracellular signaling domains.^[2] A prominent feature of DAF is extensive O-linked glycosylation in its serine/threonine-rich stalk region, spanning approximately amino acids 261 to 319, which contains 14–16 O-linked oligosaccharide chains primarily composed of GalNAc-based mucin-type structures. These modifications add approximately 20 kDa to the protein's mass and serve a protective function by shielding the stalk from protease attack, thereby enhancing DAF stability on the cell surface.^[12] In contrast, N-linked glycosylation is limited to a single site at asparagine 61 within the first complement control protein (CCP1) domain, featuring a complex biantennary glycan that contributes to proper folding and solubility but accounts for only a minor portion of the total carbohydrate content.^[2] The overall post-translational modifications result in an apparent molecular weight of ~70 kDa for membrane-bound DAF on SDS-PAGE, substantially higher than the predicted 41 kDa from its amino acid sequence due to the combined ~30 kDa from glycans. Variations in GPI anchor density across cell types or under pathological conditions can modulate DAF's surface mobility, with higher densities promoting nanoclustering in lipid rafts and improved diffusion to complement activation sites, while lower densities may reduce functional efficiency.^[2]^[10]

Genetics and expression

CD55 gene

The CD55 gene, which encodes the decay-accelerating factor (DAF) protein, is located on the long arm of chromosome 1 at the q32.2 cytogenetic band. It spans approximately 40 kb of genomic DNA and comprises 14 exons, as determined by detailed genomic analysis. This organization places CD55 within a chromosomal locus that also harbors other genes encoding complement regulatory proteins, facilitating coordinated regulation of complement pathways.^[13]^[14] The exon-intron structure of CD55 reflects the modular architecture of the DAF protein. Exon 1 encodes the N-terminal signal peptide responsible for directing the nascent polypeptide to the secretory pathway. Exons 2 through 5 each encode one of the four complement control protein (CCP) domains (CCP1–CCP4), which are short consensus repeats critical for ligand binding. Exon 6 encodes the serine/threonine-rich stalk region that provides flexibility to the extracellular domain. Finally, exons 7–9 encode the glycosylphosphatidylinositol (GPI) anchor attachment signal, enabling membrane anchoring of the mature protein, while alternative splicing in later exons can generate soluble isoforms lacking the GPI moiety. This exon arrangement supports diverse transcript variants, with at least 10 protein-coding isoforms identified.^[13]^[15]^[16] Polymorphisms in the CD55 gene primarily affect the Cromer blood group system (CROM), a collection of 16 antigens expressed on erythrocytes and other cells via DAF. These antigens arise from single nucleotide polymorphisms (SNPs), predominantly in the exons encoding CCP domains, altering epitope recognition without disrupting overall protein function in most cases. For instance, the rare Inab phenotype, characterized by complete absence of all Cromer antigens and reduced DAF expression, results from homozygous nonsense or frameshift mutations, such as the W53X mutation in exon 2 (c.159G>A), leading to premature termination and negligible protein production. Other Cromer variants, like Dr(a–), stem from missense mutations such as S165L in exon 5, which impair antigen expression but retain partial DAF activity. These genetic variants are recessive and have been mapped through family studies and sequencing of affected individuals.^[17]^[18] Transcriptional regulation of CD55 is responsive to inflammatory signals, particularly cytokines involved in immune activation. The gene's promoter region contains elements that mediate upregulation in response to interferon-gamma (IFN-γ), a key proinflammatory cytokine produced during infection and inflammation. In cell types such as colonic epithelial cells and certain tumor lines, IFN-γ treatment increases CD55 mRNA and surface protein levels, enhancing complement protection under stress conditions. This cytokine-inducible expression helps modulate local immune responses by bolstering membrane complement regulators on host cells. Additional cytokines like tumor necrosis factor-alpha (TNF-α) can synergize or antagonize this effect depending on the cellular context, underscoring CD55's role in adaptive immune homeostasis.^[19]00290-1)^[20]

Tissue distribution

Decay-accelerating factor (DAF), also known as CD55, exhibits ubiquitous expression across human cell types, serving as a key membrane-bound regulator of complement activation on the cell surface. It is prominently present on hematopoietic cells, including erythrocytes, leukocytes such as monocytes and granulocytes, and other blood cells, where it protects against autologous complement-mediated lysis. In non-hematopoietic lineages, DAF is widely distributed on cells routinely exposed to complement, notably endothelial and epithelial cells lining vascular and mucosal surfaces. This broad localization underscores its role in safeguarding diverse tissues from inadvertent immune damage.^[21]^[13]^[22] Particularly high levels of DAF expression are observed on vascular endothelium, where it contributes to the integrity of blood vessel walls amid constant complement exposure, and in the placenta, especially at the feto-maternal interface on extravillous trophoblasts throughout pregnancy. In contrast, neuronal cells display relatively low constitutive DAF expression, though it can be induced in response to inflammatory or stress signals, such as hypoxia-reoxygenation. During erythroid development, DAF expression on erythrocytes diminishes as cells mature, reflecting a shift in membrane protein profiles post-differentiation.^[22]^[3]^[23]^[24]^[25] DAF expression is dynamically regulated, with upregulation occurring in response to inflammatory stimuli via transcription factors like NF-κB, as seen in cytokine-activated endothelial and immune cells. Additionally, a soluble isoform (sDAF) is secreted from certain tissues, including epithelial linings, and circulates in plasma, saliva, tears, urine, and synovial fluid, potentially extending complement inhibitory functions beyond cell surfaces.^[26]^[27]

Biological function

Complement regulation

The decay-accelerating factor (DAF), also known as CD55, serves as a key membrane-bound regulator of the complement system by inhibiting the activation of the classical and alternative pathways at the level of C3 and C5 convertases. DAF binds directly to the C3b and C4b components of these convertases, accelerating their dissociation into inactive forms: specifically, it promotes the release of C2a from the classical pathway convertase C4b2a and Bb from the alternative pathway convertase C3bBb.^[22]^[28] This decay-accelerating activity occurs at a rate approximately 10- to 20-fold faster than spontaneous dissociation, thereby limiting the amplification of complement activation and preventing excessive deposition of C3b on host cells. By disrupting convertase stability, DAF reduces the generation of downstream effectors such as anaphylatoxins (C3a and C5a) and the membrane attack complex (MAC), protecting self-tissues from inadvertent lysis.^[6] In addition to its decay-accelerating function, DAF acts as a cofactor for the serine protease factor I, facilitating the proteolytic cleavage of surface-bound C3b to its inactivated form iC3b and C4b to C4d.^[29] This cofactor activity further dampens complement amplification by inactivating the opsonin C3b, which would otherwise promote phagocytosis and further convertase assembly, while iC3b retains limited opsonic potential but cannot sustain the cascade. Unlike some regulators, DAF's dual mechanisms—decay acceleration and cofactor function—target both pathways without directly inhibiting MAC formation, making it essential for early-stage control of complement on cell surfaces.^[6] DAF exhibits species-specific activity in complement regulation, with human DAF being ineffective at inhibiting porcine complement components, a limitation that has implications for xenotransplantation where porcine organs are at risk from human complement attack.^[30] Native porcine regulators fail to adequately control human complement, necessitating the expression of human DAF in transgenic pigs to protect grafts from hyperacute rejection.^[31] DAF functions in synergy with other complement regulators, such as CD59, which specifically inhibits MAC assembly by binding C9 and preventing pore formation, and membrane cofactor protein (MCP or CD46), which provides cofactor activity but lacks decay-accelerating capability.^[29] This coordinated action ensures comprehensive inhibition across the complement cascade: DAF and MCP at the convertase stage, complemented by CD59 at the terminal stage.^[32]

Immune modulation

Beyond its primary function in complement inhibition, decay-accelerating factor (DAF, also known as CD55) exerts complement-independent effects on immune cells, influencing innate and adaptive responses through cell surface interactions and signaling pathways.^[1] DAF serves as a ligand for the adhesion G protein-coupled receptor CD97, which is expressed on leukocytes including monocytes, granulocytes, and activated T and B cells. This interaction functions as a costimulatory signal, enhancing T cell activation by promoting proliferation of CD4+ T cells when co-engaged with the T cell receptor (CD3), as demonstrated in human peripheral blood studies where CD97-mediated stimulation of CD55 increased expression of activation markers such as CD69 and CD25.^[33] Furthermore, the CD55-CD97 binding facilitates leukocyte adhesion and migration, supporting T cell recruitment to inflammatory sites without interfering with DAF's complement regulatory activity. In innate immune modulation, DAF contributes to macrophage polarization toward an anti-inflammatory M2 phenotype through signaling cascades independent of complement. Upregulation of DAF represses Toll-like receptor (TLR) signaling and autocrine complement receptor (C3aR1/C5aR1) activation, thereby enabling adenylyl cyclase activity, cyclic AMP (cAMP) production, and protein kinase A (PKA)-mediated phosphorylation of CREB, which in turn supports Krüppel-like factor 4 (KLF4)-driven expression of M2 markers like arginase-1 (Arg-1) and resistin-like alpha (Retnla).^[34] This mechanism suppresses proinflammatory M1 responses, including reduced expression of monocyte chemoattractant protein-1 (MCP-1) and inducible nitric oxide synthase (iNOS), as evidenced in DAF-deficient macrophages where M2 polarization is impaired.^[34] Such polarization fosters a tolerogenic environment, linking DAF to resolution of inflammation. DAF also modulates adaptive lymphocyte signaling, particularly by regulating cytokine production in T cells. In murine models of antigen immunization, DAF deficiency results in hypersecretion of interleukin-2 (IL-2) by restimulated T cells, indicating that DAF normally suppresses IL-2 output to temper T cell responses; this effect is complement-dependent, as it is reversed by C3 or C5 blockade.^[35] Elevated IL-2 in DAF-null contexts persists in memory T cells, highlighting DAF's role in fine-tuning T cell immunity during recall responses.^[35] In the context of tumorigenesis, DAF overexpression on cancer cells promotes immune evasion by diminishing phagocytosis. By accelerating decay of C3 convertases, DAF limits C3b/iC3b opsonin deposition on tumor surfaces, thereby reducing recognition and engulfment by macrophages and other phagocytes, as observed in colorectal, breast, and ovarian cancers where high DAF correlates with poor prognosis and resistance to immune clearance.^[36] This protective mechanism extends to inhibition of natural killer cell activity, further shielding tumors from innate surveillance.^[36]

Disease associations

Paroxysmal nocturnal hemoglobinuria

Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematopoietic stem cell disorder caused by a somatic mutation in the PIGA gene, which encodes a key enzyme in the biosynthesis of glycosylphosphatidylinositol (GPI) anchors.^[37] This mutation, occurring in hematopoietic stem cells, results in the absence or severe deficiency of GPI-anchored proteins on the surface of blood cells, including decay-accelerating factor (DAF, or CD55) and membrane inhibitor of reactive lysis (CD59).^[38] Without these complement regulators, affected red blood cells, granulocytes, and platelets become highly susceptible to complement-mediated lysis, leading to the hallmark intravascular hemolysis of PNH.^[37] The PIGA mutation is X-linked and typically affects a single stem cell clone, which expands over time, with the proportion of PNH-type cells varying among patients.^[38] The clinical manifestations of PNH arise primarily from uncontrolled complement activation due to DAF and CD59 deficiency. Intravascular hemolysis is chronic, with paroxysmal exacerbations that were historically termed "nocturnal" because concentrated urine in the morning made hemoglobinuria more noticeable, though the hemolysis itself is continuous rather than sleep-specific. This leads to symptoms such as fatigue, dyspnea, abdominal pain, and dark urine from hemoglobinuria.^[39] Thrombosis, a major cause of morbidity and mortality, occurs in up to 40% of patients, often in unusual sites like hepatic veins, due to platelet activation and free hemoglobin's procoagulant effects.^[38] Bone marrow failure, present in about 30-50% of cases, contributes to cytopenias and may overlap with aplastic anemia or myelodysplastic syndromes.^[39] PNH has an estimated incidence of 1-2 cases per million individuals annually.^[40] Diagnosis of PNH relies on flow cytometry to detect the absence of CD55 and CD59 on peripheral blood cells, particularly granulocytes and monocytes, which provides high sensitivity and specificity for identifying the PNH clone size.^[41] Red blood cells are classified into type I (normal GPI expression), type II (partial deficiency), and type III (complete absence), with type III cells predominant in hemolytic PNH.^[37] Historical tests like the Ham acid hemolysis test, which demonstrated increased red cell lysis in acidic conditions, have been largely replaced by flow cytometry due to their lower sensitivity and technical demands.^[41] Treatment targets complement inhibition and, in select cases, addresses the underlying clonal disorder. Eculizumab, a monoclonal antibody against complement component C5, blocks the terminal complement pathway, dramatically reducing intravascular hemolysis, transfusion requirements, and thrombosis risk in most patients, as shown in pivotal trials.^[42] Long-acting C5 inhibitors like ravulizumab offer similar benefits with less frequent dosing. More recently, as of 2025, proximal complement inhibitors such as iptacopan (approved 2023) and danicopan (approved 2024), which target factor B or factor D to inhibit earlier in the pathway, and crovalimab (approved 2024), a recycling C5 inhibitor, have been approved, providing options for both intravascular and extravascular hemolysis with oral or subcutaneous administration.^[43]^[44]^[45] Eculizumab remains a foundational therapy, particularly during pregnancy. Allogeneic hematopoietic stem cell transplantation is the only curative option, eradicating the PNH clone and restoring normal hematopoiesis, particularly recommended for young patients with significant bone marrow failure or refractory disease.^[46] Supportive care, including anticoagulation for thrombosis and iron supplementation for hemoglobinuria-induced losses, complements these approaches.^[39]

Complement hyperactivation-associated protein-losing enteropathy (CHAPLE)

Complement hyperactivation-associated protein-losing enteropathy (CHAPLE) is a rare autosomal recessive disorder caused by biallelic loss-of-function mutations in the CD55 gene, leading to deficiency of membrane-bound DAF and resultant hyperactivation of the complement system.^[47] First described in 2017, CHAPLE typically presents in early childhood with gastrointestinal symptoms including chronic diarrhea, abdominal pain, and protein-losing enteropathy due to intestinal lymphangiectasia from endothelial damage by uncontrolled complement.^[48] Additional features include recurrent infections, angiopathic thrombosis (e.g., in cerebral or renal vessels), and edema from hypoalbuminemia, with an estimated prevalence of less than 1 in 1,000,000.^[49] Diagnosis involves genetic testing confirming CD55 mutations, flow cytometry showing absent DAF on blood cells, and evidence of complement hyperactivation (e.g., low C3 levels).^[47] Treatment focuses on complement inhibition; pozelimab (Veopoz), a C5 monoclonal antibody, was approved by the FDA in 2023 as the first specific therapy, administered subcutaneously weekly after an initial intravenous dose, significantly reducing protein loss and thrombosis risk in clinical trials.^[4] Supportive measures include nutritional support, anticoagulation, and infection prophylaxis.^[50]

Infectious diseases

Decay-accelerating factor (DAF, also known as CD55) serves as a cellular receptor for several picornaviruses, facilitating their attachment and entry into host cells. Specifically, DAF binds coxsackie B viruses and echoviruses through its complement control protein domains CCP3 and CCP4, which interact with viral capsid proteins to promote endocytosis.^[5]^[51] This interaction is critical for infection, as mutations in these domains abolish viral binding.^[52] Similarly, certain serotypes of enterovirus 70 utilize DAF as a primary receptor on ocular and respiratory epithelial cells, enabling conjunctivitis and respiratory infections.^[53] In malaria, DAF acts as a receptor for Plasmodium falciparum merozoites, facilitating their invasion of human erythrocytes; erythrocytes lacking CD55 (e.g., in rare Cromer blood group phenotypes) show resistance to infection, highlighting DAF's role in parasite tropism.^[54] In the context of human immunodeficiency virus type 1 (HIV-1), DAF contributes to viral evasion of complement-mediated destruction. HIV-1 particles incorporate DAF from infected host cells into their envelope during budding, where it functions to destabilize C3 and C5 convertases, thereby inhibiting complement opsonization and neutralization in serum.^[55] This incorporation enhances viral survival in the bloodstream, as demonstrated by experiments showing reduced complement sensitivity in DAF-associated virions compared to those lacking it.^[56] Bacterial pathogens also exploit DAF to modulate host immune responses. Streptococcus pneumoniae interacts with DAF to dampen complement activation, thereby resisting phagocytosis by neutrophils and macrophages.^[57] In infection models, DAF provides protective effects for the host against certain streptococcal strains by regulating excessive inflammation, although its absence can paradoxically enhance granulocyte-mediated clearance in some cases.^[58] Experimental studies using DAF-deficient mice highlight its role in viral pathogenesis. In models of coxsackievirus B3 infection, DAF knockout mice exhibit altered susceptibility to myocarditis, with reduced severity of cardiac inflammation compared to wild-type mice, underscoring DAF's contribution to viral tropism and immune cell activation in the heart.^[59]^[60]

Clinical and research applications

Therapeutic uses

Recombinant soluble forms of decay-accelerating factor (sDAF) have been investigated as therapeutics to systemically inhibit complement activation and mitigate inflammation in complement-related disorders. Preclinical studies demonstrated that sDAF effectively suppresses immune complex-mediated inflammation in models resembling rheumatoid arthritis by accelerating the decay of C3 and C5 convertases.^[61]^[62]^[63] In xenotransplantation, expression of human DAF in transgenic pigs has been a key strategy to counteract hyperacute rejection by protecting porcine endothelial cells from human complement attack. These genetically modified pigs, incorporating human DAF alongside other regulators like CD59 and thrombomodulin, have extended graft survival in preclinical nonhuman primate models.^[64] As of 2025, clinical trials are underway evaluating DAF-expressing gene-edited pig kidneys and hearts for human transplantation, with initial procedures demonstrating feasibility and reduced early rejection in end-stage organ failure patients.^[65]^[66] Cancer therapies targeting DAF leverage its overexpression on tumor cells, which promotes immune evasion by inhibiting complement-mediated lysis. Anti-CD55 monoclonal antibodies enhance antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) against DAF-expressing malignancies, such as colorectal tumors.^[67] For instance, a novel anti-CD55 antibody activated complement to suppress proliferation, invasion, and migration in colorectal cancer cells, with combination therapy alongside 5-fluorouracil amplifying antitumor effects.^[68] The 791Tgp72 antigen, identified as a glycosylated form of CD55, serves as a vaccine target in colorectal, gastric, and ovarian cancers, eliciting T-cell responses and supporting imaging and immunotherapy approaches.^[69] In paroxysmal nocturnal hemoglobinuria (PNH), where DAF deficiency exacerbates complement-driven hemolysis, DAF-mimicking strategies complement C5 inhibitors by targeting upstream convertase activity to prevent C3 opsonization and residual extravascular hemolysis. Proximal inhibitors, such as factor D blockers like danicopan, are combined with C5 inhibitors (e.g., eculizumab or ravulizumab) to restore regulation akin to DAF function, improving hemoglobin levels and reducing transfusion needs in patients with incomplete responses to C5 monotherapy.^[70]^[71] This adjunctive approach addresses the multifaceted complement dysregulation in PNH, enhancing overall disease control.^[72]

Pathogen interactions

Research on decay-accelerating factor (DAF, also known as CD55) as a target for antimicrobial interventions has highlighted its role as a cellular receptor exploited by various pathogens, enabling strategies to disrupt pathogen-host interactions and enhance immune clearance. In antiviral approaches, soluble DAF-Fc fusion proteins have demonstrated efficacy in blocking enterovirus binding and infection. Specifically, DAF-Fc inhibits coxsackievirus B3 (CVB3) infection in vitro by competing with cell-surface DAF for viral attachment, reducing plaque formation and viral replication across multiple strains.^[73] In vivo, administration of DAF-Fc in mouse models of CVB3-induced myocarditis attenuates viral load in the heart, decreases myocardial inflammation, and improves survival rates when given early post-infection, suggesting its potential as a therapeutic trap for enteroviral diseases.^[74] These findings have prompted exploration of DAF-targeted receptor traps for vaccine development against coxsackieviruses, where soluble forms could neutralize circulating virus and elicit protective immunity without full viral replication.^[75] In HIV research, DAF incorporated into virions during budding from infected cells shields the virus from complement-mediated lysis, contributing to immune evasion. Soluble DAF constructs have been investigated to counteract this protection; in vitro studies show that DAF-Fc fusion proteins bind to HIV-1 particles, displacing membrane-anchored DAF and restoring susceptibility to antibody-dependent complement-mediated cytotoxicity, thereby enhancing viral lysis under complement-sufficient conditions.^[76] This approach leverages DAF's dual role in pathogen attachment and complement regulation, potentially amplifying the efficacy of neutralizing antibodies in clearing HIV-infected cells.^[77] For bacterial pathogens, DAF serves as an adherence receptor for certain strains, and its blockade diminishes infection in relevant models. Analogous mechanisms apply to Gram-negative bacteria like diffusely adhering Escherichia coli (DAEC), which use Afa/Dr adhesins to bind DAF on epithelial cells, facilitating colonization and invasion. In vitro blockade of DAF with monoclonal antibodies significantly reduces DAEC adherence to host cells, inhibiting biofilm formation and bacterial internalization.^[78] Emerging investigations into DAF's involvement in COVID-19 immunopathology reveal its upregulation in severe cases, correlating with dysregulated complement activation and poor outcomes. In patients with severe SARS-CoV-2 infection, CD55 expression is elevated on monocytes, CD4+ T cells, and CD8+ T cells, suppressing type I interferon responses and promoting excessive inflammation via unchecked complement deposition.^[79] SARS-CoV-2 hijacks host CD55 for incorporation into virions, impairing antibody-dependent complement-mediated lysis and exacerbating endothelial damage and thrombosis.^[80] Therapeutic targeting of upregulated DAF, such as through monoclonal antibodies or soluble inhibitors, restores complement sensitivity in vitro, suggesting potential interventions to mitigate immunopathology in critical COVID-19 by enhancing viral clearance and reducing hyperinflammation.^[81]

References

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Jan 1, 2007 · Decay-accelerating factor (DAF; CD55) inhibits the complement (C) cascade by dissociating the multimolecular C3 convertase enzymes central to amplification.Missing: system | Show results with:system
[28]
The Role of Membrane Bound Complement Regulatory Proteins in ...
May 21, 2019 · CD55, CD46, and CD59 are known to exert control on all three pathways of complement activation. CD55, also known as DAF, accelerates the decay ...
[29]
Prevention of hyperacute rejection by human decay accelerating ...
As a potential source of organs for xenotransplantation, pigs that are transgenic for human decay accelerating factor (DAF) have been bred in order to overcome ...
[30]
Xenotransplantation: where are we today? - PMC - NIH
In view of the putative species incompatibility of porcine complement regulating proteins, pigs have been generated which express human complement regulators.
[31]
The Inhibitory Effect of CD46, CD55, and CD59 on Complement ...
Apr 1, 2002 · Only the combination of anti-CD55 and anti-CD59 resulted in an increase in lysis, and the effect was more additive than synergistic. These ...
[32]
https://www.nature.com/articles/3780441
[33]
https://doi.org/10.4049/jimmunol.177.2.1070
[34]
https://doi.org/10.3389/fimmu.2023.1290684
[35]
https://doi.org/10.1084/jem.20040863
[36]
Paroxysmal Nocturnal Hemoglobinuria: A Complement ... - PMC - NIH
SUMMARY. PNH is caused by a somatic mutation in PIGA that leads to a marked deficiency or absence of the complement regulatory proteins CD55 and CD59. The ...
[37]
Paroxysmal nocturnal hemoglobinuria: pathophysiology, natural ...
PIG-A mutations: mutation occurring in the PIG-A gene may affect the synthesis or the function of the encoded protein, resulting in the impairment of the first ...
[38]
Paroxysmal Nocturnal Hemoglobinuria - StatPearls - NCBI Bookshelf
Traditionally PNH was characterized by recurrent episodes of intravascular hemolysis, venous thrombosis, and cytopenias associated with bone marrow failure.
[39]
The Incidence and Prevalence of Paroxysmal Nocturnal ...
Nov 16, 2006 · 76 PNH patients were diagnosed during this time period giving an incidence of 0.13/100,000/year. Based on incidence and survival rates, the ...
[40]
Diagnosis of Paroxysmal Nocturnal Hemoglobinuria - PMC - NIH
Various tests like modified Ham's test, sucrose lysis test, gel card technique (GCT) and flow cytometry-based testing are available for making diagnosis [9–12].
[41]
The Complement Inhibitor Eculizumab in Paroxysmal Nocturnal ...
Excessive or persistent intravascular hemolysis in patients with PNH causes anemia, hemoglobinuria, and complications related to the presence of plasma free ...
[42]
Paroxysmal nocturnal hemoglobinuria: current treatments and ...
Currently, the only cure for paroxysmal nocturnal hemoglobinuria (PNH) is an allogeneic hematopoietic stem cell transplantation. Stem cell transplantation ...
[43]
Stem cell transplantation for paroxysmal nocturnal hemoglobinuria
Eculizumab is highly effective in reducing intravascular hemolysis in paroxysmal nocturnal hemoglobinuria and markedly reduces the risk for thrombosis;– it does ...
[44]
Echoviruses and coxsackie B viruses that use human decay ...
Echoviruses and coxsackie B viruses that use human decay-accelerating factor (DAF) as a receptor do not bind the rodent analogues of DAF ... CD55 Antigens ...
[45]
Human Diffusely Adhering <italic toggle='yes'>Escherichia coli ...
the majority of CD55-binding enteroviruses require CCP3 and. CCP4 (47), although EV7 binding may require CCP2, CCP3, and CCP4 (11, 21). The specificity of ...
[46]
The HeLa cell receptor for enterovirus 70 is decay-accelerating ...
Decay-accelerating factor (DAF, CD55) is a 70- to 75-kDa GPI-anchored membrane protein that is involved in the regulation of complement and has also been ...
[47]
Role of virion-associated glycosylphosphatidylinositol-linked ... - NIH
These results show that CD55 and CD59 are incorporated into HIV-1 particles and function to protect virions from complement-mediated destruction, and they are ...
[48]
Acquisition of Complement Resistance through Incorporation of ...
Human immunodeficiency virus (HIV) is known to develop resistance to human complement through the incorporation of DAF, CD46, and CD59 to the viral particles ( ...
[49]
A Novel Role for CD55 in Granulocyte Homeostasis and Anti ... - NIH
Oct 3, 2011 · Cd55-/- mice have an increased resistance against Streptococcal pneumoniae infection. Figure 4 · Open in a new tab. Wild-type and Cd55 -/- mice ...
[50]
A Novel Role for CD55 in Granulocyte Homeostasis and Anti ...
These data suggest that complement-independent interaction of CD55 with CD97 is functionally relevant and involved in granulocyte homeostasis and host defense.
[51]
Decay-accelerating factor (CD55) promotes CD1d expression and ...
... Decay-accelerating factor (CD55) promotes CD1d expression and Vgamma4+ T-cell activation in coxsackievirus B3-induced myocarditis. Viral Immunol. 2006 Summer ...
[52]
Autoimmunity in Coxsackievirus B3 induced myocarditis
Studies using DAF knockout mice confirm that this receptor is important for myocarditis but not pancreatitis [153]. DAF expression is enhanced by estrogen ...
[53]
Coupling complement regulators to immunoglobulin domains ... - NIH
... soluble DAF was released from DAF-Ig using papain. The sDAF produced this way had identical activity to sDAF secreted from CHO cells (Fig. 3b). The ability ...
[54]
Human recombinant soluble decay accelerating factor inhibits ...
mDAF is a more potent inhibitor of C-mediated hemolysis than either sDAF or seDAF, suggesting that incorporation into cell membranes greatly enhances the ...
[55]
Controlling the complement system in inflammation - ScienceDirect
Attempts to efficiently inhibit complement include the application of endogenous soluble complement inhibitors (C1-inhibitor, recombinant soluble complement ...
[56]
2025: status of cardiac xenotransplantation including preclinical ...
Apr 15, 2025 · Hearts from transgenic pigs constructed with CD59/DAF genomic clones demonstrate improved survival in primates. Xenotransplantation. (1999) ...
[57]
https://pmc.ncbi.nlm.nih.gov/articles/PMC3184942/
[58]
The generation and evaluation of TKO/hCD55/hTM/hEPCR gene ...
Jan 20, 2025 · This study investigates the generation of TKO/hCD55/hTM/hEPCR (6GE) pigs and evaluates their compatibility with human immune and coagulation systems.<|separator|>
[59]
A novel therapeutic anti‑CD55 monoclonal antibody inhibits the ...
The CD55 antibody treatment activated complement and therefore suppressed the proliferation, invasion and migration of colorectal cancer cells.
[60]
A novel therapeutic anti‑CD55 monoclonal antibody inhibits the ...
Sep 26, 2019 · Among complement regulatory proteins, the present study focused on decay-accelerating factor (CD55 or DAF or 791Tgp72), an inhibitor of ...Statistical Analysis · Results · Upregulation Of Cd55 During...<|control11|><|separator|>
[61]
Decay Accelerating Factor (CD55): A Target for Cancer Vaccines?1
CD55 inhibits the complement cascade by inactivating C3 convertases and preventing C3b deposition on cell membranes. C3b is a powerful stimulus of phagocytosis ...
[62]
https://pubmed.ncbi.nlm.nih.gov/1380537/
[63]
Paroxysmal nocturnal hemoglobinuria: Where are we going
Feb 16, 2023 · In this case, combination treatments, with proximal complement inhibitors and C5 inhibitors, may be ideal for the treatment of PNH.
[64]
Pharmacological Therapies in Paroxysmal Nocturnal ... - NIH
Sep 23, 2025 · The majority of cases of PNH are caused by a mutation of the PIGA gene [6–8]. PIGA is required for the formation of the glycophosphatidyl (GPI) ...Missing: etiology | Show results with:etiology
[65]
Inhibition of Coxsackie B Virus Infection by Soluble Forms of Its ...
The top row represents virus infection of cells in the absence of inhibitor, while a fivefold dilution of monomeric DAF (1.0 μM to 16 nM) or dimeric DAF-Fc (0.5 ...
[66]
Soluble Recombinant Coxsackievirus and Adenovirus Receptor ...
We have shown elsewhere that early DAF-Fc treatment attenuates CVB3-induced myocarditis and virus replication. Methods: CAR was synthesized as a soluble IgG1-Fc ...
[67]
Coxsackievirus B3-Associated Myocardial Pathology and Viral Load ...
DAF-Fc may be a novel therapeutic agent for active myocarditis and acute dilated cardiomyopathy if given early in the infectious period.
[68]
A novel approach to inhibit HIV-1 infection and enhance lysis of HIV ...
This regulation is mediated by proteins such as cell surface-like membrane cofactor protein (MCP), decay accelerating factor (DAF) and protectin (CD59), and the ...
[69]
HIV and human complement: inefficient virolysis and effective ...
In this review, we focus on the interaction of HIV with the human complement system, regarding the mechanisms responsible for the inefficient complement- ...
[70]
Binding of Escherichia coli adhesin AfaE to CD55 triggers ... - PNAS
For blockade of bacterial adhesion, CD55-specific mAb BRIC216 or an Ig-isotypic control (10 μg/ml) was incubated with targets before bacterial infection. In ...
[71]
Pathogenesis of Afa/Dr Diffusely Adhering Escherichia coli - PMC
In this review, the focus is on Afa/Dr DAEC strains that have been found to be associated with urinary tract infections and with enteric infection.<|control11|><|separator|>
[72]
Upregulation of CD55 complement regulator in distinct PBMC ...
Oct 7, 2022 · The present study identifies a COVID-19 specific CD55 expression pattern in PBMC subpopulations that coincides with reduced interferon responses.Results · Pbmc Transcriptomic... · Cd55 Upregulation In Severe...
[73]
SARS-CoV-2 hijacks host CD55, CD59 and factor H to impair ...
Oct 22, 2024 · These include the plasma membrane-resident protectin (CD59) and decay accelerating factor (DAF, CD55) as well as the fluid-phase regulator ...
[74]
Full article: SARS-CoV-2 hijacks host CD55, CD59 and factor H to ...
Here, we demonstrate that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) hijacks host cellular RCA members CD55 and CD59 and serum-derived Factor ...