Tools
Duffy Blood Group System
Introduction
The Duffy blood group system is complex, highly immunogenic glycoprotein antigens found on the surface of Red Blood Cells (RBC), vasculature endothelial cells, alveolar epithelial cells, collecting tubules of the kidney, and on the surface of Purkinje cells in the brain, but are absent on the adult liver. Duffy antigens are absent on platelets, lymphocytes, monocytes, and granulocytes.[1][2]
Duffy antigens act as receptors for chemokines and attract immune system cells. Duffy antigens also act as receptors for the Plasmodium species responsible for malaria. Antibodies against the Duffy blood group antigens are implicated in hemolytic transfusion reactions (HTR) and hemolytic disease of the fetus and newborn (HDFN).
Duffy blood group system International Society of Blood Transfusion (ISBT) symbol: FY
ISBT Number: 008
Duffy blood group antigen (Fy) was first discovered in 1950 in a patient named Duffy with multiple transfusions who presented with hemolytic transfusion reactions by Cutbush et al.[3] Duffy glycoprotein or CD234 (Cluster of Differentiation 234) is a multi-pass protein. It spans the RBC membrane seven times with an exocellular N- terminal and an endocellular C-terminal, while multi-pass proteins in the other blood group system, both N and C terminals, are endocellular.[4]
The Duffy antigens, FYa and FYb, are the gene products of DARC (Duffy antigen chemokine receptor; AKA ACKR1, atypical chemokine receptor 1).
Atypical Chemokine Receptor 1 (ACKR1) gene encodes the glycoprotein expressing the Duffy blood group antigens, or CD234 protein (Cluster of Differentiation 234 protein) and is encoded by a gene located at 1q23.2 position on the long arm of chromosome 1.[5] This ACKR1 gene produces two mRNA variants and yields two protein isoforms with 338 and 336 amino acids. The Duffy antigens, i.e., Fya and Fyb, are encoded by FYA and FYB codominant alleles, respectively, which differ at position 125, where guanine in Fy-a is replaced by adenosine in Fy-b, which changes the glycine amino acid to aspartic amino acid at position 42 in Duffy glycoprotein.[6]
Duffy antigens gene locus is syntenic to the gene locus for Rh antigen gene locus at chromosome 1.[7] In most Duffy negative individuals, a silent Fy-b allele with T to C substitution near the gene transcription initiation site at nucleotide-46 is present. It impairs the promoter activity in human erythroid cells by disrupting the binding site for the erythroid transcription factor, i.e., GATA1. Still, the same gene is transcribed in the nonerythroid cells due to substitution mutation.[6]
ACKRs receptors do not couple with G-proteins as its structure Asp-Arg-Tyr-Leu-Ala-Ile-Val (DRYLAIV) motif is absent on the second intracellular loop, leading to no GPCR dependant signaling pathways and chemotaxis. However, they function as scavenge, transport, and regulator of the bioavailability of chemokines.[8][9][10]
A total of five antigens are present in the Duffy blood group system: Fya, Fyb, Fy3, Fy5, and Fy6.[11][12][13]
- ISBT symbol: FY1
- ISBT number: 008.001
- Antithetical antigen: Fyb (FY2)
- The expression on the cord blood RBCs: Expressed
- The antigen can be demonstrated on the fetal RBCs as early as six weeks gestation. The adult level of Fya expression is attained approximately 12 weeks after birth.
- Fya antigens are sensitive to ficin, papain, and α-chymotrypsin and resistant to trypsin.
- ISBT symbol: FY2
- ISBT number: 008.002
- Antithetical antigen: Fy(FY1)
- Expression on the cord blood RBCs: Expressed.
- Effect of enzymes: Fyb antigens are sensitive to ficin, papain, and α-chymotrypsin and resistant to trypsin.
- ISBT symbol: FY3
- ISBT number: 008003
- Expression on the cord blood RBCs: Expressed and increases with age.
- Effect of enzymes: Fy3 antigens are resistant to ficin, papain, trypsin, and α-chymotrypsin.
- ISBT symbol: FY5
- ISBT number: 008005
- The expression on the cord blood RBCs: Expressed
- Weak antigenic expression on D negative RBCs and absence in Rh null phenotype red cells show possible interaction between Duffy and Rh proteins.
- Effect of enzymes: Fy5 antigens are resistant to ficin and papain.
- ISBT symbol: FY6
- ISBT number: 008.006
- The expression on the cord blood RBCs
- Effect of enzymes: Fy6 antigens are sensitive to ficin, papain, and α-chymotrypsin and resistant to trypsin.
- Epitopes of Fy6 antigen are required for invasion of P. vivax.
- Only murine monoclonal antibodies have defined this antigen, not human antibodies.
Note: Fy4 antigen is obsolete in this system due to no evidence of antibodies against this antigen.[13]
- Antibodies in the Duffy blood group system are mainly IgG type, and IgM type is rare. Duffy antibodies generally do not bind to complement, but some anti-Fyantibodies have been reported to bind with complement. These antibodies are not naturally occurring and are acquired by exposure to blood transfusion, pregnancy, and transplantation. Fya antibody is most common among other Duffy antibodies.[14][15]
- The majority of Duffy antibodies show their reactivity at body temperature; hence they may cause red hemolysis and are clinically significant. These clinically significant antibodies can lead to both acute and delayed types of HTR and hemolytic disease of the fetus and newborn (HDFN).[16][17]
- Dosage phenomena: Duffy blood group system shows dosage phenomena where Duffy antibodies react more strongly to homozygous cells {Fy(a−b+) or Fy(a+b−)} than heterozygous {Fy(a+b+)}.[18]
Four major Duffy phenotypes: - Fy(a+b-), Fy(a+b+), Fy(a-b+), Fy(a-b-): The Fya and Fyb antigens are found commonly in Europeans (Fya 66% and Fyb 83%) and Asians (Fya 99% and Fyb18.5%), while less common in Africans (Fya 10% and Fyb 23%). Further, Fy(a-b-) phenotype in African origins is found in two-thirds of populations and rare in Europeans.[19][20] Major antigenic frequencies are shown in Table 1.
Additionally, a minor Duffy phenotype is the Fyx or [Fy(b+x)]. In this phenotype, the antigen is weakly expressed as Fyb and is determined by serological adsorption and elution techniques and DNA sequencing. FYX allele encodes weakly expressed Fyb antigen, which sometimes may not be detected by anti-Fy. The Fy(a–b–) phenotype, most commonly found in Blacks, occurs primarily due to a GATA promoter region mutation upstream of the FY allele. This mutation prevents the expression of Duffy glycoprotein on erythrocytes only while permitting expression on nonerythroid cells.[21][22]
|
Antigenic frequencies |
European (white) |
African (Black) |
Arabic | Indians | Chinese | Brazilian |
| Fy (FY1) | 66% | 10% | 36% | 87% | 99.8% | 39% |
| Fy (FY2) | 83% | 23% | 40% | 58% | 9% | 50% |
Function
Register For Free And Read The Full Article
Search engine and full access to all medical articles- 10 free questions in your specialty
- Free CME/CE Activities
- Free daily question in your email
- Save favorite articles to your dashboard
- Emails offering discounts
Learn more about a Subscription to StatPearls Point-of-Care
Function
Functional Role of Duffy Glycoprotein
Duffy glycoprotein acts as a "Duffy antigen receptor for chemokines" (DARC), which binds with the chemicals secreted during the inflammatory process, thereby affecting the intensity of inflammation and the degree of neutrophil recruitment.[23]
DARC ( AKA CD234; ACKR 1) is homologous to the G-protein chemokine receptor (GPCR) family and functions as a scavenger in inflammatory and proinflammatory conditions. The Duffy antigen (DARC) is found on erythrocytes, capillaries, and postcapillary venule endothelial cells. DARC acts as a sort of a repository, retaining or releasing chemokines, thereby reducing or augmenting local inflammation.
During inflammation, DARC releases chemokines that bind to and progress through the endothelium. This promotes transendothelial neutrophil migration. The DARC binds with both the classes of chemokines, i.e., CC (chronic inflammation chemokine), CXC (acute inflammation chemokine), melanoma growth stimulatory activity-alpha (MGSA-α/CXCL1), interleukin 8 (CXCL8), monocyte chemotactic protein-1 (CCL2), RANTES (regulated upon activation normal T-expressed & secreted (CCL5), neutrophil-activating protein 2 and 3, epithelial neutrophil-activating peptide-78, (CXCL5), growth-related gene alpha, and angiogenesis-related platelet factor-1.[24]
Issues of Concern
Transfusion: If the patient has an antibody against the Duffy blood group system, they must be transfused red blood cells which are Duffy antigen-negative and cross-match compatible. Further, in case of mother has been sensitized to Duffy antigens from his previous pregnancy and had developed Duffy antibodies may cause HDFN in subsequent pregnancies.
In such fetuses, intrauterine transfusion of Duffy negative blood must be transfused to improve fetal anemia and outcomes. Further after the baby's birth, their exchange transfusion should be planned with the Duffy antigen-negative and cross-match compatible blood units.
Duffy antibodies (mostly Anti-Fya and Anti-Fyb) have been implicated in causing HTRs and HDFN. Such recipients who have been detected with antibodies should be issued corresponding Duffy antigen-negative blood after compatibility testing for better transfusion outcomes. In a few cases with Fy(a–b–) phenotype, recipients had been found to develop Anti-Fy3, Fy4, Fy5, and Fy6 antibodies and should be transfused Fy(a–b–) phenotyped blood whenever transfusion is needed. HTRs in the Duffy blood group system are primarily due to IgG (mostly IgG1 type), but IgM antibodies have also been reported.
HDFN is rare and mild with the Duffy blood group system after maternal immunization with Duffy antigen-positive fetal red cells. Most of the reported cases are due to anti-Fya antibodies.[14][25]
Clinical Significance
Duffy Antigens and Malaria: The Duffy status plays a pivotal role in global survival from plasmodial infections.[26]
The two most common Plasmodia globally are P. vivax and P. falciparum. P. falciparum manifestations are more severe, and the clinical outcomes are more baleful. P. vivax has more temperature tolerance and can adapt to a dormant (hypnozoite) form, ensuring relapses. Initially, patients are bitten by the Anopheles mosquito, after which sporozoites in the skin enter the circulation and eventually the liver. Within the liver, the sporozoites replicate into merozoites that enter the circulation and infect red blood cells, causing their lysis and renewing the infectious cycle again. A dormant hypnozoite state can exist in the liver for weeks to months.
The Duffy blood group antigens are the portals by which the erythrocytes are infected. Primaquine and 8-Aminoquineline are useful antimalarials that can clear the hypnozoites and prevent relapses. However, they also cause hemolysis in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. DARC is considered an essential GPCR to enter malarial parasites, Plasmodium vivax and Plasmodium knowlesi, in the red blood cells. The ligand-receptor interactions mediate the invasion of the red cell by Plasmodium between merozoites and host erythrocytes. The Duffy binding protein (DBP) on the merozoite surface interacts with DARC over the surface of the reticulocyte triggering the formation of a junction for parasitic invasion.[27]
In the West African population, many peoples were resistant to Plasmodium vivax infection due to the expression of the Fy(a-b-) phenotype on red cells. This phenotype in the African population results from the point mutation in the GATA promoter region at the FY*B gene at (–67, T to C), which disrupts the binding site for the GATA-1 erythroid transcription factor. The ligand-receptor interactions mediate the invasion of plasmodia between merozoites and host erythrocytes.
The Duffy binding protein (DBP) on the merozoite surface interacts with DARC over the surface of the reticulocyte triggering the formation of a junction for parasitic invasion. The intraerythrocytic killing of malarial parasites by platelet factor-4 (PF4) is demonstrated in vitro in erythrocytes expressing DARC on their surface, leading to accumulation of PF4 by endocytosis which results in lysis of parasitic digestive vacuoles. The protective effect does not cover the P. falciparum parasites, which can infect all phenotypic variants of the Duffy blood group system.[28][29][30]
Epidemiologically, the absence of the Duffy system (AKA "Duffy- negative or -null; Fy (a-b-) has been seen in many nations across the continents.[31][32][33] Clinical data suggests that the lack of the Duffy antigens confers a degree of resistance to Plasmodium vivax infection. However, the prevalence of P. vivax infections in Duffy negative populations is still not zero.
There are likely Duffy-independent pathways that can secondarily promote infection. These alternatives are thought to include Transferrin receptor 1 (TfR1 or CD71) and CD98. The lack of Duffy blood group antigens obstructs the invasion of Plasmodium vivax. The absence of Duffy expression is believed to be a consequence of a point mutation (c.1-67, T>C; rs2814778) in the GATA-1 transcription binding site of the DACR gene promoter. This results in the "Duffy-null," the Duffy-negative variant.
A multitude of clinical studies exist, many under the auspices of the World Health Organization, to develop malarial vaccines. Research is presently underway to develop a malarial vaccine based on the Duffy system.[34][35]
A vaccine has been created against region 2 of the Plasmodium vivax Duffy-binding protein (PvDBP2). It has a recombinant format with a glucopyranosyl lipid adjuvant-stable emulsion (GLA-SE). The vaccine elicited antigen-specific binding -inhibitory antibodies. The antibodies also have activity against a spectrum of PvDBP alleles. In a small phase I trial where malaria naive patients received a three-dose protocol, it was revealed that all patients developed inhibitory antibodies that were largely persistent. The vaccine, known as PvDBP2/GLA-SE, is safe and well-tolerated.
Duffy Antigens and HIV: The Duffy system is believed to affect HIV infections.[36] Duffy antigen receptors for chemokines (DARC) on red blood cells influence plasma levels of HIV-1 suppressive and proinflammatory chemokines 9eg. CCL5/RANTES). CCL5 (RANTES) and CCR5 enhance HIV infectivity. HIV interacts with surface receptors of macrophages and dendrites, which protect the virus from degradation and promote its dissemination.
Similarly, HIV-1 adsorbs onto the DARC on erythrocyte surfaces and is transported to its target cells (CD4+/CCR5+ T-lymphocytes). With the transport, the virus still retains its viability.[37] The red blood cells thereby act as HIV-1 carriers. Patients with the Duffy null phenotype (-467 C/C) have noted a 40% increase in HIV-1 infection (possibly as less HIV is bound); however, in Duffy negative patients already infected with HIV-1, there is a slower disease progression.
Some clinical research has suggested that African-Americans harboring a Duffy-null genotype had malarial resistance and an HIV-survival advantage compared to the general population.[38] Arguments against these studies stated that adjustments were (incorrectly) made to account for non-African test subjects. It was felt that Afro-American subjects could have European source material interspersed in their ranks and thus cannot be used.[39] They surmise that the DARC negative phenotype caused by -46 C/C cannot have their data admixed with African observations.
Duffy Antigens and COVID: The Duffy system is thought to play a role in the presence and severity of COVID infections.[40] DARC mediates the effects of proinflammatory chemokines on the endothelial cells lining the post-capillary venules as well as on the neutrophil emigration to the inflammatory sites. It also mediates chemokine transcytosis to facilitate the movement of cytokines across the endothelium, enhancing neutrophil recruitment into the lung. By these means, it enhances chemokine-induced leukocyte extravasation.[41]
In normal situations, the Duffy-null accounts for benign ethnic neutropenia amongst African-Americans, but it also exerts proinflammatory effects that can accentuate leukocyte migration into the lung. With no Duffy system to hold or modulate cytokine activity, the effects of cytokines appear more pronounced than in a Duffy-positive state. This was the reason to suspect that Duffy-null states would promote COVID-19 pneumonia and accentuate the severity of the acute lung injury. Relative to other patients, erythroid Duffy-null patients had a 17% higher risk of mortality as well as fewer ventilator-free and organ failure-free days.
Duffy Antigens and Hematopoiesis: Duffy antigen expression is associated with the hematopoiesis process. The hematopoietic stem cells and red cell precursors in bone marrow express DARC. Erythrocyte Fy dampens leukocyte activation. Endothelial (vascular) Fy concentrates chemokines, thereby promoting leukocyte diapedesis to and through the vessel border towards the inflammatory site. Phenotypically altered neutrophils (benign ethnic neutropenia with persistently lower leucocyte) are observed in otherwise healthy Africans without DARC on hematopoietic cells.[42]
The Duffy negative or null trait does not affect neutrophil function.[43] But, ironically, it portends a greater HIV infectivity though it protects against malaria.[44]
Role of DARC in organ transplantation: In a mouse model study, it is observed that mice with DARC negative showed enhanced chemokine production and inflammatory response in the absence of DARC, which leads to immunological and non-immunological injuries due to excess leucocyte recruitment.[45][46]
The UNOS database further confirms this in African Americans, who had more deleterious effects on delayed graft function than Caucasians due to the absence of DARC on renal tissues.[47] More recent data speaks of a greater antibody-mediated renal allograft rejection and reduced graft survival in DARC-positive patients compared to DARC-negative subjects.[48] In conclusion, the prominence of DARC was felt to be associated with, though NOI specific for, antibody-mediated rejection.
DARC in Atherosclerosis; ACKR1 has a role in the inflammatory process and atherosclerosis. ACKR1 on the Red cells controls inflammation, leukocyte migration, and endothelial function. ACKR1 presented CXCL2 enables unidirectional neutrophil diapedesis.[49][50]
Recent studies have demonstrated the role of a high-fat diet in inducing endothelial dysfunction due to increased CCL2 bound with the red cells expressing ACKR1, which promotes interaction between endothelial cells and leukocytes which may favor in development of atherosclerosis plaque. Wan et al. showed that mice with absent ACKR1 after gene knockout had reduced atherosclerotic plaque size in an experimental animal model.[51][52]
Enhancing Healthcare Team Outcomes
This is one condition where both laboratory and clinical personnel are of equal necessity and value. Research into the predictive and protective nature of the Duffy entity is needed as new viral threats come to the forefront of global attention. The nursing team must check for Duffy antigen-negative blood units in addition to all the pretransfusion checks before the red blood cell transfusion in the patient known to have the Duffy antibody.
Staff must also be alert that, with the Duffy system, transfusion reactions can be delayed, sometimes upwards of two weeks later.[53] By its very nature, the Duffy system may belay medical attention. In truth, it only seems to be of secondary importance.
Nursing, Allied Health, and Interprofessional Team Monitoring
The nursing team must check for Duffy antigen-negative blood unit in addition to all the pre-transfusion checks before red blood transfusion in the patient known to have Duffy antibody.
References
Horuk R, Martin AW, Wang Z, Schweitzer L, Gerassimides A, Guo H, Lu Z, Hesselgesser J, Perez HD, Kim J, Parker J, Hadley TJ, Peiper SC. Expression of chemokine receptors by subsets of neurons in the central nervous system. Journal of immunology (Baltimore, Md. : 1950). 1997 Mar 15:158(6):2882-90 [PubMed PMID: 9058825]
Neote K, Mak JY, Kolakowski LF Jr, Schall TJ. Functional and biochemical analysis of the cloned Duffy antigen: identity with the red blood cell chemokine receptor. Blood. 1994 Jul 1:84(1):44-52 [PubMed PMID: 7517217]
CUTBUSH M, MOLLISON PL. The Duffy blood group system. Heredity. 1950 Dec:4(3):383-9 [PubMed PMID: 14802995]
Lu ZH, Wang ZX, Horuk R, Hesselgesser J, Lou YC, Hadley TJ, Peiper SC. The promiscuous chemokine binding profile of the Duffy antigen/receptor for chemokines is primarily localized to sequences in the amino-terminal domain. The Journal of biological chemistry. 1995 Nov 3:270(44):26239-45 [PubMed PMID: 7592830]
Level 3 (low-level) evidenceDonahue RP, Bias WB, Renwick JH, McKusick VA. Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proceedings of the National Academy of Sciences of the United States of America. 1968 Nov:61(3):949-55 [PubMed PMID: 5246559]
Tournamille C, Colin Y, Cartron JP, Le Van Kim C. Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nature genetics. 1995 Jun:10(2):224-8 [PubMed PMID: 7663520]
Colledge KI, Pezzulich M, Marsh WL. Anti-Fy5, and antibody disclosing a probable association between the Rhesus and Duffy blood group genes. Vox sanguinis. 1973 Mar:24(3):193-9 [PubMed PMID: 4632152]
Ulvmar MH, Hub E, Rot A. Atypical chemokine receptors. Experimental cell research. 2011 Mar 10:317(5):556-68. doi: 10.1016/j.yexcr.2011.01.012. Epub 2011 Jan 25 [PubMed PMID: 21272574]
Level 3 (low-level) evidenceSánchez-Martín L, Sánchez-Mateos P, Cabañas C. CXCR7 impact on CXCL12 biology and disease. Trends in molecular medicine. 2013 Jan:19(1):12-22. doi: 10.1016/j.molmed.2012.10.004. Epub 2012 Nov 12 [PubMed PMID: 23153575]
Benredjem B, Girard M, Rhainds D, St-Onge G, Heveker N. Mutational Analysis of Atypical Chemokine Receptor 3 (ACKR3/CXCR7) Interaction with Its Chemokine Ligands CXCL11 and CXCL12. The Journal of biological chemistry. 2017 Jan 6:292(1):31-42. doi: 10.1074/jbc.M116.762252. Epub 2016 Nov 14 [PubMed PMID: 27875312]
Pogo AO, Chaudhuri A. The Duffy protein: a malarial and chemokine receptor. Seminars in hematology. 2000 Apr:37(2):122-9 [PubMed PMID: 10791881]
Chaudhuri A, Zbrzezna V, Johnson C, Nichols M, Rubinstein P, Marsh WL, Pogo AO. Purification and characterization of an erythrocyte membrane protein complex carrying Duffy blood group antigenicity. Possible receptor for Plasmodium vivax and Plasmodium knowlesi malaria parasite. The Journal of biological chemistry. 1989 Aug 15:264(23):13770-4 [PubMed PMID: 2668273]
Level 3 (low-level) evidenceStorry JR, Castilho L, Daniels G, Flegel WA, Garratty G, Francis CL, Moulds JM, Moulds JJ, Olsson ML, Poole J, Reid ME, Rouger P, van der Schoot E, Scott M, Smart E, Tani Y, Yu LC, Wendel S, Westhoff C, Yahalom V, Zelinski T. International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report. Vox sanguinis. 2011 Jul:101(1):77-82. doi: 10.1111/j.1423-0410.2010.01462.x. Epub 2011 Mar 14 [PubMed PMID: 21401621]
Geifman-Holtzman O, Wojtowycz M, Kosmas E, Artal R. Female alloimmunization with antibodies known to cause hemolytic disease. Obstetrics and gynecology. 1997 Feb:89(2):272-5 [PubMed PMID: 9015034]
Caren LD, Bellavance R, Grumet FC. Demonstration of gene dosage effects on antigens in the Duffy, Ss, and Rh systems using an enzyme-linked immunosorbent assay. Transfusion. 1982 Nov-Dec:22(6):475-8 [PubMed PMID: 6815840]
Olteanu H, Gerber D, Partridge K, Sarode R. Acute hemolytic transfusion reaction secondary to anti-Fy3. Immunohematology. 2005:21(2):48-52 [PubMed PMID: 15981343]
Level 3 (low-level) evidencePeiper SC, Wang ZX, Neote K, Martin AW, Showell HJ, Conklyn MJ, Ogborne K, Hadley TJ, Lu ZH, Hesselgesser J, Horuk R. The Duffy antigen/receptor for chemokines (DARC) is expressed in endothelial cells of Duffy negative individuals who lack the erythrocyte receptor. The Journal of experimental medicine. 1995 Apr 1:181(4):1311-7 [PubMed PMID: 7699323]
Sun XL, Yu Y, Guan XZ, Chen LF, Wang DQ. [Influence of "dosage effect" on unexpected antibody identification]. Zhongguo shi yan xue ye xue za zhi. 2015 Feb:23(1):222-7. doi: 10.7534/j.issn.1009-2137.2015.01.042. Epub [PubMed PMID: 25687077]
Thakral B, Saluja K, Sharma RR, Marwaha N. Phenotype frequencies of blood group systems (Rh, Kell, Kidd, Duffy, MNS, P, Lewis, and Lutheran) in north Indian blood donors. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 2010 Aug:43(1):17-22. doi: 10.1016/j.transci.2010.05.006. Epub 2010 Jun 16 [PubMed PMID: 20558108]
De Silva JR, Lau YL, Fong MY. Genotyping of the Duffy blood group among Plasmodium knowlesi-infected patients in Malaysia. PloS one. 2014:9(9):e108951. doi: 10.1371/journal.pone.0108951. Epub 2014 Sep 30 [PubMed PMID: 25268233]
Level 2 (mid-level) evidenceHöher G, Fiegenbaum M, Almeida S. Molecular basis of the Duffy blood group system. Blood transfusion = Trasfusione del sangue. 2018 Jan:16(1):93-100. doi: 10.2450/2017.0119-16. Epub 2017 Jan 30 [PubMed PMID: 28151395]
Nickel RG, Willadsen SA, Freidhoff LR, Huang SK, Caraballo L, Naidu RP, Levett P, Blumenthal M, Banks-Schlegel S, Bleecker E, Beaty T, Ober C, Barnes KC. Determination of Duffy genotypes in three populations of African descent using PCR and sequence-specific oligonucleotides. Human immunology. 1999 Aug:60(8):738-42 [PubMed PMID: 10439320]
Lee JS, Frevert CW, Wurfel MM, Peiper SC, Wong VA, Ballman KK, Ruzinski JT, Rhim JS, Martin TR, Goodman RB. Duffy antigen facilitates movement of chemokine across the endothelium in vitro and promotes neutrophil transmigration in vitro and in vivo. Journal of immunology (Baltimore, Md. : 1950). 2003 May 15:170(10):5244-51 [PubMed PMID: 12734373]
Level 3 (low-level) evidenceNeote K, Darbonne W, Ogez J, Horuk R, Schall TJ. Identification of a promiscuous inflammatory peptide receptor on the surface of red blood cells. The Journal of biological chemistry. 1993 Jun 15:268(17):12247-9 [PubMed PMID: 8389755]
Vescio LA, Fariña D, Rogido M, Sóla A. Hemolytic disease of the newborn caused by anti-Fyb. Transfusion. 1987 Jul-Aug:27(4):366 [PubMed PMID: 3603669]
Level 3 (low-level) evidenceLo E, Russo G, Pestana K, Kepple D, Abagero BR, Dongho GBD, Gunalan K, Miller LH, Hamid MMA, Yewhalaw D, Paganotti GM. Contrasting epidemiology and genetic variation of Plasmodium vivax infecting Duffy-negative individuals across Africa. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases. 2021 Jul:108():63-71. doi: 10.1016/j.ijid.2021.05.009. Epub 2021 May 12 [PubMed PMID: 33991680]
Cowman AF, Crabb BS. Invasion of red blood cells by malaria parasites. Cell. 2006 Feb 24:124(4):755-66 [PubMed PMID: 16497586]
Level 3 (low-level) evidenceMiller LH, Mason SJ, Clyde DF, McGinniss MH. The resistance factor to Plasmodium vivax in blacks. The Duffy-blood-group genotype, FyFy. The New England journal of medicine. 1976 Aug 5:295(6):302-4 [PubMed PMID: 778616]
McMorran BJ, Wieczorski L, Drysdale KE, Chan JA, Huang HM, Smith C, Mitiku C, Beeson JG, Burgio G, Foote SJ. Platelet factor 4 and Duffy antigen required for platelet killing of Plasmodium falciparum. Science (New York, N.Y.). 2012 Dec 7:338(6112):1348-51. doi: 10.1126/science.1228892. Epub [PubMed PMID: 23224555]
Love MS, Millholland MG, Mishra S, Kulkarni S, Freeman KB, Pan W, Kavash RW, Costanzo MJ, Jo H, Daly TM, Williams DR, Kowalska MA, Bergman LW, Poncz M, DeGrado WF, Sinnis P, Scott RW, Greenbaum DC. Platelet factor 4 activity against P. falciparum and its translation to nonpeptidic mimics as antimalarials. Cell host & microbe. 2012 Dec 13:12(6):815-23. doi: 10.1016/j.chom.2012.10.017. Epub [PubMed PMID: 23245326]
Level 3 (low-level) evidenceBrown CA, Pappoe-Ashong PJ, Duah N, Ghansah A, Asmah H, Afari E, Koram KA. High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana. Malaria journal. 2021 Feb 17:20(1):99. doi: 10.1186/s12936-021-03618-0. Epub 2021 Feb 17 [PubMed PMID: 33596926]
Haiyambo DH, Aleksenko L, Mumbengegwi D, Bock R, Uusiku P, Malleret B, Rénia L, Quaye IK. Children with Plasmodium vivax infection previously observed in Namibia, were Duffy negative and carried a c.136G } A mutation. BMC infectious diseases. 2021 Aug 21:21(1):856. doi: 10.1186/s12879-021-06573-y. Epub 2021 Aug 21 [PubMed PMID: 34418990]
Hongfongfa P, Kuesap J. Genotyping of ABO and Duffy blood groups among malaria patients in Thailand. Journal of parasitic diseases : official organ of the Indian Society for Parasitology. 2022 Mar:46(1):178-185. doi: 10.1007/s12639-021-01432-8. Epub 2021 Aug 11 [PubMed PMID: 35299921]
Singh K, Mukherjee P, Shakri AR, Singh A, Pandey G, Bakshi M, Uppal G, Jena R, Rawat A, Kumar P, Bhardwaj R, Yazdani SS, Hans D, Mehta S, Srinivasan A, Anil K, Madhusudhan RL, Patel J, Singh A, Rao R, Gangireddy S, Patil R, Kaviraj S, Singh S, Carter D, Reed S, Kaslow DC, Birkett A, Chauhan VS, Chitnis CE. Malaria vaccine candidate based on Duffy-binding protein elicits strain transcending functional antibodies in a Phase I trial. NPJ vaccines. 2018:3():48. doi: 10.1038/s41541-018-0083-3. Epub 2018 Sep 28 [PubMed PMID: 30302285]
Ntumngia FB, Pires CV, Barnes SJ, George MT, Thomson-Luque R, Kano FS, Alves JRS, Urusova D, Pereira DB, Tolia NH, King CL, Carvalho LH, Adams JH. An engineered vaccine of the Plasmodium vivax Duffy binding protein enhances induction of broadly neutralizing antibodies. Scientific reports. 2017 Oct 23:7(1):13779. doi: 10.1038/s41598-017-13891-2. Epub 2017 Oct 23 [PubMed PMID: 29062081]
He W, Neil S, Kulkarni H, Wright E, Agan BK, Marconi VC, Dolan MJ, Weiss RA, Ahuja SK. Duffy antigen receptor for chemokines mediates trans-infection of HIV-1 from red blood cells to target cells and affects HIV-AIDS susceptibility. Cell host & microbe. 2008 Jul 17:4(1):52-62. doi: 10.1016/j.chom.2008.06.002. Epub [PubMed PMID: 18621010]
Walton RT, Rowland-Jones SL. HIV and chemokine binding to red blood cells--DARC matters. Cell host & microbe. 2008 Jul 17:4(1):3-5. doi: 10.1016/j.chom.2008.06.006. Epub [PubMed PMID: 18621004]
Kulkarni H, Marconi VC, He W, Landrum ML, Okulicz JF, Delmar J, Kazandjian D, Castiblanco J, Ahuja SS, Wright EJ, Weiss RA, Clark RA, Dolan MJ, Ahuja SK. The Duffy-null state is associated with a survival advantage in leukopenic HIV-infected persons of African ancestry. Blood. 2009 Sep 24:114(13):2783-92. doi: 10.1182/blood-2009-04-215186. Epub 2009 Jul 20 [PubMed PMID: 19620399]
Level 2 (mid-level) evidenceWinkler CA, An P, Johnson R, Nelson GW, Kirk G. Expression of Duffy antigen receptor for chemokines (DARC) has no effect on HIV-1 acquisition or progression to AIDS in African Americans. Cell host & microbe. 2009 May 8:5(5):411-3; author reply 418-9. doi: 10.1016/j.chom.2009.04.010. Epub [PubMed PMID: 19454340]
Level 3 (low-level) evidenceHebbel RP, Vercellotti GM. SARS-CoV-2 severity in African Americans - A role for Duffy Null? Haematologica. 2020 Dec 1:105(12):2892. doi: 10.3324/haematol.2020.269415. Epub 2020 Dec 1 [PubMed PMID: 33054139]
Kircheis R, Schuster M, Planz O. COVID-19: Mechanistic Model of the African Paradox Supports the Central Role of the NF-κB Pathway. Viruses. 2021 Sep 21:13(9):. doi: 10.3390/v13091887. Epub 2021 Sep 21 [PubMed PMID: 34578468]
Duchene J, Novitzky-Basso I, Thiriot A, Casanova-Acebes M, Bianchini M, Etheridge SL, Hub E, Nitz K, Artinger K, Eller K, Caamaño J, Rülicke T, Moss P, Megens RTA, von Andrian UH, Hidalgo A, Weber C, Rot A. Atypical chemokine receptor 1 on nucleated erythroid cells regulates hematopoiesis. Nature immunology. 2017 Jul:18(7):753-761. doi: 10.1038/ni.3763. Epub 2017 May 29 [PubMed PMID: 28553950]
Level 3 (low-level) evidenceNaidoo KK, Ngubane A, Gaza P, Moodley A, Ndung'u T, Thobakgale CF. Neutrophil Effector Functions Are Not Impaired in Duffy Antigen Receptor for Chemokines (DARC)-Null Black South Africans. Frontiers in immunology. 2019:10():551. doi: 10.3389/fimmu.2019.00551. Epub 2019 Mar 26 [PubMed PMID: 30972057]
Rappoport N, Simon AJ, Amariglio N, Rechavi G. The Duffy antigen receptor for chemokines, ACKR1,- 'Jeanne DARC' of benign neutropenia. British journal of haematology. 2019 Feb:184(4):497-507. doi: 10.1111/bjh.15730. Epub 2018 Dec 27 [PubMed PMID: 30592023]
Dawson TC, Lentsch AB, Wang Z, Cowhig JE, Rot A, Maeda N, Peiper SC. Exaggerated response to endotoxin in mice lacking the Duffy antigen/receptor for chemokines (DARC). Blood. 2000 Sep 1:96(5):1681-4 [PubMed PMID: 10961863]
Level 3 (low-level) evidenceAkalin E, Neylan JF. The influence of Duffy blood group on renal allograft outcome in African Americans. Transplantation. 2003 May 15:75(9):1496-500 [PubMed PMID: 12792503]
Katznelson S, Gjertson DW, Cecka JM. The effect of race and ethnicity on kidney allograft outcome. Clinical transplants. 1995:():379-94 [PubMed PMID: 8794281]
Kläger J, Eskandary F, Böhmig GA, Kozakowski N, Kainz A, Colin Aronovicz Y, Cartron JP, Segerer S, Regele H. Renal allograft DARCness in subclinical acute and chronic active ABMR. Transplant international : official journal of the European Society for Organ Transplantation. 2021 Aug:34(8):1494-1505. doi: 10.1111/tri.13904. Epub 2021 Jun 25 [PubMed PMID: 33983671]
Unruh D, Srinivasan R, Benson T, Haigh S, Coyle D, Batra N, Keil R, Sturm R, Blanco V, Palascak M, Franco RS, Tong W, Chatterjee T, Hui DY, Davidson WS, Aronow BJ, Kalfa T, Manka D, Peairs A, Blomkalns A, Fulton DJ, Brittain JE, Weintraub NL, Bogdanov VY. Red Blood Cell Dysfunction Induced by High-Fat Diet: Potential Implications for Obesity-Related Atherosclerosis. Circulation. 2015 Nov 17:132(20):1898-908. doi: 10.1161/CIRCULATIONAHA.115.017313. Epub 2015 Oct 14 [PubMed PMID: 26467254]
Wan W, Liu Q, Lionakis MS, Marino AP, Anderson SA, Swamydas M, Murphy PM. Atypical chemokine receptor 1 deficiency reduces atherogenesis in ApoE-knockout mice. Cardiovascular research. 2015 Jun 1:106(3):478-87. doi: 10.1093/cvr/cvv124. Epub 2015 Apr 8 [PubMed PMID: 25858253]
Level 3 (low-level) evidenceThiriot A, Perdomo C, Cheng G, Novitzky-Basso I, McArdle S, Kishimoto JK, Barreiro O, Mazo I, Triboulet R, Ley K, Rot A, von Andrian UH. Differential DARC/ACKR1 expression distinguishes venular from non-venular endothelial cells in murine tissues. BMC biology. 2017 May 19:15(1):45. doi: 10.1186/s12915-017-0381-7. Epub 2017 May 19 [PubMed PMID: 28526034]
Level 3 (low-level) evidenceGirbl T, Lenn T, Perez L, Rolas L, Barkaway A, Thiriot A, Del Fresno C, Lynam E, Hub E, Thelen M, Graham G, Alon R, Sancho D, von Andrian UH, Voisin MB, Rot A, Nourshargh S. Distinct Compartmentalization of the Chemokines CXCL1 and CXCL2 and the Atypical Receptor ACKR1 Determine Discrete Stages of Neutrophil Diapedesis. Immunity. 2018 Dec 18:49(6):1062-1076.e6. doi: 10.1016/j.immuni.2018.09.018. Epub 2018 Nov 13 [PubMed PMID: 30446388]
Level 3 (low-level) evidenceKim HH, Park TS, Oh SH, Chang CL, Lee EY, Son HC. Delayed hemolytic transfusion reaction due to anti-Fyb caused by a primary immune response: a case study and a review of the literature. Immunohematology. 2004:20(3):184-6 [PubMed PMID: 15373650]
Level 3 (low-level) evidence