Duguid JP, Smith W, Dempster G, Edmunds PN. Nonflagellar filamentous appendages (“fimbriae”) and haemagglutinating activity in Bacterium coli. Pathol Bacteriol 1955;70:335–48.10.1002/path.170070021013295908Search in Google Scholar
Kuijpers TW. Terminal glycosyltransferase activity: a selective role in cell adhesion (review article). Blood 1993;81(4): 873–82.10.1182/blood.V81.4.873.873Search in Google Scholar
Sharon N, Lis H. Carbohydrates in cell recognition. Scientific American 1993;268:82–9.10.1038/scientificamerican0193-827678182Search in Google Scholar
Sharon N, Lis H. Lectins as cell recognition molecules. Science 1989;246:227–34.10.1126/science.25525812552581Search in Google Scholar
Knutton S, Lloyd DR, David CA, Candy A, McNeish AS. Ultrastructural study of adhesion of enterotoxigenic Escherichia coli to erythrocytes and human intestinal epithelial cells. Infect Immun 1984;44:519–27.10.1128/iai.44.2.519-527.19842635516143731Search in Google Scholar
Källenius G, Mollby R, Svenson SB, et al. The P antigen as receptor for the hemagglutinin of pyelonephritic Escherichia coli. FEMS Microbiol Lett 1980;7:297–302.10.1111/j.1574-6941.1980.tb01608.xSearch in Google Scholar
Moulds JM, Woods LL, eds. Blood groups: P, I, Sda and Pr. Arlington, VA: American Association of Blood Banks, 1991.Search in Google Scholar
Nowicki B, Moulds J, Hull R, Hull S. A hemagglutinin of uropathogenic Escherichia coli recognizes the Dr blood group antigen. Infect Immun 1988;56:1057–60.10.1128/iai.56.5.1057-1060.19882597612895740Search in Google Scholar
Loomes LM, Uemura K-I, Childs RA, et al. Erythrocyte receptors for Mycoplasma pneumoniae are sialylated oligosaccharides of Ii antigen type. Nature 1984;307:560–3.10.1038/307560a06420710Search in Google Scholar
König AL, Kreft H, Hengge U, Braun RW, Roelcke D. Coexisting anti-I and anti-FI/Gd cold agglutinins in infections by Mycoplasma pneumoniae. Vox Sang 1988;55:176–80.10.1111/j.1423-0410.1988.tb05088.x2853491Search in Google Scholar
van Alphen L, Poole J, Overbeeke M. The Anton blood group antigen is the erythrocyte receptor for Haemophilus influenzae. FEMS Microbiol Lett 1986;37:69–71.Search in Google Scholar
Daniels G. The Lutheran blood group system: monoclonal antibodies, biochemistry and the effect of In(Lu). In: Pierce SR, Macpherson CR, eds. Blood group systems: Duffy, Kidd, and Lutheran. Arlington, VA: American Association of Blood Banks, 1988:119–47.Search in Google Scholar
van Alphen L, Poole J, Geelen L, Zanen HC. The erythrocyte and epithelial cell receptors for Haemophilus influenzae are expressed independently. Infect Immun 1987;55:2353–8.10.1128/iai.55.10.2355-2358.19872607122888731Search in Google Scholar
Poole J, Levene C, Bennett M, Sela R, van Alphen L, Spruell PJ. A family showing inheritance of the Anton blood group antigen AnWj and independence of AnWj from Lutheran. Transfusion Medicine 1991;1:245–51.10.1111/j.1365-3148.1991.tb00040.xSearch in Google Scholar
van Alphen L, Levene C, Geelen-van den Broek L, Poole J, Bennett M, Dankert J. Combined inheritance of epithelial and erythrocyte receptors for Haemophilus influenzae. Infect Immun 1990;58:3807–9.10.1128/iai.58.11.3807-3809.1990Search in Google Scholar
Parsons SF, Jones J, Poole J, Anstee DJ, Illum N, Wickramasinghe SN. An In(a-b-) individual whose red cells are deficient in CD44 glycoprotein also lacks the high incidence antigen AnWj. Transfusion Medicine 1992;2:65.Search in Google Scholar
Nowicki B, Holthöfer H, Saraneva T, Rhen M, Väisänen-Rhen V, Korhonen T. Location of adhesion sites for P-fimbriated and for 075X-positive Escherichia coli in the human kidney. Microbial Pathogenesis 1986;1:169–80.10.1016/0882-4010(86)90019-7Search in Google Scholar
Karr JF, Nowicki BJ, Truong LD, Hull RA, Moulds JJ, Hull SI. pap-2 encoded fimbriae adhere to the P blood group-related glycosphingolipid stage-specific embryonic antigen 4 in the human kidney. Infect Immun 1990;58:4055–62.10.1128/iai.58.12.4055-4062.19903137761979319Search in Google Scholar
Lomberg H, Hansen LA, Jacobsson B, et al. Correlation of P blood group, vesicoureteral reflux, and bacterial attachment in patients with recurrent pyelonephritis. N Engl J Med 1983;308:1189–92.10.1056/NEJM1983051930820036341837Search in Google Scholar
Sheinfeld J, Schaeffer AJ, Cordon-Cardo C, Rogatko A, Fair WR. Association of the Lewis blood-group phenotype with recurrent urinary tract infections in women. N Engl J Med 1989;320:773–7.10.1056/NEJM1989032332012052922027Search in Google Scholar
Lomberg H, Cedergren B, Leffler H, et al. Influence of blood groups on the availability of receptors for attachment of uropathogenic Escherichia coli. Infect Immun 1986;51:919–26.10.1128/iai.51.3.919-926.19862609862868993Search in Google Scholar
Lurie S, Sigler E, Fenakel K. The ABO, Lewis, or P blood group phenotypes are not associated with recurrent pelvic inflammatory disease. Gynecol Obstet Invest 1991 ;31:158–60.10.1159/0002931392071054Search in Google Scholar
Johnson JR, Swanson JL, Neill MA. Avian P1 antigens inhibit agglutination mediated by P fimbriae of uropathogenic Escherichia coli. Infect Immun 1992;60:578–83.10.1128/iai.60.2.578-583.19922576671346125Search in Google Scholar
Storr JR. Serology and genetics of the Cromer blood group system. In: Moulds JM, Laird-Fryer B, eds. Blood groups: Ch/Rg, Kn/McC/Yk, Cromer. Bethesda, MD: American Association of Blood Banks, 1992:31–43.Search in Google Scholar
Telen MJ. Cromer blood group antigens on decay-accelerating factor. In: Moulds JM and Laird-Fryer B, eds. Blood groups: Ch/Rg, Kn/McC/Yk, Cromer. Bethesda, MD: American Association of Blood Banks, 1992:45–63.Search in Google Scholar
Telen MJ. Phosphatidylinositol-linked red blood cell membrane proteins and blood group antigens. Immunohematology 1991;7:(3)65–72.10.21307/immunohematology-2019-1014Search in Google Scholar
Nowicki B, Truong L, Moulds J, Hull R. Presence of the Dr receptor in normal human tissues and its possible role in the pathogenesis of ascending urinary tract infection. Am J Pathol 1988;133:1–4.Search in Google Scholar
Hadley TJ, Miller LH, Haynes JD. Recognition of red cells by malaria parasites: the role of erythrocyte-binding proteins. Transfusion Medicine Reviews 1991;V(2):108–22.10.1016/S0887-7963(91)70198-3Search in Google Scholar
Valko DA. The Duffy blood group system: biochemistry and role in malaria. In: Pierce SR, Macpherson CR, eds. Blood group systems: Duffy, Kidd, and Lutheran. Arlington, VA: American Association of Blood Banks, 1988:27–52.Search in Google Scholar
Young M, Eyles D, Burgess R, Jeffrey G. Experimental testing of the immunity of Negroes to Plasmodium vivax. J Parasitol 1955;41:315–8.10.2307/3274214Search in Google Scholar
Sanger R, Race R, JackJ. The Duffy blood groups of New York Negroes: the phenotype Fy(a-b-). Br J Haematol 1955;1:370–4.10.1111/j.1365-2141.1955.tb05523.x13269673Search in Google Scholar
Miller LH, Mason SJ, Dvorak JA, McGinniss MH, Rothman IK. Erythrocyte receptors for (Plasmodium knowlesi) malaria: Duffy blood group determinants. Science 1975;189:561–3.10.1126/science.11452131145213Search in Google Scholar
Miller L, Aikawa M, Johnson J, Shiroishi T. Interaction between cytochalasin B-treated malarial parasites and erythrocytes: attachment and junction formation. J Exp Med 1979;149: 172–84.10.1084/jem.149.1.1722184746105074Search in Google Scholar
Mason SJ, Miller LH, Shiroishi T, Dvorak JA, McGinniss MH. The Duffy blood group determinants: their role in the susceptibility of human and animal erythrocytes to Plasmodium knowlesi malaria. Br J Haematol 1977;36:327–35.10.1111/j.1365-2141.1977.tb00656.x70210Search in Google Scholar
Nichols ME, Rubinstein P, Barnwell J, de Cordoba SR, Rosenfield RE. A new human Duffy blood group specificity defined by a murine monoclonal antibody. Immunogenetics and association with susceptibility to Plasmodium vivax. J Exp Med 1987;166:776–85.10.1084/jem.166.3.77621886972442291Search in Google Scholar
Hadley T, David P, McGinnis M, Miller L. Identification of an erythrocyte component carrying the Duffy blood group Fya antigen. Science 1984;223:597–9.10.1126/science.66951716695171Search in Google Scholar
Horuk R, Chitnis C, Darbonne W, Colby T, Rybicki A, Hadley T, Miller L. A receptor for the malarial parasite Plasmodium vivax: the erythrocyte chemokine receptor. Science 1993;261:1182–4.10.1126/science.76892507689250Search in Google Scholar
Miller L, Haynes J, McAuliffe F, Shiroishi T, Durocher J, McGinnis M. Evidence for differences in erythrocyte surface receptors for the malarial parasites Plasmodium falciparum and Plasmodium knowlesi. J Exp Med 1977;146:277–81.10.1084/jem.146.1.2772180731327014Search in Google Scholar
Pasvol G, Waincoat J, Weatherall D. Erythrocytes deficient in glycophorin resist invasion by the malarial parasite Plasmodium falciparum. Nature 1982;297:64–6.10.1038/297064a0Search in Google Scholar
Hermentin P, Enders B, Neunziger G, et al. Wr(a+b-) red blood cells are fully susceptible to invasion by Plasmodium falciparum (letter). Lancet 1984;2:466.10.1016/S0140-6736(84)92942-8Search in Google Scholar
Rhen M, Klemm P, Korhonen TK. Identification of two new hemagglutinins of Escherichia coli, N-acetyl-D-glucosamine-specific fimbriae and a blood group M-specific agglutinin, by cloning the corresponding genes in Escherichia coli K-12. J Bacteriol 1986;168:1234–42.10.1128/jb.168.3.1234-1242.1986Search in Google Scholar
Cooper NR. Complement evasion strategies of microorganisms. Immunol Today 1991;12:327–31.10.1016/0167-5699(91)90010-QSearch in Google Scholar
Norris KA, Bradt BM, Cooper NR. Inhibition of alternative complement pathway activation by a 160-kDa binding protein of Trypanosoma cruzi (abstract). Complement Inflamm 1991;8:200.Search in Google Scholar
Boren T, Falk P, Roth KA, Larson G, Normark S. Attachment of Helicobacter pylori to human gastric epithelium mediated by blood group antigens. Science 1993;262:1892–5.10.1126/science.80181468018146Search in Google Scholar
Brown KE, Anderson SM, Young NS. Erythrocyte P antigen: cellular receptor for B19 parvovirus. Science 1993;262: 114–7.10.1126/science.82111178211117Search in Google Scholar
Brown KE, Hibbs JR, Gallinell G, et al. Resistance to parvovirus B19 infection due to lack of virus receptor (erythrocyte P antigen). N Engl J Med 1994;330:1192–6.10.1056/NEJM1994042833017048139629Search in Google Scholar
