H-deficient Bombay and para-Bombay red blood cells are most strongly agglutinated by the galactophilic lectins of Aplysia and Pseudomonas aeruginosa that detect I and P1 antigens
Morgan WTJ, Watkins WM. The inhibition of the haemagglutinins in plant seeds by human blood group substances and simple sugars. Br J Exp Pathol 1953;34:94-103.Search in Google Scholar
Kabat EA. The blood group substances. New York: Academic Press, 1956:1-330.10.1016/B978-1-4832-2933-1.50004-7Search in Google Scholar
Race RR, Sanger R. Blood groups in man. Oxford: Blackwell Scientific Publications, 1975.Search in Google Scholar
Daniel GL. Human blood groups. 2nd ed. Oxford, UK: Blackwell Science, 2002.Search in Google Scholar
Judd WJ. The role of lectins in blood group serology. Crit Rev Clin Lab Sci 1980;12:171-214.10.3109/10408368009108729Search in Google Scholar
Bird GWG. Lectins in immunohematology. Transfus Med Rev 1989;3:55-62.10.1016/S0887-7963(89)70068-7Search in Google Scholar
Levene C, Gilboa-Garber N, Garber NC. Lectin-blood group interactions. In: Doyle RJ, Slifkin M, eds. Lectin-microorganism interactions. New York: Marcel Dekker, Inc., 1994:327-93.Search in Google Scholar
Hindsgaul O, Khare DP, Bach M, Lemieux RU. Molecular recognition. III. The binding of the H-type 2 human blood group determinant by the lectin 1 of Ulex europaeus. Can J Chem 1985;63:2653-8.10.1139/v85-440Search in Google Scholar
Bhende YM, Deshpande CK, Bhatia HM, et al. A “new” blood-group character related to the ABO system. Lancet 1952;1:903-4.Search in Google Scholar
Bird GWG. Anti-T in peanuts. Vox Sang 1964;25:748-9.10.1111/j.1423-0410.1964.tb04072.xSearch in Google Scholar
Bird GWG. Relationship of the blood sub-groups A1, A2 and A1B, A2B to haemagglutinins present in the seeds of Dolichos biflorus. Nature 1952;170:674.10.1038/170674a0Search in Google Scholar
Bird GWG, Wingham J. Seed agglutinin for rapid identification of Tn-polyagglutination. Lancet 1973;1:677.Search in Google Scholar
Hakomori S. Aberrant glycosylation in tumors and tumor-associated carbohydrate antigens. Adv Cancer Res 1989;52:257-331.10.1016/S0065-230X(08)60215-8Search in Google Scholar
Hakomori S. Blood group ABH and Ii antigens of human erythrocytes: chemistry, polymorphism, and their developmental change. Semin Hematol 1981;18:39-62.Search in Google Scholar
Sarkar M, Wu AM, Kabat EA. Immunochemical studies on the carbohydrate specificity of Maclura pomifera lectin. Arch Biochem Biophys 1981;209:204-18.10.1016/0003-9861(81)90273-3Search in Google Scholar
Gilboa-Garber N, Susswein AJ, Mizrahi L, Avichezer D. Purification and characterization of the gonad lectin of Aplysia depilans. FEBS Lett 1985; 181:267-70.10.1016/0014-5793(85)80273-8Search in Google Scholar
Gilboa-Garber N, Wu AM. Binding properties and applications of Aplysia gonad lectin. Adv Exp Med Biol 2001;491:109-26.10.1007/978-1-4615-1267-7_814533793Search in Google Scholar
Gilboa-Garber N. Inhibition of broad spectrum hemagglutinin from Pseudomonas aeruginosa by D-galactose and its derivatives. FEBS Lett 1972; 20:242-4.10.1016/0014-5793(72)80805-6Search in Google Scholar
Gilboa-Garber N, Katcoff DJ, Garber NC. Identification and characterization of Pseudomonas aeruginosa PA-IIL lectin gene and protein compared to PA-IL. FEMS Immunol Med Microbiol 2000;29:53-7.10.1111/j.1574-695X.2000.tb01505.xSearch in Google Scholar
Gilboa-Garber N. Pseudomonas aeruginosa lectins. Methods Enzymol 1982;83:378-85.10.1016/0076-6879(82)83034-6Search in Google Scholar
Garber N, Guempel U, Gilboa-Garber N, Doyle RJ. Specificity of the fucose-binding lectin of Pseudomonas aeruginosa. FEMS Microbiol Lett 1987;48:331-4.10.1111/j.1574-6968.1987.tb02619.xSearch in Google Scholar
Gilboa-Garber N, Sudakevitz D, Sheffi M, Sela R, Levene C. PA-I and PA-II lectin interactions with the ABO(H) and P blood group glycosphingolipid antigens may contribute to the broad spectrum adherence of Pseudomonas aeruginosa to human tissues in secondary infections. Glycoconj J 1994;11:414-7.10.1007/BF007312767696845Search in Google Scholar
Mitchell E, Houles C, Sudakevitz D, et al. Structural basis for oligosaccharide-mediated adhesion of Pseudomonas aeruginosa in the lung of cystic fibrosis patients. Nature Struct Biol 2002;9:918-21.10.1038/nsb86512415289Search in Google Scholar
Gilboa-Garber N, Sudakevitz D. Usage of Aplysia lectin interactions with T antigen and poly N-acetyllactosamine for screening of E. coli strains which bear glycoforms cross-reacting with cancer-associated antigens. FEMS Immunol Med Microbiol 2001;30:235-40.10.1111/j.1574-695X.2001.tb01576.x11335144Search in Google Scholar
Wu AM, Song S-C, Chen Y-Y, Gilboa-Garber N. Defining the carbohydrate specificities of Aplysia gonad lectin exhibiting a peculiar D-galacturonic acid affinity. J Biol Chem 2000;275:14017-24.10.1074/jbc.275.19.1401710799474Search in Google Scholar
Sudakevitz D, Levene C, Gilboa-Garber N. The galactophilic lectins of Pseudomonas aeruginosa and Aplysia differentiate between I-positive and I-negative human erythrocytes. In: Van Driessche E, Rouge P, Beeckmans TC, Bog-Hansen TC, eds. Lectins: biology, biochemistry, clinical biochemistry. Hellerup (Denmark): Textop, 1996: 207-11.Search in Google Scholar
Bausch JN, Poretz RD. Purification and properties of the hemagglutinin from Maclura pomifera seeds. Biochemistry 1977;16:5790-4.10.1021/bi00645a023588553Search in Google Scholar
Allen FHJ, Marsh WL, Jensen L, Fink J. Anti-IP: an antibody defining another product of interaction between the genes of the I and P blood group systems. Vox Sang 1974;27:422-6.10.1111/j.1423-0410.1974.tb02440.x4607508Search in Google Scholar
Sudakevitz D, Levene C, Sela R, Gilboa-Garber N. Differentiation between human erythrocytes of PK and p blood types using Pseudomonas aeruginosa PA-I lectin. Transfusion 1996;36:113-6.10.1046/j.1537-2995.1996.36296181921.xSearch in Google Scholar
Lotan R, Skutelsky E, Danon D, Sharon N. The purification, composition, and specificity of the anti-T lectin from peanut (Arachis hypogaea). J Biol Chem 1975;250:8518-23.10.1016/S0021-9258(19)40790-4Search in Google Scholar
Debray H, Decout D, Strecker G, Spik G, Montreuil J. Specificity of twelve lectins towards oligosaccharides and glycopeptides related to N-glycosylproteins. Eur J Biochem 1981;117:41-55.10.1111/j.1432-1033.1981.tb06300.x7262089Search in Google Scholar
Chen C-P, Song SC, Gilboa-Garber N, Chang KSS, Wu AM. Studies on the binding site of the galactose-specific agglutinin PA-IL from Pseudomonas aeruginosa. Glycobiology 1998; 8:7-16.10.1093/glycob/8.1.79451010Search in Google Scholar
Moulds JM, Nowicki S, Moulds JJ, Nowicki BJ. Human blood groups: incidental receptors for viruses and bacteria. Transfusion 1996;36:362-74.10.1046/j.1537-2995.1996.36496226154.x8623141Search in Google Scholar
Oriol R, Danilovs J, Hawkins BR. A new genetic model proposing that the Se gene is a structural gene closely linked to the H gene. Am J Hum Genet 1981;33:421-31.Search in Google Scholar
Chen DP, Tseng CP, Wang WT, et al. Two prevalent h alleles in para-Bombay haplotypes among 250,000 Taiwanese. Ann Clin Lab Sci 2004;34: 314-8.Search in Google Scholar
Daniels GL, Anstee DJ, Cartron JP, et al. International Society of Blood Transfusion Working Party on Terminology for Red Cell Surface Antigens. Vox Sang 2001;80:193-7.10.1046/j.1423-0410.2001.00024.x11449960Search in Google Scholar
Yip SP, Chee KY, Chan PY, Chow EY, Wong HF. Molecular genetic analysis of para-Bombay phenotypes in Chinese: a novel non-functional FUT1 allele is identified. Vox Sang 2002;83:258-62.10.1046/j.1423-0410.2002.00184.x12366770Search in Google Scholar
Kaneko M, Nishihara S, Shinya N, et al. Wide variety of point mutations in the H gene of Bombay and para-Bombay individuals that inactivate H enzyme. Blood 1997;90:839-49.10.1182/blood.V90.2.839Search in Google Scholar
Kelly RJ, Ernst LK, Larsen RD, et al. Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals. Proc Natl Acad Sci U S A 1994;91:5843-7.10.1073/pnas.91.13.5843440937912436Search in Google Scholar
Herron R, Greenwell P, Westwood MC, et al. An H-deficient blood with normal H transferase levels. Vox Sang 1980;39:186-94.10.1111/j.1423-0410.1980.tb01856.x7210607Search in Google Scholar
Shechter Y, Etzioni A, Levene C, Greenwell P. A Bombay individual lacking H and Le antigens but expressing normal levels of alpha-2- and alpha-4-fucosyltransferases. Transfusion 1995;35:773-6.10.1046/j.1537-2995.1995.35996029164.xSearch in Google Scholar
Khare DP, Hindsgaul O, Lemieux RU. The synthesis of monodeoxy derivatives of lacto-N-biose I and N-acetyl-lactosamine to serve as substrates for the differentiation of α-L-fucosyl transferases. Carbohydr Res 1985;136:285-308.10.1016/0008-6215(85)85204-6Search in Google Scholar
Le Pendu J, Cartron JP, Lemieux RU, Oriol R. The presence of at least two different H-blood-group-related beta-D-gal alpha-2-L-fucosyltransferases in human serum and the genetics of blood group H substances. Am J Hum Genet 1985;37:749-60.Search in Google Scholar
Sarnesto A, Kohlin T, Thurin J, Blaszczyk-Thurin M. Purification of H gene-encoded beta-galactoside alpha 1-2 fucosyltransferase from human serum. J Biol Chem 1990;265:15067-75.10.1016/S0021-9258(18)77224-4Search in Google Scholar
Naiki M, Marcus DM. An immunochemical study of the human blood group P1, P, and PK glycosphingolipid antigens. Biochemistry 1975;14:4837-41.10.1021/bi00693a0101182122Search in Google Scholar
Tippett P, Noades J, Sanger R, Race RR, Laima S. Further studies of the I antigen and antibody. Vox Sang 1960;5:107-21.10.1111/j.1423-0410.1960.tb04668.xSearch in Google Scholar
Beck ML. The I blood group collection. In: Moulds JM, Woods LL, eds. Blood groups: P, I, Sda and Pr. Arlington, VA: American Association of Blood Banks, 1991:23-52.Search in Google Scholar
Feizi T, Kabat EA, Vicari G, Anderson B, Marsh WL. Immunochemical studies on blood groups. XLIX. The I antigen complex: specificity differences among anti-I sera revealed by quantitative precipitin studies; partial structure of the I determinant specific for one anti-I serum. J Immunol 1971;106:1578-92.10.4049/jimmunol.106.6.1578Search in Google Scholar
Imberty A, Wimmerova M, Mitchell EP, Gilboa-Garber N. Structures of the lectins from Pseudomonas aeruginosa: insights into the molecular basis for host glycan recognition. Microbes Infect 2004;6:221-8.10.1016/j.micinf.2003.10.01615049333Search in Google Scholar
