The LW blood group system: not just “tagging along” with D

1. Gahmberg CG, Valmu L, Kotovuori A, et al. Leukocyte adhesion: an integrated molecular process at the leukocyte plasma membrane. Biosci Rep 1999;19:273–81. Gahmberg CG Valmu L Kotovuori A . Leukocyte adhesion: an integrated molecular process at the leukocyte plasma membrane . Biosci Rep 1999 ; 19 : 273 – 81 . Search in Google Scholar

2. Hermand P, Gane P, Callebaut I, Kieffer N, Cartron J-P, Bailly P. Integrin receptor specificity for human red cell ICAM-4 ligand. Eur J Biochem 2004;271:3729–40. Hermand P Gane P Callebaut I Kieffer N Cartron J-P Bailly P . Integrin receptor specificity for human red cell ICAM-4 ligand . Eur J Biochem 2004 ; 271 : 3729 – 40 . Search in Google Scholar

3. Lee G, Lo A, Short SA, et al. Targeted gene deletion demonstrates that the cell adhesion molecule ICAM-4 is critical for erythroblastic island formation. Blood 2006;108:2064–71. Lee G Lo A Short SA . Targeted gene deletion demonstrates that the cell adhesion molecule ICAM-4 is critical for erythroblastic island formation . Blood 2006 ; 108 : 2064 – 71 . Search in Google Scholar

4. Hermand P, Gane P, Huet M, et al. Red cell ICAM-4 is a novel ligand for platelet-activated αIIbβ3 integrin. J Biol Chem 2003;278:4892–8. Hermand P Gane P Huet M . Red cell ICAM-4 is a novel ligand for platelet-activated α_IIbβ₃ integrin . J Biol Chem 2003 ; 278 : 4892 – 8 . Search in Google Scholar

5. Ihanus E, Uotila LM, Toivanen A, Varis M, Gahmberg CG. Red-cell ICAM-4 is a ligand for the monocyte/macrophage integrin CD11c/CD18: characterization of the binding sites on ICAM-4. Blood 2006;109:802–10. Ihanus E Uotila LM Toivanen A Varis M Gahmberg CG . Red-cell ICAM-4 is a ligand for the monocyte/macrophage integrin CD11c/CD18: characterization of the binding sites on ICAM-4 . Blood 2006 ; 109 : 802 – 10 . Search in Google Scholar

6. Levine P, Celano MJ, Wallace J, Sanger R. A human ‘D-like’ antibody. Nature 1963;198:596–7. Levine P Celano MJ Wallace J Sanger R. A human ‘D-like’ antibody . Nature 1963 ; 198 : 596 – 7 . Search in Google Scholar

7. Hermand P, Le Pennec PY, Rouger P, Cartron JP, Bailly P. Characterization of the gene encoding the human LW blood group protein in LW+ and LW– phenotypes. Blood 1996;87:2962–7. Hermand P Le Pennec PY Rouger P Cartron JP Bailly P . Characterization of the gene encoding the human LW blood group protein in LW+ and LW– phenotypes . Blood 1996 ; 87 : 2962 – 7 . Search in Google Scholar

8. Hermand P, Gane P, Mattei MG, Sistonen P, Cartron JP, Bailly P. Molecular basis and expression of the LWa/LWb blood group polymorphism. Blood 1995;86:1590–4. Hermand P Gane P Mattei MG Sistonen P Cartron JP Bailly P . Molecular basis and expression of the LWa/LWb blood group polymorphism . Blood 1995 ; 86 : 1590 – 4 . Search in Google Scholar

9. Sistonen P, Virtaranta-Knowles K, Denisova R, Kucinskas V, Ambrasiene D, Beckman L. The LWb blood group as a marker of prehistoric Baltic migrations and admixture. Hum Hered 1999;49:154–8. Sistonen P Virtaranta-Knowles K Denisova R Kucinskas V Ambrasiene D Beckman L . The LWb blood group as a marker of prehistoric Baltic migrations and admixture . Hum Hered 1999 ; 49 : 154 – 8 . Search in Google Scholar

10. Srivastava K, Almarry NS, Flegel WA. Genetic variation of the whole ICAM4 gene in Caucasians and African Americans. Transfusion 2014;54:2315–24. Srivastava K Almarry NS Flegel WA . Genetic variation of the whole ICAM4 gene in Caucasians and African Americans . Transfusion 2014 ; 54 : 2315 – 24 . Search in Google Scholar

11. Yin Q, Srivastava K, Schneider JB, Gebremedhin A, Makuria AT, Flegel WA. Molecular analysis of the ICAM4 gene in an autochthonous East African population. Transfusion 2019;59:1880–1. Yin Q Srivastava K Schneider JB Gebremedhin A Makuria AT Flegel WA . Molecular analysis of the ICAM4 gene in an autochthonous East African population . Transfusion 2019 ; 59 : 1880 – 1 . Search in Google Scholar

12. Lopez GH, Wilson B, Millard GM, et al. A new high-prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant. Vox Sang 2022;117:958–65. Lopez GH Wilson B Millard GM . A new high-prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant . Vox Sang 2022 ; 117 : 958 – 65 . Search in Google Scholar

13. Gauthier E, Kappler-Gratias S, Vallet D, et al. LW null phenotype: identification of two novel mutations in the LW gene. AABB Abstracts 2012;158A. Gauthier E Kappler-Gratias S Vallet D . LW null phenotype: identification of two novel mutations in the LW gene . AABB Abstracts 2012 ; 158A . Search in Google Scholar

14. Grandstaff Moulds MK. The LW blood group system: a review. Immunohematology 2011; 27:136–42. Grandstaff Moulds MK . The LW blood group system: a review . Immunohematology 2011 ; 27 : 136 – 42 . Search in Google Scholar

15. Storry JR. Review: the LW blood group system. Immunohematology 1992;8:87–93. Storry JR . Review: the LW blood group system . Immunohematology 1992 ; 8 : 87 – 93 . Search in Google Scholar

16. Sistonen P, Tippett P. A ‘new’ allele giving further insight into the LW blood group system. Vox Sang 1982;42:252–5. Sistonen P Tippett P. A ‘new’ allele giving further insight into the LW blood group system . Vox Sang 1982 ; 42 : 252 – 5 . Search in Google Scholar

17. Gibbs MB. The quantitative relationship of the Rh-like (LW) and D antigens of human erythrocytes. Nature 1966;210: 642–3. Gibbs MB . The quantitative relationship of the Rh-like (LW) and D antigens of human erythrocytes . Nature 1966 ; 210 : 642 – 3 . Search in Google Scholar

18. Merron BM, Maguire K, Morris K. When is an anti-D antibody not an anti-D antibody? Transfus Med 2015;25:115–7. Merron BM Maguire K Morris K . When is an anti-D antibody not an anti-D antibody? Transfus Med 2015 ; 25 : 115 – 7 . Search in Google Scholar

19. Miola MP, Cervo SV, Fachini RM, Ricci Júnior O. Do not confuse anti-LW autoantibodies with anti-D. Rev Bras Hematol Hemoter 2013;35:198. Miola MP Cervo SV Fachini RM Ricci Júnior O . Do not confuse anti-LW autoantibodies with anti-D . Rev Bras Hematol Hemoter 2013 ; 35 : 198 . Search in Google Scholar

20. Konigshaus GJ, Holland TI. The effect of dithiothreitol on the LW antigen. Transfusion 1984;24:536–7. Konigshaus GJ Holland TI . The effect of dithiothreitol on the LW antigen . Transfusion 1984 ; 24 : 536 – 7 . Search in Google Scholar

21. Bailly P, Hermand P, Callebaut I, et al. The LW blood group glycoprotein is homologous to intercellular adhesion molecules. Proc Natl Acad Sci U S A 1994;91:5306–10. Bailly P Hermand P Callebaut I . The LW blood group glycoprotein is homologous to intercellular adhesion molecules . Proc Natl Acad Sci U S A 1994 ; 91 : 5306 – 10 . Search in Google Scholar

22. Fraser NS, Knauth CM, Schoeman EM, et al. Investigation of the variable In(Lu) phenotype caused by KLF1 variants. Transfusion 2018;58:2414–20. Fraser NS Knauth CM Schoeman EM . Investigation of the variable In(Lu) phenotype caused by KLF1 variants . Transfusion 2018 ; 58 : 2414 – 20 . Search in Google Scholar

23. Zhang J, Abiraman K, Jones SM, Lykotrafitis G, Andemariam B. Regulation of active ICAM-4 on normal and sickle cell disease RBCs via AKAPs is revealed by AFM. Biophys J 2017;112:143–52. Zhang J Abiraman K Jones SM Lykotrafitis G Andemariam B . Regulation of active ICAM-4 on normal and sickle cell disease RBCs via AKAPs is revealed by AFM . Biophys J 2017 ; 112 : 143 – 52 . Search in Google Scholar

24. Zennadi R, Whalen EJ, Soderblom EJ, et al. Erythrocyte plasma membrane–bound ERK1/2 activation promotes ICAM-4–mediated sickle red cell adhesion to endothelium. Blood 2012;119:1217–27. Zennadi R Whalen EJ Soderblom EJ . Erythrocyte plasma membrane–bound ERK1/2 activation promotes ICAM-4–mediated sickle red cell adhesion to endothelium . Blood 2012 ; 119 : 1217 – 27 . Search in Google Scholar

25. MacKinney A, Woska E, Spasojevic I, Batinic-Haberle I, Zennadi R. Disrupting the vicious cycle created by NOX activation in sickle erythrocytes exposed to hypoxia/reoxygenation prevents adhesion and vasoocclusion. Redox Biol 2019;25:101097. MacKinney A Woska E Spasojevic I Batinic-Haberle I Zennadi R . Disrupting the vicious cycle created by NOX activation in sickle erythrocytes exposed to hypoxia/reoxygenation prevents adhesion and vasoocclusion . Redox Biol 2019 ; 25 : 101097 . Search in Google Scholar

26. McMahon TJ, Shan S, Riccio DA, et al. Nitric oxide loading reduces sickle red cell adhesion and vaso-occlusion in vivo. Blood Adv 2019;3:2586–97. McMahon TJ Shan S Riccio DA . Nitric oxide loading reduces sickle red cell adhesion and vaso-occlusion in vivo . Blood Adv 2019 ; 3 : 2586 – 97 . Search in Google Scholar

27. Bennett-Guerrero E, Veldman TH, Doctor A, et al. Evolution of adverse changes in stored RBCs. Proc Natl Acad Sci U S A 2007;104:17063–8. Bennett-Guerrero E Veldman TH Doctor A . Evolution of adverse changes in stored RBCs . Proc Natl Acad Sci U S A 2007 ; 104 : 17063 – 8 . Search in Google Scholar

28. Cowman AF, Tonkin CJ, Tham WH, Duraisingh MT. The molecular basis of erythrocyte invasion by malaria parasites. Cell Host Microbe 2017;22:232–45. Cowman AF Tonkin CJ Tham WH Duraisingh MT . The molecular basis of erythrocyte invasion by malaria parasites . Cell Host Microbe 2017 ; 22 : 232 – 45 . Search in Google Scholar

29. Bhalla K, Chugh M, Mehrotra S, et al. Host ICAMs play a role in cell invasion by Mycobacterium tuberculosis and Plasmodium falciparum. Nat Commun 2015;6:6049. Bhalla K Chugh M Mehrotra S . Host ICAMs play a role in cell invasion by Mycobacterium tuberculosis and Plasmodium falciparum . Nat Commun 2015 ; 6 : 6049 . Search in Google Scholar