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Alloimmunity

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proinflammatory Th1, Th17 lymphocytes and anti-inflammatory regulatory T cells. This is influenced by cytokine microenvironment, as mentioned before, where CD4 T-lymphocytes are activated and also by inflammation level (because pathogens invading organism activate the immune system to various degrees and causing proinflammatory cytokine secretion, therefore they support the rejection). Immunosuppressive drugs are used to suppress the immune response, but the effect is not specific. Therefore, organism can be affected by the infection much more easily. The goal of the future therapies is to suppress the alloimmune response specifically to prevent these risks. The tolerance could be achieved by elimination of most or all alloreactive T cells and by influencing alloreactive effector-regulatory T-lymphocytes ratio in favor of regulatory cells which could inhibit alloreactive effector cells. Another method would be based on costimulatory signal blockade during alloreactive T-lymphocytes activation.
426:). This promotes APC maturation which leads to amplification of T-cell alloreactivity by means of direct and also indirect pathway of alloantigen recognition (as described below). NK cells are able to kill Foxp3 regulatory T-lymphocytes as well and shift the immune response from graft tolerance toward its rejection. Besides the ability of NK cells to influence APC maturation and T cell development, they can probably reduce or even prevent alloimmune response to transplanted tissue – either by killing the Donor APCs or by anti-inflammatory cytokine IL-10 and TGF-β secretion. However it is important to note that NK cell sub-populations differ in alloreactivity rate and in their immunomodulatory potential. Concerning 422:) family bind concrete MHC class I molecules. If the graft has these ligands on its surface, NK cell cannot be activated (KIR receptors provide inhibitory signal). So if these ligands are missing, there is no inhibitory signal and NK cell becomes activated. It recognizes target cells by "missing-self strategy" and induces their apoptosis by enzymes perforin and granzymes released from its cytotoxic granules. Alloreactive NK cells also secrete proinflammatory cytokines IFN-γ and TNF-α to increase expression of MHC molecules and costimulatory receptors on the surface of APCs ( 460:– recipient's APCs infiltrate transplanted tissue, then they process and present, as any other foreign peptides, donor's MHC glycoproteins by MHC class II molecules. Mechanism of indirect allorecognition and therefore the involvement of CD4 T-lymphocytes is the main cause of graft rejection. That is why the compatibility between donor and recipient MHC class II molecules is the most important factor concerning transplantation. 477:
signaling resulting in IL-2 production, clonal expansion and therefore development of effector and memory T-lymphocytes. In contrast, there are also such receptors on T-lymphocytes that cause inhibition of T-cell activation (for instance CD152/CTLA-4 receptor which binds CD80 and CD86 as well). If T-lymphocyte does not receive costimulatory signal, its activation fails and it becomes
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Lafferty KJ, Prowse SJ, Simeonovic CJ, Warren HS (1983), Immunobiology of tissue transplantation: a return to the passenger leukocyte concept. Annu Rev Immunol.1:143-73 – according to Archbold JK, Ely LK, Kjer-Nielsen L, Burrows SR, Rossjohn J, McCluskey J, Macdonald WA (2008), T-cell allorecognition
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development. These cells may represent a serious problem after the transplantation. As the effect of being exposed to various infections in the past, antigen-specific T-lymphocytes have developed in patient's body. Part of them is kept in organism as memory cells and these cells could be a reason for
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Ashton-Chess J, Giral M, Brouard S, Soulillou JP (2007), Spontaneous operational tolerance after immunosuppressive drug withdrawal in clinical renal allotransplantation. Transplantation. 84(10):1215-9 – according to Sánchez-Fueyo A, Strom TB (2011), Immunologic basis of graft rejection and tolerance
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Jenkins MK, Taylor PS, Norton SD, Urdahl KB (1991), CD28 delivers a costimulatory signal involved in antigen-specific IL-2 production by human T cells. J Immunol. 147(8):2461-6 – according to Priyadharshini B, Greiner DL, Brehm MA (2012), T-cell activation and transplantation tolerance. Transplant
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Transplanted tissue is accepted by immunocompetent recipient if it is functional in the absence of immunosuppressive drugs and without histologic signs of rejection. Host can accept another graft from the same donor but reject graft from different donor. Graft acceptance depends on the balance of
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Walunas TL, Lenschow DJ, Bakker CY, Linsley PS, Freeman GJ, Green JM, Thompson CB, Bluestone JA (1994), CTLA-4 can function as a negative regulator of T cell activation. Immunity. ;1(5):405-13 – according to Priyadharshini B, Greiner DL, Brehm MA (2012), T-cell activation and transplantation
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T-lymphocytes must receive costimulatory signal. There are costimulatory molecules on T-cell surface and APCs express their ligands (e.g. molecule CD28, which is on the surface of all naĂŻve CD4 and CD8 T-lymphocytes, can bind ligands CD80 and CD86). Receptor-ligand engagement triggers T-cell
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is impaired. In many instances the maternal immune system attacks the fetal blood cells, resulting in fetal anemia. HDN ranges from mild to severe. Severe cases require intrauterine transfusions or early delivery to survive, while mild cases may only require phototherapy at birth.
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De Maria A, Fogli M, Mazza S, Basso M, Picciotto A, Costa P, Congia S, Mingari MC, Moretta L (2007), Increased natural cytotoxicity receptor expression and relevant IL-10 production in NK cells from chronically infected viremic HCV patiens. Eur J Immunol.
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Humoral (antibody-mediated) type of rejection is caused by recipient's B-lymphocytes which produce alloantibodies against donor MHC class I and II molecules. These alloantibodies can activate the complement – this leads to target cell
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McNerney ME, Lee KM, Zhou P, Molinero L, Mashayekhi M, Guzior D, Sattar H, Kuppireddi S, Wang CR, Kumar V, Alegre ML (2006), Role of natural killer cell subsets in cardiac allograft rejection. Am J Transplant.
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through Fc receptors of mononuclear leukocytes. Mechanism of humoral rejection is relevant for hyperacute, accelerated and chronic rejection. Alloimmunity can be also regulated by neonatal B cells.
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NK cells can also directly target the transplanted tissue. It depends on the balance of activating and inhibitory NK cell receptors and on their ligands expressed by the graft. Receptors of KIR (
450:– occurs when donor's APCs are presenting graft antigens. Recipient's T-lymphocytes can identify either MHC molecules alone or complex MHC molecule-foreign peptide as alloantigens. Specific 688:
Korn T, Bettelli E, Gao W, Awasthi A, Jäger A, Strom TB, Oukka M, Kuchroo VK (2007), IL-21 initiates an alternative pathway to induce proinflammatory T(H)17 cells. Nature 448(7152):484-7
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Jenkins MK, Schwartz RH (1987), Antigen presentation by chemically modified splenocytes induces antigen-specific T cell unresponsiveness in vitro and in vivo. J Exp Med. 165(2):302-19
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Fangmann J, Dalchau R, Fabre JW (1992), Rejection of skin allografts by indirect allorecognition of donor class I major histocompatibility complex peptides. J Exp Med. 175(6):1521-9
454:(TCR) of CD8 T-lymphocytes recognize these peptides when form the complex with MHC class I molecules and TCR of CD4 T-lymphocytes recognize a complex with MHC class II molecules. 490:"cross-reactivity" – immune response against unrelated but similar graft alloantigens. This immune response is called secondary and is faster, more efficient and more robust. 629:
Fang Li, Mary E. Atz, Elaine F. Reed (2009), Human leukocyte antigen antibodies in chronic transplant vasculopathy-mechanisms and pathways. Curr Opin Immunol. 21(5): 557–562
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Sánchez-Fueyo A, Strom TB (2011), Immunologic basis of graft rejection and tolerance following transplantation of liver or other solid organs. Gastroenterology 140(1):51-64
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Alloimmune response can be enhanced by proinflammatory cytokines and by CD4 T-lymphocytes that are responsible for APC maturation and IL-2 production. IL-2 is crucial for
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Williams MA, Tyznik AJ, Bevan MJ (2006), Interleukin-2 signals during priming are required for secondary expansion of CD8 memory T cells. Nature. 441(7095):890-3
1307: 189:. They recognize transplanted tissue because of expression of alloantigens. A transplant is rejected during first several days or weeks after transplantation. 1444: 843:
Ahmed EB, Daniels M, Alegre ML, Chong AS (2011), Bacterial infections, alloimmunity, and transplantation tolerance. Transplant Rev (Orlando). 25(1):27-35
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Yu G, Xu X, Vu MD, Kilpatrick ED, Li XC (2006), NK cells promote transplant tolerance by killing donor antigen-presenting cells. J Exp Med. 203(8):1851-8
560: 1149: 221:. This type of rejection is very fast, the graft is rejected in a few minutes or hours after the transplantation. Accelerated rejection leads to 906: 852:
Ford ML, Larsen CP (2009), Translating costimulation blockade to the clinic - lessons learned from three pathways. Immunol Rev. 229(1):294-306
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Li XC, Rothstein DM, Sayegh MH (2009), Costimulatory pathways in transplantation: challenges and new developments. Immunol Rev. 229(1):271-93
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Seetharam A, Tiriveedhi V, Mohanakumar T (2010), Alloimmunity and autoimmunity in chronic rejection. Curr Opin Organ Transplant 15(4):531-536
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Gould DS, Auchincloss H Jr (1999), Direct and indirect recognition: the role of MHC antigens in graft rejection. Immunol Today. 20(2):77-82
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Hyperacute and accelerated rejection is antibody-mediated immune response to the allograft. Recipient's blood already contains circulating
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of the blood vessels is being damaged, therefore the graft is not sufficiently supplied with blood and is replaced with fibrous tissue (
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Villard J. (2011), The role of natural killer cells in human solid organ and tissue transplantation. J Innate Immun. 3(4): 395-402
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Walsh PT, Strom TB, Turka LA (2004), Routes to transplant tolerance versus rejection: the role of cytokines. Immunity (20):121-131
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is similar to a transfusion reaction in that the mother's antibodies cannot tolerate the fetus's antigens, which happens when the
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Curtsinger JM, Mescher MF (2010), Inflammatory cytokines as a third signal for T cell activation. Curr Opin Immunol. 22(3):333-40
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along with other mononuclear leukocytes (their exact function regarding the topic is not known) participate in the rejection.
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that bind Fc parts of antibodies. Graft rejection occurs within 3 to 5 days. This type of rejection is a typical response to
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Welsh RM, Selin LK (2002), No one is naive: the significance of heterologous T-cell immunity. Nat Rev Immunol. 2(6):417-26
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T-lymphocytes must recognize complex MHC-alloantigen presented by APC through direct or indirect allorecognition pathway.
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Chronic rejection is not yet fully understood, but it is known that it is associated with alloantibody and
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Alloantigen on APC surface can be recognized by recipient's T-lymphocytes through two different pathways:
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gene in the absence of proinflammatory cytokines and thus differentiation of CD4 T-lymphocytes into
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T-lymphocytes recognize alloantigens significantly influences polarization of the immune response.
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following transplantation of liver or other solid organs. Gastroenterology 140(1):51-64
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can result in alloantibodies reacting towards the transfused cells, resulting in a
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and MHC-restriction – A case of Jekyll and Hyde? Mol Immunol. 45(3):583-98
304:. Alternatively, donor cells are coated with alloantibodies that initiate 1272: 1099: 935: 250: 230: 1794: 1547: 1453: 1200: 1012: 47: 1852: 1557: 1452: 1277: 1159: 1048: 581: 568: 222: 120:, of the donor and graft recipient. These products are recognized by 112:
Alloimmunity is caused by the difference between products of highly
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Immune response to nonself antigens from members of the same species
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along with TGF-β, CD4 T-lymphocytes acquire tissue-destructive
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T-lymphocytes are fully activated under two conditions:
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Cellular rejection – CD4 and CD8 T-lymphocytes, NK cells
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is an immune response to the self's own antigens. (The
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Acute rejection is caused by antigen-specific Th1 and
592: 538:by Abul K. Abbas, Andrew H. Lichtman, Shiv Pillai, 788:tolerance. Transplant Rev (Orlando). 26(3):212-22 698: 696: 694: 229:activation (not of the complement) through their 1865: 1150:Transfusion-associated graft versus host disease 385:and TGF-β which ensures the allograft tolerance. 638: 691: 536:Cellular and Molecular Immunology, 7th edition 363:. Then allograft tolerance is mostly observed. 1438: 900: 217:; moreover, the reaction can be enhanced by 54:antigens. In alloimmunity, the body creates 1145:Transfusion associated circulatory overload 632: 1445: 1431: 1155:Febrile non-hemolytic transfusion reaction 1028:International Society of Blood Transfusion 907: 893: 260: 165:Hemolytic disease of the fetus and newborn 160:Hemolytic disease of the fetus and newborn 128:which infiltrate the graft and damage it. 877:at the U.S. National Library of Medicine 867:at the U.S. National Library of Medicine 656: 131: 420:Killer-cell immunoglobulin-like receptor 639:Walker WE, Goldstein DR (August 2007). 175: 136: 1866: 280:and cytokines also play a role in it. 152:, there is a risk of reaction against 62:) against the alloantigens, attacking 46:. Two major types of alloantigens are 1426: 1140:Transfusion related acute lung injury 888: 337:(which is usually secreted by mature 324:CD4 T-lymphocytes differentiate into 201:before the transplantation – either 519:Neonatal alloimmune thrombocytopenia 240: 193:Hyperacute and accelerated rejection 205:or antibodies incurred by previous 13: 493: 180: 14: 1890: 1183:Transfusion transmitted infection 858: 348:and destroy the allograft tissue. 287:Humoral rejection – B-lymphocytes 524:Hemolytic disease of the newborn 433: 316:Cytokine microenvironment where 294: 118:major histocompatibility complex 846: 837: 827: 818: 809: 800: 791: 781: 771: 762: 753: 744: 734: 724: 715: 705: 1772:Immunoglobulin class switching 682: 673: 623: 614: 574: 551: 116:genes, primarily genes of the 1: 545: 529: 169:immune tolerance of pregnancy 1072:Intraoperative blood salvage 388:However, in the presence of 311: 7: 1088:Blood compatibility testing 778:Rev (Orlando). 26(3):212-22 658:10.4049/jimmunol.179.3.1700 502: 465:Activation of T-lymphocytes 413: 355:, CD4 T-lymphocytes become 150:blood compatibility testing 97:means "other", whereas the 10: 1895: 1601:Polyclonal B cell response 1835: 1793: 1735: 1636: 1566: 1474: 1467: 1191: 1135:Transfusion hemosiderosis 1123: 1080: 1041: 1005: 926: 154:human blood group systems 34:from members of the same 1115:Monocyte monolayer assay 879:Medical Subject Headings 869:Medical Subject Headings 458:Indirect allorecognition 424:antigen-presenting cells 343:proinflammatory cytokine 990:Granulocyte transfusion 439:Alloantigen recognition 428:immunosuppressive drugs 261:Mechanisms of rejection 187:cytotoxic T-lymphocytes 156:other than ABO and Rh. 68:allotransplanted tissue 1715:Tolerance in pregnancy 1457:adaptive immune system 586:allaboutantibodies.com 448:Direct allorecognition 369:induces expression of 132:Types of the rejection 126:mononuclear leukocytes 101:prefix means "self".) 82:) response results in 1750:Somatic hypermutation 1584:Polyclonal antibodies 1579:Monoclonal antibodies 1125:Transfusion reactions 341:). Th1 cells produce 148:. Even with standard 1767:Junctional diversity 1535:Antigen presentation 1105:Kleihauer–Betke test 1067:Exchange transfusion 946:Platelet transfusion 920:transfusion medicine 176:Transplant rejection 146:transfusion reaction 137:Transfusion reaction 1762:V(D)J recombination 1745:Affinity maturation 1497:Antigenic variation 1193:Blood group systems 1128:and adverse effects 963:Fresh frozen plasma 514:Allotransplantation 359:secreting IL-4 and 333:in the presence of 38:, which are called 563:2016-10-09 at the 540:Saunders Copyright 509:Allograft diseases 375:regulatory T cells 209:(e.g. by repeated 52:histocompatibility 22:(sometimes called 1861: 1860: 1789: 1788: 1539:professional APCs 1420: 1419: 997:Blood substitutes 985:White blood cells 916:Blood transfusion 487:memory CD8 T cell 270:CD8 T-lymphocytes 241:Chronic rejection 211:blood transfusion 142:Blood transfusion 1886: 1755:Clonal selection 1727:Immune privilege 1722:Immunodeficiency 1677:Cross-reactivity 1667:Hypersensitivity 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593: 580: 579: 575: 565:Wayback Machine 556: 552: 548: 532: 505: 496: 494:Graft tolerance 436: 416: 339:dendritic cells 314: 297: 263: 243: 235:xenotransplants 195: 183: 181:Acute rejection 178: 162: 139: 134: 107:isoimmunization 84:graft rejection 74:in some cases. 70:, and even the 28:immune response 17: 12: 11: 5: 1892: 1882: 1881: 1876: 1859: 1858: 1856: 1855: 1850: 1845: 1839: 1837: 1833: 1832: 1830: 1829: 1824: 1823: 1822: 1812: 1811: 1810: 1799: 1797: 1791: 1790: 1787: 1786: 1784: 1783: 1774: 1769: 1764: 1759: 1758: 1757: 1752: 1741: 1739: 1737:Immunogenetics 1733: 1732: 1730: 1729: 1724: 1719: 1718: 1717: 1712: 1707: 1702: 1697: 1685: 1684: 1682:Co-stimulation 1679: 1674: 1669: 1664: 1659: 1654: 1649: 1642: 1640: 1634: 1633: 1631: 1630: 1625: 1623:Immune complex 1619: 1618: 1613: 1608: 1603: 1598: 1597: 1596: 1591: 1586: 1581: 1570: 1568: 1564: 1563: 1561: 1560: 1555: 1550: 1545: 1543:Dendritic cell 1531: 1530: 1525: 1524: 1523: 1521:Conformational 1518: 1507: 1506: 1501: 1500: 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1602: 1599: 1595: 1594:Microantibody 1592: 1590: 1587: 1585: 1582: 1580: 1577: 1576: 1575: 1572: 1571: 1569: 1565: 1559: 1556: 1554: 1551: 1549: 1546: 1544: 1540: 1536: 1533: 1532: 1529: 1526: 1522: 1519: 1517: 1514: 1513: 1512: 1509: 1508: 1505: 1502: 1498: 1495: 1493: 1490: 1488: 1485: 1484: 1483: 1480: 1479: 1477: 1473: 1470: 1466: 1462: 1458: 1455: 1448: 1443: 1441: 1436: 1434: 1429: 1428: 1425: 1413: 1410: 1408: 1405: 1403: 1400: 1398: 1395: 1393: 1390: 1388: 1385: 1383: 1380: 1378: 1374: 1371: 1369: 1366: 1364: 1361: 1359: 1356: 1354: 1351: 1349: 1346: 1344: 1341: 1339: 1336: 1334: 1331: 1329: 1326: 1324: 1321: 1318: 1314: 1311: 1309: 1306: 1304: 1301: 1299: 1296: 1294: 1291: 1289: 1286: 1284: 1281: 1279: 1276: 1274: 1271: 1269: 1266: 1264: 1261: 1259: 1256: 1254: 1251: 1249: 1246: 1244: 1241: 1239: 1236: 1234: 1231: 1229: 1228:Chido-Rodgers 1226: 1224: 1221: 1219: 1216: 1212: 1209: 1208: 1207: 1204: 1202: 1199: 1198: 1196: 1194: 1190: 1184: 1181: 1179: 1176: 1172: 1169: 1167: 1164: 1163: 1161: 1158: 1156: 1153: 1151: 1148: 1146: 1143: 1141: 1138: 1136: 1133: 1132: 1130: 1126: 1122: 1116: 1113: 1111: 1108: 1106: 1103: 1101: 1098: 1094: 1091: 1090: 1089: 1086: 1085: 1083: 1079: 1073: 1070: 1068: 1065: 1062: 1061:leukapheresis 1058: 1054: 1050: 1047: 1046: 1044: 1040: 1034: 1031: 1029: 1026: 1024: 1021: 1019: 1016: 1014: 1011: 1010: 1008: 1004: 998: 995: 991: 988: 987: 986: 983: 979: 976: 974: 971: 969: 966: 964: 961: 960: 959: 956: 954: 951: 947: 944: 943: 942: 939: 937: 934: 933: 931: 929: 925: 921: 917: 910: 905: 903: 898: 896: 891: 890: 887: 880: 876: 873: 870: 866: 863: 862: 849: 840: 830: 821: 812: 803: 794: 784: 774: 765: 756: 747: 737: 727: 718: 708: 699: 697: 695: 685: 676: 668: 664: 659: 654: 650: 646: 642: 635: 626: 617: 608: 606: 604: 602: 600: 598: 596: 587: 583: 577: 570: 566: 562: 559: 554: 550: 541: 537: 534: 533: 525: 522: 520: 517: 515: 512: 510: 507: 506: 500: 491: 488: 480: 475: 472: 471: 470: 467: 466: 459: 456: 453: 449: 446: 445: 444: 441: 440: 434:T-lymphocytes 431: 429: 425: 421: 408: 404: 401: 400: 395: 391: 387: 384: 380: 376: 372: 368: 365: 362: 358: 354: 350: 347: 344: 340: 336: 332: 331: 327: 323: 322: 321: 319: 309: 307: 303: 295:B-lymphocytes 289: 286: 283: 282: 281: 279: 275: 274:B-lymphocytes 271: 267: 258: 256: 252: 248: 238: 236: 232: 228: 224: 220: 216: 212: 208: 204: 200: 190: 188: 173: 170: 166: 157: 155: 151: 147: 143: 129: 127: 123: 122:T-lymphocytes 119: 115: 110: 108: 104: 100: 96: 93: 89: 85: 81: 77: 73: 69: 65: 61: 57: 53: 50:antigens and 49: 45: 41: 37: 33: 29: 25: 21: 1672:Inflammation 1657:Alloimmunity 1656: 1652:Autoimmunity 1637:Immunity vs. 1589:Autoantibody 1487:Superantigen 848: 839: 829: 820: 811: 802: 793: 783: 773: 764: 755: 746: 736: 731:37(2):445-55 726: 717: 707: 684: 675: 648: 644: 634: 625: 616: 585: 576: 553: 539: 535: 497: 486: 484: 468: 464: 463: 457: 447: 442: 438: 437: 417: 405:and secrete 402: 397: 378: 356: 351:If there is 330:helper cells 328: 325: 315: 306:phagocytosis 298: 264: 249:production. 244: 231:Fc receptors 207:immunization 196: 184: 163: 140: 111: 106: 102: 98: 91: 88:autoimmunity 79: 75: 59: 43: 40:alloantigens 39: 23: 20:Alloimmunity 19: 18: 1795:Lymphocytes 1454:Lymphocytic 1201:Blood types 1100:Coombs test 936:Whole blood 865:Alloantigen 712:6(3):505-13 251:Endothelium 219:neutrophils 114:polymorphic 48:blood group 44:isoantigens 30:to nonself 24:isoimmunity 1874:Immunology 1868:Categories 1836:Substances 1700:Peripheral 1688:Inaction: 1567:Antibodies 1548:Macrophage 1461:complement 1013:Blood bank 875:Isoantigen 645:J. Immunol 571:Dictionary 558:Isoantigen 546:References 530:Literature 215:complement 199:antibodies 124:and other 76:Alloimmune 56:antibodies 1853:Cytolysin 1843:Cytokines 1690:Tolerance 1639:tolerance 1558:Immunogen 1218:Augustine 1162:reaction 1160:Hemolytic 1049:Apheresis 941:Platelets 569:eMedicine 403:phenotype 357:Th2 cells 312:Cytokines 290:Cytokines 223:phagocyte 80:isoimmune 1879:Antigens 1803:Cellular 1647:Immunity 1645:Action: 1628:Paratope 1616:Idiotype 1606:Allotype 1574:Antibody 1528:Mimotope 1492:Allergen 1475:Antigens 1468:Lymphoid 1343:Lutheran 1248:Dombrock 1033:ISBT 128 667:17641036 561:Archived 503:See also 414:NK cells 278:NK cells 255:fibrosis 247:cytokine 58:(called 32:antigens 26:) is an 1848:Opsonin 1827:NK cell 1815:Humoral 1695:Central 1662:Allergy 1611:Isotype 1511:Epitope 1482:Antigen 1382:Scianna 1268:Gerbich 1171:delayed 1042:Methods 479:anergic 227:NK cell 36:species 1820:B cell 1808:T cell 1553:B cell 1516:Linear 1504:Hapten 1293:Indian 1238:Cromer 1233:Colton 958:Plasma 881:(MeSH) 871:(MeSH) 665:  582:"Home" 95:prefix 1412:Other 1338:Lewis 1328:Knops 1308:KANNO 1253:Duffy 1243:Diego 1166:acute 1081:Tests 407:IL-17 394:IL-21 383:IL-10 371:Foxp3 367:TGF-β 346:IFN-Îł 335:IL-12 302:lysis 99:auto- 92:allo- 72:fetus 1459:and 1392:T-Tn 1377:RHAG 1375:and 1368:Raph 1363:P1PK 1323:Kidd 1313:Kell 1278:GLOB 1263:FORS 1223:CD59 968:PF24 918:and 663:PMID 399:Th17 390:IL-6 379:Treg 361:IL-5 353:IL-4 268:and 225:and 1781:HLA 1777:MHC 1397:Vel 1387:Sid 1353:MNS 1333:Lan 1303:JMH 1273:GIL 1206:ABO 653:doi 649:179 567:at 392:or 326:Th1 318:CD4 266:CD4 203:IgM 42:or 1870:: 1541:: 1407:Yt 1402:Xg 1373:Rh 1358:OK 1348:LW 1317:Xk 1298:JR 1288:Ii 1283:Hh 1258:Er 1059:, 1055:, 693:^ 661:. 647:. 643:. 594:^ 584:. 276:, 237:. 66:, 1779:/ 1537:/ 1446:e 1439:t 1432:v 1319:) 1315:( 1063:) 1051:( 908:e 901:t 894:v 669:. 655:: 588:. 481:. 409:. 377:( 105:( 78:(

Index

immune response
antigens
species
blood group
histocompatibility
antibodies
transfused blood
allotransplanted tissue
fetus
graft rejection
autoimmunity
prefix
polymorphic
major histocompatibility complex
T-lymphocytes
mononuclear leukocytes
Blood transfusion
transfusion reaction
blood compatibility testing
human blood group systems
Hemolytic disease of the fetus and newborn
immune tolerance of pregnancy
cytotoxic T-lymphocytes
antibodies
IgM
immunization
blood transfusion
complement
neutrophils
phagocyte

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