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Lenfoproliferatif Hastalıklar

Year 2006, Volume: 4 Issue: 2, 34 - 39, 01.06.2006

Abstract

Programlanmış hücre ölümü apoptozis immün sistemin homeostazının korunmasında büyük öneme sahiptir. Periferik matür T hücrelerinin antijen cevabının düzenlenmesi ve homeostazının sağlanmasında da apoptozisin rolü olduğu yapılan çalışmalarda gösterilmiştir.

References

  • 1. Leonardo M, Chan FK, Hornung F, et al. Mature lymphocyte apoptosis-immune regulation in a dynamic and unpredictable antigenic enviroment. Annu Rev Immunol 1999; 17:221-53.
  • 2. Strauss S.E., Sneller M, Leonardo M.J. et al. An inherited disorder of lymphocyte apoptosis: The autoimmune lymphoproliferative syndrome. Annals of ‹nternal Med 1999; 130: 591-601.
  • 3. Pan TQ, Atkinson TP, Makris CM, et al. ALPS (autoimmune lymphoproliferative syndrome) associated with a mutation in Fas-Ligand (abstract 48). In: Programs and Abstracts of the 14th Annual Conference on Clinical Immunology and 5th International Symposium on Clinical Immunology. Washington; DC; 1999. p. 442.
  • 4. Wang J, Zheng L, Lobito A, et al. Inherited human caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome II. Cell 1999; 98:47-58.
  • 5. Jackson CE, Fischer RE, Hsu AP, et al. Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance. Am J Hum Genet 1999; 64:1002-14.
  • 6. Fisher G.H, Rosenberg F.J., Straus S.E. et al. Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. Cell 1995; 81:935-46.
  • 7. ‹nfante A.J, Britton H.A., DeNapoli T., Middelton L.A. et al. The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a fas mutation that impairs lymphocyte apoptosis. J. Pediatr 1998; 133:629-33.
  • 8. Sneller MC, Straus SE, Jaffe ES, et al. A novel autoimmune lymphoproliferative syndrome resembling murine lpr/gld disease. J Clin Invest 1992; 90:334-41.
  • 9. Takahashi T, Tanaka M, Brannan CL, et al. Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand. Cell 1994;76:969-76.
  • 10. Bleesing J.J, Straus S.E., Fleisher T.A. Autoimmune lymphoproliferative syndrome. A human disorder of abnormal lympocyte. Pediatr Clin North Am 2000; Dec; 47: 1291-310.
  • 11. Watanabe- Fukunaga R, Brannan CI,Copeland NG, et al. Lymphoproliferation disorder in mice explained by defects in fas antigen that mediates apoptosis. Nature 1992; 356:314-7.
  • 12. Behrmann I, Walczak H, Krammer PH. Structure of the human APO-1 gene. Eur J Immunol 1994; 24:3057-362.
  • 13. Martin DA, Zheng L, Siegel RM, et al. Defective CD95/APO-1/Fas signal complex formation in the human autoimmune lymphoproliferative syndrome, type Ia. Proc Natl Acad Sci USA 1999; 96:4552-7.
  • 14. Rieux-Laucat F, Le Deist, Hivbroz C, et al. Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity. Science 1995; 268:1347-9.
  • 15. Sleight BJ, Prasad VS, DeLaat C, et al. Correction of autoimmune lymphoproliferative syndrome by bone marrow transplantation. Bone Marrow Transplant 1998; 22:375-80.
  • 16. Van der Burg M, de Groot R, Comans-Bitter WM, et al. Autoimmune lymphoproliferative syndrome (ALPS) in a child from consanguineous parents: a dominant or recessive disease? Pediatr Res 2000; 47:336-43.
  • 17. Kasahara Y, Wada T, Nida Y, et al. Novel Fas (CD95/APO-1) mutations in infants with a lymphoproliferative disorder. Int Immunol 1998; 10:195-202.
  • 18. Vaishnaw AK, Toubi E, Ohsako S, et al. The spectrum of apoptotic defects and clinical manifestations , including systemic lupus erythematosus, in humans with CD95 (Fas/APO-1)) mutations. Arthritis Rheum 1999; 42:1833-42.
  • 19. Bader-Meunier B, Rieux-Laucat F, Croisille L, et al. Dyserythropoisesis associated with a Fas deficient condition in childhood. Br J Haematol 2000;108:300-4
  • 20. Hetts SW. To die or not to die: an overview of apoptosis and its role disease. JAMA 1998; 279:300-7.
  • 21. Griffith TS, Brunner T, Fletcher SM, et al. Fas ligand-induced apoptosis as a mechanism of immune privilege. Science 1995; 270:1189-92.
  • 22. Siegel RM, Chan FK, Chum HJ, et al. The multifaceted role of Fas signaling in immune cell homeostasis and autoimmunity. Nat Immunol 2000; 1:1469-74.
  • 23. Sneller MC, Wang J, Dale JK, et al. Clinical, immünologic and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocyte apoptosis. Blood 1997; 89:1341-8.
  • 24. Bekerrou M, Le Deist F, de Villartay JP, et al. Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation. Eur J Immunol 1997; 27:2043-7.
  • 25. Chanock SJ, Foster CB. SNPing away at innate immunity. J Clin Invest 1999; 104:369-70.
  • 26. Straus SE, Jaffe ES, Puck JM, et al. The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis. Blood 2001; 98:194-200.
  • 27. Purtilo DT, Cassel CK, Yang JPS, et al. X-linked recessive progressive combined variable immundeficiency (Duncan's disease). Lancet 1975; 1:935-41.
  • 28. Brandau O, Schuster V, Weiss M, et al. Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP). Hum Mol gen 1999; 8:2407-13.
  • 29. Sumegi J , Huang D, lanyi A, et al. Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease. Blood 2000; 96:3118-25.
  • 30. Coffey AJ, Brooksbank RA, Brandau O, et al. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat genet 1998; 20:129-35.
  • 31. Seemayer TA, Gross TG , Egeler RM, et al. X-linked lymphoproliferative disease: twenty-five years after the discovery. Pediatr Res 1995; 38:471-8.
  • 32. Dutz JP, Benoit L, Wang X, et al. Lymphocytic vasculitis in X-linked lymphoproliferative disease. Blood 2001; 97:95-100.
  • 33. Okano M, Pirrucello SJ, Grierson HL, et al. Immunovirological studies of natal infectious mononucleosis in apatient with X-linked lymphoproliferative syndrome treated with intravenous immunoglobulin and interferon-alpha. Clin Immunol Immunopathol 1990; 54:410-8.
  • 34. Amrolia P, Gaspar HB, Hassan A, et al. Nonmyeloablative stem cell transplantation for congenital immunodeficiencies. Blood 2000; 96:1239-46.
  • 35. Grierson H, Purtilo DT. Epstein-Barr virus infection in males with X-linked lymphoproliferative syndrome. Ann Int Med 1987; 106:538-45.
  • 36. Schuster J, Gross TG, Seemayer TA. The molecular genetics Xlinked lymphoproliferative (Duncan's) disease. Cancer J Sci Am 1999; 5:57-62.
  • 37. Harrington DS, Weisenburger DD, Purtilo DT. Malignant lymphoma in the X-linked lymphoproliferative syndrome. Cancer 1987; 59:1419-29.
  • 38. Purtilo DT, Sakamoto K, Barnabei V, et al. Epstein-Barr virus-induced diseases in boys with the X-linked lymphoproliferative syndrome (XLP): update on studies of the registry. Am J Med 1982; 73:49-56.
  • 39. Grierson HL, Skare J, Hawk J, Pauzo M, Purtilo DT. Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease. Am J Med Genet 1991; 40:294-7.
  • 40. Purtilo DT, Grierson HL, Ochs H, Skare J. Detection of X-linked lymphoproliferative disease using molecular and immunovirologic markers. Am J Med 1989; 87:421-4.
Year 2006, Volume: 4 Issue: 2, 34 - 39, 01.06.2006

Abstract

References

  • 1. Leonardo M, Chan FK, Hornung F, et al. Mature lymphocyte apoptosis-immune regulation in a dynamic and unpredictable antigenic enviroment. Annu Rev Immunol 1999; 17:221-53.
  • 2. Strauss S.E., Sneller M, Leonardo M.J. et al. An inherited disorder of lymphocyte apoptosis: The autoimmune lymphoproliferative syndrome. Annals of ‹nternal Med 1999; 130: 591-601.
  • 3. Pan TQ, Atkinson TP, Makris CM, et al. ALPS (autoimmune lymphoproliferative syndrome) associated with a mutation in Fas-Ligand (abstract 48). In: Programs and Abstracts of the 14th Annual Conference on Clinical Immunology and 5th International Symposium on Clinical Immunology. Washington; DC; 1999. p. 442.
  • 4. Wang J, Zheng L, Lobito A, et al. Inherited human caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome II. Cell 1999; 98:47-58.
  • 5. Jackson CE, Fischer RE, Hsu AP, et al. Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance. Am J Hum Genet 1999; 64:1002-14.
  • 6. Fisher G.H, Rosenberg F.J., Straus S.E. et al. Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. Cell 1995; 81:935-46.
  • 7. ‹nfante A.J, Britton H.A., DeNapoli T., Middelton L.A. et al. The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a fas mutation that impairs lymphocyte apoptosis. J. Pediatr 1998; 133:629-33.
  • 8. Sneller MC, Straus SE, Jaffe ES, et al. A novel autoimmune lymphoproliferative syndrome resembling murine lpr/gld disease. J Clin Invest 1992; 90:334-41.
  • 9. Takahashi T, Tanaka M, Brannan CL, et al. Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand. Cell 1994;76:969-76.
  • 10. Bleesing J.J, Straus S.E., Fleisher T.A. Autoimmune lymphoproliferative syndrome. A human disorder of abnormal lympocyte. Pediatr Clin North Am 2000; Dec; 47: 1291-310.
  • 11. Watanabe- Fukunaga R, Brannan CI,Copeland NG, et al. Lymphoproliferation disorder in mice explained by defects in fas antigen that mediates apoptosis. Nature 1992; 356:314-7.
  • 12. Behrmann I, Walczak H, Krammer PH. Structure of the human APO-1 gene. Eur J Immunol 1994; 24:3057-362.
  • 13. Martin DA, Zheng L, Siegel RM, et al. Defective CD95/APO-1/Fas signal complex formation in the human autoimmune lymphoproliferative syndrome, type Ia. Proc Natl Acad Sci USA 1999; 96:4552-7.
  • 14. Rieux-Laucat F, Le Deist, Hivbroz C, et al. Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity. Science 1995; 268:1347-9.
  • 15. Sleight BJ, Prasad VS, DeLaat C, et al. Correction of autoimmune lymphoproliferative syndrome by bone marrow transplantation. Bone Marrow Transplant 1998; 22:375-80.
  • 16. Van der Burg M, de Groot R, Comans-Bitter WM, et al. Autoimmune lymphoproliferative syndrome (ALPS) in a child from consanguineous parents: a dominant or recessive disease? Pediatr Res 2000; 47:336-43.
  • 17. Kasahara Y, Wada T, Nida Y, et al. Novel Fas (CD95/APO-1) mutations in infants with a lymphoproliferative disorder. Int Immunol 1998; 10:195-202.
  • 18. Vaishnaw AK, Toubi E, Ohsako S, et al. The spectrum of apoptotic defects and clinical manifestations , including systemic lupus erythematosus, in humans with CD95 (Fas/APO-1)) mutations. Arthritis Rheum 1999; 42:1833-42.
  • 19. Bader-Meunier B, Rieux-Laucat F, Croisille L, et al. Dyserythropoisesis associated with a Fas deficient condition in childhood. Br J Haematol 2000;108:300-4
  • 20. Hetts SW. To die or not to die: an overview of apoptosis and its role disease. JAMA 1998; 279:300-7.
  • 21. Griffith TS, Brunner T, Fletcher SM, et al. Fas ligand-induced apoptosis as a mechanism of immune privilege. Science 1995; 270:1189-92.
  • 22. Siegel RM, Chan FK, Chum HJ, et al. The multifaceted role of Fas signaling in immune cell homeostasis and autoimmunity. Nat Immunol 2000; 1:1469-74.
  • 23. Sneller MC, Wang J, Dale JK, et al. Clinical, immünologic and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocyte apoptosis. Blood 1997; 89:1341-8.
  • 24. Bekerrou M, Le Deist F, de Villartay JP, et al. Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation. Eur J Immunol 1997; 27:2043-7.
  • 25. Chanock SJ, Foster CB. SNPing away at innate immunity. J Clin Invest 1999; 104:369-70.
  • 26. Straus SE, Jaffe ES, Puck JM, et al. The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis. Blood 2001; 98:194-200.
  • 27. Purtilo DT, Cassel CK, Yang JPS, et al. X-linked recessive progressive combined variable immundeficiency (Duncan's disease). Lancet 1975; 1:935-41.
  • 28. Brandau O, Schuster V, Weiss M, et al. Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP). Hum Mol gen 1999; 8:2407-13.
  • 29. Sumegi J , Huang D, lanyi A, et al. Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease. Blood 2000; 96:3118-25.
  • 30. Coffey AJ, Brooksbank RA, Brandau O, et al. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat genet 1998; 20:129-35.
  • 31. Seemayer TA, Gross TG , Egeler RM, et al. X-linked lymphoproliferative disease: twenty-five years after the discovery. Pediatr Res 1995; 38:471-8.
  • 32. Dutz JP, Benoit L, Wang X, et al. Lymphocytic vasculitis in X-linked lymphoproliferative disease. Blood 2001; 97:95-100.
  • 33. Okano M, Pirrucello SJ, Grierson HL, et al. Immunovirological studies of natal infectious mononucleosis in apatient with X-linked lymphoproliferative syndrome treated with intravenous immunoglobulin and interferon-alpha. Clin Immunol Immunopathol 1990; 54:410-8.
  • 34. Amrolia P, Gaspar HB, Hassan A, et al. Nonmyeloablative stem cell transplantation for congenital immunodeficiencies. Blood 2000; 96:1239-46.
  • 35. Grierson H, Purtilo DT. Epstein-Barr virus infection in males with X-linked lymphoproliferative syndrome. Ann Int Med 1987; 106:538-45.
  • 36. Schuster J, Gross TG, Seemayer TA. The molecular genetics Xlinked lymphoproliferative (Duncan's) disease. Cancer J Sci Am 1999; 5:57-62.
  • 37. Harrington DS, Weisenburger DD, Purtilo DT. Malignant lymphoma in the X-linked lymphoproliferative syndrome. Cancer 1987; 59:1419-29.
  • 38. Purtilo DT, Sakamoto K, Barnabei V, et al. Epstein-Barr virus-induced diseases in boys with the X-linked lymphoproliferative syndrome (XLP): update on studies of the registry. Am J Med 1982; 73:49-56.
  • 39. Grierson HL, Skare J, Hawk J, Pauzo M, Purtilo DT. Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease. Am J Med Genet 1991; 40:294-7.
  • 40. Purtilo DT, Grierson HL, Ochs H, Skare J. Detection of X-linked lymphoproliferative disease using molecular and immunovirologic markers. Am J Med 1989; 87:421-4.
There are 40 citations in total.

Details

Primary Language Turkish
Journal Section Research Article
Authors

Yasin Karalı This is me

Sara Şebnem Kılıç This is me

Publication Date June 1, 2006
Published in Issue Year 2006 Volume: 4 Issue: 2

Cite

APA Karalı, Y., & Kılıç, S. Ş. (2006). Lenfoproliferatif Hastalıklar. Güncel Pediatri, 4(2), 34-39.
AMA Karalı Y, Kılıç SŞ. Lenfoproliferatif Hastalıklar. Güncel Pediatri. June 2006;4(2):34-39.
Chicago Karalı, Yasin, and Sara Şebnem Kılıç. “Lenfoproliferatif Hastalıklar”. Güncel Pediatri 4, no. 2 (June 2006): 34-39.
EndNote Karalı Y, Kılıç SŞ (June 1, 2006) Lenfoproliferatif Hastalıklar. Güncel Pediatri 4 2 34–39.
IEEE Y. Karalı and S. Ş. Kılıç, “Lenfoproliferatif Hastalıklar”, Güncel Pediatri, vol. 4, no. 2, pp. 34–39, 2006.
ISNAD Karalı, Yasin - Kılıç, Sara Şebnem. “Lenfoproliferatif Hastalıklar”. Güncel Pediatri 4/2 (June 2006), 34-39.
JAMA Karalı Y, Kılıç SŞ. Lenfoproliferatif Hastalıklar. Güncel Pediatri. 2006;4:34–39.
MLA Karalı, Yasin and Sara Şebnem Kılıç. “Lenfoproliferatif Hastalıklar”. Güncel Pediatri, vol. 4, no. 2, 2006, pp. 34-39.
Vancouver Karalı Y, Kılıç SŞ. Lenfoproliferatif Hastalıklar. Güncel Pediatri. 2006;4(2):34-9.