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2022, Número 4

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Rev Cubana Hematol Inmunol Hemoter 2022; 38 (4)


Caracterización fisiopatológica de las anemias hemolíticas autoinmunes

Soler NG
Texto completo Cómo citar este artículo Artículos similares

Idioma: Español
Referencias bibliográficas: 55
Paginas: 1-22
Archivo PDF: 690.69 Kb.


PALABRAS CLAVE

anemia hemolítica autoinmune, autoanticuerpos eritrocitarios, autoinmunidad, hemólisis, prueba de antiglobulina directa.

RESUMEN

Introducción: La anemia hemolítica autoinmune se define como el aumento de la destrucción de los eritrocitos en presencia de autoanticuerpos dirigidos contra antígenos de grupos sanguíneos eritrocitarios.
Objetivo: Caracterizar las anemias hemolíticas autoinmunes teniendo en cuenta las características fisiopatológicas, manifestaciones clínicas y el diagnóstico de laboratorio.
Métodos: Se realizó una revisión de la literatura en inglés y español de artículos publicados en los últimos 10 años sobre anemia hemolítica autoinmune.
Conclusiones: La anemia hemolítica autoinmune es una enfermedad muy heterogénea. El diagnóstico suele ser fácil, pero los casos difíciles pueden ser un desafío. La definición de cada tipo es fundamental ya que la terapia es diferente y se enfoca más con la comprensión de los mecanismos patogénicos.


REFERENCIAS (EN ESTE ARTÍCULO)

  1. Petz LD, Garratty G. Immune Hemolytic Anemias. 2nd ed. Philadelphia: Churchill Livingstone; 2004.

  2. Hill QA, Stamps R, Massey E, Grainger JD, Provan D, Hill A. British Society for Haematology. The diagnosis and management of primary autoimmune haemolyticanaemia. Br J Haematol. 2017; 176: 395-411. DOI: https://10.1111/bjh.144782.

  3. Jäger U, Barcellini W, Broome CM, Gertz MA, Hill A, Hill QA, et al. Diagnosis and treatment of autoimmune hemolytic anemia in adults: Recommendations from the First International Consensus Meeting. Blood Rev. 2019;41:100648. DOI: https://10.1016/j.blre.2019.1006483.

  4. Barcellini W, Giannotta J, Fattizzo B. Autoimmune hemolytic anemia in adults: primary risk factors and diagnostic procedures. Expert Rev Hematol. 2020;13(6):585-97. DOI: https://10.1080/17474086.2020.17547914.

  5. Berentsen S. New insights in the pathogenesis and therapy of cold agglutinin mediated autoimmune hemolytic Anemia. Front Immunol. 2020;11:590. DOI: https://10.3389/fimmu.2020.005905.

  6. Williams JD, Jayaprakash RK, Kithany H, Tighe MP. How to use Donath-Landsteiner test to diagnose paroxysmal cold haemoglobinuria (PCH). Arch Dis Child Educ Pract Ed. 2021;0:1-8. . DOI: https://10.1136/archdischild-2020-3195686.

  7. Shulman IA, Branch DR, Nelson JM, Thompson JC, Saxena S, Petz LD. Autoimmune hemolytic anemia with both cold and warm autoantibodies. JAMA. 1985;253(12):1746-8. . DOI: https://10.1001/jama.1985.033503600720217.

  8. Takahashi T. direct antiglobulina test-negative autoimmune hemolytic anemia. Acta Haematol. 2018;140:18-9. . DOI: https://10.1159/0004892538.

  9. Fung MK, Eder AF, Spitalnik S, Westhoff CM, eds. The Technical Manual.19th ed. Bethesda:AABB; 2017

  10. Habibi B, Homberg JC, Schaison G, Salmon C. Autoimmune hemolytic anemia in children. A review of 80 cases. Am J Med. 1974;56(1):61-9. DOI: https://10.1016/0002-9343(74)90751-710.

  11. Garratty G, Arndt P, Domen R, Clarke A, Sutphen-Shaw D, Clear J, et al. Severe autoimmune hemolytic anemia associated with IgM warm autoantibodies directed against determinants on or associated with glycophorin A. Vox Sang. 1997;72(2):124-30. DOI: https://10.1046/j.1423-0410.1997.7220124.x11.

  12. Ravetch JV. Fc receptors. Curr Opin Immunol. 1997;9(1):121-5. . DOI: https://10.1016/S0952-7915(97)80168-912.

  13. Vidarsson G, Dekkers G, Rispens T. IgG subclasses and allotypes: from structure to effector functions. Front Immunol. 2014;5:520. DOI: https://10.3389/fimmu.2014.0052013.

  14. Van den Akker M, Smolders D, Mahieu S, Bonouvrie K, van der Werf Ten Bosch J. Primary IgA-mediated Autoimmune Hemolytic Anemia in an Infant Successfully Treated with Rituximab. J Pediatr Hematol Oncol. 2020;42:e615-9. DOI: https://doi.org/10.1097/MPH.000000000000176514.

  15. Ha S, Ou Y, Vlasak J, Li Y, Wang S, Vo K, et al. Isolation and characterization of IgG1 with asymmetrical Fc glycosylation. Glycobiology. 2011. 21;8:1087-96. . DOI: https://doi.org/10.1093/glycob/cwr04715.

  16. Sachs UJ, Roder L, Santoso S, Bein G. Does a negative direct antiglobulin test exclude warm autoimmune haemolyticanaemia? A prospective study of 504 cases. Br J Haematol. 2006;132(5):655-6. . DOI: https://10.1111/j.1365-2141.2005.05955.x16.

  17. Hamer HM, Beckers EA, Henskens YM. Haemolysis: role of the direct antiglobulin test and eluate. Ned Tijdschr Geneeskd. 2018;161:D1290. Dutch.

  18. Parker V, Tormey CA. The Direct Antiglobulin Test: Indications, Interpretation, and Pitfalls. Arch Pathol Lab Med.2017;141(2):305-10. . DOI: https://10.5858/arpa.2015-0444-RS18.

  19. Michalak SS, Olewicz-Gawlik A, Rupa-Matysek J, Wolny-Rokicka E, Nowakowska E, Gil L. Autoimmune hemolytic anemia: current knowledge and perspectives. Immun Ageing. 2020;17:38.. DOI: https://10.1186/s12979-020-00208-719.

  20. Barrera-Vargas A, Campos-Guzmán J, Govea-Peláez S, García-Ramos A, Demichelis-Gómez R, Bourlon C, et al. THU0260 systemic lupus erythematosus and cytopenias: the key findings in bone marrow. Ann Rheum Dis.2019;78:408. DOI: https://10.1136/annrheumdis-2019-eular.651520.

  21. Chalayer E, Costedoat-Chalumeau N, Beyne-Rauzy O, Ninet J, Durupt S, Tebib J, et al. Bone marrow involvement in systemic lupus erythematosus. QJM. 2017 Nov 1;110(11):701-11. DOI: https://10.1093/qjmed/hcx10221.

  22. Virot E, Duclos A, Adelaide L, Miailhes P, Hot A, Ferry T, et al. Autoimmune diseases and HIV infection: A cross-sectional study. Medicine (Baltimore). 2017;96(4):e5769. DOI: https://10.1097/MD.000000000000576922.

  23. Pellicano C, Leodori G, Innocenti GP, Gigante A, Rosato E. Microbiome, Autoimmune Diseases and HIV Infection: Friends or Foes? Nutrients.2019;11:2629. DOI: https://10.3390/nu1111262923.

  24. Yazdani R, Habibi S, Sharifi L, Azizi G, Abolhassani H, Olbrich P, et al. Common variable immunodeficiency: epidemiology, pathogenesis, clinical manifestations, diagnosis, classification and management. J Investig Allergol Clin Immunol. 2020;30(1):14-34. DOI: https://10.18176/jiaci.038824.

  25. Rieux-Laucat F, Magérus-Chatinet A, Neven B. The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions. J Clin Immunol. 2018;38:558-68. DOI: https://10.1007/s10875-018-0523-x25.

  26. Sharma D, Sharma ZP, Sharma R, Saraswat D. Evans Syndrome- An Unresolved Tale. J Med Biomed App Sci. 2020; 8(3):352-3. DOI: https://10.15520/jmbas.v8i3.21426.

  27. Vitale C, Montalbano MC, Salvetti C, Boccellato E, Griggio V, Boccadoro M, et al. Autoimmune Complications in Chronic Lymphocytic Leukemia in the Era of Targeted Drugs. Cancers.2020; 12(2):282. DOI: https://10.3390/cancers1202028227.

  28. Pejsa V, Lucijanic M, Vrkljan VA, Stoos-Veic T, Jaksic O, Zeljko J, et al. Prolonged methylprednisolone premedication prior too binutuzumab in patients with chronic lymphocytic leukemia. Leuk Lymphoma. 2020;61(4):934-9. DOI: https://10.1080/10428194.2019.170218228.

  29. Visco C, Barcellini W, Maura F, Neri A, Cortelezzi A, Rodeghiero F. Autoimmune cytopenias in chronic lymphocytic leukemia. Am J Hematol. 2014;89(11):1055-62. DOI: https://doi:org/10.1002/ajh.2378529.

  30. Arndt PA. Drug-induced immune hemolytic anemia: the 30 years of changes. Immunohematology. 2014;30:44-54

  31. Hill QA, Stamps R, Massey E, grainger JD, Provan D, Hill A. British Society for Haematology Guidelines: Guidelines on the management of drug-induced immune and secundary autoimmune haemolyticanaemia. Br J Haematol.2017; 177:208-20. DOI: https://10.1111/bjh.1465431.

  32. Garratty G. Drug-induced immune hemolytic anemia. Hematology Am Soc Hematol Educ Program. 2009:73-9. DOI: https://10.1182/asheducation-2009.1.7332.

  33. Salama A, Santoso S, Mueller-Eckhardt C. Antigenic determinants responsible for the reactions of drug-dependent antibodies with blood cells. Br J Haematol. 1991;78(4):535-9.

  34. Barcellini W. Fattizzo B. How I treat warm autoinmune hemolytic anemia. Blood. 2021;137(10):1283-94. DOI: https://10.1111/j.1365-2141.1991.tb04484.x34.

  35. Michel M, Jaeger U. Autoimmune hemolytic anemia. In: Hoffman R, Benz E, Silberstein LE, Heslop H, Weitz J, Anastasi J, eds. Hematology. Basic Principles and Practice. 7th Ed. Philadelphia: Elsevier; 2017.p.648-62.

  36. Liesveld JL, Rowe JM, Lichtman MA. Variability of the erythropoietic response in autoimmune hemolytic anemia: analysis of 109 cases. Blood. 1987;69(3):820-6. DOI: https://10.1182/blood.V69.3.820.82036.

  37. Shih AW, McFarlane A, Verhovsek M. Haptoglobin testing in hemolysis: measurement and interpretation. Am J Hematol. 2014;89(4):443-7. DOI: https://10.1002/ajh.2362337.

  38. Soler Noda G, González Guldriz M, Forrellat Barrios M. Diagnóstico diferencial de las anemias hemolíticas. Rev Cubana Hematol Inmunol Hemoter. 2020 [acceso 25/01/2021];36(4):e1097. Disponible en: http://www.revhematologia.sld.cu/index.php/hih/article/view/109738.

  39. Arndt PA, Leger RM, Garratty G. Serologic findings in autoimmune hemolytic anemia associated with immunoglobulin M warm autoantibodies. Transfusion. 2009;49:235-42. DOI: https://10.1111/j.1537-2995.2008.01957.x39.

  40. Berentsen S, Röth A, Randen U, Jilma B, Tjønnfjord GE. Coldagglutinin disease: current challenges and further prospects. J Blood Med. 2019;10:93-103. DOI: https://10.2147/JBM.S17762140.

  41. Berentsen S. How I manage patients with cold agglutinin disease. Br J Haematol. 2018;181:320-30. DOI: https://10.1111/bjh.1510941.

  42. Ahmed-Balola AH, Mayer B, Bartolmäs T, Salama A. Sublytic Terminal Complement Components Induce Eryptosis in Autoimmune HaemolyticAnaemia Related to IgM Autoantibodies. Cell Physiol Biochem. 2019;53:453-64. DOI: https://10.33594/00000015042.

  43. Jenkins WJ, Marsh WL, Noades J, Tippett P, Sanger R, Race RR. The I antigen and antibody. Vox Sang. 1960;5:97-121. DOI: https://10.1111/j.1423-0410.1960.tb04667.x43.

  44. Marsh WL. Anti-i: a cold antibody defining the Ii relationship in human red cells. Br J Haematol. 1961;7:200-9. DOI: https://10.1111/j.1365-2141.1961.tb00329.x44.

  45. Randen U, Trøen G, Tierens A, Steen C, Warsame A, Beiske K, et al. Primary cold agglutinin-associated lymphoproliferative disease: a B-cell lymphoma of the bone marrow distinct from lymphoplasmacytic lymphoma. Haematologica. 2014;99(3):497-504. DOI: https://10.3324/haematol.2013.09170245.

  46. Stein B, DeCredico N, Hillman L. Evaluation of the Direct Antiglobulin Test (DAT) in the Setting of Mycoplasma pneumoniae Infection. JAMA. 2018;319(13):1377-1378. DOI: https://10.1001/jama.2018.196946.

  47. Crickx E, Poullot E, Moulis G, Goulabchand R, Fieschi Claire, Galicier L, et al. Clinical spectrum, evolution, and management of autoimmune cytopenias associated with angioimmunoblastic T-cell lymphoma. Eur J Haematol. 2019;103(1):35-42. DOI: https://10.1111/ejh.1323947.

  48. Dasanu CA, Bockorny B, Grabska J,Codreanu J. Prevalence and Pattern of Autoimmune Conditions in Patients with Marginal Zone Lymphoma: A Single Institution Experience. Conn Med. 2015;79(4):197-200.

  49. Gelbenegger G, Schoergenhofer C, Derhaschnig U, Buchtele N, Sillaber C, Fillitz M, et al. Inhibition of complement C1s in patients with cold agglutinin disease: lessons learned from a named patient program. Blood Adv. 2020;4(6):997-1005. DOI: https://10.1182/bloodadvances.201900132149.

  50. Bertoni F, Rossi D, Zucca E. Recent advances in understanding the biology of marginal zone lymphoma. F1000Res.2018;7:406. DOI: https://10.12688/f1000research.13826.150.

  51. Sokol RJ, Hewitt S, Stamps BK, Hitchen PA. Autoimmune haemolysis in childhood and adolescence. Acta Haematol. 1984;72(4):245-57. DOI: https://10.1159/00020639751.

  52. Williams JD, Jayaprakash RK, Kithany H, Tighe MP. How to use Donath- Landsteiner test to diagnose paroxysmal cold haemoglobinuria (PCH). Arch Dis Child Educ Pract Ed. 2021;0:1-8. DOI: https://10.1136/archdischild-2020-31956852.

  53. Lau-Braunhut SA, Stone H, Collins G, Berentsen S, Zinter M, Braun B.et al. Paroxysmal cold hemoglobinuria successfully treated with complement inhibition. Blood Adv. 2019;3:3575-8. DOI: https://10.1182/blood-2019-12636553.

  54. Aladjidi N, Jutand MA, Beaubois C, Fernandes H, Jeanpetit J, Coureau G, et al. Reliable assessment of the incidence of childhood autoimmune hemolytic anemia. Pediatr Blood Cancer.2017;64:e26683. DOI: https://10.1002/pbc.2668354.

  55. Qiao L, Chen J, Leng XM, Zhang W, Han B, Zhao Y, et al. Agranulocytosis and mixed-type autoimmune hemolytic anemia in primary Sjogren's syndrome: a case report and review of the literature. Int J Rheum Dis. 2016;19(12):1351-3. DOI: https://10.1111/1756-185X.1280355.




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