Rh Isoimmunization in Low Responders: Case report
Abstract
Introduction. Rh isoimmunization consists of a Rh negative pregnant woman producing maternal antibodies against the antigens of fetal Rh-positive erythrocytes due to fetomaternal hemorrhage. 15% of the pregnant population is Rh negative, and the severity of fetal effects is related to a series of immunological processes and the obstetric history. If a Rh-negative pregnant woman at risk of isoimmunization does not receive a prophylaxis of Anti-D immunolobulin, 16% are immunized in the first pregnancy, 30% in the second and 50% after the third. In this case report we will describe the subgroup of low responder pregnant patients with Rh isoimmunization. Case Presentation. G9P5C1A2Gem1V7, 43 years old, referred on the 30th week of pregnancy due to Rh isoimmunization. She did not receive Anti-D immunolobulin during this pregnancy, nor in her previous pregnancies, nor during postpartum. Indirect Coombs report of 1/4, which increases to 1/16. Ultrasound monitoring is normal. At week 35.3 she presented mild fetal anemia, and because the pregnancy was near its term, it was ended by cesarean section. Newborn with adequate weight considering the gestational age, who was then discharged after 72 hours with satisfactory evolution. Discussion. Low responder pregnant women with Rh isoimmunization are sensitized with high blood volumes but without hemodynamic repercussions in utero, producing a mild fetal hemolytic disease. This immune response is infrequent and is associated with protective factors; however, further studies are required to support this condition. Conclusions. Prenatal control and serialized quantitative indirect Coombs testing are the main tools for the prevention of isoimmunization. Knowledge of the immunological response enables identifying the subgroup of low responders who present a milder clinical evolution and lower newborn morbidity.
References
Fundación medicina fetal Barcelona. Isoinmunización y transfusión intrauterina [Internet]. Medicina Fetal Barcelona. Recuperado a partir de: https://medicinafetalbarcelona.org/protocolos/es/patologia-fetal/isoinmunizacion-y-transfusion-intrauterina.html
Liumbruno GM, D’Alessandro A, Rea F, Piccinini V, Catalano L, Calizzani G, et al. The role of antenatal immunoprophylaxis in the prevention of maternal-foetal anti-Rh(D) alloimmunisation. Blood Transfus [Internet]. 2010;8(1):8-16. doi: https://doi.org/10.2450/2009.0108-09
Sulochana PV, Rajesh A, Mathai J, Sathyabhama S. Blocked D phenomenon, a rare condition with Rh D haemolytic disease of newborn - a case report. Int J Lab Hematol [Internet]. 2008;30(3):244-47. doi: https://doi.org/10.1111/j.1751-553X.2007.00943.x
Gabbe SG, Niebyl JR, Simpson JL, Landon MB, Galan HL, Jauniaux ERM, et al. Obstetricia: Embarazos normales y de riesgo [Internet]. 7a ed. Barcelona, España. 2019 Niebyl JR, editor. Elsevier; 770-785 p. Recuperado a partir de: https://www.elsevier.com/books/obstetricia/978-84-9113-358-2 (4).
Esan AJ. Hemolytic Disorders of the Newborn, Current Methods of Diagnosis and Treatment: A Review Study. J Hematol Blood Transfus Disord [Internet]. 2016;3(1):1-18. doi: https://doi.org/10.24966/HBTD-2999/100008
Palmeira P, Quinello C, Silveira-Lessa AL, Zago CA, Carneiro-Sampaio M. IgG placental transfer in healthy and pathological pregnancies. Clin Dev Immunol [Internet]. 2012;2012:985646:1-13. doi: https://doi.org/10.1155/2012/985646
Ibañez-Burillo P, Hernández-Bretón P, González-Bosquet E, Fabre-González E. Isoinmunización eritrocitaria y plaquetaria materno-fetal. Obstetricia [Internet]. 7ª ed. Barcelona, España. 2018:457-468. Recuperado a partir de: https://dialnet.unirioja.es/servlet/articulo?codigo=7228166
Velkova E. Correlation between the Amount of Anti-D Antibodies and IgG Subclasses with Severity of Haemolytic Disease of Foetus and Newborn. Open Access Maced J Med Sci [Internet]. 2015;3(2):293-297. doi: https://doi.org/10.3889/oamjms.2015.058
Hildén JO, Gottvall T, Lindblom B. HLA phenotypes and severe Rh(D) immunization. Tissue Antigens [Internet]. 1995;46(4):313-5. doi: https://doi.org/10.1111/j.1399-0039.1995.tb02498.x
Neppert J, Witzleben-Schürholz EV, Zupanska B, Bartz L, Greve O, Eichler H, et al. High incidence of maternal HLA A, B and C antibodies associated with a mild course of haemolytic disease of the newborn. Eur J Haematol [Internet]. 1999;63(2):120-125. doi: https://doi.org/10.1111/j.1600-0609.1999.tb01125.x
Dooren MC, Kuijpers RW, Joekes EC, Huiskes E, Goldschmeding R, Overbeeke MA, et al. Protection against immune haemolytic disease of newborn infants by maternal monocyte-reactive IgG alloantibodies (anti-HLA-DR). Lancet [Internet]. 1992;339(8801):1067-70. doi: https://doi.org/10.1016/0140-6736(92)90661-l
Hadley AG, Kumpel BM. The role of Rh antibodies in haemolytic disease of the newborn. Baillieres Clin Haematol [Internet]. 1993;6(2):423-44. doi: https://doi.org/10.1016/s0950-3536(05)80153-2
Agrawal A, Hussain KS, Kumar A. Minor blood group incompatibility due to blood groups other than Rh(D) leading to hemolytic disease of fetus and newborn: a need for routine antibody screening during pregnancy. Intractable Rare Dis Res [Internet]. 2020;9(1):43-7. doi: https://doi.org/10.5582/irdr.2019.01094
Moise KJ. Management of rhesus alloimmunization in pregnancy. Obstet Gynecol [Internet]. 2002;100(3):600-11. doi: http://doi.org/10.1016/s0029-7844(02)02180-4
Eichler H, Zieger W, Neppert J, Kerowgan M, Melchert F, Goldmann SF. Mild course of fetal RhD haemolytic disease due to maternal alloimmunisation to paternal HLA class I and II antigens. Vox Sang [Internet]. 1995;68(4):243-7. doi: http://dx.doi.org/10.1111/j.1423-0410.1995.tb02581.x
Downloads
Copyright (c) 2023 MedUNAB

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
| Article metrics | |
|---|---|
| Abstract views | |
| Galley vies | |
| PDF Views | |
| HTML views | |
| Other views | |


























