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면역혈액학_6과_정리레포트

6. Rh Antibodies
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한컴오피스
최초등록일 2024.02.15 최종저작일 2019.06
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면역혈액학_6과_정리레포트
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    소개

    6. Rh Antibodies

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    본문내용

    General Characteristics 일반적인 성격
    Rh 항체는 반드시 수혈이나 임신을 통해서 rh 항원을 가지고 있는 적혈구가 몸에 들어와서 면역 시스템에 노출이 되었을 때만 만들어진다. (정상적으로는 rh 항체가 내 몸에 있으면 안됨. 있다고 하면 외부에서 rh 항원이 들어온 경우. 임신 시기 태아도 타인이라고 할 수 있다)
    IgG, 37도에서 항원 항체 반응을 하고, Indirect anti-globulin test 에 의해서만 응집이 된다. IgG 타입의 대부분이 그러하듯이 complement 가 activate 되지 않는다.
    Dosage effect: 양쪽에 Large C 가 있을 때 더 강하게 반응한다.

    (2) Clinical Considerations
    1) 지연성용혈성수혈부작용 (Delayed hemolytic transfusion reactions): Rh 항체가 생겨난 이후에 수혈을 받으면 ABO 타입 혈액형처럼 바로 보체가 형성되어 용혈성 작용이 일어나는 것이 아니라 비장으로 간 이후에 혈관 밖 용혈이 일어난다(혈관내용혈은 ABO – acute, 급성 용혈성 수혈 부작용).

    2) Hemolytic disease of the fetus and newborn (D-positive baby vs D-negative mother) 태아 신생아 용혈성 질환

    Initial pregnancy: anti-D production in mother 임신 중에 태아의 혈액이 모체로 갈 수도 있고, 분만 중에 태아의 혈액이 역류해서 모체에게 갈 수도 있다. 그리고 이렇게 노출되게 되면 면역계가 anti-D 를 외부 물질로 인식해서 항체가 생긴다. 첫번째 임신에서는 문제가 없는데, 두번째 아이가 만약 또 D-positive 라고 하면 IgG 타입의 anti-D 항체를 가진 모체의 혈액이 태반을 통과해서 아이가 가지고 있는 D 항원에 결합해서 태아의 용혈이 일어나 적혈구가 파괴되고, 용혈성 질환이 일어나게 된다.

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  • AI와 토픽 톺아보기

    • 1. Rh Antibodies
      Rh antibodies are a critical component of the Rh blood group system, which is one of the most important blood group systems in transfusion medicine. These antibodies can be produced by individuals who lack the Rh antigen on their red blood cells, typically the D antigen, and can cause severe hemolytic reactions in individuals who possess the Rh antigen. The formation of Rh antibodies is a complex process that involves the immune system's recognition of foreign Rh antigens and the subsequent production of antibodies to neutralize them. Rh antibodies can be particularly problematic in the context of pregnancy, where they can cross the placenta and cause hemolytic disease of the newborn, a potentially life-threatening condition. Understanding the mechanisms behind Rh antibody formation and their clinical implications is crucial for ensuring safe and effective blood transfusions and managing Rh-related complications during pregnancy. Ongoing research in this field aims to improve our understanding of Rh antibodies and develop more effective strategies for their prevention and management.
    • 2. LW Blood Group System
      The LW blood group system is a relatively rare and lesser-known blood group system, but it is still an important consideration in transfusion medicine. The LW antigen is expressed on the surface of red blood cells and can elicit the production of antibodies in individuals who lack this antigen. These antibodies can potentially cause hemolytic transfusion reactions and, in rare cases, hemolytic disease of the newborn. The clinical significance of the LW blood group system is primarily related to the potential for alloimmunization and the need for careful antigen matching during blood transfusions. While the prevalence of LW antibodies is low, it is crucial for healthcare providers to be aware of this blood group system and to consider it when managing patients who may require blood transfusions or have a history of pregnancy-related complications. Ongoing research in this area aims to further elucidate the role of the LW blood group system in clinical practice and to develop more effective strategies for its management.
    • 3. Kell Blood Group System
      The Kell blood group system is one of the most clinically significant blood group systems after the ABO and Rh systems. The Kell antigen is expressed on the surface of red blood cells and can elicit the production of antibodies in individuals who lack this antigen. These Kell antibodies can cause severe hemolytic transfusion reactions and, in the context of pregnancy, can lead to hemolytic disease of the newborn, a potentially life-threatening condition. The Kell blood group system is particularly important in the management of patients with sickle cell disease, as Kell-negative blood is often preferred for transfusions to minimize the risk of alloimmunization. Additionally, the Kell system has been implicated in various other clinical scenarios, such as autoimmune hemolytic anemia and neonatal alloimmune thrombocytopenia. Ongoing research in this field aims to further elucidate the role of the Kell blood group system in clinical practice and to develop more effective strategies for its management, including the potential use of Kell-matched blood products and the development of novel therapeutic approaches.
    • 4. Kx Blood Group System
      The Kx blood group system is a relatively rare and specialized blood group system that is primarily associated with the McLeod phenotype, a condition characterized by the absence or reduced expression of the Kx antigen on red blood cells. The Kx antigen is closely linked to the Kell blood group system, and individuals with the McLeod phenotype may also exhibit neurological and hematological abnormalities. The clinical significance of the Kx blood group system lies in its potential to cause alloimmunization and subsequent hemolytic transfusion reactions, particularly in individuals who require frequent blood transfusions. Additionally, the Kx system has been implicated in the development of autoimmune hemolytic anemia and other rare hematological disorders. Ongoing research in this field aims to further elucidate the genetic and molecular mechanisms underlying the Kx blood group system and to develop more effective strategies for its management, including the identification of Kx-negative blood donors and the potential use of targeted therapies for individuals with the McLeod phenotype.
    • 5. Duffy Blood Group System
      The Duffy blood group system is an important consideration in transfusion medicine and the management of certain infectious diseases. The Duffy antigen serves as a receptor for the Plasmodium vivax and Plasmodium knowlesi parasites, which can cause malaria in humans. Individuals who lack the Duffy antigen (Duffy-negative) are generally resistant to infection by these parasites, making the Duffy blood group system clinically relevant in regions where these malaria strains are prevalent. In the context of transfusion medicine, Duffy antibodies can cause hemolytic transfusion reactions and, in rare cases, hemolytic disease of the newborn. Understanding the Duffy blood group system and its implications for transfusion safety and infectious disease management is crucial for healthcare providers, particularly in regions where Duffy-negative individuals are more common. Ongoing research in this field aims to further elucidate the role of the Duffy system in disease susceptibility and to develop more effective strategies for its management in both transfusion and infectious disease contexts.
    • 6. Kidd Blood Group System
      The Kidd blood group system is an important consideration in transfusion medicine due to its potential to cause alloimmunization and subsequent hemolytic transfusion reactions. The Kidd antigen is expressed on the surface of red blood cells and can elicit the production of antibodies in individuals who lack this antigen. These Kidd antibodies can be particularly problematic in the context of pregnancy, where they can cross the placenta and cause hemolytic disease of the newborn, a potentially life-threatening condition. Additionally, the Kidd blood group system has been implicated in various other clinical scenarios, such as autoimmune hemolytic anemia and neonatal alloimmune thrombocytopenia. Understanding the Kidd blood group system and its clinical implications is crucial for healthcare providers to ensure safe and effective blood transfusions and to manage Kidd-related complications during pregnancy. Ongoing research in this field aims to further elucidate the role of the Kidd system in clinical practice and to develop more effective strategies for its management, including the potential use of Kidd-matched blood products and the development of novel therapeutic approaches.
    • 7. Lutheran Blood Group System
      The Lutheran blood group system is a relatively rare and lesser-known blood group system, but it is still an important consideration in transfusion medicine. The Lutheran antigen is expressed on the surface of red blood cells and can elicit the production of antibodies in individuals who lack this antigen. These Lutheran antibodies can potentially cause hemolytic transfusion reactions and, in rare cases, hemolytic disease of the newborn. The clinical significance of the Lutheran blood group system is primarily related to the potential for alloimmunization and the need for careful antigen matching during blood transfusions. While the prevalence of Lutheran antibodies is low, it is crucial for healthcare providers to be aware of this blood group system and to consider it when managing patients who may require blood transfusions or have a history of pregnancy-related complications. Ongoing research in this area aims to further elucidate the role of the Lutheran blood group system in clinical practice and to develop more effective strategies for its management.
    • 8. Lewis Blood Group System
      The Lewis blood group system is a unique and complex blood group system that is primarily associated with the expression of the Lewis antigens on the surface of red blood cells and other tissues. Unlike most other blood group systems, the Lewis antigens are not inherently expressed on red blood cells but are rather acquired through the action of specific enzymes. This makes the Lewis system particularly interesting from a biological and clinical perspective. The Lewis antigens can elicit the production of antibodies in individuals who lack these antigens, and these antibodies can potentially cause hemolytic transfusion reactions. Additionally, the Lewis system has been implicated in various other clinical scenarios, such as the development of certain types of cancer and the susceptibility to certain infectious diseases. Ongoing research in this field aims to further elucidate the complex mechanisms underlying the Lewis blood group system and to explore its potential clinical applications, including the development of targeted therapies and diagnostic tools.
    • 9. I Blood Group System
      The I blood group system is a unique and complex blood group system that is primarily associated with the expression of the I antigen on the surface of red blood cells. The I antigen is a carbohydrate structure that is synthesized by a series of enzymatic reactions, and its expression can be influenced by various genetic and environmental factors. The clinical significance of the I blood group system lies in its potential to cause alloimmunization and subsequent hemolytic transfusion reactions, particularly in individuals who lack the I antigen. Additionally, the I system has been implicated in various other clinical scenarios, such as the development of certain types of cancer and the susceptibility to certain infectious diseases. Ongoing research in this field aims to further elucidate the complex mechanisms underlying the I blood group system and to explore its potential clinical applications, including the development of targeted therapies and diagnostic tools. Understanding the I blood group system and its implications for transfusion medicine and other clinical areas is crucial for healthcare providers to ensure safe and effective patient care.
    • 10. P Blood Group System
      The P blood group system is a relatively rare and specialized blood group system that is primarily associated with the expression of the P antigen on the surface of red blood cells. The P antigen is a carbohydrate structure that can elicit the production of antibodies in individuals who lack this antigen, and these antibodies can potentially cause hemolytic transfusion reactions. The clinical significance of the P blood group system is primarily related to its potential for alloimmunization and the need for careful antigen matching during blood transfusions. Additionally, the P system has been implicated in various other clinical scenarios, such as the development of certain types of cancer and the susceptibility to certain infectious diseases. Ongoing research in this field aims to further elucidate the complex mechanisms underlying the P blood group system and to explore its potential clinical applications, including the development of targeted therapies and diagnostic tools. Understanding the P blood group system and its implications for transfusion medicine and other clinical areas is crucial for healthcare providers to ensure safe and effective patient care.
    • 11. MNS Blood Group System
      The MNS blood group system is one of the most complex and clinically significant blood group systems after the ABO and Rh systems. The MNS system is characterized by the expression of the M, N, and S antigens on the surface of red blood cells, and these antigens can elicit the production of antibodies in individuals who lack them. These MNS antibodies can potentially cause hemolytic transfusion reactions and, in the context of pregnancy, can lead to hemolytic disease of the newborn, a potentially life-threatening condition. The MNS blood group system is particularly important in the management of patients with sickle cell disease, as MNS-matched blood is often preferred for transfusions to minimize the risk of alloimmunization. Additionally, the MNS system has been implicated in various other clinical scenarios, such as autoimmune hemolytic anemia and neonatal alloimmune thrombocytopenia. Ongoing research in this field aims to further elucidate the complex genetic and molecular mechanisms underlying the MNS blood group system and to develop more effective strategies for its management, including the potential use of MNS-matched blood products and the development of novel therapeutic approaches.
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