Blood type

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Blood type is determined, in part, by the ABO blood group antigens present on red blood cells
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Blood type is determined, in part, by the ABO blood group antigens present on red blood cells

A total of 29 human blood group systems are recognized by the International Society of Blood Transfusion (ISBT).[1] The most important of these are the ABO blood group system and the Rhesus blood group system.

Each blood group is represented by a substance on the surface of red blood cells (RBCs). These substances are important because they contain specific sequences of amino acid and carbohydrate which are antigenic. As well as being on the surface of RBCs, some of these antigens are also present on the cells of other tissues. A complete blood type describes the set of 29 substances on the surface of RBCs, and an individual's blood type is one of the many possible combinations of blood group antigens; usually only the ABO blood group system and the presence or absence of the Rhesus D antigen (also known as the Rhesus factor) are determined and used to describe the blood type. Over 600 different blood group antigens have been found,[2] many of these being very rare. If an individual is exposed to a blood group antigen that is not recognised as self, the individual can become sensitized to that antigen; the immune system makes specific antibodies which binds specifically to a particular blood group antigen and an immunological memory against that particular antigen is formed. These antibodies can bind to antigens on the surface of transfused red blood cells (or other tissue cells) often leading to destruction of the cells by recruitment of other components of the immune system. Knowledge of an individual's blood type is important to identify appropriate blood for transfusion or tissue for organ transplantation.

Several different RBC surface antigens stemming from one allele (or very closely linked genes) are collectively labeled as a blood group system (or blood group). The two most important blood group systems were discovered during early experiments with blood transfusion, the ABO group in 1901[3] and the Rhesus group in 1937.[4] These two blood groups are reflected in the common nomenclature A positive, O negative, etc. with letters referring to the ABO group and positive/negative to the presence/absence of the RhD antigen of the Rhesus group. Development of the Coombs test in 1945[5] and the advent of transfusion medicine led to discovery of more blood groups. The Coombs test is used routinely in the screening of blood for blood group antibodies in the preparation of blood for transfusion.

Blood types are inherited and represent contributions from both parents. Some blood types are rare, and are primarily found in certain ethnic groups. Some blood types are associated with inheritance of other diseases, for example the Kell antigen is associated with McLeod syndrome.[6] Certain blood types may affect susceptibility to infections, an example being the resistance to specific malaria species seen in individuals lacking the Duffy antigen.[7] Very rarely, a person's blood type changes through addition or suppression of an antigen in infection or malignancy.[citation needed]Transfusion reactions can occur if a person is transfused with blood of a different blood type. Mismatches involving minor antigens or weak antibodies may lead to minor problems; however, more serious incompatibilities can lead to a more vigorous immune response with massive RBC destruction, low blood pressure, and even death.

Often, pregnant women carry a fetus with a different blood type to their own, and sometimes the mother forms antibodies against the red blood cells of the fetus, which causes hemolysis of fetal RBCs and leads to low fetal blood counts, a condition known as hemolytic disease of the newborn.

Contents

[edit] Introduction

ABO blood group system - diagram showing the carbohydrate chains which determine the ABO blood group
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ABO blood group system - diagram showing the carbohydrate chains which determine the ABO blood group

[edit] ABO and Rhesus: the two main blood group systems

The ABO system is the most important blood group system in human blood transfusion. The associated anti-A antibodies and anti-B antibodies are usually IgM antibodies. ABO IgM antibodies are produced in the first years of life by sensitization to environmental substances such as food, bacteria and viruses. The "O" in ABO is often replaced by 0 (zero/null) in other languages.[8]

The Rhesus system is the second most important blood group system in human blood transfusion. The most important Rhesus antigen is the RhD antigen because it is the most immunogenic of the five main rhesus antigens; however, anti-RhD antibodies are not usually produced by sensitization against environmental substances. It is common for RhD negative individuals not to have any anti-RhD IgG or IgM antibodies; nevertheless, RhD negative individuals can produce IgG antibodies when they are transfused with RhD positive RBCs.

The agglutination of IgM is stronger due to the relatively large size of the IgM antibody, but the nature of the bodily reaction as a result of agglutination with IgG can be more dramatic

[edit] Table of ABO and Rh distribution by nation

ABO and Rh blood type distribution by nation (averages for each population)
Population O+ A+ B+ AB+ O− A− B− AB−
Australia[9] 40% 31% 8% 2% 9% 7% 2% 1%
Canada[10] 39.0% 36.0% 7.6% 2.5% 7.0% 6.0% 1.4% 0.5%
Denmark[11] 35% 37% 8% 4% 6% 7% 2% 1%
Finland[12] 27% 38% 15% 7% 4% 6% 2% 1%
France[citation needed] 36% 37% 9% 3% 6% 7% 1% 1%
Korea, South[13] 27.4% 34.4% 26.8% 11.2% 0.1% 0.1% 0.1% 0.05%
Sweden[14] 32% 37% 10% 5% 6% 7% 2% 1%
UK[15] 37% 35% 8% 3% 7% 7% 2% 1%
USA[16] 38% 34% 9% 3% 7% 6% 2% 1%

[edit] Other human blood group systems

The International Society of Blood Transfusion currently recognizes 29 blood group systems[1] (including the ABO and Rh systems). Thus, in addition to the ABO antigens and Rhesus antigens, many other antigens are expressed on the RBC surface membrane. For example, an individual can be AB RhD positive, and at the same time M and N positive (MNS system), K positive (Kell system), Lea or Leb positive (Lewis system), and so on for each blood group system. Many of the blood group systems were named after the patients in whom the corresponding antibodies were initially encountered.

[edit] Importance for transfusions

Main article: Blood transfusion

Transfusion medicine is a specialized branch of hematology that is concerned with the study of blood group antigens and blood group antibodies, along with the work of a blood bank to provide a transfusion service for blood and other blood products. Across the world blood products must be prescribed by a medical doctor (licensed physician or surgeon) in a similar way to medicines. In the USA blood products are tightly regulated by the Food and Drug Administration.

Blood transfusions between donor and recipient of incompatible blood types can cause severe acute immunological reactions, hemolysis (RBC destruction), renal failure, shock, and sometimes death. Antibodies can be highly active and can attack RBCs and bind components of the complement system to cause massive hemolysis of the transfused blood.

[edit] Hemolytic disease of the newborn

An antenatal woman can make IgG blood group antibodies if her fetus has a blood group antigen that she does not. This can happen if some of the fetus' blood cells pass into the mother's blood circulation (e.g. a small fetomaternal hemorrhage at the time of child birth) or sometimes after a therapeutic blood transfusion. This can lead to Rh disease or another forms of hemolytic disease of the newborn (HDN) in her current baby or in subsequent pregnancies. Some blood groups can cause severe HDN, some can only cause mild HDN and others are not known to cause HDN.

[edit] Compatibility

[edit] Blood products

In order to provide maximum benefit from each blood donation and to extend shelf-life, blood banks fractionate whole blood into several products. The most common of these products are packed RBCs, plasma, platelets, cryoprecipitate, and fresh frozen plasma (FFP). FFP is quick-frozen to retain labile clotting factors V and VIII and usually administered to patients who have a potentially fatal clotting problem caused by a condition such as advanced liver disease, overdose of anticoagulant, or disseminated intravascular coagulation (DIC).

Clotting factors synthesized by modern recombinant methods are now in routine clinical use for hemophilia, as the risks of infection transmission that occur with pooled blood products are avoided.

[edit] Cross matching blood

Main article: Cross-matching

Patients should ideally receive their own blood or type-specific blood products to minimize the chance of a transfusion reaction. If time allows, the risk will further be reduced by cross-matching blood, in addition to blood typing both recipient and donor. Cross-matching involves mixing a sample of the recipient's blood with a sample of the donor's blood and checking to see if the mixture agglutinates, or forms clumps. Blood bank technicians usually check for agglutination with a microscope, and if it occurs, that particular donor's blood cannot be transfused to that particular recipient. Blood transfusion is a potentially risky medical procedure and it is vital that all blood specimens are correctly identified, so in cross-matching labeling is standardized using a barcode system known as ISBT 128.

[edit] RBC compatibility

  • Blood group AB individuals have both A and B antigens on the surface of their RBCs, and their blood serum does not contain any antibodies against either A or B antigen. Therefore, an individual with type AB blood can receive blood from any group (with AB being preferable), but can only donate blood to another group AB individual.
  • Blood group A individuals have the A antigen on the surface of their RBCs, and blood serum containing IgM antibodies against the B antigen. Therefore, a group A individual can only receive blood from individuals of groups A or O (with A being preferable), and can donate blood to individuals of groups A or AB.
  • Blood group B individuals have the B antigen on their surface of their RBCs, and blood serum containing IgM antibodies against the A antigen. Therefore, a group B individual can only receive blood from individuals of groups B or O (with B being preferable), and can donate blood to individuals of groups B or AB.
  • Blood group O (or blood group zero in some countries) individuals do not have either A or B antigens on the surface of their RBCs, but their blood serum contains IgM antibodies against both A and B antigens. Therefore, a group O individual can only receive blood from a group O individual, but they can donate blood to individuals of any ABO blood group (ie A, B, O or AB). O- is therefore used when an emergency transfusion is necessary and there has not been enough time to verify the patient's blood type.
Donors of blood type O can give to A, B & AB; donors of types A & B can give to AB.
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Donors of blood type O can give to A, B & AB; donors of types A & B can give to AB.
RBC compatibility table
Recipient blood type Donor must be
AB+ Any blood type
AB- O- A- B- AB-
A+ O- O+ A- A+
A- O- A-    
B+ O- O+ B- B+
B- O- B-    
O+ O- O+    
O- O-      

An RhD negative patient (who has not been sensitized to RhD positive RBCs and who does not have any anti-D antibodies) can receive RhD positive blood cells, but there is a high probability that this would sensitize the patient to the RhD antigen, and a female patient would risk HDN. Therefore RhD positive blood is never given to RhD negative women of childbearing age, and is only given to other RhD negative patients in extreme circumstances, such as a major bleed when RhD negative red cells are running short. If a RhD negative patient has developed anti-D antibodies, a second exposure to RhD positive blood would lead to a potentially dangerous transfusion reaction. Occasionally, for transfusion of males or women above child-bearing age, RhD positive blood is given to a RhD negative individual (who do not have atypical red cell antibodies) when it is necessary to conserve RhD negative blood stocks in the blood bank for use in people where sensitisation to RhD antigens could cause serious problems. The converse is not true: RhD positive patients do not react to RhD negative blood.

[edit] Plasma compatibility

Plasma from type AB can be given to A, B & O; plasma from types A & B can be given to O.
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Plasma from type AB can be given to A, B & O; plasma from types A & B can be given to O.

Donor-recipient compatibility for blood plasma is the reverse from that of RBCs. Plasma extracted from type AB blood can be transfused to individuals of any blood group, but type O plasma can only be used by type O recipients.

Rhesus D antibodies are not usually naturally occurring, so generally both RhD negative and RhD positive blood do not contain anti-RhD antibodies. RhD negative or RhD positive donor blood plasma can therefore generally be transfused into both RhD negative and RhD positive recipients. Consequently RhD positive or RhD negative is irrelevant in the table below. If anti-RhD antibodies have developed in a donor these would be detected by antibody screening in the blood bank. Donor blood containing anti-RhD antibodies would not be suitable for transfusion into a RhD positive patient, but anyone with any strong atypical blood group antibodies would not be accepted as a blood donor.

Plasma compatibility table
Recipient blood type Donor must be
AB AB
A A or AB
B B or AB
O Any blood type

[edit] Universal donors and universal recipients

Individuals with blood type O negative are often called universal donors and individuals with type AB positive blood are called universal recipients, but the terms universal donor and universal recipient are not very useful, because they only consider the reaction of the patient's antibodies to received red blood cells, and not the antibodies present in the transfused blood. These terms may be generally true for transfusions of packed red cells, where as much of the plasma as possible has been removed. Thus, although a transfusion of O negative blood to a patient of blood group A or B is unlikely to produce an immune reaction due to the recipient's antibodies, the transfused blood may itself contain antibodies to the patient's A and B antigens; this can cause an adverse reaction, although the risk is far less than that of an O negative patient receiving types A or B. For this reason an exact ABO-type match is preferable where circumstances allow. Additionally, the other red blood cell surface antigens that belong to blood groups other than the ABO blood group system might cause an adverse reaction if they can bind the corresponding antibodies.

With respect to transfusions of plasma this situation is reversed. Type O plasma can only be given to O recipients, while AB plasma (which does not contain anti-A or anti-B antibodies) can be given to patients of any ABO blood group.

Transfusions are further complicated because platelets and white blood cells (WBCs) have their own systems of surface antigens. Sensitization to platelet or WBC antigens can occur as a result of transfusion.

[edit] Miscellaneous

  • For RhD negative people, there is a risk associated with travelling to parts of the world where supplies of RhD negative blood are rare, particularly East Asia. Correspondingly, blood services in these areas may look to encourage westerners to donate blood.[17]
  • Some blood types may offer protection from certain disorders and illnesses. For example, Duffy blood group is related to immunity against some kinds of malaria, and is more common in ethnic groups from areas with a high incidence of malaria as a result of natural selection.[18]
  • The Japanese blood type theory of personality is a popular belief that a person's ABO blood type is predictive of their personality, character, and compatibility with others, according to books by Masahiko Nomi. This belief has carried over to certain extent in other parts of East Asia such as South Korea and Taiwan. In Japan, asking someone their blood type is considered as normal as asking their astrological sign. It is also common for Japanese-made video games (especially Role-Playing Games) and manga series to include blood type with character descriptions.
  • Some front-line military personnel choose to be tattooed with their blood type in case they should need an emergency blood transfusion. This was especially the case with frontline German Waffen SS troops fighting on the Eastern Front against the Russians during the Second World War, ironically this was an easy form of SS identification.[19]
  • Rare blood types can cause supply problems for blood banks and hospitals. For example, U-negative and Duffy-negative are two blood groups which occur much more frequently in people of African origin.[20] The rarity of these factors in the rest of the population can result in a shortage of U-negative and Duffy-negative blood for patients of African ethnicity.
  • The ABO antigen is also expressed on the von Willebrand factor (vWF) glycoprotein,[21] which participates in hemostasis (control of bleeding). In fact, having type O blood predisposes to bleeding,[22] as 30% of the total genetic variation observed in plasma vWF is explained by the effect of the ABO blood group,[23] and individuals with group O blood normally have significantly lower plasma levels of vWF (and Factor VIII) than do non-O individuals.[24][25] In addition, vWF is degraded more rapidly due the higher prevalence of blood group O with the Cys1584 variant of vWF (an amino acid polymorphism in VWF):[26] the gene for ADAMTS13 (vWF-cleaving protease) maps to the ninth chromosome (9q34), the same locus as ABO blood type. Higher levels of vWF are more common amongst people who have had ischaemic stroke (from blood clotting) for the first time.[27] The results of this study found that the occurrence was not affected by ADAMTS13 polymorphism, and the only significant genetic factor was the person's blood group.
  • The blood type diet is a system whereby people modify their food intake and lifestyle according to their ABO blood group and secretor status for health.[28]

[edit] References

  1. ^ a b Table of blood group systems. International Society of Blood Transfusion (October 2006). Retrieved on 2006-11-14.
  2. ^ American Red Cross Blood Services, New England Region, Maine, Massachusetts, New Hampshire, Vermont. American Red Cross Blood Services - New England Region (2001). Retrieved on 2006-11-14. “there are more than 600 known antigens besides A and B that characterize the proteins found on a person's red cells”
  3. ^ Landsteiner K. Zur Kenntnis der antifermentativen, lytischen und agglutinierenden Wirkungen des Blutserums und der Lymphe. Zentralblatt Bakteriologie 1900;27:357-62.
  4. ^ Landsteiner K, Wiener AS. An agglutinable factor in human blood recognized by immune sera for rhesus blood. Proc Soc Exp Biol Med 1940;43:223-224.
  5. ^ Coombs RRA, Mourant AE, Race RR. A new test for the detection of weak and "incomplete" Rh agglutinins. Brit J Exp Path 1945;26:255-66.
  6. ^ Allen FH Jr, Krabbe SM, Corcoran PA. A new phenotype (McLeod) in the Kell blood-group system. Vox Sang. 1961 Sep;6:555-60. PMID 13477267
  7. ^ Miller LH, Mason SJ, Clyde DF, McGinniss MH. "The resistance factor to Plasmodium vivax in blacks. The Duffy-blood-group genotype, FyFy." N Engl J Med. 1976 Aug 5;295(6):302-4 PMID 778616
  8. ^ Your blood – a textbook about blood and blood donation (PDF) 63. Retrieved on 2006-11-21.
  9. ^ Blood Types - What Are They?, Australian Red Cross http://www.giveblood.redcross.org.au/Donor/aboutblood/bloodtypes.asp
  10. ^ Types & Rh System, Canadian Blood Services http://www.bloodservices.ca/CentreApps/Internet/UW_V502_MainEngine.nsf/page/Blood%20Types%20and%20Rh%20System?OpenDocument
  11. ^ Fordeling af blodtyper http://www.bloddonor.dk/index.php?id=513
  12. ^ Suomalaisten veriryhmäjakauma http://www.veripalvelu.fi/asp/system/empty.asp?P=1275
  13. ^ Statistics on annual blood donations 2002-2005, Gyung Nam Blood Center. http://www.gnbc.or.kr/sub01_07_03.html
  14. ^ Frequency of major blood groups in the Swedish population. http://www.geblod.nu/general.aspx?PageId=10
  15. ^ Frequency of major blood groups in the UK population. http://www.blood.co.uk/pages/all_about.html
  16. ^ Census CounterParts. http://www.census.gov/sdc/www/ccp0601.pdf
  17. ^ Bruce, MG (May 2002). BCF - Members - Chairman's Annual Report. The Blood Care Foundation. Retrieved on 2006-11-16. “As Rhesus Negative blood is rare amongst local nationals, this Agreement will be of particular value to Rhesus Negative expatriates and travellers”
  18. ^ Kwiatkowski, DP (Aug 2005). "How Malaria Has Affected the Human Genome and What Human Genetics Can Teach Us about Malaria". Am J Hum Genet. 77 (2): 171-192. Full text at PMC: 1224522. Retrieved on 2006-11-16."The different geographic distributions of α thalassemia, G6PD deficiency, ovalocytosis, and the Duffy-negative blood group are further examples of the general principle that different populations have evolved different genetic variants to protect against malaria".
  19. ^ German Intelligence Agents and Suspected Agents. Highlights of Freedom of Information releases in September 2005. The National Archives (September 2005). Retrieved on 2006-11-20. “... the trademark SS tattoo under his arm of his blood group”
  20. ^ Nickel, RG, Willadsen SA, Freidhoff LR, et. al (1999 Aug). "Determination of Duffy genotypes in three populations of African descent using PCR and sequence-specific oligonucleotides". Hum Immunol. 60 (8): 738-42. PMID 10439320.
  21. ^ Sarode, R, Goldstein J, Sussman II, Nagel RL, Tsai HM (2000 Jun). "Role of A and B blood group antigens in the expression of adhesive activity of von Willebrand factor". Br J Haematol. 109 (4): 857-64. PMID 10929042.
  22. ^ O'Donnell, J, Laffan MA (2001 Aug). "The relationship between ABO histo-blood group, factor VIII and von Willebrand factor". Transfus Med. 11 (4): 343-51. DOI:10.1046/j.1365-3148.2001.00315.x. PMID 11532189.
  23. ^ O'Donnell, J, Boulton FE, Manning RA, Laffan MA (2002 Feb 1). "Amount of H antigen expressed on circulating von Willebrand factor is modifiedby ABO blood group genotype and is a major determinant of plasma von Willebrand factor antigen levels". Arterioscler Thromb Vasc Biol. 22 (2): 335-41. PMID 11834538.
  24. ^ Gill, JC, Endres-Brooks J, Bauer PJ, Marks WJ, Montgomery RR (1987 Jun). "The effect of ABO blood group on the diagnosis of von Willebrand disease". Blood 69 (6): 1691-5. PMID 3495304.
  25. ^ Shima, M, Fujimura Y, Nishiyama T et. al (1995). "ABO blood group genotype and plasma von Willebrand factor in normal individuals". Vox Sang 68 (4): 236–40. PMID 7660643.
  26. ^ Bowen, DJ, Collins PW, Lester W, et. al (2005 Mar). "The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotype". Br J Haematol 128 (6): 830-6. DOI:10.1111/j.1365-2141.2005.05375.x. PMID 15755288.
  27. ^ Bongers T, de Maat M, van Goor M, et. al (2006). "High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability.". Stroke 37 (11): 2672-7. PMID 16990571.
  28. ^ D'Adamo, Dr. Peter J, Catherine Whitney (1996). Eat Right 4 Your Type: The Individualized Diet Solution to Staying Healthy, Living Longer and Achieving Your Ideal Weight. New York: Penguin Group (USA). ISBN 039914255X.

[edit] Further reading

  • Mollison PL, Engelfriet CP and Contreras M. "Blood Transfusion in Clinical Medicine." 1997. 10th edition. Blackwell Science, Oxford, UK. ISBN 0865428816

[edit] External links

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Transfusion medicine
Apheresis  (Plasmapheresis — Plateletpheresis — Leukapheresis) | Blood transfusion | Coombs test | Cross-matching | Exchange transfusion | International Society of Blood Transfusion | Intraoperative blood salvage | ISBT 128 | Transfusion reactions
Human blood group systems - Blood type
ABO | Colton | Duffy | Hh | Kell | Kidd | Kx | Rhesus |Yt
Blood products
Blood | Blood donation | Blood substitutes | Cryoprecipitate | Platelets | Plasma | Red blood cells