Human blood group systems
<templatestyles src="Module:Hatnote/styles.css"></templatestyles>
Lua error in package.lua at line 80: module 'strict' not found.
The term human blood group systems is defined by International Society of Blood Transfusion as systems in the human species where cell-surface antigens—in particular, those on blood cells—are "controlled at a single gene locus or by two or more very closely linked homologous genes with little or no observable recombination between them",[1] and include the common ABO and Rh- (Rhesus) antigen systems, as well as many others; thirty-five major human systems are identified as of November 2014.[2] In addition to the ABO and Rh systems, the antigens expressed on blood cell membrane surfaces include 346 red blood cell antigens and 33 platelet antigens, as defined serologically.[3][better source needed] The genetic basis for most of these antigens lie in 45 red blood cell and 6 platelet genes.[citation needed] An individual, for example, can be AB RhD positive, and at the same time M and N positive in the MNS system, K positive in the Kell system, and Lea or Leb positive in the Lewis system,[citation needed] where these and many of the systems are named for patients in whom the corresponding antibodies were first detected.[citation needed]
Contents
Blood grouping postulates
Lua error in package.lua at line 80: module 'strict' not found. Blood is composed of cells suspended in a liquid called plasma. Suspended in the plasma are three types of cells:
- Red blood cells carry oxygen
- White blood cells fight infection
- Platelets stop bleeding in injuries
The most common type of grouping is the ABO (either uppercase or lowercase) grouping. The varieties of glycoprotein coating on red blood cells divides blood into four groups:
- A (A oligosaccharide is present)
- B (B oligosaccharide is present)
- AB (A and B oligosaccharides are present)
- O (neither A nor B, only their precursor H oligosaccharide present)
There are subtypes under this grouping (listed as A1, A2, A1B or A2B…) some of which are quite rare. Apart from this there is a protein which plays an important part in the grouping of blood. This is called the Rh factor. If this is present, the particular blood type is called positive. If it is absent, it is called negative. Thus we have the following broad categories:[4][dubious ][better source needed]
- A1 Negative (A1 −ve)
- A1 Positive (A1 +ve)
- A1B Negative (A1B −ve)
- A1B Positive (A1B +ve)
- A2 Negative (A2 −ve)
- A2 Positive (A2 +ve)
- A2B Negative (A2B −ve)
- A2B Positive (A2B +ve)
- B Negative (B −ve)
- B Positive (B +ve)
- B1 Positive (B1 +ve)
- O Negative (O −ve)
- O Positive (O+ve)
Rare blood types
Lua error in package.lua at line 80: module 'strict' not found. In the "ABO" system, (and Rhesus D system) all blood belongs to one of four major groups: A+/−, B+/−, AB+/−, or O+/−. The presence (+) or absence (−) of the RhD (Rhesus D) antigen is indicated by the plus or minus following the ABO type. But there are more than two hundred minor blood groups that can complicate blood transfusions. These are known as rare blood types. Whereas common blood types are expressed in a letter or two, which may be a plus or a minus, a smaller number of people express their blood type in an extensive series of letters in addition to their 'AB-' type designation. The h/h blood group, also known as Oh or the Bombay blood group, is a rare blood type.[5][citation needed]
Blood group systems
This table was borrowed in significant part from a tabular ISBT document available via the web (columns 1, 2, 3 and 5),[2] with column 4, regarding epitopes and entry notes, being largely unsourced (and therefore suspect material not in compliance with Wikipedia policies).[6] That and other unsourced information—i.e., not appearing in the ISBT table cited, or new to the table since publication of the ISBT table—should be considered as currently unverifiable by this encyclopedia's standards.
ISBT №[2] | System name | System symbol | Epitope or carrier, notes[citation needed] | Chromosome |
---|---|---|---|---|
001 | ABO | ABO | Carbohydrate (N-Acetylgalactosamine, galactose). A, B and H antigens mainly elicit IgM antibody reactions, although anti-H is very rare, see the Hh antigen system (Bombay phenotype, ISBT #18). | 9q34.2 |
002 | MNS | MNS | GPA / GPB (glycophorins A and B). Main antigens M, N, S, s. | 4q31.21 |
003 | P | P | Glycolipid. Three antigens: P1, P, and Pk | 22q13.2 |
004 | Rh | RH | Protein. C, c, D, E, e antigens (there is no "d" antigen; lowercase "d" indicates the absence of D). | 1p36.11 |
005 | Lutheran | LU | Protein (member of the immunoglobulin superfamily). Set of 21 antigens. | 19q13.32 |
006 | Kell | KEL | Glycoprotein. K1 can cause hemolytic disease of the newborn (anti-Kell), which can be severe. | 7q34 |
007 | Lewis | LE | Carbohydrate (fucose residue). Main antigens Lea and Leb — associated with tissue ABH antigen secretion. | 19p13.3 |
008 | Duffy | FY | Protein (chemokine receptor). Main antigens Fya and Fyb. Individuals lacking Duffy antigens altogether are immune to malaria caused by Plasmodium vivax and Plasmodium knowlesi. | 1q23.2 |
009 | Kidd | JK | Protein (urea transporter). Main antigens Jka and Jkb. | 18q12.3 |
010 | Diego | DI | Glycoprotein (band 3, AE 1, or anion exchange). Positive blood is found only among East Asians and Native Americans. | 17q21.31 |
011 | Yt | YT | Protein (AChE, acetylcholinesterase). | 7q22.1 |
012 | XG | XG | Glycoprotein. | Xp22.33 |
013 | Scianna | SC | Glycoprotein. | 1p34.2 |
014 | Dombrock | DO | Glycoprotein (fixed to cell membrane by GPI, or glycosyl-phosphatidyl-inositol). | 12p12.3 |
015 | Colton | CO | Aquaporin 1. Main antigens Co(a) and Co(b). | 7p14.3 |
016 | Landsteiner-Wiener | LW | Protein (member of the immunoglobulin superfamily). | 19p13.2 |
017 | Chido | CH | C4A C4B (complement fractions). | 6p21.3 |
018 | Hh | H | Carbohydrate (fucose residue). | 19q13.33 |
019 | XK | XK | Glycoprotein. | Xp21.1 |
020 | Gerbich | GE | GPC / GPD (Glycophorins C and D). | 2q14.3 |
021 | Cromer | CROM | Glycoprotein (DAF or CD55, regulates complement fractions C3 and C5, attached to the membrane by GPI). | 1q32.2 |
022 | Knops | KN | Glycoprotein (CR1 or CD35, immune complex receptor). | 1q32.2 |
023 | Indian | IN | Glycoprotein (CD44 adhesion function?). | 11p13 |
024 | Ok | OK | Glycoprotein (CD147). | 19p13.3 |
025 | Raph | RAPH | Transmembrane glycoprotein. | 11p15.5 |
026 | JMH | JMH | Protein (fixed to cell membrane by GPI). Also known as Semaphorin 7A or CD108. | 15q24.1 |
027 | Ii | I | Branched (I) / unbranched (i) polysaccharide. | 6p24.2 |
028 | Globoside | GLOB | Glycolipid. Antigen P. | 3q26.1 |
029 | GIL | GIL | Aquaporin 3.[citation needed] | 9p13.3 |
030 | Rh-associated glycoprotein | RHAg | Rh-associated glycoprotein.[citation needed] | 6p21-qter |
031 | Forssman | FORS | Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (GBGT1)[citation needed] | 9q34.13 |
032 | Langereis[7] | LAN | ABCB6, human ATP-binding cassette (ABC) transporter, mitochondrial porphyrin transporter.[7] | 2q36 |
033 | Junior | JR | ABCG2. Multi-drug transporter protein.[citation needed] | 4q22 |
034 | Vel | Vel | Human red cell antigens[citation needed] | 1p36.32 |
035 | CD59 | CD59 | — | 11p13 |
References
<templatestyles src="Reflist/styles.css" />
Cite error: Invalid <references>
tag; parameter "group" is allowed only.
<references />
, or <references group="..." />
External links
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- ISBT Table of blood group antigens within systems, updated August 2008.
- BGMUT Blood Group Antigen Gene Mutation Database at NCBI, NIH.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ 2.0 2.1 2.2 Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.[non-primary source needed][full citation needed]
- ↑ Indian Red Cross Society, Tamil Nadu Branch.[dubious ]
- ↑ This blood phenotype was first discovered in Bombay, now known as Mumbai, in India, by Dr. Y. M. Bhende in 1952.[citation needed]
- ↑ See WP:VERIFY and WP:OR.
- ↑ 7.0 7.1 Lua error in package.lua at line 80: module 'strict' not found.
- Pages with reference errors
- Medicine articles needing expert attention
- Articles lacking reliable references from February 2016
- Articles with unsourced statements from February 2016
- All accuracy disputes
- Articles with disputed statements from February 2016
- Blood antigen systems
- Transfusion medicine
- Wikipedia articles needing factual verification from February 2016