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Topic:Major Histocompatibility Complex (MHC)

The Major Histocompatibility Complex (MHC) in horses is a group of genes that play a significant role in the immune system by encoding proteins responsible for antigen presentation. These proteins are essential for the recognition of foreign molecules by the immune system, facilitating the differentiation between self and non-self entities. In horses, the MHC is located on equine chromosome 20 and is divided into several regions, including class I and class II, which present antigens to different subsets of T cells. Variability in the MHC genes is associated with susceptibility or resistance to various diseases, influencing immune responses and vaccine efficacy. This page compiles peer-reviewed research studies and scholarly articles that explore the genetic diversity, expression patterns, and implications of MHC in equine health and disease.
Joint report of the Third International Workshop on Lymphocyte Alloantigens of the Horse, Kennett Square, Pennsylvania, 25-27 April 1984.
Animal genetics    January 1, 1986   Volume 17, Issue 4 363-373 doi: 10.1111/j.1365-2052.1986.tb00730.x
Antczak DF, Bailey E, Barger B, Guerin G, Lazary S, McClure J, Mottironi VD, Symons R, Templeton J, Varewyck H.The Third International Workshop on Lymphocyte Alloantigens of the Horse was held on 25-27 April 1984 in Kennett Square, Pennsylvania. Twelve laboratories from five countries participated. The principal purpose of this Workshop was to determine the phenotypic and gene frequencies of the 10 equine lymphocyte antigens (ELA) and a non-ELA lymphocyte antigen, ELY-2.1, in several breeds of horse. A total of 86 alloantisera characterized in previous workshops were tested against lymphocytes from 1179 horses. In addition, several experimental antisera were also tested against the same panel of lympho...
Segregation distortion within the equine MHC; analogy to a mouse T/t-complex trait.
Immunogenetics    January 1, 1986   Volume 24, Issue 4 225-229 doi: 10.1007/BF00364526
Bailey E.Segregation distortion was found for a haplotype of the equine lymphocyte antigen (ELA) system in an extended family of American Standardbred horses. In one sire family, consisting of a stallion and his 17 sons and grandsons, the gene for ELA-A10 (A10) was transmitted to 57.7% of 638 offspring scored (P = 0.001). Significant segregation distortion was not seen for mares or for unrelated stallions, regardless of the ELA markers they possessed. Since the effect was seen for this one sire family and not seen for other stallions with A10, it is unlikely that the gene for A10 is the cause of this p...
A soluble class I molecule analogous to mouse Q10 in the horse and related species.
Immunogenetics    January 1, 1986   Volume 23, Issue 5 277-283 doi: 10.1007/BF00398789
Lew AM, Valas RB, Maloy WL, Coligan JE.Horse serum is shown to contain a soluble class I molecule analogous to the secreted Q10 molecule in the mouse. This molecule has several similarities to the recently described mouse Q10 molecule: it is smaller than membrane-bound equine class I molecules; it occurs in a high molecular mass complex of 200-300 kd in serum; and the serum levels of the equine molecule are similar to that of the Q10 molecule (about 30 micrograms/ml). A soluble molecule is also detected in the sera of species related to the horse; it has in fact been found in all the wild members of the order Perissodactyla so far ...
DNA polymorphism in the major histocompatibility complex of man and various farm animals.
Animal genetics    January 1, 1986   Volume 17, Issue 2 113-133 doi: 10.1111/j.1365-2052.1986.tb00732.x
Vaiman M, Chardon P, Cohen D.In the past few years it has been possible by combining enzymatic cleavage of genomic DNA and the Southern blot hybridization technique to explore the endonuclease recognition site polymorphism of the MHC. HLA class I and DR and DQ alpha and beta class II specific probes as well as human C4 and Bf class III probes were used. All these probes were shown to cross-hybridize with DNA from pigs, cattle, sheep and horses. Hybridization of human genomic DNA with a class I probe showed 15-25 bands per genome depending on the enzyme used. Distinct endonucleases generated clusters of restriction fragmen...
Equine leukocyte antigens: relationships with sarcoid tumors and laminitis in two pure breeds.
Immunogenetics    January 1, 1986   Volume 23, Issue 4 221-225 doi: 10.1007/BF00373016
Meredith D, Elser AH, Wolf B, Soma LR, Donawick WJ, Lazary S.Frequencies of equine leukocyte antigen distribution were determined by complement-mediated cytotoxicity testing among populations of Thoroughbred and Standardbred horses, including animals affected with equine sarcoid and laminitis. A highly significant association is described between the presence or history of sarcoid lesions in Thoroughbreds and the expression of the major histocompatibility complex (MHC)-encoded antigens, W3 and B1. No association was found between antigenic expression frequencies and laminitis in either breed. These findings suggest that a strong relationship exists betw...
Equine leucocyte antigen system: progress and potential.
Equine veterinary journal    July 1, 1985   Volume 17, Issue 4 265-268 doi: 10.1111/j.2042-3306.1985.tb02493.x
Matthews SM.Leucocyte antigens are cell-surface glycoproteins, the structure of which is under the genetic control of a chromosome region called the major histocompatibility complex. Progress in the study of the equine leucocyte antigen (ELA) system has been achieved in two ways; first by the fact that the ELA system is intensively investigated in different laboratories all over the world and parallels can be drawn to the information gained from research in more extensively studied species, and secondly by the collaborative efforts of the participants in three international workshops. The potential applic...
Equine leucocyte antigens in sarcoid-affected horses.
Equine veterinary journal    July 1, 1985   Volume 17, Issue 4 283-286 doi: 10.1111/j.2042-3306.1985.tb02498.x
Lazary S, Gerber H, Glatt PA, Straub R.The distribution of equine leucocyte antigens (ELA) in horses affected by equine sarcoid tumours was determined and compared with unaffected controls. ELA-haplotype W3,B1 occurred more frequently in affected riding horses of Irish, Swiss and French background. The combined data for the three breeds resulted in a chi 2 value of 20.35 (P less than 0.0005 after correction). Simultaneously, ELA-specificity W11 was more frequently found in horses of Irish background, while W5 was found in Swiss and French horses with sarcoids. The combined data for haplotype W3,B1 and/or W5 specificity demonstrated...
Equine lymphocyte antigens in four major Belgian horse populations. Contribution to serology and antigen distribution.
Animal blood groups and biochemical genetics    January 1, 1985   Volume 16, Issue 3 217-228 doi: 10.1111/j.1365-2052.1985.tb01472.x
Varewyck H, Bouquet Y, Lazary S, Guérin G, Van de Weghe A, Van Zeveren A.158 Belgian Saddlebreds, 130 Belgian Trotters, 108 Belgian Draft horses and 92 Shetland ponies have been typed for serologically defined antigens at the ELA and ELY systems. Gene frequencies were estimated in each breed for the internationally established ELA, ELY-1 and ELY-2 alleles as well as for locally assigned additional ELA markers and for subtypes of ELA-W3, W9 and W11. The distribution of ELA alleles was in agreement with the expected Hardy-Weinberg equilibrium for the 4 horse breeds described here. Differences in gene frequencies between these main Belgian horse populations were obser...
Usefulness of lymphocyte typing to exclude incorrectly assigned paternity in horses.
American journal of veterinary research    October 1, 1984   Volume 45, Issue 10 1976-1978 
Bailey E.Lymphocyte typing can be used to detect incorrectly identified parentage of horses. Efficacies of lymphocyte typing to solve paternity questions were calculated using gene frequency estimates of equine lymphocyte antigen (ELA) markers for Thoroughbreds and Standardbreds. Probabilities that ELA typing will detect an incorrectly assigned sire were 68.7% in Thoroughbreds, 67.9% in pacing Standardbreds, and 62.0% in trotting Standardbreds. These calculations demonstrate that ELA typing is among the most efficacious genetic systems for solving paternity questions in horses. Likewise, it could also ...
Lymphocyte alloantigens of the horse. II. Antibodies to ELA antigens produced during equine pregnancy.
Journal of reproductive immunology    August 1, 1984   Volume 6, Issue 5 283-297 doi: 10.1016/0165-0378(84)90028-7
Antczak DF, Miller JM, Remick LH.Evidence is presented for a reproducible maternal immune response to histocompatibility antigens during equine pregnancy. Mares were stimulated as a result of pregnancy to produce cytotoxic antibodies to paternal lymphocyte alloantigens. The majority of these antibodies were directed against antigens of the equine lymphocyte antigen (ELA) system, which is the major histocompatibility complex (MHC) of the horse. In 16 experimental pregnancies produced using 12 mares and 4 stallions which had been typed for ELA antigens, there was correlation between ELA incompatibility between sire and dam and ...
Xenogeneic monoclonal antibodies to cell surface antigens of equine lymphocytes.
American journal of veterinary research    April 1, 1984   Volume 45, Issue 4 626-632 
Newman MJ, Beegle KH, Antczak DF.Monoclonal antibodies to equine lymphocyte antigens were produced, using normal peripheral blood lymphocytes as the immunogen and standard hybridoma techniques. Antibody producing hybridomas were detected by a solid-phase enzyme-linked immunosorbent assay. Antibodies produced by 6 cloned hybrids were characterized further by microlymphocytotoxicity, indirect immunofluorescence, and agglutination assays on peripheral blood lymphocytes, platelets, and erythrocytes. Reaction patterns on leukocytes indicated that these antibodies may recognize at least 3 different cell-surface antigens: (1) an ant...
Lymphocyte alloantigens of the horse. III. ELY-2.1: a lymphocyte alloantigen not coded for by the MHC.
Animal blood groups and biochemical genetics    January 1, 1984   Volume 15, Issue 2 103-115 doi: 10.1111/j.1365-2052.1984.tb01105.x
Antczak DF.A new polymorphic locus of the horse which has several unusual properties is described. The suggested name for the locus is ELY-2. The gene product of one allele at this locus, designated ELY-2.1, has been identified with antisera raised as a result of pregnancy. Antibody to ELY-2.1 was first detected on day 55 after conception in the serum of a mare in first pregnancy. This early onset of antibody is similar to that seen for antibody to ELA antigens, and suggests that the source of the antigenic stimulus may be the tissue of the equine endometrial cups. The antisera identifying ELY-2.1 are cy...
Histocompatibility polymorphisms of domestic animals.
Advances in veterinary science and comparative medicine    January 1, 1983   Volume 27 1-76 
Newman MJ, Antczak DF.No abstract available
Population studies on the ELA system in American standardbred and thoroughbred mares.
Animal blood groups and biochemical genetics    January 1, 1983   Volume 14, Issue 3 201-211 doi: 10.1111/j.1365-2052.1983.tb01073.x
Bailey E.336 Standardbred mares and 334 Thoroughbred mares in the vicinity of Lexington, Kentucky, were lymphocyte typed for 11 allelic antigenic specificities of the equine lymphocyte antigen (ELA) system. The Standardbred mares were divided into a population of pacers and a population of trotters. Substantial differences in ELA gene frequencies were found between the 3 groups. When the distribution of antigens within populations were compared to Hardy-Weinberg equilibrium expectations, relatively good agreement was found.
Joint report of the First International Workshop on Lymphocyte Alloantigens of the Horse held 24-29 October 1981.
Animal blood groups and biochemical genetics    January 1, 1983   Volume 14, Issue 2 119-137 doi: 10.1111/j.1365-2052.1983.tb01067.x
Bull RW.Six equine lymphocyte alloantigen (ELA) specificities were defined by an international antiserum comparison test and workshop held in 1981. Twelve laboratories from four countries submitted 195 antisera for analysis. The antisera were exchanged among the 12 laboratories and tested in a standard lymphocyte microcytoxicity assay against the isolated lymphocytes at 1009 horses of several breeds. The data was pooled and analysed by a single computer analysis. The calculated chi 2 values of all cells with all antisera provided comparisons between antisera. Fifteen antisera clusters were formed by t...
Structure and function of the major histocompatibility complex in domestic animals.
Journal of the American Veterinary Medical Association    November 15, 1982   Volume 181, Issue 10 1030-1036 
Antczak DF.The major histocompatibility complex (MHC) is a genetic region that has been intensively studied for the past 2 decades. Interest in the MHC has been high because of (i) the particular involvement of the MHC in transplantation reactions, including organ allograft rejection in human beings; and (ii) the more general role of MHC gene products in the genetic control of immune responses in all mammals. The MHC has several remarkable properties that include a distinctive genetic structure which has been well-preserved through evolution, and the extreme plasticity of form of the principal MHC genes,...
Equine leucocyte antigen system. III. Non-MHC linked alloantigenic system in horses.
Journal of immunogenetics    October 1, 1982   Volume 9, Issue 5 327-334 doi: 10.1111/j.1744-313x.1982.tb00990.x
Lazary S, Gerber H, de Weck AL, Arnold P.A new, non-MHC linked alloantigenic membrane antigen on the equine lymphocytes is described. This antigen was characterized with alloantisera in the two-stage microcytotoxicity test and designated as ELy-1 antigen. The frequency of ELy-1 antigen positive animals in various populations is close to 50%. ELy-1 shows an autosomal, dominant inheritance. Since an allelic antigen (s) could not be demonstrated in family studies, it is assumed that only two alleles ELy-1+ and ELy-1- exist. The ELy-1 antigen in positive animals is expressed on both T and B lymphocytes but it is not present on erythrocyt...
Equine lymphocyte antigens in a Welsh pony family.
American journal of veterinary research    October 1, 1982   Volume 43, Issue 10 1859-1862 
Swift RV, Mottironi VD.Lymphocytes from an extended family of Welsh ponies were tested in a microcytotoxicity test against Thoroughbred and Arabian horse-derived antisera, which defined 4 and 6 equine lymphocyte antigen (ELA) specificities, respectively. Mixed leukocyte culture (MLC) tests were also performed. Welsh pony lymphocytes reacted to the Thoroughbred antisera. Most of the ponies' lymphocytes showed reactivity to 2 of the Thoroughbred ELA specificities, the offspring inheriting 1 antigen from each parent. Antigenic determinants were only partially demonstrated with Arabian antisera, although results indicat...
Lymphocyte alloantigens of the horse. I. Serologic and genetic studies.
Tissue antigens    September 1, 1982   Volume 20, Issue 3 172-187 doi: 10.1111/j.1399-0039.1982.tb00343.x
Antczak DF, Bright SM, Remick LH, Bauman BE.A genetic system controlling lymphocyte alloantigens of the horse is described. Alloantisera to paternal histocompatibility antigens induced as a result of pregnancy in mares were used in an antibody-mediated complement-dependent microcytotoxicity assay to define 15 Equine Leukocyte Antigen (ELA) specificities using cluster analysis. In this study 369 sera were screened for alloantibody using lymphocytes from 10 randomly selected, unrelated horses. A high proportion (83%) of these sera were found to be positive for antibody to lymphocyte alloantigens. After initial cluster analysis, 120 of the...
Maternal anti-fetal cytotoxic antibody responses of equids during pregnancy.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 361-369 
Kydd J, Miller J, Antczak DF, Allen WR.The maternal immunological response to the developing equine fetus was investigated in 69 pregnancies of various genotypes. In normal intraspecies horse pregnancy (N = 16), 94% of mares produced strong cytotoxic antibody responses to paternal histocompatibility antigens which were first detectable between 44 and 70 days after ovulation. In all other types of pregnancy examined (intraspecies donkey, N = 19; interspecies mule, N = 6; interspecies hinny, N = 2; extraspecies horse-in-donkey, N = 3; and extraspecies donkey-in-horse, N = 21), antibody production was observed less frequently, and som...
Major histocompatibility locus in the Arabian horse.
Transplantation    April 1, 1981   Volume 31, Issue 4 290-294 doi: 10.1097/00007890-198104000-00011
Mottironi VD, Perryman LE, Pollara B, Mickey MR, Swift R, McGrath P.Combined immunodeficiency disease (CID) is a genetic disorder of T and B lymphocyte production which results in a nonfunctional immune system. It is inherited as an autosomal recessive trait and has been reported in humans and in horses of the Arabian breed. Arabian horses known to have the CID gene and horses of unknown carrier status were tested using a microlymphocytotoxicity technique. Computer chi 2 analysis distinguished six serologically defined specificities. The study of unrelated horses and a limited number of families showed that the specificities behave as codominant alleles segreg...
Equine leukocyte antigen system. II. Serological and mixed lymphocyte reactivity studies in families.
Transplantation    September 1, 1980   Volume 30, Issue 3 210-215 
Lazary S, Bullen S, Müller J, Kovacs G, Bodo I, Hockenjos P, De Weck AL.Mono- and oligospecific lymphocytotoxic alloantibodies from primiparous mares were tested on cells from horse families of various breeds in the two-step microcytotoxicity assay. The results showed that the detected antigens were inherited co-dominantly and autosomally as simple Mendelian traits. The membrane antigens showed different linkage with one or more other antigens and seem to be coded by a limited number of loci (at least three) from one chromosome. In the families tested one recombinant for the serologically defined antigens was recognized. The mixed leukocyte reactions of cells from...
Identification and genetics of horse lymphocyte alloantigens.
Immunogenetics    January 1, 1980   Volume 11, Issue 5 499-506 doi: 10.1007/BF01567818
Bailey E.Six hundred horses were tested with lymphocytotoxic antisera derived from 550 parous mares and 58 antisera produced by alloimmunization with horse blood cells. Seven equine lymphocyte specificities were identified using correlation analysis of the test data, absorption analysis and lysostripping. These specificities are expressed on lymphocytes and platelets, but not on red blood cells (RBC). Therefore, these specificities do not appear to be products of any of the eight known blood group systems of the horse. The distribution of these specificities in 113 Thoroughbred horses and 57 Arabian ho...
Linkage of loci controlling alloantigens on red blood cells and lymphocytes in the horse.
Science (New York, N.Y.)    June 22, 1979   Volume 204, Issue 4399 1317-1319 doi: 10.1126/science.451540
Bailey E, Stormont C, Suzuki Y, Trommershausen Smith A.A system of equine lymphocyte alloantigens designated ELA, is identified, and it is shown that the locus or loci controlling these markers must be closely linked to the locus controlling markers in the A system of horse blood groups. Among 29 offspring in two stallion families there was evidence for one recombinant. Lod scores for linkage between the A and ELA loci in the two families were 3.61 and 3.33, respectively, for theta equal to 0.
Lymphocyte specificity to protein antigens. II. Fine specificity of T-cell activation with cytochrome c and derived peptides as antigenic probes.
The Journal of experimental medicine    February 1, 1979   Volume 149, Issue 2 436-447 doi: 10.1084/jem.149.2.436
Corradin G, Chiller JM.Murine T-lymphocyte specificity was determined in a system of antigen driven in vitro T-cell proliferation using cytochrome c molecules from different species, their derived peptides and reconstituted hybrid proteins. It was observed that primed T cells could discriminate between peptide fragments which differed from each other at a single amino acid residue. These conclusions were substantiated by the pattern of cross-reactivity noted in the response of closely related cytochrome c proteins as well as when artificial hybrid molecules reconstituted by the covalent linkage of peptide fragments ...
Microculture method for mixed lymphocyte cultures in the horse.
American journal of veterinary research    February 1, 1978   Volume 39, Issue 2 337-339 
McClure JJ, Muscoplat CC, Johnson DW, Senogles DR.A miniaturized method for the mixed lymphocyte culture test in the horse is described. The test is performed in either round- or flat-bottom microtitration tissue culture plates. Concentrations of responsing and stimulating cells are varied, depening on the experiment. Significant discrimination between isogeneic and allogenic mixtures is possible after 120 hours' culture when cells are labeled ([3H]thymidine) for the last 16 to 18 hours of the test.
[Immunogenetic studies on horses].
Wiener tierarztliche Monatsschrift    June 1, 1967   Volume 54, Issue 6 375-389 
Schmid DO.No abstract available
[Tissue antigens of the digestive tract in man and animals. II. Antigens of the colon].
Pathologie et biologie    April 1, 1967   Volume 15, Issue 7 359-367 
Zweibaum A, Halpern B, Veyre C, Oriol-Palou R.No abstract available
[Immunogenetic studies on English half-bred horses in Yugoslavia].
Zentralblatt fur Veterinarmedizin. Reihe A    April 1, 1965   Volume 12, Issue 3 243-249 
Schmid DO, Mancić D.No abstract available
Genetic Systems of Blood Groups in Horses.
Genetics    November 1, 1964   Volume 50, Issue 5 915-929 doi: 10.1093/genetics/50.5.915
STORMONT C, SUZUKI Y.No abstract available
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