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Topic:Antigen

Antigens are substances that can induce an immune response in horses, typically by being recognized as foreign by the immune system. These substances can include proteins, polysaccharides, or lipids, and are often components of pathogens such as bacteria, viruses, or parasites. In horses, antigens are essential for the activation of both the innate and adaptive immune responses, leading to the production of antibodies and the activation of immune cells. The study of antigens in equines encompasses understanding their structure, the mechanisms by which they are recognized by the immune system, and their role in vaccine development. This page compiles peer-reviewed research studies and scholarly articles that explore the identification, characterization, and immunological impact of antigens in equine health and disease.
A primary immune response to dextran B512 is followed by a period of antigen-specific immunosuppression caused by autoanti-idiotypic antibodies.
Scandinavian journal of immunology    January 1, 1980   Volume 11, Issue 1 53-62 doi: 10.1111/j.1365-3083.1980.tb00208.x
Fernandez C, Möller G.After a primary immune response to the alpha 1-6 epitope of dextran B512, dextran high responder strains exhibit a specific inability to produce IgM and IgG antibodies against this epitope, although they gave an expected secondary response to horse erythrocytes. Spleen cells from dextran-primed and-suppressed mice responded well to dextran after transfer to lethally irradiated previously untreated mice, indicating that tolerance or exhaustive proliferation of dextran reactive B cells is not responsible. Thymus-dependent dextran-protein conjugates also induced specific suppression. Suppression ...
Topographic antigenic determinants on cytochrome c. Immunoadsorbent separation of the rabbit antibody populations directed against horse cytochrome.
The Journal of biological chemistry    December 25, 1979   Volume 254, Issue 24 12706-12716 
Jemmerson R, Margoliash E.Seven populations of site-specific antibodies were isolated from each of three sera of rabbits immunized against glutaraldehyde-polymerized horse cytochrome c. The antibodies were separated using an immunoadsorption scheme which employed the following cytochromes c: horse, beef, guanaco, rabbit, mouse testicular, pigeon, and the cyanogen-bromide cleaved fragment of the rabbit protein containing residues 1 to 65. The monovalent, antigen-binding fragments of the antibodies (Fab') gave 1:1 stoichiometries with native horse cytochrome c in fluorescence quenching assays. Cross-reactivities with het...
The effects of sodium cromoglycate on antigen inhalation challenge in two horses affected with chronic obstructive pulmonary disease (COPD).
Veterinary immunology and immunopathology    November 1, 1979   Volume 1, Issue 1 89-95 doi: 10.1016/0165-2427(79)90010-2
Murphy JR, McPherson EA, Lawson GH.80 mg sodium cromoglycate (SCG) was administered by inhalation to two COPD-affected animals known to have respiratory hypersensitivity to Micropolyspora faeni. SCG treatment 20-30 minutes prior to inhalation challenge with M. faeni prevented exacerbation of respiratory disease, usually seen 4-8 hours after challenge. duration of protection against antigen challenge after a single SCG treatment was 4-5 days. The duration of protection was not prolonged by reducing the frequency of antigen challenge. Multiple antigen challenge, using M. faeni and Aspergillus fumigatus, shortened the protective p...
Equine IgG and IgG(T) antibodies: dependence of precipitability on both antigen and antibody structure.
Molecular immunology    October 1, 1979   Volume 16, Issue 10 787-790 doi: 10.1016/0161-5890(79)90156-1
McGuire TC, Archer BG, Crawford TB.No abstract available
Identification of alpha1-lipoproteins in crossed immunoelectrophoresis.
Clinical chemistry    October 1, 1979   Volume 25, Issue 10 1749-1756 
Cline LJ, Crowle AJ.Evans Blue dye binds selectively, but with different avidities, to five major antigens in human serum. The anodic mobility of the antigen-dye complexes is greater than that of the antigens alone in crossed immunoelectrophoresis, which is of practical value for identification. We used this characteristic to show that in some human sera there is a population of alpha1-lipoprotein molecules that migrates electrophoretically in the beta-lipoprotein region, where in conventional zone electrophoresis it could be mistaken for beta-lipoprotein. We also demonstrate that horses, unlike rabbits, rarely m...
The presence of precipitating antibodies in the sera of horses with chronic obstructive pulmonary disease (COPD).
Equine veterinary journal    July 1, 1979   Volume 11, Issue 3 172-176 doi: 10.1111/j.2042-3306.1979.tb01334.x
Lawson GH, McPherson EA, Murphy JR, Nicholson JM, Wooding P, Breeze RG, Pirie HM.The sera of horses affected and not affected with chronic obstructive pulmonary disease (COPD) were examined for precipitins to Micropolyspora faeni and Aspergillus fumigatus. Precipitins to both antigens were not restricted to COPD cases but occurred more frequently in animals affected with COPD. Many animals without detectable precipitins responded clinically to inhalation challenge with these antigens.
Chronic obstructive pulmonary disease (COPD) in horses: aetiological studies: responses to intradermal and inhalation antigenic challenge.
Equine veterinary journal    July 1, 1979   Volume 11, Issue 3 159-166 doi: 10.1111/j.2042-3306.1979.tb01330.x
McPherson EA, Lawson GH, Murphy JR, Nicholson JM, Breeze RG, Pirie HM.Micropolyspora faeni and Aspergillus fumigatus were identified as common causes of respiratory hypersensitivity in horses affected with chronic obstructive pulmonary disease (COPD). Rye grass pollen and an Actinomycete evoked respiratory allergy in a few horses. Not infrequently, individual horses were found to have respiratory hypersensitivity to two or more antigens. The methods used to examine for allergy were intradermal testing and inhalation challenge with environmental antigens. An intradermal test using an M faeni extract was demonstrated to be suitable for diagnostic use in horses pre...
Viral respiratory disease.
The Veterinary clinics of North America. Large animal practice    May 1, 1979   Volume 1, Issue 1 59-72 doi: 10.1016/s0196-9846(17)30198-2
Coggins L.No abstract available
Persistent infection of a human lymphoblastoid cell line with equine herpesvirus 1.
Infection and immunity    May 1, 1979   Volume 24, Issue 2 539-544 doi: 10.1128/iai.24.2.539-544.1979
Roumillat LF, Feorino PM, Lukert PD.Infection of a human lymphoblastoid cell line (Jijoye line derived from a Burkitt lymphoma which contains Epstein-Barr virus) with equine herpesvirus 1, maintained and observed for 53 days, was characterized by the continuous production of infectious extracellular and intracellular virus. Maximum virus production correlated with active cell multiplication. Less than 15% of the cells possessed viral capsid antigen at any one time. Five percent of the cells in the Jijoye line possess Epstein-Barr viral capsid antigen; 80% of the Epstein-Barr viral caspid-containing cells also contained equine he...
Comparative serologic study of equine piroplasmosis, with card and complement-fixation tests.
American journal of veterinary research    April 1, 1979   Volume 40, Issue 4 529-531 
Amerault TE, Frerichs WM, Stiller D.An agglutinating antigen and a rapid card test (CT) for equine piroplasmosis was developed. The antigen for the CT was prepared from lyophilized Babesia caballi complement-fixation (CF) antigen. Serum and plasma samples for testing were obtained from known B caballi-infected horses and clinically normal horses maintained at the laboratory. Serum samples also were obtained from horses outside the continental United States, in areas where piroplasmosis is endemic. Comparative CT and CF tests were done on all samples. The CT correctly identified 85% of 192 plasma samples from known infected and n...
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 ...
Evaluation of the use of “thermoresistant” antigen Patoc 1, in the diagnosis of human and animal leptospirosis. Preliminary report.
Bollettino dell\'Istituto sieroterapico milanese    January 31, 1979   Volume 57, Issue 6 707-712 
Cinco Del Fabbro M, Dougan R, Jelincic A, Piacentini I.The macroagglutination test, according Mailloux, was investigated for its feasibility in the rapid diagnosis of human and animal leptospirosis. Suspected sera examinated by Mailloux test, were also examinated by Complement Fixation and Microagglutination; the results suggest that: Mailloux macroagglutination is the serological test of choice, for screening of animal and human sera, mostly if it is not needed to know the infecting serovar.
The characterization of equine prealbumin (Pr) proteins by antigen-antibody crossed electrophoresis.
Acta veterinaria Scandinavica    January 1, 1979   Volume 20, Issue 2 180-190 doi: 10.1186/BF03546610
Ek N. Acta vet. scand. 1979, , 180–190. — Selected equine Pr phenotypes from a total of 55 horses of mixed breeds were investigated. The horse sera were subjected to acid starch gel electrophoresis at pH 4.8, followed by right angle electrophoresis in agarose gels containing rabbit-produced anti-Pr protein. This technique gives peaks in the agarose gels corresponding to the Pr zones in acid gels. The investigation revealed patterns of the Pr protein which were more complex than those seen when using ordinary acid starch gel electrophoresis. The phenotypes FF, II and LL showed a total of eight p...
[Myocardial changes following experimental protein sensitization].
Arkhiv patologii    January 1, 1979   Volume 41, Issue 9 17-22 
Frolov VA, Derx H, Riguer P.Guinea pigs were sensitized by three subcutaneous injections of 0.1 ml native horse serum at 2-day intervals, 21 days after the third injection the animals developed marked sensitization to this antigen which was manifested by anaphylactic reaction to the subcutaneous challenge with this antigen. At this time, the myocardium of the sensitized animals showed signs of extra- and intracellular oedema, a sharp increase in the number of lysosomes, damage of their membranes, 2 1/2 months after sensitization the animals showed no anaphylactic reaction to the challenge dose of the antigen. There were ...
Studies on equine adenovirus. II. Isolation of hexon antigen.
Nihon juigaku zasshi. The Japanese journal of veterinary science    December 1, 1978   Volume 40, Issue 6 733-737 doi: 10.1292/jvms1939.40.733
Harasawa R, Konishi SI, Ogata M.No abstract available
Antibody response of horses to Mycoplasma mycoides subsp capri.
American journal of veterinary research    November 1, 1978   Volume 39, Issue 11 1734-1737 
Stalheim OH, Stone SS, Blackburn BO, Foley J.In horses given whole cultures or cells of Mycoplasma mycoides subsp capri (by subcutaneous and intravenous injections), antibody responses were measured by serologic procedures. During an immunization period of 22 weeks, horses produced an antiserum that was used to identify M mycoides subsp capri by agglutination, complement-fixation, and fluorescent antibody (FA) tests, but not by the growth-inhibition test. Horses that were injected with whole cultures of M mycoides subsp capri responded better than horses that were injected with only cells, ie, antibodies were detectable sooner by agar ge...
[Heterophile haemagglutinogens on pig, canine and human thymocytes (author’s transl)].
Annales d\'immunologie    October 1, 1978   Volume 129 C, Issue 6 847-854 
Salmon H.Immunization of sheep or horse with pig, canin or horse thymocytes produces heteroagglutinating antibodies, which allow to define two heterophile antigens:--the first one, HC, immunogen for sheep, is localized on pig, human and canin thymocytes, as well as on red blood cells of the two latter species;--the other, HCP, immunogen for horses, is situated on the red blood cells and thymocytes of the same three species. HC is distributed on various cells and in similar fashion in pig and human, except for the pig red blood cells.
Radioimmunoassay for quantitation of antibodies to alphaviruses with staphylococcal protein A.
Journal of clinical microbiology    July 1, 1978   Volume 8, Issue 1 54-60 doi: 10.1128/jcm.8.1.54-60.1978
Jahrling PB, Hesse RA, Metzger JF.A radioimmunoassay (RIA) procedure is described for measuring antibodies to alphaviruses in human and other mammalian sera. The test employed protein Abearing Staphylococcus aureus as a solid-phase immunoadsorbent for (3)H-labeled viruses complexed with immunoglobulin G. Using antibodies produced in humans and guinea pigs, the RIA procedure clearly differentiated among antibodies to Venezuelan, western, and eastern equine encephalomyelitis viruses. Sensitivity of the RIA depended on the concentrations of labeled viruses employed. The dilution of serum that effected binding of 50% of the (3)H-l...
Evaluation of delayed hypersensitivity responses in normal horses and immunodeficient foals.
American journal of veterinary research    July 1, 1978   Volume 39, Issue 7 1161-1167 
Hodgin EC, McGuire TC, Perryman LE, Grant BD.Delayed hypersensitivity (DH) responses of normal and immunodeficient horses were evaluated with antigens [dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH)] and phytolectins [phytohemagglutinin (PHA), concanavalin A (Con A)]. Immunologically normal horses sensitized with 5 daily applications of 2 mg of DNCB developed positive skin reactions upon challenge with 0.4 mg of DNCB. The delayed onset of the reaction and the predominately mononuclear cell infiltration at the test site indicated these were DH reactions. Normal horses sensitized with 500 microgram of KLH and challenged with ...
Antigenic homogeneity of equine adenoviruses.
Australian veterinary journal    May 1, 1978   Volume 54, Issue 5 263-264 doi: 10.1111/j.1751-0813.1978.tb05559.x
Studdert MJ.No abstract available
Induction of a cell membrane antigen by equine infectious anemia virus.
American journal of veterinary research    March 1, 1978   Volume 39, Issue 3 385-386 
McGuire TC, Crawford TB.Equine fibroblasts persistently infected with equine infectious anemia virus acquire a new cell membrane antigen demonstrable by indirect radioimmunoassay, using infected horse serum as an antibody source.
[Immunochemical investigations on the gene expression of horse serum carboxylesterase (author’s transl)].
Annales d'immunologie    February 1, 1978   Volume 129, Issue 2-3 353-365 
Méténier L, Kaminski M.Immunochemical and enzymatic analyses of horse serum carboxylesterase were carried out with respect to the existence of a silent gene. Sera with positive phenotypic expression of esterase, both heterozygotes and presumed homozygotes, were compared with:--sera with positive phenotypic expression but genotypically +/O;--sera with a negative phenotypic expression, i. e. genotypically O/O;--sera of natural +/O "hemi-zygotes": mules (donkey lacking the esterase);--positive sera heated at 60 degrees C;--positive sera after specific inhibition of enzymatic activity. Titration by immunocompetition has...
Synthetic antigens. Horse “natural” antibodies against interpolymer of styrene and maleic acid (PSM).
Archivum immunologiae et therapiae experimentalis    January 1, 1978   Volume 26, Issue 1-6 67-71 
Ugorski M, Mikulska J, Skibiński G, Wieczorek Z, Lisowski J.Properties of horse natural anti-PSM antibodies are described. The antibodies were of IgG class. Electrostatic forces were mainly involved in reaction of PSM with horse antibodies. The reaction was inhibited by low molecular compounds resembling structural unit of PSM. Studies of difference spectra and ORD and CD spectra showed no major conformational changes in horse antibodies after reaction with PSM.
Preparation of hemagglutinating antigen of equine infectious anemia virus from infected equine leukocyte cultures.
National Institute of Animal Health quarterly    January 1, 1978   Volume 18, Issue 1 39-40 
Sentsui H, Kono Y.No abstract available
[Diagnosis of infectious anemia in horses using the Coggins test].
Veterinarno-meditsinski nauki    January 1, 1978   Volume 15, Issue 3 19-25 
Tekerlekov P, Dilovski M, Enchev S, Peneva I.Coggins' immune diffusion test was modified, and was applied as a screening one in the study of the epizootic status. The positive reactions were characterized by the production of a precipitation line between the antigen and the respective serum that was tested. The appearance of such a line was associated with that formed with the use of the positive control serum, pointing to a reaction of identity. With the weakly positive reactions the ends of the precipitin lines, formed with the use of the positive control serum, were found to deviate slightly toward the site where the antigen had been ...
Antigenic relatedness of equine herpes virus types 1 and 3.
Archives of virology    January 1, 1978   Volume 56, Issue 1-2 33-45 doi: 10.1007/BF01317281
Gutekunst DE, Malmquist WA, Becvar CS.Antiserums prepared in specific pathogen free (SPF) ponies were used in direct and indirect immunofluorescence, immunodiffusion, complement fixation and serum neutralization procedures to study the interrelationships of the three types of equine herpes viruses (EHV-1, EHV-2, and EHV-3). Equine cell cultures infected with each type virus fluoresced when stained with homologous conjugated antiserum. In reciprocal tests EHV-1 and EHV-3 cross-fluoresced, but EHV-2 did not cross-fluoresce. Non-infected cell cultures did not fluoresce when stained with the 3 conjugates. EHV-1 and EHV-3 cross-fluores...
Analysis of a complex antigenic site on horse cytochrome c.
Advances in experimental medicine and biology    January 1, 1978   Volume 98 119-129 doi: 10.1007/978-1-4615-8858-0_6
Jemmerson R, Margoliash E.Of the antigenic determinants so far identified for cytochrome c, only one involves more than a single amino acid substitution between the immunogen and host proteins. Both a threonine at position 89 and a glutamic acid at position 92 control one of the three antigenic sites identified in horse cytochrome c, as expressed in rabbits. Three antibody subpopulations, all directed against this region of the molecule, were isolated from the serum of a single rabbit by adsorption on a series of insolubilized cytochromes c. Antibody fluorescence quenching titrations with a variety of cytochromes c wer...
Antigenic relationship between the Tokyo and the Miami strains of equine influenza subtype 2 virus.
Nihon juigaku zasshi. The Japanese journal of veterinary science    October 1, 1977   Volume 39, Issue 5 571-574 doi: 10.1292/jvms1939.39.571
Goto H, Shimizu K.The first outbreak of equine influenza (EI) infection in Japan was recognized during the period December 1971 to January 1972 [1, 6]. No evidence of the disease had been found before then [2,6]. The etiological agent of this epizootic was identified by hemagglutination-inhibition (HI) and neutralization tests with chicken or ferret antiserum as the subtype 2 of EI virus (6, 7). However, the isolate, A/equine/Tokyo/71 (Tokyo) strain, was not completely identical to the prototypic A/equine/Miami /63 (Miami) strain of the subtype 2, since antibody responses of convalescent horses were 2 to 16 tim...
[Pathogenesis of equine infectious anemia (with reference to similar chronic viral infection)].
Bulletin der Schweizerischen Akademie der Medizinischen Wissenschaften    September 1, 1977   Volume 33, Issue 4-6 249-263 
Hallauer C.1. Equine infectious anemia (EIA) is an immunologically-medicated disease. Immune complexes formed in blood and tissues are responsible for most symptoms and lesions (anemia, splenomegaly, lymphadenopathy, glomerulonephritis, etc.). In addition, a state of cellular hypersensitivity of the delayed type is involved in the pathogenesis. 2. Periodical attacks of pyrexia and clinical illness in the presence of immunity are caused by antigenically-modified variants of virus. By means of immunosuppressive treatments similar relapses of fever associated with the appearance of new virus variants can be...
Characterization of a retravirus isolated from squirrel monkeys.
Journal of virology    August 1, 1977   Volume 23, Issue 2 384-393 doi: 10.1128/JVI.23.2.384-393.1977
Schochetman G, Fine D, Arthur L, Gilden R, Heberling R.A new retravirus (SMRV) isolated from a squirrel monkey, Saimiri sciureus, has an Mg2+-dependen reverse transcriptase and a buoyant density of 1.17 g/cm3 in sucrose and 1.21 g/cm3 in cesium chloride, similar to the mouse mammary tumor virus and the Mason-Pfizer monkey virus. The polypeptide patter of SMRV as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis was distinct from the reported polypeptide patterns of known retraviruses. Four major polypeptides of molecular weights 40,000, 20,000, 14,000 and 8,000 were resolved in virus propagated in human, mink, and canine cell...
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