Analyze Diet

Topic:Immunology

The equine immune system is a complex network of cells, tissues, and organs that work collaboratively to defend against pathogens and maintain homeostasis. It consists of innate and adaptive components, each with distinct functions and mechanisms. The innate immune system provides the first line of defense through physical barriers, phagocytic cells, and the complement system. The adaptive immune system involves lymphocytes, such as B cells and T cells, which generate specific responses to antigens and provide immunological memory. Research in equine immunology explores the interactions between these components, the impact of genetic and environmental factors on immune function, and the development of vaccines and therapeutics. This page gathers peer-reviewed studies and scholarly articles focusing on the mechanisms, regulation, and clinical applications of the equine immune system in health and disease.
N-Terminal sequences of equine and human immunoglobulin heavy chains.
Biochimica et biophysica acta    February 17, 1970   Volume 200, Issue 2 258-266 doi: 10.1016/0005-2795(70)90169-8
Montgomery PC, Bello AC, Rockey JH.N-terminal tetrapeptides from heavy chains of equine γGab- and γT-globulins, and of human γG and γA myeloma proteins and a γM macroglobulin, have been studied. The equine and human heavy chains lacked free α-amino-terminal groups. After mild alkaline hydrolysis, glutamic acid was identified as the terminal amino acid by reaction with dimethylaminonaphthalenesulfonyl chloride, tentatively identifying pyrrolid-2-one-5-carboxylic acid (PCA) as the unreactive terminal residue of each heavy chain. Peptides lacking a free α-amino group were isolated from subtilisin and pronase digests of the ...
Cross-reactivity studies of horse, goat and rabbit anti-lymphocyte globulin.
Clinical and experimental immunology    February 1, 1970   Volume 6, Issue 2 279-289 
Ameniya H, Kashiwagi N, Putnam CW, Starzl TE.In the sera of ten normal humans and twenty-eight candidates for organ transplantation, the passive haemagglutination test detected a 50% incidence of preformed antibodies of low titre directed against horse serum. Such antibodies were also found to cross react with goat or rabbit sera in most instances. Seventeen of the organ recipients were later studied after the institution of treatment with horse antihuman-lymphocyte globulin (ALG). The incidence of anti-horse-serum antibodies rose to 100%. At the same time, an increased activity against goat serum developed; cross-reactions against rabbi...
Changes in pathogenicity of equine infectious anemia virus during passages in horse leukocyte cultures.
National Institute of Animal Health quarterly    January 1, 1970   Volume 10, Issue 3 106-112 
Kono Y, Kobayashi K.No abstract available
Growth characteristics of equine infectious anemia virus in horse leukocyte cultures. Brief report.
Archiv fur die gesamte Virusforschung    January 1, 1970   Volume 30, Issue 2 252-256 doi: 10.1007/BF01250196
Kono Y, Yoshino T, Fukanaga Y.No abstract available
The plasmapheresis of hyperimmunized horses.
Bulletin of the World Health Organization    January 1, 1970   Volume 42, Issue 6 998-1000 
Levine L, Broderick EJ.No abstract available
Characterization of the Erysipelothrix rhusiopathiae protective-antigen production-enhancing effect of horse serum.
Texas reports on biology and medicine    January 1, 1970   Volume 28, Issue 3 337-345 
White RR, Verwey WF.No abstract available
Cellular response to equine encephalomyelitis vaccine in skin window of horses.
American journal of veterinary research    January 1, 1970   Volume 31, Issue 1 97-102 
Zarrilli LW, Calhoun ML.No abstract available
Nature of complement-fixing antibodies in horses infected with equine rhinopneumonitis virus.
National Institute of Animal Health quarterly    January 1, 1970   Volume 10, Issue 3 123-128 
Suzuki T, Nakano K, Shimizu Y, Isayama Y, Kawakami Y.No abstract available
[Production of antilymphocyte globulin].
Langenbecks Archiv fur Chirurgie    January 1, 1970   Volume 327, Issue 1 281-284 doi: 10.1007/BF01259028
Heide K, Seiler FR, Schwick HG.No abstract available
Production of human antilymphocytic serum in horse with thoracic duct lymphocytes and peripheral blood lymphocytes.
Federation proceedings    January 1, 1970   Volume 29, Issue 1 108-110 
Traeger J, Fries D, Revillard JP, Durix A, Carraz M, Plan M.No abstract available
Further studies on M-components with antistreptolysin O activity. The inactivating effect on different oxygen-labile haemolysins.
Acta pathologica et microbiologica Scandinavica. Section B: Microbiology and immunology    January 1, 1970   Volume 78, Issue 4 467-472 doi: 10.1111/j.1699-0463.1970.tb04329.x
Mansa B, Kjems E.No abstract available
Reactivities to horse anti-lymphocyte globulin. I. Induction of immunologic tolerance in man.
International archives of allergy and applied immunology    January 1, 1970   Volume 39, Issue 2-3 113-120 doi: 10.1159/000230340
Gewurz H, Moberg A, Simmons R, Pollara B, Soll R, Najarian S.No abstract available
Demonstration of equine infectious anemia viral antigen by immunofluorescence.
National Institute of Animal Health quarterly    January 1, 1970   Volume 10, Issue 2 90-91 
Ushimi C, Nakajima H, Tanaka S.No abstract available
[Epizootiology of pasteurellosis].
Archiv fur experimentelle Veterinarmedizin    January 1, 1970   Volume 24 179-185 
Stryszak A.No abstract available
The response of ponies to Myxovirus influenzae A-equi 2. I. Serum and nasal antibody titres following exposure. Rouse BT, Ditchfield WJ.The antibody response in serum and nasal secretions of groups of ponies vaccinated or infected with Myxovirus influenzae A-equi 2 was examined. Following infection by aerosol with live virus, a weak antibody response was recorded in both serum and secretions. Antibody levels were undetectable in secretions at 31 days after infection. After primary intramuscular vaccination with killed virus, using sodium alginate as an adjuvant, antibody was detected only in the serum. However, following revaccination, a pronounced antibody response was demonstrated in both serum and secretions. Antibody was s...
The response of ponies to Myxovirus influenzae A-equi 2. II. Immunoglobulin classes of antibody to the virus in serum and nasal secretions. Rouse BT, Ditchfield WJ.Nasal secretions and serum were collected from ponies in order to determine the types of immunoglobulins responsible for antibody activity against Myxovirus influenzae A-equi 2. Using specific antisera to remove each immunoglobulin, the antiviral activity of serum was shown to be a property of IgG globulin, whereas in nasal secretions activity was found in both IgG and IgG(T) globulins. However in secretions the predominant activity was attributed to IgG(T) globulin. Because of its sensitivity to 2 mercaptoethanol, early serum antibody was assumed to belong to the IgM class of immunoglobulins....
Isolation of herpesvirus from equine leukocytes: comparison with equine rhinopneumonitis virus.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    January 1, 1970   Volume 34, Issue 1 59-65 
Kemeny L, Pearson JE.An agent which possessed the properties of herpesviruses was isolated from the leukocytes of 71 out of 80 (88.7%) apparently normal Iowa horses. It was ether- and heat-sensitive, DNA type, and produced type-A intranuclear inclusion bodies in cell cultures. Electron micrographs revealed a virion of typical herpesvirus structure. Leukocyte isolate virus could be differentiated from equine rhinopneumonitis virus (ERV) by serum neutralization, by growth differences in rabbit kidney cells, and by fluorescent antibody staining. Specific neutralizing antibody against this agent was found in a pooled ...
WHO collaborative studies on enterovirus reference antisera. Third report.
Bulletin of the World Health Organization    January 1, 1970   Volume 42, Issue 6 847-863 
Melnick JL, Hampil B.This paper smmarizes the results of the third part of co-operative studies undertaken by the WHO International Reference Centre for Enteroviruses and a number of WHO Regional Virus Reference Centres and WHO Virus Collaborating Laboratories and other laboratories in a comprehensive testing programme of enterovirus equine antisera prepared for long-term use as reference antisera. The studies were designed to appraise the specificity of the immune serum of horses inoculated with prototype enteroviruses (coxsackie-viruses A1, A5, A6, A12 and A22 and echoviruses 5, 6, 13-16, 18-20, 22-26, 29 and 32...
Comparative studies on the haemolytic and Treponema pallidum immobilizing complement activity in the serum of different species.
Immunology    January 1, 1970   Volume 18, Issue 1 13-18 
Müller F, Segerling M.Complement activity in the serum of eight species has been studied in two ways: by immobilization of sensitized with human or rabbit antibody and by haemolysis of sheep red cells sensitized with rabbit antibody. Serum of the pig, monkey and man was actively haemolytic but contained a heatlabile factor that immobilized unsensitized in the presence of guinea-pig complement and precluded the detection of immune immobilizing activity. Sera of other species, although without action on unsensitized treponemes, even with added guinea-pig complement, differed in their relative haemolytic and immobil...
On the relationship between bluetongue, African horsesickness and reoviruses: hybridization studies.
The Onderstepoort journal of veterinary research    December 1, 1969   Volume 36, Issue 2 175-179 
Verwoerd DW, Huismans H.No abstract available
[Comparative research concerning the heterohemagglutinant capacity of the human serum].
Revue canadienne de biologie    December 1, 1969   Volume 28, Issue 4 263-265 
Acalugaritei G, Vrabiescu A.No abstract available
The occurrence of complement fixing antibody to the Chlamydia group anti- gen in horses.
Australian veterinary journal    December 1, 1969   Volume 45, Issue 12 595-596 
Studdert MJ.No abstract available
Impaired bone marrow response in equine infectious anemia.
American journal of veterinary research    December 1, 1969   Volume 30, Issue 12 2099-2104 
McGuire TC, Henson JB, Quist SE.No abstract available
Induction of tolerance in man to horse-IgG.
Lancet (London, England)    November 22, 1969   Volume 2, Issue 7630 1141-1142 doi: 10.1016/s0140-6736(69)90744-2
Brendel W, Land W, Hopf U, Seifert J.No abstract available
[Veterinary-zootechnical control in equestrian sports].
Veterinariia    November 1, 1969   Volume 46, Issue 11 89-90 
Zaĭtsev VI, Bobylev IF.No abstract available
Experimental infection of horses with A-equi 2-Miami-1-63 and human A2-Hong Kong 1-68 influenza viruses. II. Antibody response to the infection.
Acta virologica    November 1, 1969   Volume 13, Issue 6 507-514 
Blaskovic D, Sabó A, Kapitáncik B, Styk B, Vrtiak O, Kaplan M.No abstract available
[Isolation of the major antitoxic fraction of horse immunoserums]. Audibert F, Sandor G.No abstract available
A comparative study of the temporal patterns of cutaneous water vapour loss from some domesticated mammals with epitrichial sweat glands.
Comparative biochemistry and physiology    October 15, 1969   Volume 31, Issue 2 347-363 doi: 10.1016/0010-406x(69)91659-4
Allen TE, Bligh J.1. The temporal patterns of cutaneous water vapour loss from the skin of the sheep, goat, ox, horse, donkey and llama during exposure to 40°C Ta and during i.v. injections and infusions of adrenaline are examined. 2. It is concluded that there are marked species variations in the extent to which the discharge of sweat is affected by periodic contractions of the myoepithelium, or by simple displacement of fluid from the filled lumen as more fluid is secreted into it.
Enhanced humoral immunity in mice infected with attenuated Venezuelan equine encephalitis virus.
Journal of immunology (Baltimore, Md. : 1950)    October 1, 1969   Volume 103, Issue 4 699-707 
Howard RJ, Craig CP, Trevino GS, Dougherty SF, Mergenhagen SE.No abstract available
Electron microscopy of equine infectious anemia virus.
Journal of virology    October 1, 1969   Volume 4, Issue 4 521-527 doi: 10.1128/JVI.4.4.521-527.1969
Tajima M, Nakajima H, Ito Y.Equine infectious anemia (EIA) virus was observed in thin sections of infected cultured horse leukocytes by electron microscopy. The virus particles had a spherical shape and were between 80 and 120 nm in diameter. Most of them contained an electron-dense nucleoid 40 to 60 nm in diameter. They were observed to form by a process of budding from the plasma membrane and appeared to have thin surface projections. The particles described were not detected in uninfected cultured cells, and their appearance could be prevented by adding EIA immune serum to the inoculum. The implications of these findi...