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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.
The functional competence of uterine-derived polymorphonuclear neutrophils (PMN) from mares resistant and susceptible to chronic uterine infection: a sequential migration analysis.
Biology of reproduction    December 1, 1986   Volume 35, Issue 5 1168-1174 doi: 10.1095/biolreprod35.5.1168
Liu IK, Cheung AT, Walsh EM, Ayin S.The functional competence of uterine-derived polymorphonuclear neutrophils (PMNs) from 28 mares was measured for migration responsiveness by use of a chamber (filter) assay. Uterine infection was induced with Streptococcus zooepidemicus in mares considered resistant to chronic uterine infection (Grade I). In sequential analysis of uterine flushings obtained from these mares 5, 12, 15, 20, and 25 h after infection was induced, PMNs showed an initial rise at 12 h (from 5), then a general decline in migration response and in concentration of cells per ml from 12 through 25 h post-inoculation. In ...
Clinical survey of antibodies against red blood cells in horses after homologous blood transfusion.
American journal of veterinary research    December 1, 1986   Volume 47, Issue 12 2566-2571 
Wong PL, Nickel LS, Bowling AT, Steffey EP.Serum samples of 20 horses were evaluated for antibodies against RBC after homologous blood transfusion. Transfusion-associated antibodies against RBC were detected in 10 horses. Antibodies recognizing horse blood group antigens Aa, Ae, Db, and Dc were identified. Antibodies against Aa were found in all samples from Aa-negative horses that were transfused with Aa-positive RBC. Antibodies against Aa persisted for at least 1 year after transfusion. Antibodies against Ae were detected in 7 of 8 horses transfused with Ae-positive RBC. Initial appearance and persistence of antibodies against Ae dif...
Nucleotide and deduced amino acid sequence of the influenza neuraminidase genes of two equine serotypes.
Virology    December 1, 1986   Volume 155, Issue 2 460-468 doi: 10.1016/0042-6822(86)90207-2
Dale B, Brown R, Miller J, White RT, Air GM, Cordell B.Equine influenza is caused by two serotypes of type A influenza virus, EIV-A1 and EIV-A2. The complete nucleotide sequence of the neuraminidase (NA) genes of both the A1 (N7 subtype) and A2 (N8 subtype) serotype has been determined following cloning of full-length viral NA cDNAs into pBR322. Analysis of the deduced amino acid sequences reveals that the N7 and N8 genes share expected extensive homologies with the previously sequenced N1, N2, and N9 NA subtypes. These homologies include conservation of basic NA gene and protein structure, cysteine residues, potential glycosylation sites, and res...
Resistance of horse alpha 1-proteinase inhibitor to perchloric acid denaturation and a simplified purification procedure resulting therefrom.
Biochimica et biophysica acta    November 21, 1986   Volume 874, Issue 2 144-149 doi: 10.1016/0167-4838(86)90111-1
Pellegrini A, Hägeli G, von Fellenberg R.Addition of perchloric acid (6.4% w/v final concentration) to horse alpha 1-proteinase inhibitor or to horse plasma neither precipitated nor inactivated alpha 1-proteinase inhibitor. None of the isoinhibitors of alpha 1-proteinase inhibitor was altered by dilute perchloric acid. This unexpected behavior led to a simplified procedure for the purification of horse alpha 1-proteinase inhibitor, consisting of removal of the bulk of plasma proteins, by perchloric acid precipitation and by gel filtration on Sephadex G-75 and G-200. The resulting preparations of alpha 1-proteinase inhibitor were immu...
Investigation of the antigenic relationship between equine IgG and IgGT.
Veterinary immunology and immunopathology    November 1, 1986   Volume 13, Issue 3 255-259 doi: 10.1016/0165-2427(86)90077-2
Widders PR, Stokes CR, Bourne FJ.The antigenic cross reactivity between equine IgG and IgGT was investigated. On the basis of immunodiffusion and immunoelectrophoresis reactions using an antiserum raised against the Fc fraction of IgGT, this equine immunoglobulin can be unequivocally classified as a subclass of IgG.
Milk and the neonatal gut: comparative lessons to be learnt.
Equine veterinary journal    November 1, 1986   Volume 18, Issue 6 427-429 doi: 10.1111/j.2042-3306.1986.tb03677.x
Weaver LT.No abstract available
Shedding and interspecies type sero-reactivity of the envelope glycopolypeptide gp120 of the human immunodeficiency virus.
The Journal of general virology    November 1, 1986   Volume 67 ( Pt 11) 2533-2538 doi: 10.1099/0022-1317-67-11-2533
Schneider J, Kaaden O, Copeland TD, Oroszlan S, Hunsmann G.Two glycopolypeptides with molecular weights 160,000 and 120,000 (gp120) are regularly recognized by human immunodeficiency virus (HIV)-specific antisera in lysates of cells persistently infected with HIV. In the present study, gp120 was characterized as the major envelope glycopolypeptide of HIV. Gp120 was identified as the external viral glycoprotein by radiosequencing and by its presence in purified virus. However gp120 was predominantly shed as a soluble protein into the culture fluid. Furthermore gp120 was precipitated by sera from horses infected with equine infectious anaemia virus (EIA...
Use of indirect and competitive ELISAs to compare isolates of equine influenza A virus.
Journal of virological methods    November 1, 1986   Volume 14, Issue 3-4 253-265 doi: 10.1016/0166-0934(86)90027-3
Denyer MS, Crowther JR.Antigenic differences within equine-1 and equine-2 isolates of influenza were studied by haemagglutination inhibition tests, indirect ELISA and competition ELISA, using the same antisera. Better differentiation was obtained with the competition ELISA than with the other two tests. All three methods produced similar relationships within the equine-1 isolates but differed in their ability to differentiate the equine-2 isolates where the competition ELISA was superior and produced epidemiologically sensible results. In all three tests, post-infection ferret and horse sera were more useful in disc...
Single step purification procedure for the rapid separation of equine leucocytes.
Veterinary research communications    November 1, 1986   Volume 10, Issue 6 445-452 doi: 10.1007/BF02214007
Sedgwick AD, Morris T, Russell BA, Lees P.Percoll gradients have been used to separate relatively pure populations of viable equine polymorphonuclear (PMN) and mononuclear (MN) cells. In preliminary studies, a continuous density gradient of 70% Percoll solution was used to separate two distinct leucocyte-rich bands. After measurement of the density of each band on the continuous gradient, discontinuous Percoll gradients, using 60% and 75% Percoll solutions, were used to provide a rapid means of separating PMN and MN cells. The yield of viable cells per ml of blood was 3.0 X 10(6) and 3.2 X 10(6) for MN and PMN cells, respectively. Cor...
Serum protein changes in ponies on different parasite control programmes.
Equine veterinary journal    November 1, 1986   Volume 18, Issue 6 453-457 doi: 10.1111/j.2042-3306.1986.tb03686.x
Herd RP, Kent JE.Serum protein responses were examined in 52 ponies divided into five groups and subjected to various control strategies that resulted in pasture infectivity ranging from 706 to 18,486 infective third stage, cyathostome and Trichostrongylus axei larvae per kilogram of herbage (L3/kg) by 17 September 1984. Major protein changes occurred only in young ponies (Groups 4 and 5) and were observed before exposure to maximum numbers of pasture larvae (Group 4; 10,210 L3/kg, Group 5: 10,042 L3/kg) on 17 September. It appeared that a primary infection of T axei was a greater stimulus to serum beta-globul...
Influence of vitamin E and selenium supplement on antibody production in horses.
Equine veterinary journal    November 1, 1986   Volume 18, Issue 6 472-474 doi: 10.1111/j.2042-3306.1986.tb03694.x
Baalsrud KJ, Overnes G.Fifteen horses used for serum production were maintained on low vitamin E and selenium diets. They were divided into four groups receiving: Group 1 no supplements, Group 2 vitamin E, Group 3 selenium and Group 4 both vitamin E and selenium. The humoral immune response to novel antigens, such as tetanus toxoid and equine influenza virus, was increased in groups receiving either vitamin E or selenium/vitamin E. No effects were recorded on the titres against Escherichia coli or the levels of immunoglobulin G.
Molecular cloning and physical characterization of integrated equine infectious anemia virus: molecular and immunologic evidence of its close relationship to ovine and caprine lentiviruses.
Virology    October 15, 1986   Volume 154, Issue 1 1-8 doi: 10.1016/0042-6822(86)90424-1
Yaniv A, Dahlberg J, Gazit A, Sherman L, Chiu IM, Tronick SR, Aaronson SA.Molecular clones of the integrated form of the genome of equine infectious anemia virus (EIAV), the etiologic agent of a naturally occurring, worldwide disease of horses, were obtained. The restriction map of a full-length genome was determined. Additional evidence for the close evolutionary relationship between EIAV and a prototype lentivirus (caprine arthritis encephalitis virus) was acquired by Southern blotting and immunological analyses. An interspecies radioimmunoassay was developed in which EIAV and ovine and caprine lentiviruses could be detected equally well. These studies make availa...
[Application of the passive hemagglutination test to the study of equine rhinopneumonitis. II. Serologic study in horses].
Revista latinoamericana de microbiologia    October 1, 1986   Volume 28, Issue 4 339-343 
Berrios P, Ibarra L, Riquelme S.No abstract available
Enzyme-linked immunosorbent assay for the detection of antibodies to equid herpesvirus type 1 (EHV-1).
Nihon juigaku zasshi. The Japanese journal of veterinary science    October 1, 1986   Volume 48, Issue 5 1045-1048 doi: 10.1292/jvms1939.48.1045
Hohdatsu T, Eiki T, Ide S, Yamagishi H.No abstract available
Passive transfer of mucosal antibody to Streptococcus equi in the foal.
Infection and immunity    October 1, 1986   Volume 54, Issue 1 202-206 doi: 10.1128/iai.54.1.202-206.1986
Galan JE, Timoney JF, Lengemann FW.Passive transfer of mucosal antibody to Streptococcus equi was studied in foals during the first 2 months of life. Immunoglobulin G (IgG) and IgA antibodies were found in sera and nasal secretions of foals shortly after colostrum intake. Titers were highest 2 days after birth; IgG predominated in sera, and IgA predominated in nasal washes. Intragastrically administered 99mTc-labeled IgA was transported from the bloodstream to the nasal mucosa of a newborn foal within a few hours of colostrum intake. Western blot analysis of the specificities of colostral and serum antibodies showed that select...
Molecular cloning and expression in Escherichia coli of equine type I interferons.
DNA (Mary Ann Liebert, Inc.)    October 1, 1986   Volume 5, Issue 5 345-356 doi: 10.1089/dna.1986.5.345
Himmler A, Hauptmann R, Adolf GR, Swetly P.Using human interferon-alpha 2 (IFN-alpha 2) and IFN-beta DNA to probe an equine genomic library we isolated recombinant phages containing genes for equine interferon-alpha (EqIFN-alpha), interferon-beta (EqIFN-beta), and interferon-omega (EqIFN-omega). Sequence and hybridization analyses of these genes reveal that the equine genome contains gene families of each of these three type I interferon classes. The mature proteins of EqIFN-alpha are 71-77% homologous to human IFN-alpha polypeptides, and, when expressed in E. coli, possess antiviral activity on both equine and human cells. By contrast...
Cell types in the pineal gland of the horse: an ultrastructural and immunocytochemical study.
The Anatomical record    October 1, 1986   Volume 216, Issue 2 165-174 doi: 10.1002/ar.1092160208
Cozzi B.A combined ultrastructural and immunocytochemical study was performed on the pineal gland of the horse in order to identify the cell types present and describe their characteristics. Comparisons have been made with other mammals. Two main cell types are present: pinealocytes and glial cells. Pinealocytes display different degrees of electron density in the nucleus and the cytoplasm, yet no ultrastructural feature supports the idea of separate populations. Putative secretory materials are stored in vesicles related to the Golgi apparatus. A variety of electron-dense bodies are present in the cy...
Echinococcus granulosus of equine origin from different countries possess uniform morphological characteristics.
International journal for parasitology    October 1, 1986   Volume 16, Issue 5 529-540 doi: 10.1016/0020-7519(86)90089-5
Kumaratilake LM, Thompson RC, Eckert J.Echinococcus granulosus of equine origin from different countries possess uniform morphological characteristics. International Journal for Parasitology16: 529–540. Detailed comparative studies on isolates of larval and adult Echinococcus granulosus of equine origin from England, Scotland, Ireland, Belgium, Switzerland, South Africa and New Zealand demonstrated the morphological uniformity of the equine parasite. The morphological features of the equine strain of E. granulosus were fully characterized and it was found that on the basis of morphology alone, this strain could be differentiated ...
Immunoglobulin and neutrophil defense against uterine infection in mares resistant and susceptible to chronic endometritis: a review.
Journal of the American Veterinary Medical Association    September 15, 1986   Volume 189, Issue 6 700-702 
Liu IK, Cheung AT.No abstract available
Hemagglutination-inhibiting antibodies to equine influenza viruses in Japanese horses and antigenic variation of the viruses.
The Kitasato archives of experimental medicine    September 1, 1986   Volume 59, Issue 3 49-55 
Kudo H, Ohde H, Yamanaka T, Ohtsuka Y, Matumoto M.No abstract available
Allergic skin reactions in the horse: response to intradermal challenge with fractionated Culicoides.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    September 1, 1986   Volume 33, Issue 7 508-517 doi: 10.1111/j.1439-0450.1986.tb00062.x
Morrow AN, Quinn PJ, Baker KP.No abstract available
Observations on the long term effects of Brucella abortus infection in the horse, including effects during pregnancy and lactation.
Equine veterinary journal    September 1, 1986   Volume 18, Issue 5 388-390 doi: 10.1111/j.2042-3306.1986.tb03661.x
MacMillan AP, Cockrem DS.Five mares and a stallion were studied from three to 30 months after experimental infection with Brucella abortus strain 544. The mares bred normally. No organisms were recovered from horses or from pregnant Friesian heifer contacts. Titres of serum antibody in the antiglobulin (Coombs) and complement fixation tests fell more slowly than those assessed by other tests. The serum of one foal yielded maternal antibody. An intradermal test was positive in infected adults only, and negative in all foals.
Isolation of piliated Escherichia coli from diarrheic foals.
Veterinary microbiology    September 1, 1986   Volume 12, Issue 3 221-228 doi: 10.1016/0378-1135(86)90051-9
Ward AC, Sriranganathan N, Evermann JF, Traub-Dargatz JL.Escherichia coli was isolated from the feces and intestines of foals with and without diarrhea. Piliation of isolates was demonstrated by electron microscopy and agglutination in antisera having specificity for K88, K99, P987 and F41 pili. Piliation was also demonstrated by electron microscopy on organisms which did not react with any of the antisera.
Elastase-producing microorganisms in horse lungs: their possible role in the pathogenesis of chronic pulmonary disease in the horse.
Equine veterinary journal    September 1, 1986   Volume 18, Issue 5 396-400 doi: 10.1111/j.2042-3306.1986.tb03665.x
Grünig G, Von Fellenberg R, Maier R, Corboz L.Seventeen out of 21 horses had pulmonary microbial organisms which reached considerable numbers in seven cases. Elastase-producing microorganisms from the environment (Streptomyces species and to a lesser extent Bacillus species) constituted 22 per cent to 99 per cent (mean 79 per cent) of the total growth. There was a considerable number of microorganisms with in vitro-produced elastases which were not or only slightly affected by horse serum. There was no correlation between numbers of organisms and pulmonary histopathological findings thus the significance of these microorganisms in the pat...
[Concentration of the Venezuelan equine encephalomyelitis virus in a 2-phase system of water-soluble polymers].
Voprosy virusologii    September 1, 1986   Volume 31, Issue 5 584-587 
Pomelova VG, Gaĭdamovich SIa, Demenev VA, Kadoshnikov IuP.A three-step concentration of Venezuelan equine encephalomyelitis (VEE) virus from tissue culture fluid was carried out in a two-phase system of polyethyleneglycol (PEG)--sodium dextran sulphate (SDS). The concentration method was based on the dependence of virus distribution coefficient upon NaCl content in the system which allowed alternating transfer of the virus from one phase of the system into the other. The infectious activity of the virus increased approximately 100-fold after the first step, 190-fold after the second, and 300-fold after the third step. The process of concentration was...
Identification and antigenic comparison of equine arteritis virus isolated from an outbreak of epidemic abortion of mares.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    August 1, 1986   Volume 33, Issue 6 413-417 doi: 10.1111/j.1439-0450.1986.tb00051.x
Golnik W, Moraillon A, Golnik J.No abstract available
Equine leucocyte antigen system. IV. Recombination within the major histocompatibility complex (MHC).
Journal of immunogenetics    August 1, 1986   Volume 13, Issue 4 315-325 doi: 10.1111/j.1744-313x.1986.tb01116.x
Lazary S, Dubath ML, Luder C, Gerber H.A case of recombination between the putative class I ELA antigen series and the structure(s) governing mixed lymphocyte reactivity in an informative horse family is described. The results of serological typing, 'lysostripping' and mixed lymphocyte culture tests strongly suggest that the recombination took place between two loci and is not intragenic. An alloantigenic membrane structure, provisionally called B1, which does not belong to the known ELA series, was also involved in the cross-over. The B1 antigen resembles the class II gene products of other species in two respects: it is not prese...
Other parasites. Recent advances.
The Veterinary clinics of North America. Equine practice    August 1, 1986   Volume 2, Issue 2 329-336 doi: 10.1016/s0749-0739(17)30719-8
Klei TR.This article briefly reviews new information on trichostrongylid stomach worms, spirurid stomach worms, tapeworms, threadworms, pinworms, intestinal protozoa, lungworms, eye worms, and numerous other aberrant parasites as it relates to prevalence, pathogenesis of diseases, and treatments.
Parasitic skin diseases.
The Veterinary clinics of North America. Equine practice    August 1, 1986   Volume 2, Issue 2 403-437 doi: 10.1016/s0749-0739(17)30725-3
Foil L, Foil C.In this discussion of parasitic skin diseases of horses, details on life cycles are given to aid the understanding and development of control strategies.
Equine arteritis virus-induced polypeptide synthesis.
The Journal of general virology    August 1, 1986   Volume 67 ( Pt 8) 1543-1549 doi: 10.1099/0022-1317-67-8-1543
van Berlo MF, Rottier PJ, Spaan WJ, Horzinek MC.Intracellular virus-specific proteins induced by equine arteritis virus (EAV) have been compared with in vitro translation products of virion and intracellular EAV RNAs. In infected BHK-21 cells, the two major virion proteins (C and E1) and polypeptides with mol. wt. of 60,000 (p60), 42,000 (p42) and 30,000 (p30) were found. There were no indications that the viral proteins were processed from a larger precursor as shown by pulse-chase, amino acid analogue and protease inhibitor experiments. The six polyadenylated RNAs that occur in EAV-infected cells were isolated and translated in an mRNA-de...