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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.
Immunohistochemical localisation of alpha-1-protease inhibitor in the horse.
Research in veterinary science    May 1, 1989   Volume 46, Issue 3 354-357 
Winder NC, Pellegrini A, von Fellenberg R.Using a peroxidase anti-peroxidase technique alpha-1-protease inhibitor (alpha-1-PI) was identified in normal equine hepatocytes in formalin-fixed liver sections, and in airway secretions and macrophages in formalin-fixed lung sections of horses with chronic small airway disease and chronic bronchointerstitial pneumonia. In addition, it was identified occasionally in macrophages in bronchoalveolar lavage samples from clinically healthy horses and from horses with chronic small airway disease. Equine peripheral blood leucocytes and formalin-fixed lung sections with normal histology were negativ...
[The possibility of using equine serum albumin in place of bovine serum albumin and ovalbumin in radioimmunological and immunoenzyme analyses and in virological practice].
Zhurnal mikrobiologii, epidemiologii i immunobiologii    May 1, 1989   Issue 5 47-50 
Kolmakova MV, Kuskova ZR, Ratner GM, Laptakova LM.Horse serum albumin has been shown to meet the requirements to protein preparations for microanalysis and thus to be suitable for use in kits of reagents for the radioimmunological determination of insulin and myoglobin, for the determination of tick-borne encephalitis virus antigen by the method of the enzyme immunoassay and for the stabilization of proteins in the hemagglutination test and the hemagglutination inhibition test.
Identification of the gB homologues of equine herpesvirus types 1 and 4 as disulphide-linked heterodimers and their characterization using monoclonal antibodies.
The Journal of general virology    May 1, 1989   Volume 70 ( Pt 5) 1161-1172 doi: 10.1099/0022-1317-70-5-1161
Meredith DM, Stocks JM, Whittaker GR, Halliburton IW, Snowden BW, Killington RA.Equine herpesvirus types 1 and 4 (EHV-1 and EHV-4) labelled with [14C]glucosamine were purified from infected cell culture medium and profiles of their structural proteins were obtained that enabled identification of the major glycoproteins. Nine glycosylated polypeptides were identified for each virus. Preparations of the purified viruses each contained a glycoprotein which was linked by disulphide bonds, as determined by diagonal gel electrophoresis under reducing/non-reducing conditions. High Mr forms of this glycoprotein were detected for EHV-1 when the sample was not heated. The EHV-1 pro...
Detection of hypogammaglobulinaemia in neonatal foals using the glutaraldehyde coagulation test.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    May 1, 1989   Volume 36, Issue 3 168-174 doi: 10.1111/j.1439-0450.1989.tb00587.x
Saikku A, Koskinen E, Sandholm M.The glutaraldehyde coagulation test was adapted to foal serum to determine adequacy of the colostral-intestinal transfusion of IgG. The test is performed simply by mixing one volume of reagent with 10 volumes of serum and observing the coagulation time. The required glutaraldehyde concentration was established for various threshold levels of IgG as determined by radial immunodiffusion. The analysis consisted of 140 serum samples from foals. Sera with low IgG levels require high glutaraldehyde concentrations and vice versa. The 4 g/l threshold generally accepted for IgG adequacy, was achieved a...
Nonequivalence of the two subunits of horse erythrocyte glutathione transferase in their reaction with sulfhydryl reagents.
The Journal of biological chemistry    April 5, 1989   Volume 264, Issue 10 5462-5467 
Ricci G, Del Boccio G, Pennelli A, Aceto A, Whitehead EP, Federici G.Glutathione transferase (EC 2.5.1.18) from horse erythrocytes has been purified and some molecular and kinetic properties have been investigated. It appears to be a dimeric protein composed of subunits of about 23 kDa, indistinguishable either in sodium dodecyl sulfate or in urea electrophoresis. Amino acid composition, substrate specificities, sensitivity to inhibitors, CD spectra, and immunological studies provide evidence that the horse enzyme is related to the pi class transferases. This enzyme has only two reactive thiol groups/dimer whose integrity appears to be essential for the activit...
Pathways between lymph vessels and sinuses in lymph nodes: a study in horses.
The Anatomical record    April 1, 1989   Volume 223, Issue 4 420-424 doi: 10.1002/ar.1092230411
Heath TJ, Perkins NR.The pathways through which lymph flows from terminal afferent lymphatics to the lymph sinuses, and from the sinuses to initial efferent lymphatics, were studied in horse lymph nodes by using Microfil casts and electron microscopy. Terminal afferent lymphatics are continuous with the subcapsular sinus through oval holes, about 3 microns wide, along their length, and through larger openings near their end. Other terminal afferents penetrate into the node within trabeculae and are supported by processes across the lumen. They connect with trabecular and medullary sinuses through oval or round hol...
Colostral volume and immunoglobulin G and M determinations in mares.
American journal of veterinary research    April 1, 1989   Volume 50, Issue 4 466-470 
Lavoie JP, Spensley MS, Smith BP, Mihalyi J.Colostral volume and IgG and IgM concentrations were determined in 6 multiparous mares at foaling and them every 2 hours from 16 to 20 hours after parturition. Serum IgG and IgM concentrations at foaling also were determined in each mare. The rate of mammary secretion was 292 +/- 26 ml/h (range, 202 to 389 ml/h), and the colostral volume was 5.1 +/- 0.5 L (range, 3.2 to 7.0 L). The colostral IgG and IgM contents were 440 +/- 106 g (range, 199 to 855 g) and 3.1 +/- 0.9 g (range, 0.7 g to 7.1 g), respectively. There was no significant correlation between serum and initial colostral IgG and IgM c...
Immunoglobulin lambda-light-chain-derived amyloidosis (A lambda) in two horses.
Blut    March 1, 1989   Volume 58, Issue 3 129-132 doi: 10.1007/BF00320431
Linke RP, Trautwein G.Tumorous amyloid deposits in the nasal mucosa of two horses differed from generalized AA-amyloidosis with respect to clinical features, organ distribution, and resistance to KMnO4 treatment. Using a panel of antibodies directed against different human amyloid fibril proteins and employing the peroxidase-anti-peroxidase (PAP) technique, we showed the described equine amyloid to be A lambda-type, as demonstrated by immunohistochemical cross-reactivity. Consequently, we identified a second amyloid class in horses and showed that immunoglobulin light-chain-derived amyloid may also be present in an...
Surface antigens on equine sarcoid cells and normal dermal fibroblasts as assessed by xenogeneic antisera.
Research in veterinary science    March 1, 1989   Volume 46, Issue 2 172-179 
Brostroöm H, Paulie S, Perlmann P.To characterise the expression of surface antigens on equine sarcoid cells compared to normal equine fibroblasts, immune sera were produced in rabbits against transformed cells of a virus-containing sarcoid cell line (Mc-1) and normal dermal fibroblasts, respectively. The specificities of the sera were analysed by antibody-dependent cellular cytotoxicity against 51Cr-labelled target cells using human lymphocytes as effector cells. Anti-Mc-1 antiserum induced strong cytotoxicity against transformed cells of two sarcoid cell lines (Mc-1 and Bay Mc-1), whereas the cytotoxicity against transformed...
Purification of chicken liver ferritin by two novel methods and structural comparison with horse spleen ferritin.
The Biochemical journal    March 1, 1989   Volume 258, Issue 2 413-419 doi: 10.1042/bj2580413
Passaniti A, Roth TF.Ferritin was purified from chicken liver by two different methods: gel filtration on controlled-pore glass beads, and immunoaffinity chromatography employing a chicken ferritin-specific monoclonal antibody that did not cross-react with horse spleen ferritin. This antibody recognizes intact ferritin and an oligomeric 240 kDa form of the molecule after protein transfer to nitrocellulose, but not the 22 kDa chicken ferritin subunit. Chicken liver ferritin purified by these methods exhibited reduced migration on non-denaturing polyacrylamide gels compared with horse spleen ferritin. These results ...
A monoclonal antibody against horse kidney (Na+ + K+)-ATPase inhibits sodium pump and E2K to E1 conversion of (Na+ + K+)-ATPase from outside of the cell membrane.
Biochimica et biophysica acta    February 2, 1989   Volume 994, Issue 2 104-113 doi: 10.1016/0167-4838(89)90149-0
Satoh K, Nakao T, Nagai F, Kano I, Nakagawa A, Ushiyama K, Urayama O, Hara Y, Nakao M.Monoclonal antibodies against horse kidney outer medulla (Na+ + K+)-ATPase were prepared. One of these antibodies (M45-80), was identified as an IgM, recognized the alpha subunit of the enzyme. M45-80 had the following effects on horse kidney (Na+ + K+)-ATPase: (1) it inhibited the enzyme activity by 50% in 140 mM Na+ and by 80% in 8.3 mM Na+; (2) it increased the Na+ concentration necessary for half-maximal activation (K0.5 for Na+) from 12.0 to 57.6 mM, but did not affect K0.5 for K+; (3) it slightly increased the K+-dependent p-nitrophenylphosphatase (K-pNPPase) activity; (4) it inhibited p...
Immunohistochemical demonstration of somatostatin-containing cells in the equine thyroid and parathyroid glands.
Nihon juigaku zasshi. The Japanese journal of veterinary science    February 1, 1989   Volume 51, Issue 1 228-230 doi: 10.1292/jvms1939.51.228
Tanimura N, Tateyama S, Yamaguchi R, Nosaka D.No abstract available
Antigenic relationship between Pythium insidiosum de Cock et al. 1987 and its synonym Pythium destruens Shipton 1987.
Mycoses    February 1, 1989   Volume 32, Issue 2 73-77 doi: 10.1111/j.1439-0507.1989.tb02205.x
Mendoza L, Marin G.Antigens and rabbit-antisera from holotypes of Pythium insidiosum and P. destruens were prepared to elucidate their antigenic relationship. The antigens and rabbit-antisera of P. insidiosum as well as P. destruens used as a reference system showed that both shared three precipitin bands in common. The antigen and rabbit-antisera of P. destruens and P. insidiosum used as a reference system against other strains isolated from humans and animals with pythiosis, also showed three precipitin bands in common. When we used sera taken from horses with proven pythiosis against antigens of P. insidiosum...
[A western blot test for the serological diagnosis of equine infectious anemia]. Rossmanith W, Horvath E.After electrophoretic separation in SDS-PAGE structural proteins of the virus of Equine Infectious Anemia (EIA) were easily blotted by the semi-dry-blotting method onto nitrocellulose filters. Strips of these filters were used for antibody demonstration, and positive reactions thereof were intensified by a biotin-avidin-peroxidase system. Sensitivity of this system was so high as to allow readable interpretation of bands up to the dilution of 1:6,400 of a strongly positive serum. Frequently this procedure allowed to make a firm diagnostic Western-Blot diagnosis on far weaker equine sera. Inter...
Immunocytochemical component of endocrine cells in pancreatic islets of horses.
Nihon juigaku zasshi. The Japanese journal of veterinary science    February 1, 1989   Volume 51, Issue 1 35-43 doi: 10.1292/jvms1939.51.35
Furuoka H, Ito H, Hamada M, Suwa T, Satoh H, Itakura C.The endocrine cell components in the pancreatic islets of the following 4 pancreatic regions of the horse were investigated by immunohistochemical methods: lobus pancreatis sinister (left lobe); lobus pancreatis dexter (right lobe); and 2 regions of Corpus pancreatis (body), the duodenal lobe which lies along the cranial duodenal flexure and descending duodenum, and the intermediate lobe which is situated around the portal vein. The islets in the left and intermediate lobes contained a central mass of glucagon cells surrounded by insulin cells, a few somatostatin cells and sporadic pancreatic ...
Identification and nucleotide sequence of a gene in equine herpesvirus 1 analogous to the herpes simplex virus gene encoding the major envelope glycoprotein gB.
The Journal of general virology    February 1, 1989   Volume 70 ( Pt 2) 383-394 doi: 10.1099/0022-1317-70-2-383
Whalley JM, Robertson GR, Scott NA, Hudson GC, Bell CW, Woodworth LM.A gene in equine herpesvirus 1 (EHV-1; equine abortion virus) equivalent to the gB glycoprotein gene of herpes simplex virus (HSV) has been identified by DNA hybridization and nucleotide sequencing. A 4.3 kbp EHV-1 PstI-ClaI sequence (0.40 to 0.43 map units) contained an open reading frame flanked by appropriate control elements and was capable of encoding a polypeptide of 980 amino acids. This had 50 to 60% identity over a 617 amino acid conserved region with the gB gene products of HSV and three other alphaherpesviruses, and 20 to 30% identity with those of human cytomegalovirus and Epstein-...
The structure and properties of horse muscle acylphosphatase in solution. Mobility of antigenic and active site regions.
FEBS letters    January 2, 1989   Volume 242, Issue 2 225-232 doi: 10.1016/0014-5793(89)80474-0
Saudek V, Williams RJ, Ramponi G.The solution structure of acylphosphatase determined by proton nuclear magnetic resonance spectroscopy is described. The results allow us to discuss the fold of the protein (101 amino acids), to correlate the exposure and the mobility of the backbone with the antigenicity, and to locate the active site.
Production of monoclonal antibodies against equine influenza: application to a comparative study of various strains of the virus.
Annales de recherches veterinaires. Annals of veterinary research    January 1, 1989   Volume 20, Issue 3 243-250 
Crucière C, Guillemin MC, Roseto A, Wirbel A, Plateau E.Monoclonal antibodies (Mo Abs) were prepared against influenza/A/equine/Prague/1/56 (H7N7) and influenza/A/equine/Miami/1/63 (H3N8) reference strains of equine influenza virus. These monoclonals were tested against the 2 reference strains, 8 field strains of equine influenza virus, 3 human influenza viruses possessing the H3 hemagglutinin, and one virus of human origin possessing the H1 hemagglutinin. Two antibodies were obtained in one fusion against the Prague/1/56 strain and reacted only with this strain. Four anti/A/equine/Miami/1/63 Mo Abs were obtained in one fusion. They differentiated ...
Comparison of diagnostic tests for the detection of equine infectious anemia antibody. Matsushita T, Hesterberg LK, Porter JP, Smith BJ, Newman LE.Two diagnostic tests are approved for detecting antibody to equine infectious anemia virus: the agar-gel immunodiffusion (AGID) test and the competitive enzyme-linked immunosorbent assay (ELISA). A total of 420 sera from National Veterinary Services Laboratories check sets were tested with the AGID and competitive ELISA. A 100% correlation was obtained. The AGID and competitive ELISA were further used to test difficult samples with low levels of equine infectious anemia antibody (weak positives). A third test (Western blot) was also used with these weak positive samples to resolve any discorda...
Immunocytochemical localization of carbonic anhydrase isozyme III in equine thymus.
Histochemistry    January 1, 1989   Volume 91, Issue 1 39-42 doi: 10.1007/BF00501908
Nishita T, Matsushita H.Sections of equine thymus were examined for the presence of carbonic anhydrase (CA) isozymes by an immunohistochemical method. Carbonic anhydrase III, a major enzyme of skeletal muscle, was localized in some of the epithelial-reticular cells of the equine thymus. This finding suggests the presence of a new type of cell in the thymic cortex. The concentration of CA-III in the thymus was 17 micrograms/g wet tissue. CA-I and CA-II were not found in equine thymus.
T and B lymphocytes in horses persistently infected with equine infectious anaemia virus.
Veterinary research communications    January 1, 1989   Volume 13, Issue 1 57-65 doi: 10.1007/BF00366853
Valpotić I, Kastelan M, Rudolf M, Gerencer M, Jukić B, Basić I.The percentage of T and B lymphocytes in the peripheral blood of horses chronically infected with equine infectious anaemia (EIA) virus was determined and the results were compared with the percentage of these cells in healthy uninfected horses. Cells with membrane receptors for sheep erythrocytes (T and active T lymphocytes) were determined by E and A rosette techniques, while cells with receptors for the C3b component of complement and those with receptors for mouse erythrocytes (B lymphocytes), were determined by the EAC rosette method. The percentage of Fe positive cells was assayed by the...
Equine lymphocyte antigens and reproduction in the Standardbred mare.
Animal genetics    January 1, 1989   Volume 20, Issue 1 99-104 doi: 10.1111/j.1365-2052.1989.tb00847.x
Park CA, Hines HC, Threlfall WR.Equine lymphocyte antigen (ELA) gene frequencies were estimated for pacing and trotting Standardbred mares residing on a breeding farm in central Ohio. The ELA gene frequencies for Ohio Standardbreds did not differ significantly from the ELA gene frequencies of Kentucky Standardbreds, determined by Bailey (1983). No significant differences were found in the distribution of ELA class I antigens in horses with lower overall fertility or a history of abortion on the investigated breeding farm. Likewise, no significant association was observed when the ELA types of both the mare and the stallion t...
Dermatographism in a horse.
The Cornell veterinarian    January 1, 1989   Volume 79, Issue 1 109-116 
Cornick JL, Brumbaugh GW.An eight-year-old Thoroughbred gelding with dermatographic urticaria is presented. Forelimb edema and generalized urticaria were the presenting clinical signs. All hematologic and serum biochemical values were normal. Immunologic and histologic evaluation failed to reveal specific abnormalities. During hospitalization, an urticarial response to mechanical pressure (dermatographism) was identified. Clinical responses to corticosteroid and antihistaminic (H1) therapy were equivocal. The condition resolved in five weeks and an etiology was not discovered. A discussion of the pathogenesis, diagnos...
Purification of F(ab’)2 anti-snake venom by caprylic acid: a fast method for obtaining IgG fragments with high neutralization activity, purity and yield.
Toxicon : official journal of the International Society on Toxinology    January 1, 1989   Volume 27, Issue 3 297-303 doi: 10.1016/0041-0101(89)90177-3
dos Santos MC, D'Império Lima MR, Furtado GC, Colletto GM, Kipnis TL, Dias da Silva W.Pooled horse plasma containing antibodies against Crotalus durissus terrificus whole venom were digested with pepsin at an enzyme-substrate ratio of 8:1, pH 3.1, for 40 min and the F(ab')2M fragments purified by adding 8.7% caprylic acid (pH 5.0). For comparison, F(ab')2B purified by precipitation with ammonium sulphate and uncleaved IgG purified with caprylic acid were also prepared. Fab' fragments were obtained by reduction and alkylation of F(ab')2B. The anti-whole C.d. terrificus venom titers, determined by Dot-Blot were 12,800 (IgG), 6400 [F(ab')2B], 4800 [F(ab')2M] and 3200 (Fab'B). Immu...
Maternal immunological recognition of pregnancy in equids.
Journal of reproduction and fertility. Supplement    January 1, 1989   Volume 37 69-78 
Antczak DF, Allen WR.There is little evidence for maternal immunological recognition of pregnancy in most species with the striking exception of the members of the genus Equus. Almost all mares make strong cytotoxic antibody responses to paternally inherited fetal antigens by Day 60 of gestation. Most of these responses are directed against antigens of the Major Histocompatibility Complex (MHC), which constitutes the primary immunogenetic barrier to successful organ transplantation. The source of fetal MHC antigens in the pregnant mare appears to be the specialized trophoblast cells of the chorionic girdle region ...
Equine herpes virus 1 (EHV-1) in liver, spleen, and lung as demonstrated by immunohistology and electron microscopy.
Acta veterinaria Scandinavica    January 1, 1989   Volume 30, Issue 2 141-146 doi: 10.1186/BF03548050
Jönsson L, Beck-Friis J, Renström LH, Nikkilä T, Thebo P, Sundquist B.Ten aborted foals, diagnosed as infected with Equine Herpes Virus 1 (EHV-1) on histopathological criteria, were examined for the presence of EHV-1 using immunohistology as the investigative instrument. The primary reagent was an antiserum specific for viral envelope glycoproteins. Immunohistology localised EHV-1 to areas of liver necrosis and to the cytoplasm of infected Kupffer cells and hepatocytes. Cytoplasmic immunolabelling was also prominent in reticular cells of the red pulp of the spleen and in intact and degenerated bronchiolar epithelium. Cytoplasmic immunolabelling was seen in morph...
Topography of oxytocin and vasopressin neurons in the forebrain of Equus caballus: further support of proposed evolutionary relationships for proopiomelanocortin, oxytocin and vasopressin neurons.
Brain, behavior and evolution    January 1, 1989   Volume 33, Issue 4 193-204 doi: 10.1159/000115928
Melrose PA, Knigge KM.The present study describes the topography of immunoreactive (ir) oxytocin (OXY) and vasopressin (AVP) neurons in the forebrain of Equus caballus and the coexistence of ir proopiomelanocortin (POMC)-derived peptides in the same cells. These data are compared to those for other mammalian species and the possible significance of species variations is considered. As expected, magnocellular neurons of the equine hypothalamus, which contain ir OXY or AVP, have prominent discernible projections to the neurohypophysis. Further, as in other mammalian species, the field of ir OXY perikarya generally ex...
Immunoglobulin concentration in the blood serum of foals suffering from pneumonia associated with mycoplasma infection.
Archiv fur experimentelle Veterinarmedizin    January 1, 1989   Volume 43, Issue 5 747-750 
Antal A, Szabó I, Vajda G, Antal VD, Polner A, Totth B, Szollár I, Stipkovits L.Clinical, microbiological, haematological, and immunological investigations were carried out in mares and their foals of 2 studs. A considerable number of foals fell ill with pneumonia, the mortality rate was high. Mycoplasmas were mostly isolated from nasal swabs and from the lungs. The isolation rate of bacteria was lower. Serum IgG concentration was reduced in the diseased or dead foals compared to that of healthy animals, the data stress in importance of IgG in the development of respiratory diseases also in foals.
Comparative effects of cholera toxin, Salmonella typhimurium culture lysate, and viable Salmonella typhimurium in isolated colon segments in ponies.
American journal of veterinary research    January 1, 1989   Volume 50, Issue 1 22-28 
Murray MJ, Doran RE, Pfeiffer CJ, Tyler DE, Moore JN, Sriranganathan N.Isolated segments of left dorsal colon and a side-to-side colocolostomy (between the left ventral colon and left dorsal colon) were surgically created in 6 adult ponies. Four segments, each separated by an empty segment, were inoculated (20 ml) with 1 of the following 4 solutions: phosphate buffered saline solution (PBSS)/1% polyethylene glycol (PEG); purified cholera toxin in PBSS/1% PEG (5 micrograms cholera toxin/ml of PBSS/1% PEG); lyophilized Salmonella typhimurium UCD 1755 culture lysate, reconstituted in PBSS/1% PEG; and viable S typhimurium UCD 1755 (10(8) organisms/ml of PBSS/1% PEG)....
[Experimental equine fascioliasis: evolution of serologic, enzymatic and parasitic parameters].
Annales de recherches veterinaires. Annals of veterinary research    January 1, 1989   Volume 20, Issue 3 295-307 
Soulé C, Boulard C, Levieux D, Barnouin J, Plateau E.Three, four, and one horses were respectively infected with 100, 1,000, and 5,000 metacercariae of Fasciola hepatica. Six of them were reinfected 38 weeks later with 1,000 metacercariae each. Specific antibodies assayed by counter-electrophoresis, passive hemagglutination and ELISA tests appeared three to six weeks post-infection and peaked 10 to 17 weeks post-infection. Horses infected by 1,000 metacercariae and more showed 17.6% of positive samples by counter-electrophoresis, 49.2% by ELISA, and 75.6% by passive hemagglutination. Plasma glutamate dehydrogenase and gamma-glutamyltransferase l...