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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.
Production of antibody to homologous -fetoprotein in rabbits, rats and horses by immunization with human -fetoprotein.
Journal of immunology (Baltimore, Md. : 1950)    November 1, 1972   Volume 109, Issue 5 957-960 
Nishi S, Watabe H, Hirai H.The production of antibody to homologous alpha fetoprotein (AFP) in rabbits, rats, and horses by immunication with human AFP is reported. The antigens were administered subcutaneously 5 times at intervals of 7-10 days. Rabbits and dogs received 1 mg of human AFP/ml of the homologous pooled newborn serum with each injection while the rats received 1/2 of the dose. The horses received 5 mg/ml/injection. 2 weeks after the last injection, antisera were collected and immunologic assays were performed by the Ouchterlony method and the reversed version of the Mancini method. High titered antibodies w...
A DNA-binding protein in the serum of certain mammalian species.
Proceedings of the National Academy of Sciences of the United States of America    November 1, 1972   Volume 69, Issue 11 3327-3330 doi: 10.1073/pnas.69.11.3327
Thoburn R, Hurvitz AI, Kunkel HG.Various mammalian species contain an anionic serum protein that reacts specifically with native DNA. It is considerably less reactive with single-strand DNA and does not react with monodeoxyribonucleotides, homopolyribonucleotides, or duplexes of homopolyribonucleotides. Synthetic dA.dT was an effective inhibitor of the reaction with native DNA, while Micrococcus luteus DNA and dG.dC were not inhibitory. This protein was encountered in the course of studies on DNA antibodies. Although it reacted with red cells coated with DNA and gave agar precipitation bands, it was clearly distinct from DNA ...
Persistence of neutralizing antibody in Equidae vaccinated with Venezuelan equine encephalomyelitis vaccine strain TC-83.
Journal of the American Veterinary Medical Association    October 15, 1972   Volume 161, Issue 8 916-918 
Walton TE, Johnson KM.No abstract available
Effect of back passage of Venezuelan equine encephalomyelitis TC-83 vaccine virus on clinical, virologic, and immune responses in horses.
Journal of the American Veterinary Medical Association    October 1, 1972   Volume 161, Issue 7 824-831 
Luedke AJ, Barber TL, Foster NM, Batalla D, Mercado S.No abstract available
[Mechanisms of action of interferon].
Antibiotiki    October 1, 1972   Volume 17, Issue 10 940-945 
Tazulakhova EB, Ershov FI.No abstract available
Prevention of tetanus.
Journal of the Indian Medical Association    October 1, 1972   Volume 59, Issue 7 294-295 
Sen B.No abstract available
Equine infectious anemia: activity of liquid antigen extracts in the agar-gel immunodiffusion and complement-fixation tests.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    October 1, 1972   Volume 36, Issue 4 377-379 
Carrier SP, Bannister GL, Boulanger P.Twenty-nine lots of acetone-ether extracted liquid antigen were prepared from the pulp of 11 spleens collected from horses at the acute phase of experimental infection. The lots prepared from the highly reactive pulp resulted in general in a liquid antigen of greater activity than those extracted from weakly reactive pulps. Some variations in activity between lots of antigen prepared from the same spleen were also observed. No matter what the results, given a wide enough variation, all results were reproducible. The procedure permitted production of a greater number of antigen test doses from ...
Identification and quantitation of equine serum and secretory immunoglobulin A.
Infection and immunity    October 1, 1972   Volume 6, Issue 4 610-615 doi: 10.1128/iai.6.4.610-615.1972
McGuire TC, Crawford TB.Immunoglobulin A (IgA) was demonstrated in equine serum and secretions. This immunoglobulin had a molecular weight extending from 150,000 to 700,000 and reacted with specific antihuman alpha-chain antiserum. Antigenic determinants specific for secretory IgA were demonstrated and found to be absent on serum IgA. Antigen binding activity was detected in IgA from tears. Purified IgA was antigenically distinct from equine IgG, IgM, IgG(T), and aggregating immunoglobulin. Quantitative studies demonstrated that IgA was the predominant immunoglobulin in tears and milk but not in colostrum. The electr...
Immunological studies on the organ and species specificity of ferritin from horse, rabbit and pig.
Comparative biochemistry and physiology. B, Comparative biochemistry    September 15, 1972   Volume 43, Issue 1 217-221 doi: 10.1016/0305-0491(72)90218-0
Marsden RJ, Ducker HA, Douglas TA, Renton JP.No abstract available
Equine anaphylaxis.
Journal of the American Veterinary Medical Association    September 1, 1972   Volume 161, Issue 5 438 
Mansmann RA.No abstract available
Demonstration of antigenic identity between purified equine infectious anemia virus and an antigen extracted from infected horse spleen.
Infection and immunity    September 1, 1972   Volume 6, Issue 3 416-417 doi: 10.1128/iai.6.3.416-417.1972
Nakajima H, Norcross NL, Coggins L.Antigenic relationship between purified equine infectious anemia (EIA) virus and spleen-derived antigen from EIA-infected horses was examined by immunodiffusion. Identical antigenicity of these two antigens has been proven because precipitation lines formed between the two antigens and EIA antiserum connected with each other. The results indicate that the antigenic substance derived from infected spleen is a component of EIA virus.
[Research on identification and titration of gonadotropins for therapeutic use by immunologic methods. 3. Experimental research on preparations of equine origin: serum gonadotropin or PMSG].
Journal de pharmacie de Belgique    September 1, 1972   Volume 27, Issue 5 519-542 
Beys-L'Hoest B.No abstract available
Comparison of immunization methods for producing reference adenovirus antisera in horses.
Applied microbiology    September 1, 1972   Volume 24, Issue 3 398-404 doi: 10.1128/am.24.3.398-404.1972
Hierholzer JC, Gamble WC, Quist KD, Chappell WA.Horses were immunized by a variety of inoculation procedures designed to determine the most efficient method of producing antisera to adenovirus types 25 to 31. The procedures evaluated included immunization by (i) direct intravenous (iv) injection, (ii) iv infusion, (iii) intramuscular (im) injection of virus with and without Freund's incomplete adjuvant, (iv) combined iv and im injections, and (v) combined iv infusion and im injection. The im schedule (no. 3) was superior to the others in terms of immunizing antigen and time required, and hemagglutination-inhibition (HI) and serum-neutralizi...
Equine pulmonary emphysema: a bronchopulmonary mould allergy.
The Veterinary record    August 5, 1972   Volume 91, Issue 6 134-140 doi: 10.1136/vr.91.6.134
Eyre P.No abstract available
Elimination of repeated clot formation in mouse ascitic fluid containing arbovirus antibodies.
Applied microbiology    August 1, 1972   Volume 24, Issue 2 288-289 doi: 10.1128/am.24.2.288-289.1972
Chiewsilp D, McCown JM.Repeated clot formation in mouse ascitic fluids containing antiviral antibody was eliminated by acid precipitation of the fibrinogen.
Japanese encephalitis in horses in Japan.
Equine veterinary journal    July 1, 1972   Volume 4, Issue 3 155-156 doi: 10.1111/j.2042-3306.1972.tb03900.x
Nakamura H.No abstract available
A study of different equine influenza vaccination schedules in seronegative foals and in horses.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    July 1, 1972   Volume 20, Issue 5 361-366 doi: 10.1111/j.1439-0450.1973.tb01137.x
Petermann HG, Stellmann C, Graveline P.No abstract available
Isolation and partial characterization of mare milk lysozyme.
Archives of biochemistry and biophysics    July 1, 1972   Volume 151, Issue 1 353-355 doi: 10.1016/0003-9861(72)90507-3
Jauregui-Adell J, Cladel G, Ferraz-Pina C, Rech J.No abstract available
The fluorescent antibody technique in the diagnosis of equine rhinopneumonitis virus abortion. Smith IM, Girard A, Corner AH, Mitchell D.Using two known positive equine viral rhinopneumonitis (EVR) sera, conjugates were prepared with fluorescein isothiocyanate and tested for specificity using EVR infected tissue culture cells. The conjugate was then applied to selected tissues from 32 aborted fetuses and foals submitted during a natural outbreak of EVR. Antigen was detected in various tissues by immunofluorescence in 20 cases (62.5%). In 24 cases bovine fetal kidney cell monolayers were inoculated with a pool of lung and liver and EVR virus was isolated from 15 (62.5%). Histological examination of various tissues from 29 cases ...
Pathologic changes in experimental equine anaphylaxis.
Journal of the American Veterinary Medical Association    June 15, 1972   Volume 160, Issue 12 1632-1636 
McGavin MD, Gronwall RR, Mia AS.No abstract available
[Autoantibodies and autoimmune diseases in animals].
DTW. Deutsche tierarztliche Wochenschrift    June 15, 1972   Volume 79, Issue 12 306-310 
Trautwein G.No abstract available
Specific anti-antibodies.
Experientia    June 15, 1972   Volume 28, Issue 6 692-694 doi: 10.1007/BF01944983
Radoiu N, Zydeck FA, Bennett RR.No abstract available
Immunologically mediated glomerulitis of horses. II. Antiglomerular basement membrane antibody and other mechanisms in spontaneous disease.
Laboratory investigation; a journal of technical methods and pathology    June 1, 1972   Volume 26, Issue 6 708-715 
Banks KL, Henson JB.No abstract available
Immunologically mediated glomerulitis of horses. I. Pathogenesis in persistent infection by equine infectious anemia virus.
Laboratory investigation; a journal of technical methods and pathology    June 1, 1972   Volume 26, Issue 6 701-707 
Banks KL, Henson JB, McGuire TC.No abstract available
The evolution of an equine allergist.
The Journal of asthma research    June 1, 1972   Volume 9, Issue 4 249-250 doi: 10.3109/02770907209105654
Mansmann JA.No abstract available
Inhibition of the mixed lymphocyte reaction by antibodies.
Transplantation proceedings    June 1, 1972   Volume 4, Issue 2 173-176 
Revillard JP, Robert M, Betuel H, Latour M, Bonneau M, Brochier J, Traeger J.No abstract available
Inhibition of the interaction between fimbrial haemagglutinins and erythrocytes by D-mannose and other carbohydrates.
Journal of general microbiology    June 1, 1972   Volume 71, Issue 1 149-157 doi: 10.1099/00221287-71-1-149
Old DC.No abstract available
Hepatotoxic effects of horse anti-mouse lymphocyte serum.
Experimental and molecular pathology    June 1, 1972   Volume 16, Issue 3 302-310 doi: 10.1016/0014-4800(72)90006-8
Pisano JC, Patterson JT, Trejo R, Hoffman E, Lentz PE, Di Luzio NR.No abstract available
Study of the one-step growth curve of equine infectious anemia virus by immunofluorescence.
Infection and immunity    June 1, 1972   Volume 5, Issue 6 890-895 doi: 10.1128/iai.5.6.890-895.1972
Ushimi C, Henson JB, Gorham JR.Primary horse leukocyte cultures were inoculated with 2 or 10 50% tissue culture infective doses (TCID(50)) of equine infectious anemia (EIA) virus per cell, and the titer of cell-associated and fluid-phase virus was determined from 1 to 72 hr postinoculation (PI). Cover slips were collected from 4 to 72 hr PI and stained for EIA viral antigen by the indirect immunofluorescent (FA) technique. Viral replication was detected after a latent period of approximately 18 to 24 hr and reached peak titers of approximately 10(4.5) to 10(6) TCID(50)/0.5 ml from 48 to 72 hr PI. The fluid phase contained 1...
[Low temperature thresholds of reproduction of group A arboviruses in tissue culture].
Voprosy virusologii    May 1, 1972   Volume 17, Issue 3 283-287 
L'vov DK, Cheban DS, Tsilinskiĭ IaIa.No abstract available