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Topic:Immunoglobulins

Immunoglobulins in horses are antibodies produced by the immune system to identify and neutralize pathogens such as bacteria and viruses. These proteins are essential components of the horse's immune response and are involved in recognizing foreign antigens. The primary classes of immunoglobulins in horses include IgG, IgA, IgM, IgE, and IgD, each with distinct roles in immune function. IgG is the most abundant and plays a key role in systemic immune responses, while IgA is important for mucosal immunity. IgM is the first antibody produced in response to an antigen, and IgE is involved in allergic reactions. IgD's function is less well-defined but is thought to be involved in respiratory immune responses. This page aggregates peer-reviewed research studies and scholarly articles that explore the structure, function, and clinical relevance of immunoglobulins in equine health.
Lymphoid leukosis viruses, their recognition as ‘persistent’ viruses and comparisons with certain other retroviruses of veterinary importance.
Veterinary research communications    January 1, 1996   Volume 20, Issue 1 83-108 doi: 10.1007/BF00346580
Darcel C.Diseases caused by lymphoid leukosis virus (LLV), a retrovirus, take a long time after infection to develop and have a wide variety of pathological manifestations. This long latent period is characteristic of 'persistent virus infections'. Disease produced by LLV infection and its underlying mechanisms is compared with 'persistent' infections caused by other retroviruses in birds and mammals of veterinary importance. The diseases considered for comparison are those caused by reticuloendotheliosis, feline leukaemia, bovine leukosis and equine infectious anaemia viruses. There are significant ch...
Equine gammaherpesvirus 2 (EHV2) is latent in B lymphocytes.
Archives of virology    January 1, 1996   Volume 141, Issue 3-4 495-504 doi: 10.1007/BF01718313
Drummer HE, Reubel GH, Studdert MJ.Peripheral blood leukocytes were collected from 5 Thoroughbred horses and examined for the presence of EHV2 in sub-populations of mononuclear cells. Peripheral blood mononuclear cells were separated on Percoll gradients and then enriched for plastic adherent cells (predominantly monocytes), surface immunoglobulin positive (sIg+) B lymphocytes and T lymphocytes, using panning techniques. The purity of each cell population was assessed by fluorescence activated cell scanning. In an infectious centre assay, each cell population was inoculated onto equine foetal kidney monolayer cell cultures whic...
Value of skin testing for predicting reactions to equine rabies immune globulin.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America    September 1, 1995   Volume 21, Issue 3 660-662 doi: 10.1093/clinids/21.3.660
Tantawichien T, Benjavongkulchai M, Wilde H, Jaijaroensup W, Siakasem A, Chareonwai S, Yountong C, Sitprija V.The high cost of postexposure prophylaxis for rabies is one reason that treatment is inadequate in developing countries. This problem has kindled interest in the use of equine rabies immune globulin, which is a less expensive, yet effective, substitute for human rabies immune globulin. Fatal anaphylaxis is a feared complication of the administration of heterologous serum; therefore, authoritative sources recommend prior skin testing. However, recommendations for methods of administering such a skin test and for its interpretation vary greatly. We embarked on a long-term study to develop guidel...
Monoclonal equine IgM and IgG immunoglobulins.
Veterinary immunology and immunopathology    July 1, 1995   Volume 47, Issue 1-2 1-12 doi: 10.1016/0165-2427(94)05381-2
Wagner B, Radbruch A, Richards C, Leibold W.In order to define equine immunoglobulins (Igs) and to produce monoclonal reference Igs we fused equine peripheral blood mononuclear cells with X63-Ag8.653 non Ig producing murine myeloma cells. A total of 29 equine Ig producing equi-murine heterohybridomas were obtained, of which ten expressed equine Ig for more than 3 months. One of these heterohybridoma lines produced monoclonal IgM, an equine isotype which has not been available in monoclonal form before. Four lines secreted equine IgG of two distinct Ig heavy chain types as assessed by the molecular weight (MW), while the remaining five l...
Production of monoclonal antibodies in horses.
Methods in molecular biology (Clifton, N.J.)    January 1, 1995   Volume 45 55-60 doi: 10.1385/0-89603-308-2:55
Perryman LE, Mason PH.Monoclonal antibodies (MAbs) have been successfully used to evaluate immune responses in horses, and to target important antigens of equine infectious agents to which protective immune responses may be directed (1–5). Most of these studies are performed with murine MAb produced by fusing spleen cells from immunized mice with an appropriate myeloma cell line, as described in Chapter 3. However, there are experimental questions for which murine MAb are not adequate. These include: 1.Definition of microbial epitopes recognized by the infected host; 2.Identification of immunodominant epito...
Seroanalysis of Tyzzer’s disease in horses: implications that multiple strains can infect Equidae.
Equine veterinary journal    January 1, 1995   Volume 27, Issue 1 8-12 doi: 10.1111/j.2042-3306.1995.tb03025.x
Hook RR, Riley LK, Franklin CL, Besch-Williford CL.A monoclonal antibody based competitive inhibition assay was used to detect antibodies in horse sera to purified flagellar antigens from distinct Clostridium piliforme isolates. Sequential absorption of hyperimmune rat serum to C. piliforme isolate E (horse-origin isolate), a positive C. piliforme-immune horse serum, and other suspected immune horse sera with unrelated bacteria or C. piliforme isolates E or isolate R1 (rat-origin isolate) alone demonstrated the specificity of this assay for C. piliforme. This specificity was associated with the inhibition of monoclonal antibody binding to C. p...
The amino Acid sequence glutamine-628 to valine-646 within the A1 repeat domain mediates binding of von Willebrand factor to bovine brain sulfatides and equine tendon collagen.
Platelets    January 1, 1995   Volume 6, Issue 5 245-251 doi: 10.3109/09537109509023562
Andrews RK, Booth WJ, Bendall LJ, Berndt MC.von Willebrand Factor (vWF) is a multifunctional glycoprotein in plasma and vascular subendothelial matrix which plays a major role in cellular adhesion. vWFdependent adhesion of platelets to the subendothelium at high shear rates involves a specific platelet membrane receptor, the glycoprotein (GP) Ib-IX complex. We have previously purified a 39/34-kiloDalton (kDa) dispase fragment of vWF (Leu-480/Val-481 to Gly-718) and demonstrated that this fragment contains the binding site for the GP Ib-IX complex [Andrews R K, et al. Biochemistry 1989; 28: 8326-83361. vWF also mediates agglutination of ...
Light chain isotype regulation in the horse. Characterization of Ig kappa genes.
Journal of immunology (Baltimore, Md. : 1950)    August 1, 1994   Volume 153, Issue 3 1099-1111 
Ford JE, Home WA, Gibson DM.Horse Ig kappa genes have been characterized to determine whether there may be a structural basis for the low level of kappa expression in this species. The overall organization of the J kappa-C kappa locus is remarkably similar to that of the mouse and human loci. A single C kappa exon is separated by 2.9 kb from five J kappa segments, four of which seem functional and three of which are associated with canonical recombination signal sequences. A highly conserved intron enhancer was identified upstream of the C kappa exon and a single restriction fragment in horse genomic DNA hybridized stron...
Characterization of monoclonal antibodies specific for equine homologues of CD3 and CD5.
Immunology    August 1, 1994   Volume 82, Issue 4 548-554 
Blanchard-Channell M, Moore PF, Stott JL.Two monoclonal antibodies (mAb), UC F6G-3 and UC F13C-5, were characterized as being specific for the apparent equine homologues of CD3 and CD5, respectively. Both antibodies exhibited characteristics of pan-T-lymphocyte markers based upon immunohistology and two-colour flow cytometry. UC F6G-3 precipitated a complex of proteins (up to seven) with molecular weights ranging from 18,000 to 42,000, similar to the human and murine CD3 complex. Upon further dissociation of the precipitated complex, two proteins were identified with molecular weights of 22,000 and 27,000. Immobilized UC F6G-3 was ef...
Report of the First International Workshop on Equine Leucocyte Antigens, Cambridge, UK, July 1991.
Veterinary immunology and immunopathology    July 1, 1994   Volume 42, Issue 1 3-60 doi: 10.1016/0165-2427(94)90088-4
Kydd J, Antczak DF, Allen WR, Barbis D, Butcher G, Davis W, Duffus WP, Edington N, Grünig G, Holmes MA.The First International Workshop on Equine Leucocyte Antigens was organized and convened for the purposes of identifying immunologically relevant cell surface molecules of equine leucocytes and establishing a system of nomenclature for those molecules. Participating members of the workshop represented the majority of laboratories world-wide engaged in the tasks of production and characterization of equine leucocyte and lymphocyte markers using monoclonal antibodies. The workshop confirmed the identification of several equine CD molecules described previously by individual laboratories, and in ...
Down-regulation followed by re-expression of equine CD4 molecules in response to phorbol myristate acetate.
Veterinary immunology and immunopathology    July 1, 1994   Volume 42, Issue 1 71-82 doi: 10.1016/0165-2427(94)90090-6
Zhang CH, Grünig G, Davis W, Antczak DF.The regulatory effects of phorbol myristate acetate (PMA) on the expression of the CD4 molecule on horse T cells were investigated. On both peripheral blood lymphocytes and thymocytes, PMA resulted in a rapid and transient down-regulation of equine CD4 expression, but had no such effect on the surface expression of equine CD5, CD8 or major histocompatibility complex (MHC) class I and class II molecules. Over 75% of the surface CD4 molecules per cell were lost after a 4 h exposure to PMA at 37 degrees C. The regulation of equine CD4 expression induced by PMA was temperature dependent and revers...
An equine B cell surface antigen defined by a monoclonal antibody.
Veterinary immunology and immunopathology    July 1, 1994   Volume 42, Issue 1 91-102 doi: 10.1016/0165-2427(94)90092-2
Zhang CH, Donaldson WL, Antczak DF.A surface antigen of equine B lymphocytes was identified using the Equine Leucocyte Antigen Workshop antibody WS 65. This marker was expressed on almost all equine B cells, but not on T cells, granulocytes or thymocytes. WS 65 strongly stained cells in the follicular areas of lymph nodes and cells in the splenic nodules when tested on frozen tissue sections by immunohistochemistry. Equine leukemic T cells were not labeled by WS 65, and neither were the cells from a horse with B cell leukemia, although these latter cells carried surface immunoglobulin. Immunoprecipitation of lymphocyte membrane...
Snake antivenoms from hyperimmunized horses: comparison of the antivenom activity and biological properties of their whole IgG and F(ab’)2 fragments.
Toxicon : official journal of the International Society on Toxinology    June 1, 1994   Volume 32, Issue 6 725-734 doi: 10.1016/0041-0101(94)90341-7
Morais JF, de Freitas MC, Yamaguchi IK, dos Santos MC, da Silva WD.IgG and F(ab')2 fragments were prepared from horse plasma rich in specific antibodies against Brazilian Bothrops or Crotalus venoms. Both preparations, free of gross contamination with non-immunoglobulin proteins, were able to combine in vitro with their respective antigens, forming immune complexes at antigen excess, equivalence or antibody excess, and activating the C system, through either the classical or the alternative pathways. The IgG preparation was more effective in neutralizing the lethal factors in Bothrops or Crotalus venoms, compared with the F(ab')2 fragments. In contrast, IgG a...
Purification of a plasminogen activator from Streptococcus uberis.
FEMS microbiology letters    May 1, 1994   Volume 118, Issue 1-2 153-158 doi: 10.1111/j.1574-6968.1994.tb06818.x
Leigh JA.A protein capable of activating bovine, equine and ovine plasminogen, but not that from human or porcine plasma, was purified from culture filtrates of Streptococcus uberis (strain 0140J). Purification was achieved by ammonium sulphate precipitation followed by molecular exclusion chromatography. The elution position of the native molecule was equivalent to a molecular mass of approximately 57 kDa. However, the molecular mass, as determined by SDS-PAGE, was 29 kDa, suggesting the existence of a dimeric structure. Purified immunoglobulin from three out of five monoclonal antibodies raised to th...
Specific immune responses are required to control parasitemia in Babesia equi infection.
Infection and immunity    May 1, 1994   Volume 62, Issue 5 1909-1913 doi: 10.1128/iai.62.5.1909-1913.1994
Knowles DP, Kappmeyer LS, Perryman LE.Horses possessing a normal immune system and spleen often control infection caused by Babesia equi. However, splenectomized horses are unable to control B. equi infection and usually succumb to the infection. To investigate the role of the spleen in the control of B. equi infection in the absence of specific immune responses, two 1-month-old foals with severe combined immunodeficiency (SCID) and two age-matched normal foals were inoculated with B. equi. The SCID foals became febrile seven days postinoculation and developed terminal parasitemias of 41 and 29%. The SCID foals had greater than 50...
Caprylic acid fractionation of hyperimmune horse plasma: description of a simple procedure for antivenom production.
Toxicon : official journal of the International Society on Toxinology    March 1, 1994   Volume 32, Issue 3 351-363 doi: 10.1016/0041-0101(94)90087-6
Rojas G, Jiménez JM, Gutiérrez JM.A simple methodology for hyperimmune horse plasma fractionation, based on caprylic acid precipitation, is described. Optimal conditions for fractionation were studied; the method gives best results when concentrated caprylic acid was added to plasma, whose pH had been adjusted to 5.8, until a final caprylic acid concentration of 5% was reached. The mixture was vigorously stirred during caprylic acid addition and then for 60 min; afterwards the mixture was filtered. Non-immunoglobulin proteins precipitated in these conditions, whereas a highly enriched immunoglobulin preparation was obtained in...
Duration of protective efficacy of equine influenza immunostimulating complex/tetanus vaccines.
The Veterinary record    February 12, 1994   Volume 134, Issue 7 158-162 doi: 10.1136/vr.134.7.158
Mumford JA, Jessett DM, Rollinson EA, Hannant D, Draper ME.Seven previously untreated five-month-old New Forest ponies received two doses of equine influenza immunostimulating complex vaccines, one with and one without an immunopurified tetanus toxoid component, given by deep intramuscular injection six weeks apart, followed by a booster dose without tetanus toxoid five months later. Fifteen months after the third dose of vaccine, the ponies were challenged by exposure to an aerosol of influenza A/Equine 2/Sussex/89 (H3N8), a virus isolated from a recent outbreak of influenza A/equine 2 in Britain. The challenge produced severe clinical signs of influ...
Granulomatous enteritis and cutaneous arteritis in a horse.
Journal of the American Veterinary Medical Association    December 1, 1993   Volume 203, Issue 11 1573-1575 
Woods PR, Helman RG, Schmitz DG.A 5-year-old Quarter Horse mare was examined because of weight loss of 2 months' duration. The horse was anemic and in poor body condition, and had several areas of cutaneous ulceration, including areas on the muzzle and distal portion of the limbs. Histologic examination of a rectal mucosa biopsy specimen revealed a lymphoplasmacytic infiltrate in the lamina propria mucosa. Results of a glucose absorption test were suggestive of malabsorption. Histologic examination of a biopsy specimen from the cutaneous lesions revealed pronounced arteritis, and weak, patchy immunofluorescent staining for i...
Preventive administration of bovine colostral immunoglobulins for foal diarrhea with rotavirus.
The Journal of veterinary medical science    December 1, 1993   Volume 55, Issue 6 1039-1040 doi: 10.1292/jvms.55.1039
Watanabe T, Ohta C, Shirahata T, Goto H, Tsunoda N, Tagami M, Akita H.Foal diarrhea due to serotype 3 rotavirus broke out on a foal-raising farm in the years 1987 and 1989. In 1989, all of the foals, regardless of whether or not they suffered from diarrhea, received bovine colostral immunoglobulin (Ig) powder orally for 3 to 5 days during the epidemic. The morbidity of the diarrhea was lower than that observed in 1987, when the Ig powder was not administered to foals. These data suggested that the administration of Ig powder might partially prevent foal diarrhea with rotavirus infection.
Serologic evidence of canine and equine ehrlichiosis in northeastern United States.
Journal of clinical microbiology    November 1, 1993   Volume 31, Issue 11 2857-2860 doi: 10.1128/jcm.31.11.2857-2860.1993
Magnarelli LA, Anderson JF.In a retrospective study, indirect fluorescent-antibody staining methods were used to detect immunoglobulins to Ehrlichia canis and Ehrlichia risticii in canine and equine sera that had originally been analyzed for antibodies to Borrelia burgdorferi. Analyses of 60 dog serum specimens collected in Connecticut and New York State during 1986 revealed antibodies to E. canis in 7 (11.7%) specimens; titration endpoints ranged from 1:40 to 1:320. Three of these dogs had anemia. Of the 187 equine serum specimens obtained in Connecticut during 1985 and analyzed by indirect fluorescent-antibody stainin...
Immunologic studies of a horse with lymphosarcoma.
Veterinary immunology and immunopathology    October 1, 1993   Volume 38, Issue 3-4 229-239 doi: 10.1016/0165-2427(93)90083-g
Ansar Ahmed S, Furr M, Chickering WR, Sriranganathan N, Sponenberg DP.Immunological, clinical, and pathological investigations were conducted on a horse with lymphosarcoma. The immunological status was investigated by measuring the level of antibodies by single radial immunodiffusion test and the ability of lymphocytes to proliferate in response to mitogens. Multiple immunological abnormalities were noted in this horse. They were; (1) decreased IgM, IgG, and IgA levels in the serum despite hyperproteinemia; (2) increased in-vitro spontaneous lymphoproliferation which reflects augmented mitosis; (3) decreased lymphoproliferative response to T cell stimulants (e.g...
[The immunogenic properties of a recombinant vaccinia virus with an incorporated DNA copy of the 26S RNA of the Venezuelan equine encephalomyelitis virus].
Voprosy virusologii    September 1, 1993   Volume 38, Issue 5 222-226 
Sviatchenko VA, Agapov EV, Urmanov IKh, Serpinskiĭ OI, Frolov IV, Kolykhalov AA, Ryzhikov AB, Netesov SV.A recombinant strain of vaccinia virus (VR26) containing a DNA-copy of the subgenomic 26S RNA of Venezuelan equine encephalomyelitis virus (VEE) inserted into the coding region of thymidine kinase (TK) gene was produced. This subgenomic RNA contained the genes for all structural proteins of the VEE virus, the strain Trinidad donkey (TRD). VR26 effectively expressed VEE virus glycoproteins on the membranes of the infected cells. Blood sera of VR26-immunized animals were found to contain VEE virus-specific antibodies. VR26-immunized mice and rabbits showed a high level of resistance to subcutane...
Comparative studies of the Spi1 proteins of three equine alpha-1-proteinase inhibitor haplotypes following isolation by affinity chromatography.
The International journal of biochemistry    September 1, 1993   Volume 25, Issue 9 1263-1268 doi: 10.1016/0020-711x(93)90077-r
Pemberton AD, Miller HR, John HA, Scudamore CL.1. Antiproteinase deficiency can result in excessive proteinase-induced tissue damage. The major anti-elastase (Spi1) protein of equine alpha 1-proteinase inhibitor (alpha 1-PI) was isolated from the plasma/serum of three common haplotypes (I, L and U). 2. The N-terminal amino acid sequences of the three inhibitors were identical, but were only approx 65-77% homologous with two other published equine Spi1 sequences. 3. All three inhibitors complexed quickly and irreversibly with equine leucocyte proteinase 2A (kass = 2 x 10(7) M-1 sec-1). They were also efficient inhibitors of chymase (rat mas...
Synteny mapping in the horse using horse-mouse heterohybridomas.
Animal genetics    August 1, 1993   Volume 24, Issue 4 257-260 doi: 10.1111/j.1365-2052.1993.tb00308.x
Williams H, Richards CM, Konfortov BA, Miller JR, Tucker EM.In a study of 35 horse-mouse heterohybridoma cell lines, synteny in the horse was found between LDHB, PEPB and IGF1 and between NP, MPI and IDH2. A synteny between ADA and PEPC was also indicated. The loci for horse immunoglobulin light chain (IgL) genes and for LDHA were independent.
[Foal diseases and foal loss].
Tierarztliche Praxis    June 1, 1993   Volume 21, Issue 3 233-238 
Thein P, Essich G.An investigation was carried out upon occurrence and course of infectious and non infectious diseases as well as the mortality in foals born and raised at the State Stud Marbach/Lauter between 1982 and 1991. The foals have been investigated from birth to weaning, they consisted of 177 Thoroughbred Arabians and 285 German Warmblood foals (total 462 foals). The diseases were divided into pre-, peri- and postnatal according to their known or assumed cause and onset. There was a preponderance of prenatal diseases (11.25%) whereas the perinatal rate was 1.30% and the postnatal rate of diseases was ...
An immunohistological study of MHC class II expression and T lymphocytes in the endometrium of the mare.
Equine veterinary journal    March 1, 1993   Volume 25, Issue 2 120-124 doi: 10.1111/j.2042-3306.1993.tb02920.x
Watson ED, Dixon CE.The distribution of T lymphocytes and of cells bearing MHC Class II antigens in the endometrium of the mare was studied using an avidin-biotin-peroxidase staining method. The cells within the endometrium which expressed MHC Class II were macrophages, lymphocytes, monocytes, dendritic cells, epithelial cells and endothelial cells. MHC Class II expression increased significantly (P < 0.05) in the luminal epithelium and tended (P = 0.0573) to increase in the subepithelial layers during oestrus. Numbers of T lymphocytes did not differ between oestrus and dioestrus. MHC Class II expression and T...
L chain isotype regulation in horse. I. Characterization of Ig lambda genes.
Journal of immunology (Baltimore, Md. : 1950)    December 15, 1992   Volume 149, Issue 12 3927-3936 
Home WA, Ford JE, Gibson DM.Analysis of 10 cDNA encoding lambda L chains of horse Ig indicated that this species may employ a relatively small number of variable region (V lambda) genes in the splenic B cell population. The V lambda sequences of all of the cDNA analyzed were closely related (> 88% identity at the nucleotide level) and were characterized by a deletion of the amino acid residue at position 3 compared with V lambda sequences so far described in other species. The 10 V lambda sequences could be grouped into three groups, V lambda 1 to V lambda 3, on the basis of a number of linked substitutions. Sequences...
Selective IgM deficiency and abnormal B-cell response in a foal.
Journal of the American Veterinary Medical Association    November 1, 1992   Volume 201, Issue 9 1396-1398 
Weldon AD, Zhang C, Antczak DF, Rebhun WC.Selective IgM deficiency was diagnosed in a 3-month-old Standardbred colt that was referred for chronic respiratory tract disease. Immunoglobulin quantification revealed normal IgG and IgA concentrations, but undetectable IgM concentration. Stimulation of blood lymphocytes with the T-cell mitogens concanavalin A and phytohemagglutinin yielded results within the normal range. However, stimulation with the B-cell mitogen lipopolysaccharide produced no response. A B-cell defect similar to that associated with several immunodeficiency disorders in people was suggested as the cause of the IgM defic...
Immune responses of specific pathogen free foals to EHV-1 infection.
Veterinary microbiology    October 1, 1992   Volume 32, Issue 3-4 215-228 doi: 10.1016/0378-1135(92)90146-k
Chong YC, Duffus WP.Four foals were raised under specific pathogen free (SPF) conditions. At 3 to 4 months of age, SPF foals and 1 other non-SPF foal were intranasally inoculated with equine herpes virus type 1 (EHV-1). Clinical signs included depression, fever, inappetence and intermittent coughing. Clinical recovery was complete by seven days but high titres of virus were detected in nasal mucus for at least 10 days after inoculation. Clinical illness was less severe in the non-SPF foal. Interferon was detected in the nasal mucus of all foals from 2 days post infection (dpi), persisting until 8 or 10 dpi. ELISA...
In vitro production of specific antibody by equine peripheral blood mononuclear cells using tetanus toxoid as a recall antigen.
Research in veterinary science    September 1, 1992   Volume 53, Issue 2 184-190 doi: 10.1016/0034-5288(92)90108-e
O'Brien MA, Holmes MA, Duffus WP.Anti-tetanus toxoid (TT) antibody (Ig) levels in the supernatant of cultured, pre-immunised equine peripheral blood mononuclear cells (PBMC) were measured by an indirect enzyme-linked immunoabsorbent assay (ELISA). Optimal anti-TT Ig production occurred at concentrations of stimulating, purified TT of between 0.001 and 0.1 micrograms ml-1, which varied depending on the cell concentration. Optimal anti-TT Ig production was most consistently produced when the cell concentration was 5 x 10(6) ml-1. At this cell concentration maximal anti-TT Ig was induced using 0.1 micrograms ml-1 TT. At a cell c...
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