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  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
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  • A61K39/295—Polyvalent viral antigens; Mixtures of viral and bacterial antigens
• • A—HUMAN NECESSITIES
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• • A—HUMAN NECESSITIES
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  • A61K39/02—Bacterial antigens
  • A61K39/0225—Spirochetes, e.g. Treponema, Leptospira, Borrelia
• • A—HUMAN NECESSITIES
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• • A—HUMAN NECESSITIES
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  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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• • A—HUMAN NECESSITIES
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  • A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
• • A—HUMAN NECESSITIES
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  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
  • A61K2039/52—Bacterial cells; Fungal cells; Protozoal cells
  • A61K2039/521—Bacterial cells; Fungal cells; Protozoal cells inactivated (killed)
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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  • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
  • A61K2039/525—Virus
  • A61K2039/5254—Virus avirulent or attenuated
• • A—HUMAN NECESSITIES
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• • A—HUMAN NECESSITIES
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  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K2039/70—Multivalent vaccine
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  • C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
  • C12N2710/00011—Details
  • C12N2710/16011—Herpesviridae
  • C12N2710/16711—Varicellovirus, e.g. human herpesvirus 3, Varicella Zoster, pseudorabies
  • C12N2710/16734—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
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  • C12N2760/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses negative-sense
  • C12N2760/00011—Details
  • C12N2760/18011—Paramyxoviridae
  • C12N2760/18511—Pneumovirus, e.g. human respiratory syncytial virus
  • C12N2760/18534—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
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  • C12N2760/00011—Details
  • C12N2760/18011—Paramyxoviridae
  • C12N2760/18611—Respirovirus, e.g. Bovine, human parainfluenza 1,3
  • C12N2760/18634—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
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  • C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
  • C12N2770/00011—Details
  • C12N2770/24011—Flaviviridae
  • C12N2770/24311—Pestivirus, e.g. bovine viral diarrhea virus
  • C12N2770/24334—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S424/00—Drug, bio-affecting and body treating compositions
  • Y10S424/813—Viral vaccine for bovine species, e.g. cattle
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S424/00—Drug, bio-affecting and body treating compositions
  • Y10S424/823—Bacterial vaccine for bovine species, e.g. cattle

Definitions

• the present invention relates to compositions, uses thereof, and methods of vaccinating cattle, particularly cows and heifers, against Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) by using Leptospira interrogans serovar hardjo (type hardjoprajitno ).
• Leptospirosis is the most widespread zoonotic disease in the world. It affects most mammals and is an important cause of reproductive failure in cattle throughout the world.
• Leptospires are gram-negative, thin, helical bacteria classified into at least twelve pathogenic and four saprophytic species, with more than 250 pathogenic serovars. The bacteria may survive in the environment for up to six months, preferably in basic soils (pH of 7.2 to 8.0) and in a warm, moist environment. The bacteria rarely survive in dry or extreme cold conditions. (See Faine et al., 1999; Heath and Johnson, 1994.)
• Pathogenic species persist as chronic infections of the renal tubules of the maintenance host, sometimes causing very little or no disease. Transmission occurs through direct contact with infected urine or by contact through feed or bedding contaminated with infected urine. In cattle, common clinical signs of the disease include reproductive failure, weak calves, abortion, stillbirths, mummification, and agalactia. Shedding of the bacteria in urine may occur for extended lengths of time. Renal lesions may be the direct result of leptospiremia from infection with Leptospira serovars hardjo, pomona , and grippotyphosa . (See Faine et al., 1999; Heath and Johnson, 1994; Ellis, 1994.)
• LHP Leptospira interrogans serovar hardjo
• LHB Leptospira borgpetersenii serovar hardjo
• LHP is found primarily in Europe, whereas the most common cause of leptospirosis in cattle throughout much of the world is LHB.
• LHB is the only hardjo serovar that has been isolated to date from cattle in the United States. (Bolin, et. al., 1989(a).)
• Vaccination with whole cell inactivated leptospiral vaccine containing Leptospira serovars hardjo, canicola, pomona, grippotyphosa , and icterohaemorrhagiae is the primary means of controlling leptospirosis in cattle. Because the costs associated with the manufacture of a vaccine are directly related to the type(s) and number of components used to formulate the vaccine, it is desirable to reduce the number of components in the vaccine without loss of vaccine effectiveness.
• the present invention provides immieuxic compositions, vaccines, and related methods and uses that overcome deficiencies in the art.
• the compositions, methods, and uses provide protection against, reduction in the incidence, and/or lessen the severity of infection by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) by vaccinating with Leptospira interrogans serovar hardjo (type hardjoprajitno ).
• Immunogenic compositions and vaccines of the invention comprise a Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria capable of provoking an immune response against Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• the Leptospira interrogans serovar hardjo is a killed bacterium or bacteria.
• Immunogenic compositions and vaccines of the invention can further comprise one or more modified live viruses (MLVs) selected from the group consisting of Infectious Bovine Rhinotracheitis (IBR) virus, Bovine Virus Diarrhea (BVD) Types 1 and 2, Parainfluenza 3 (PI3) virus, and Bovine Respiratory Syncytial Virus (BRSV).
• MMVs modified live viruses selected from the group consisting of Infectious Bovine Rhinotracheitis (IBR) virus, Bovine Virus Diarrhea (BVD) Types 1 and 2, Parainfluenza 3 (PI3) virus, and Bovine Respiratory Syncytial Virus (BRSV).
• IBR Infectious Bovine Rhinotracheitis
• BBD Bovine Virus Diarrhea
• PI3 Parainfluenza 3
• BRSV Bovine Respiratory Syncytial Virus
• Preferred immunogenic compositions and vaccines include a combination of killed Leptospira interrogans serovar hardjo (type hardjoprajitno ), modified live Infectious Bovine Rhinotracheitis (IBR) virus, modified live Bovine Virus Diarrhea (BVD) Type 1 and modified live BVD Type 2—such as the licensed commercially available combination product, Express FP® 3 VL5, Boehringer Ingelheim Vetmedica, Inc., St. Joseph.
• Immunogenic compositions and vaccines of the invention may also comprise modified live Bovine Respiratory Syncytial Virus (BRSV), or a combination of killed Campylobacter Fetus, Haemophilus somnus , and any of Leptospira serovars canicola, grippotyphosa, hardjo, icterohaemorrhagiae , and pomona.
• BRSV Bovine Respiratory Syncytial Virus
• Immunogenic compositions and vaccines of the invention provide protection against, reduction in the incidence, and/or lessens the severity of infection by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) in a subject.
• the subject is a bovine, more preferably the bovine is a cow or heifer, most preferably the bovine is a heifer.
• Immunogenic compositions of the invention which comprise at least one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria as defined herein may further comprise a physiologically-acceptable vehicle such as a pharmaceutically or veterinarily acceptable carrier, adjuvant, or combination thereof.
• a physiologically-acceptable vehicle such as a pharmaceutically or veterinarily acceptable carrier, adjuvant, or combination thereof.
• Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacteria provided herewith or any immunogenic compositions comprising one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria provided herewith can be used as a medicament, preferably as a vaccine or immunogenic composition, most preferably for the prophylaxis or treatment of a subject against a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection.
• compositions used herein may incorporate known injectable, physiologically acceptable sterile solutions.
• aqueous isotonic solutions e.g. saline or plasma protein solutions
• the immunogenic and vaccine compositions of the present invention can include veterinary-acceptable carriers, diluents, isotonic agents, stabilizers, or adjuvants.
• the invention also provides methods, as well as uses of the compositions of the invention, for providing protection against, reduction in the incidence, and/or lessening the severity of infection by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) in a subject comprising administering to the subject an immunogenic composition or vaccine, wherein the immunogenic composition or vaccine includes a Leptospira interrogans serovar hardjo (type hardjoprajitno ).
• Methods of the invention, as well as uses of the compositions of the invention include, but are not limited to, a method of or use for provoking an immune response against a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection in a subject comprising the step of administering to the subject an immunogenic composition comprising one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria as defined herein.
• the immune response is provoked against more than one serotype or strain of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• compositions of the invention may be used to treat or alternatively to prevent a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection.
• a Leptospira borgpetersenii serovar hardjo type hardjo - bovis
• such immune response reduces the incidence of or severity of one or more clinical signs associated with or caused by the infection with one or more Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) serotypes.
• compositions of the invention may be administered.
• animals and humans in need of either prophylactic or treatment for a viral, microbial, parasitic, protozoan, bacterial, or fungal associated infection, disease, or condition.
• Animals in which the immune response is stimulated by use of compositions or methods of the invention include livestock, such as swine, bovines, poultry (e.g. chickens, ducks, geese, or turkeys) goats, and sheep, and domestic animals, such as mice, rabbits, dogs, cats, and horses.
• Preferred animals include bovines, most preferably cows and heifers.
• the invention also provides a method, as well as a use of the compositions of the invention, of reducing the incidence of or severity of one or more clinical signs associated with or caused by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection, comprising the step of administering an immunogenic composition of the invention that comprises one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria as provided herewith and preferably a carrier molecule, such that the incidence of or the severity of a clinical sign of the Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection is reduced by at least 10%, preferably by at least 20%, even more preferably by at least 30%, even more preferably by at least 50%, still more preferably by at least 70%, and most preferably by 100% relative to a subject that has not received the immunogenic composition as provided herewith.
• the present invention also relates to a method, as well as a use of the compositions of the invention, for the prophylaxis of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection comprising the step of administering an immunogenic composition of the invention that comprises one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) as provided herewith.
• Another aspect of the invention provides a method of producing one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria that induce an immune response against at least one serotype of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ), and more preferably two or more serotypes of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• This method comprises culturing a transformed expression vector coding for and expressing one or more of the Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria disclosed herein.
• the expressed bacterium or bacteria are either retained by the expression organism or secreted into the culture medium. Expression is conducted under conditions sufficient to produce Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacteria capable of inducing an immune response to Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• compositions of the invention may further comprise admixing one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria and a carrier molecule with a physiologically-acceptable vehicle such as a pharmaceutically- or veterinary-acceptable carrier, adjuvant, or combination thereof.
• a physiologically-acceptable vehicle such as a pharmaceutically- or veterinary-acceptable carrier, adjuvant, or combination thereof.
• the invention provides a method, as well as a use of the compositions of the invention, of diagnosing a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection in a subject.
• the method and use comprise providing one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria; contacting the one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria with a sample obtained from the subject; and identifying the subject as having a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection if an antibody capable of binding the one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria is detected in the sample.
• kits that comprise an immunogenic composition that comprises one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria, optionally together with a carrier molecule; a container for packaging the immunogenic composition; a set of printed instructions; and a dispenser capable of administering the immunogenic composition to an animal.
• the one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria and the carrier molecule may be packaged as together or as separate compounds.
• kits for vaccinating an animal comprising a set of printed instructions; a dispenser capable of administering the immunogenic composition provided herewith comprising one or more Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria to an animal; and wherein at least one of Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria effectively immunizes the animal against at least one disease associated with Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection.
• kits of the invention may further comprise a veterinary acceptable carrier, adjuvant, or combination thereof.
• the dispenser in a kit of the invention is capable of dispensing its contents as droplets; and the immunogenic composition comprises the Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria as provided herewith included in the kit is capable of reducing the severity of at least one clinical sign of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection when administered subcutaneously, intranasally, intradermally, or intramuscularly to an animal.
• the immunogenic composition comprises the Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria as provided herewith included in the kit is capable of reducing the severity of at least one clinical sign of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection when administered subcutaneously, intranasally, intradermally, or intramuscularly to an animal.
• the severity of a clinical sign is reduced by at least 10% preferably by at least 20%, even more preferably by at least 30%, even more preferably by at least 50%, still more preferably by at least 70%, and most preferably by 100% as compared to an untreated, infected animal.
• compositions of the invention for the treatment or prophylaxis of infections caused by Leptospira borgpetersenii serovar hardjo are also disclosed.
• the methods and uses comprise administering an effective amount of a Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria to a subject, wherein said treatment or prophylaxis is selected from the group consisting of reducing signs of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection, reducing the severity of or incidence of clinical signs of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection, reducing the mortality of subjects from Leptospira borgpetersenii serovar hardjo (type hardjo -bovis) infection, and combinations thereof.
• compositions of the invention further comprise a veterinarily acceptable carrier, adjuvant, or combination thereof.
• a veterinarily acceptable carrier may be used as a vaccine and comprise an attenuated vaccine, an inactivated vaccine, or combinations thereof.
• Such vaccines elicit a protective immunological response against at least one disease or clinical symptom associated with a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection.
• compositions used herein may incorporate known injectable, physiologically acceptable sterile solutions.
• aqueous isotonic solutions e.g. saline or plasma protein solutions
• the immunogenic and vaccine compositions of the present invention can include pharmaceutical- or veterinary-acceptable carriers, diluents, isotonic agents, stabilizers, or adjuvants.
• Methods and uses of the invention may also comprise admixing a composition of the invention with a veterinarily acceptable carrier, adjuvant, or combination thereof.
• a veterinarily acceptable carrier for example, a benzyl alcohol, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl, sulfonate, benzyl, sulfate, sulfate, sulfate, stearate, stearate, stearate, stearate, stearate, benzyl sulfate, sulfate, benzyl sulfate, benzyl sulfate, sulfate, benzyl sulfate, sulfate, benzyl sulfonylurea sulfonylurea sulfony
• the invention also provides a method or use of the invention for reducing the severity of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection in an animal comprising administrating to the animal a composition that comprises a Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria.
• compositions of the invention for the treatment or prophylaxis of infections caused by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) are also disclosed.
• the method comprises administering an effective amount of the Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria of the present invention to an animal.
• compositions of the invention may also be administered in two or more doses, as well as, by other routes of administration.
• routes of administration include subcutaneously, intracutaneously, intravenously, intravascularly, intraarterially, intraperitnoeally, intrathecally, intratracheally, intracardially, intralobally, intramedullarly, intrapulmonarily, or intravaginally.
• the compositions according to the invention may be administered once or several times, also intermittently, for instance on a daily basis for several days, weeks or months and in different dosages.
• kits for vaccinating an animal comprising a set of printed instructions; a dispenser capable of administering a vaccine to an animal; and at least one killed Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium or bacteria that effectively immunizes the animal against at least one disease associated with Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• Kits of the invention may further comprise a veterinarily acceptable carrier, adjuvant, or combination thereof.
• the dispenser in a kit of the invention is capable of dispensing its contents as droplets; and the isolate included in the kit is capable of reducing the severity of at least one clinical sign of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection when administered intranasally, orally, intradermally, or intramuscularly to an animal.
• the isolate is also capable of reducing the severity of at least one clinical sign of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection.
• the severity of a clinical sign is reduced by at least 10% as compared to an untreated, infected animal.
• the present invention provides immisseic compositions, vaccines, and related methods and uses that provide protection against, reduce the incidence, and/or lessen the severity of infection by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) by vaccinating with Leptospira interrogans serovar hardjo (type hardjoprajitno ).
• the present invention demonstrates the ability of the LHP component of two different combination vaccines to protect against challenge with LHB.
• Post-challenge culture results showed that none of the vaccinated heifers in either vaccine treatment group (Groups 1 and 2, Example 1) had infection as a result of challenge (see Tables 2 and 6, Example 1). These results were in sharp contrast to the placebo control vaccinated animals where 100% of the heifers became infected (see Tables 2, 3 and 5, Example 1).
• the level of protection provided by a vaccine will depend not only on the specifics of the serovar/strain of the organism contained in the vaccine, but also on the adjuvant, if any, used in the formulation of the vaccine.
• the vaccines used included an adjuvant(s).
• growth and inactivation conditions utilized for production of the strain can also impact the efficacy provided by the vaccine.
• Serovar differences combined with adjuvant formulation and organism processing for the vaccine can effect the ability of the vaccine to induce a protective immune response. Any or all of these factors combined may account for the prior failures of others and the success of the present invention.
• Vaccination with both the modified live viral/LHP bacterin combination and killed viral/LHP bacterin combination resulted in prevention of urine shedding as well as prevention of renal infection and colonization after challenge with LHB.
• the results of this study show that the L. hardjo component of the test vaccines is highly efficacious against challenge induced renal infection and colonization and associated urinary shedding due to LHB.
• “Protection against disease”, “protective immunity”, “functional immunity” and similar phrases means a response against a disease or condition generated by administration of one or more therapeutic compositions of the invention, or a combination thereof, that results in fewer deleterious effects than would be expected in a non-immunized subject that has been exposed to disease or infection. That is, the severity of the deleterious effects of the infection are lessened in a vaccinated subject. Infection may be reduced, slowed, or possibly fully prevented, in a vaccinated subject.
• complete prevention of infection is meant, it is specifically stated. If complete prevention is not stated then the term includes partial prevention.
• “reduction of the incidence and/or severity of clinical signs” or “reduction of clinical symptoms” means, but is not limited to, reducing the number of infected subjects in a group, reducing or eliminating the number of subjects exhibiting clinical signs of infection, or reducing the severity of any clinical signs that are present in one or more subjects, in comparison to wild-type infection.
• these clinical signs are reduced in one or more subjects receiving the therapeutic composition of the present invention by at least 10% in comparison to subjects not receiving the composition and that become infected. More preferably clinical signs are reduced in subjects receiving a composition of the present invention by at least 20%, preferably by at least 30%, more preferably by at least 40%, and even more preferably by at least 50%.
• the term “increased protection” herein means, but is not limited to, a statistically significant reduction of one or more clinical symptoms which are associated with infection by an infectious agent, preferably a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ), respectively, in a vaccinated group of subjects vs. a non-vaccinated control group of subjects.
• infectious agent preferably a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis )
• statically significant reduction of clinical symptoms means, but is not limited to, the frequency in the incidence of at least one clinical symptom in the vaccinated group of subjects is at least 10%, preferably 20%, more preferably 30%, even more preferably 50%, and even more preferably 70% lower than in the non-vaccinated control group after the challenge the infectious agent.
• “Long-lasting protection” shall refer to “improved efficacy” that persists for at least 3 weeks, but more preferably at least 3, 4, 5, 6, or 7 months, still more preferably 8, 9, 10, 11, or 12 months, still even more preferably 13, 14, 15, 16, 17, or 18 months, and most preferably 19 months or longer.
• livestock it is most preferred that the long lasting protection shall persist until the average age at which animals are marketed for meat.
• the long lasting protection shall persist until the average age at which the animals are retired from breeding and marketed.
• an “immunogenic or immunological composition” refers to a composition of matter that comprises at least one Leptospira interrogans serovar hardjo (type hardjoprajitno ), or immunogenic portion thereof, that elicits an immunological response in the host of a cellular or antibody-mediated immune response to the composition.
• an immunogenic composition induces an immune response and, more preferably, confers protective immunity against one or more of the clinical signs of a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection.
• an “immune response” or “immunological response” means, but is not limited to, the development of a cellular and/or antibody-mediated immune response to the composition or vaccine of interest.
• an immune or immunological response includes, but is not limited to, one or more of the following effects: the production or activation of antibodies, B cells, helper T cells, suppressor T cells, and/or cytotoxic T cells, directed specifically to an antigen or antigens included in the composition or vaccine of interest.
• the host will display either a therapeutic or a protective immunological (memory) response such that resistance to new infection will be enhanced and/or the clinical severity of the disease reduced.
• Such protection will be demonstrated by either a reduction in number of symptoms, severity of symptoms, or the lack of one or more of the symptoms associated with the infection of the pathogen, a delay in the of onset of viremia, reduced viral persistence, a reduction in the overall viral load and/or a reduction of viral excretion.
• specifically immunoreactive refers to an immunoreactive protein or polypeptide that recognizes an antigen characteristic of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection but does not react with an antigen characteristic of a strict challenge control.
• a pharmaceutical- or veterinary-acceptable carrier includes any and all solvents, dispersion media, coatings, adjuvants, stabilizing agents, diluents, preservatives, antibacterial and antifungal agents, isotonic agents, adsorption delaying agents, and the like.
• stabilizing agents for use in the present invention include stabilizers for lyophilization or freeze-drying.
• the immunogenic composition of the present invention contains an adjuvant.
• adjuvants can include aluminum hydroxide and aluminum phosphate, saponins e.g., Quil A, QS-21 (Cambridge Biotech Inc., Cambridge Mass.), GPI-0100 (Galenica Pharmaceuticals, Inc., Birmingham, Ala.), water-in-oil emulsion, oil-in-water emulsion, water-in-oil-in-water emulsion.
• the emulsion can be based in particular on light liquid paraffin oil (European Pharmacopea type); isoprenoid oil such as squalane or squalene; oil resulting from the oligomerization of alkenes, in particular of isobutene or decene; esters of acids or of alcohols containing a linear alkyl group, more particularly plant oils, ethyl oleate, propylene glycol di-(caprylate/caprate), glyceryl tri-(caprylate/caprate) or propylene glycol dioleate; esters of branched fatty acids or alcohols, in particular isostearic acid esters.
• light liquid paraffin oil European Pharmacopea type
• isoprenoid oil such as squalane or squalene
• oil resulting from the oligomerization of alkenes in particular of isobutene or decene
• the oil is used in combination with emulsifiers to form the emulsion.
• the emulsifiers are preferably nonionic surfactants, in particular esters of sorbitan, of mannide (e.g. anhydromannitol oleate), of glycol, of polyglycerol, of propylene glycol and of oleic, isostearic, ricinoleic or hydroxystearic acid, which are optionally ethoxylated, and polyoxypropylene-polyoxyethylene copolymer blocks, in particular the Pluronic products, especially L121.
• mannide e.g. anhydromannitol oleate
• glycol of polyglycerol
• propylene glycol and of oleic isostearic, ricinoleic or hydroxystearic acid, which are optionally ethoxylated, and polyoxypropylene-polyoxyethylene copolymer blocks, in particular the Pluronic products
• Vaccine 15:564-570 exemplary adjuvants are the SPT emulsion described on page 147 of “Vaccine Design, The Subunit and Adjuvant Approach” edited by M. Powell and M. Newman, Plenum Press, 1995, and the emulsion MF59 described on page 183 of this same book.
• an adjuvant is a compound chosen from the polymers of acrylic or methacrylic acid and the copolymers of maleic anhydride and alkenyl derivative.
• Advantageous adjuvant compounds are the polymers of acrylic or methacrylic acid which are cross-linked, especially with polyalkenyl ethers of sugars or polyalcohols. These compounds are known by the term carbomer (Phameuropa Vol. 8, No. 2, June 1996). Persons skilled in the art can also refer to U.S. Pat. No.
• 2,909,462 which describes such acrylic polymers cross-linked with a polyhydroxylated compound having at least 3 hydroxyl groups, preferably not more than 8, the hydrogen atoms of at least three hydroxyls being replaced by unsaturated aliphatic radicals having at least 2 carbon atoms.
• the preferred radicals are those containing from 2 to 4 carbon atoms, e.g. vinyls, allyls and other ethylenically unsaturated groups.
• the unsaturated radicals may themselves contain other substituents, such as methyl.
• the products sold under the name Carbopol; (BF Goodrich, Ohio, USA) are particularly appropriate. They are cross-linked with an allyl sucrose or with allyl pentaerythritol.
• Carbopol 974P, 934P and 971P there may be mentioned Carbopol 974P, 934P and 971P. Most preferred is the use of Cabopol 971P.
• copolymers of maleic anhydride and alkenyl derivative are the copolymers EMA (Monsanto), which are copolymers of maleic anhydride and ethylene. The dissolution of these polymers in water leads to an acid solution that will be neutralized, preferably to physiological pH, in order to give the adjuvant solution into which the immunogenic, immunological or vaccine composition itself will be incorporated.
• Suitable adjuvants include, but are not limited to, the RIBI adjuvant system (Ribi Inc.), Block co-polymer (CytRx, Atlanta Ga.), SAF-M (Chiron, Emeryville Calif.), monophosphoryl lipid A, Avridine lipid-amine adjuvant, heat-labile enterotoxin from E. coli (recombinant or otherwise), cholera toxin, IMS 1314 or muramyl dipeptide, or naturally occurring or recombinant cytokines or analogs thereof or stimulants of endogenous cytokine release, among many others.
• an adjuvant can be added in an amount of about 100 ⁇ g to about 10 mg per dose, preferably in an amount of about 100 ⁇ g to about 10 mg per dose, more preferably in an amount of about 500 ⁇ g to about 5 mg per dose, even more preferably in an amount of about 750 ⁇ g to about 2.5 mg per dose, and most preferably in an amount of about 1 mg per dose.
• the adjuvant may be at a concentration of about 0.01 to 50%, preferably at a concentration of about 2% to 30%, more preferably at a concentration of about 5% to 25%, still more preferably at a concentration of about 7% to 22%, and most preferably at a concentration of 10% to 20% by volume of the final product.
• “Diluents” can include water, saline, dextrose, ethanol, glycerol, and the like.
• Isotonic agents can include sodium chloride, dextrose, mannitol, sorbitol, and lactose, among others.
• Stabilizers include albumin and alkali salts of ethylendiamintetracetic acid, among others.
• Safety refers to the absence of adverse consequences in a vaccinated animal following vaccination, including but not limited to: potential reversion of a bacterium-based vaccine to virulence, clinically significant side effects such as persistent, systemic illness or unacceptable inflammation at the site of vaccine administration.
• vaccination or “vaccinating” or variants thereof, as used herein means, but is not limited to, a process which includes the administration of an immunogenic composition of the invention that, when administered to an animal, elicits, or is able to elicit—directly or indirectly—, an immune response in the animal against Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• “Mortality”, in the context of the present invention, refers to death caused by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infection, and includes the situation where the infection is so severe that an animal is euthanized to prevent suffering and provide a humane ending to its life.
• Attenuation means reducing the virulence of a pathogen.
• attenuation is synonymous with “avirulent”.
• an attenuated bacterium is one in which the virulence has been reduced so that it does not cause clinical signs of a Leptospirosis but is capable of inducing an immune response in the target mammal, but may also mean that the clinical signs are reduced in incidence or severity in animals infected with the attenuated Leptospira interrogans serovar hardjo (type hardjoprajitno ) in comparison with a “control group” of animals infected with non-attenuated Leptospira interrogans serovar hardjo (type hardjoprajitno ) and not receiving the attenuated bacterium.
• an attenuated, avirulent Leptospira interrogans serovar hardjo (type hardjoprajitno ) strain is one that suitable for incorporation into an immunogenic composition comprising a modified live Leptospira interrogans serovar hardjo (type hardjoprajitno ) bacterium.
• an effective dose means, but is not limited to, an amount of antigen that elicits, or is able to elicit, an immune response that yields a reduction of clinical symptoms in an animal to which the antigen is administered.
• an effective amount means, in the context of a composition, an amount of an immunogenic composition capable of inducing an immune response that reduces the incidence of or lessens the severity of infection or incident of disease in an animal. Particularly, an effective amount refers to colony forming units (CFU) per dose.
• CFU colony forming units
• the term “effective amount” refers to the amount of a therapy which is sufficient to reduce or ameliorate the severity or duration of a disease or disorder, or one or more symptoms thereof, prevent the advancement of a disease or disorder, cause the regression of a disease or disorder, prevent the recurrence, development, onset, or progression of one or more symptoms associated with a disease or disorder, or enhance or improve the prophylaxis or treatment of another therapy or therapeutic agent.
• immunological response against Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• the immunogenic compositions provided herewith may also comprise one or more adjuvants.
• Leptospira interrogans serovar hardjo type hardjoprajitno
• the adjuvant may be purified by any of the techniques described previously or known in the art.
• the preferred purification technique is silica gel chromatography, in particular the “flash” (rapid) chromatographic technique, as described by W. Clark Still et al, J. Organic Chemistry, 43, 2923-2925 (1978).
• other chromatographic methods including HPLC, may be used for purification of the adjuvant.
• Crystallization may also be used to purify the adjuvant. In some cases, no purification is required as a product of analytical purity is obtained directly from the synthesis.
• the vaccine compositions of the invention are prepared by physically mixing the adjuvant with the Leptospira interrogans serovar hardjo (type hardjoprajitno ) under appropriate sterile conditions in accordance with known techniques to produce the adjuvanted composition. Complexation of the Leptospira interrogans serovar hardjo (type hardjoprajitno ) and the adjuvant is facilitated by the existence of a net negative charge on the conjugate which is electrostatically attracted to the positive charge present on the long chain alkyl compound adjuvant.
• an adjuvant can be added in an amount of about 100 ⁇ g to about 10 mg per dose, preferably in an amount of about 100 ⁇ g to about 10 mg per dose, more preferably in an amount of about 500 ⁇ g to about 5 mg per dose, even more preferably in an amount of about 750 ⁇ g to about 2.5 mg per dose, and most preferably in an amount of about 1 mg per dose.
• the adjuvant may be at a concentration of about 0.01% to 75%, preferably at a concentration of about 2% to 30%, more preferably at a concentration of about 5% to 25%, still more preferably at a concentration of about 7% to 22%, and most preferably at a concentration of 10% to 20% by volume of the final product.
• the vaccine compositions of this invention may be formulated using techniques similar to those used for other pharmaceutical polypeptide compositions.
• the adjuvant and Leptospira interrogans serovar hardjo may be stored in lyophilized form and reconstituted in a physiologically acceptable vehicle to form a suspension prior to administration.
• the adjuvant and conjugate may be stored in the vehicle.
• Preferred vehicles are sterile solutions, in particular, sterile buffer solutions, such as phosphate buffered saline. Any method of combining the adjuvant and the conjugate in the vehicle such that improved immunological effectiveness of the immunogenic composition is appropriate.
• the volume of a single dose of the vaccine of this invention may vary but will be generally within the ranges commonly employed in conventional vaccines.
• the volume of a single dose is preferably between about 0.1 ml and about 3 ml, preferably between about 0.2 ml and about 1.5 ml, more preferably between about 0.2 ml and about 0.5 ml at the concentrations of conjugate and adjuvant noted above.
• the vaccine compositions of the invention may be administered by any convenient, suitable means.
• Immunogenic compositions comprising Leptospira interrogans serovar hardjo (type hardjoprajitno ) can be used as vaccines for immunization against Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• the vaccines comprising the immunogenic composition in a physiologically acceptable vehicle, are useful in a method of immunizing animals, preferably cattle, preferably cows, most preferably heifers, for treatment or prevention of infections by Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• Antibodies generated against immunogenic compositions of the present invention by immunization with an immunogenic composition can be used in passive immunotherapy and generation of antiidiotypic antibodies for treating or preventing infections of Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ).
• the subject to which the composition is administered is preferably an animal, including but not limited to cows, horses, sheep, pigs, poultry (e.g. chickens), goats, cats, dogs, hamsters, mice and rats, most preferably the animal is a cow or heifer.
• cows horses, sheep, pigs, poultry (e.g. chickens), goats, cats, dogs, hamsters, mice and rats, most preferably the animal is a cow or heifer.
• the formulations of the invention comprise an effective immunizing amount of one or more immunogenic compositions or antibodies thereto and a physiologically acceptable vehicle.
• Vaccines comprise an effective immunizing amount of one or more immunogenic compositions and a physiologically acceptable vehicle.
• the formulation should suit the mode of administration.
• the immunogenic composition can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents.
• the immunogenic composition can be a liquid solution, suspension, emulsion, tablet, pill, capsule, sustained release formulation, or powder.
• Oral formulation can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, etc.
• the compounds described herein can be administered to a subject at therapeutically effective doses to treat Leptospirosis-associated diseases.
• the dosage will depend upon the host receiving the vaccine as well as factors such as the size, weight, and age of the host.
• an effective immunizing amount is that amount sufficient to treat or prevent a Leptospira borgpetersenii serovar hardjo (type hardjo - bovis ) infectious disease in a subject.
• Effective doses may also be extrapolated from dose-response curves derived from animal model test systems and can vary from 0.001 mg/kg to 100 mg/kg.
• Toxicity and therapeutic efficacy of compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population).
• the dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD 50 /ED 50 .
• Compounds which exhibit large therapeutic indices are preferred. While compounds that exhibit toxic side effects can be used, care should be taken to design a delivery system that targets such compounds to the site of affected tissue in order to minimize potential damage to uninfected cells and, thereby, reduce side effects.
• the data obtained from the cell culture assays and animal studies can be used in formulating a range of dosage for use in animals, especially cattle.
• the dosage of such compounds lies preferably within a range of circulating concentrations that include the ED 50 with little or no toxicity.
• the dosage can vary within this range depending upon the dosage form employed and the route of administration utilized.
• the therapeutically effective dose can be estimated initially from cell culture assays.
• a dose can be formulated in animal models to achieve a circulating plasma concentration range that includes the IC 50 (i.e., the concentration of the test compound which achieves a half-maximal inhibition of symptoms) as determined in cell culture.
• IC 50 i.e., the concentration of the test compound which achieves a half-maximal inhibition of symptoms
• levels in plasma can be measured, for example, by high performance liquid chromatography.
• Immunogenicity of a composition can be determined by monitoring the immune response of test subjects following immunization with the composition by use of any immunoassay known in the art. Generation of a humoral (antibody) response and/or cell-mediated immunity, may be taken as an indication of an immune response.
• Test subjects may include animals such as pigs, mice, hamsters, dogs, cats, rabbits, cows, horses, sheep, poultry (e.g. chickens, ducks, geese, and turkeys), and humans.
• the immune response of the test subjects can be analyzed by various approaches such as: the reactivity of the resultant immune serum to the immunogenic conjugate, as assayed by known techniques, e.g., enzyme linked immunosorbent assay (ELISA), immunoblots, immunoprecipitations, etc.; or, by protection of immunized hosts from infection by the pathogen and/or attenuation of symptoms due to infection by the pathogen in immunized hosts as determined by any method known in the art, for assaying the levels of an infectious disease agent, e.g., the bacterial levels (for example, by culturing of a sample from the subject), or other technique known in the art.
• the levels of the infectious disease agent may also be determined by measuring the levels of the antigen against which the immunoglobulin was directed. A decrease in the levels of the infectious disease agent or an amelioration of the symptoms of the infectious disease indicates that the composition is effective.
• the therapeutics of the invention can be tested in vitro for the desired therapeutic or prophylactic activity, prior to in vivo use in animals or humans.
• in vitro assays that can be used to determine whether administration of a specific therapeutic is indicated include in vitro cell culture assays in which appropriate cells from a cell line or cells cultured from a subject having a particular disease or disorder are exposed to or otherwise administered a therapeutic, and the effect of the therapeutic on the cells is observed.
• the therapeutic may be assayed by contacting the therapeutic to cells (either cultured from a subject or from a cultured cell line) that are susceptible to infection by the infectious disease agent but that are not infected with the infectious disease agent, exposing the cells to the infectious disease agent, and then determining whether the infection rate of cells contacted with the therapeutic was lower than the infection rate of cells not contacted with the therapeutic.
• Infection of cells with an infectious disease agent may be assayed by any method known in the art.
• the therapeutic can be assessed by measuring the level of the molecule against which the antibody is directed in the animal model or human subject at suitable time intervals before, during, or after therapy. Any change or absence of change in the amount of the molecule can be identified and correlated with the effect of the treatment on the subject.
• the level of the molecule can be determined by any method known in the art.
• any binding assay known in the art can be used to assess the binding between the resulting antibody and the particular molecule. These assays may also be performed to select antibodies that exhibit a higher affinity or specificity for the particular antigen.
• Antibodies, or binding portions thereof, resulting from the use Leptospira interrogans serovar hardjo (type hardjoprajitno ) compositions of the present invention are useful for detecting in a sample the presence of Leptospira .
• This detection method comprises the steps of providing an isolated antibody or binding portion thereof raised against an Leptospira interrogans serovar hardjo (type hardjoprajitno ) of the invention, adding to the isolated antibody or binding portion thereof a sample suspected of containing a quantity of Leptospira , and detecting the presence of a complex comprising the isolated antibody or binding portion thereof bound to Leptospira.
• the antibodies or binding portions thereof resulting from the use Leptospira interrogans serovar hardjo (type hardjoprajitno ) compositions of the present invention are also useful for detecting in a sample the presence of a Leptospira .
• This detection method comprises the steps of providing an isolated antibody or binding portion thereof raised against a Leptospira interrogans serovar hardjo (type hardjoprajitno ), adding to the isolated antibody or binding portion thereof a sample suspected of containing a quantity of Leptospira , and detecting the presence of a complex comprising the isolated antibody or binding portion thereof bound to the Leptospira.
• Immunoglobulins particularly antibodies, (and functionally active fragments thereof) that bind a specific molecule that is a member of a binding pair may be used as diagnostics and prognostics, as described herein.
• the present invention provides the measurement of a member of the binding pair, and the uses of such measurements in clinical applications.
• the immunoglobulins in the present invention may be used, for example, in the detection of an antigen in a biological sample whereby subjects may be tested for aberrant levels of the molecule to which the immunoglobulin binds, and/or for the presence of abnormal forms of such molecules.
• antibodies of this invention may also be included as a reagent in a kit for use in a diagnostic or prognostic technique.
• an antibody resulting from the use Leptospira interrogans serovar hardjo (type hardjoprajitno ) compositions of the present invention that immunospecifically binds to a Leptospira may be used to diagnose, prognose or screen for a Leptospira infection.
• the invention provides a method of diagnosing or screening for the presence of a Leptospira infection or immunity thereto, comprising measuring in a subject the level of immunospecific binding of an antibody to a sample derived from the subject, in which the antibody immunospecifically binds a Leptospira peptide in which an increase in the level of said immunospecific binding, relative to the level of said immunospecific binding in an analogous sample from a subject not having the infectious disease agent, indicates the presence of S. suis.
• Suitable assays to detect the presence of Leptospira peptides or antagonists thereof include but are not limited to ELISA, radioimmunoassay, gel-diffusion precipitation reaction assay, immunodiffusion assay, agglutination assay, fluorescent immunoassay, protein A immunoassay, or immunoelectrophoresis assay.
• Immunoassays for the particular molecule will typically comprise incubating a sample, such as a biological fluid, a tissue extract, freshly harvested cells, or lysates of cultured cells, in the presence of a detectably labeled antibody and detecting the bound antibody by any of a number of techniques well-known in the art.
• a sample such as a biological fluid, a tissue extract, freshly harvested cells, or lysates of cultured cells.
• binding activity of a given antibody may be determined according to well known methods. Those skilled in the art will be able to determine operative and optimal assay conditions for each determination by employing routine experimentation.
• kits for the detection or measurement of LHB comprise in one or more containers an anti- Leptospira interrogans serovar hardjo (type hardjoprajitno ) antibody, and, optionally, a labeled binding partner to the antibody.
• the anti- Leptospira interrogans serovar hardjo (type hardjoprajitno ) antibody can be labeled (with a detectable marker, e.g., a chemiluminescent, enzymatic, fluorescent, or radioactive moiety).
• the present invention provides a diagnostic kit comprising, an anti- Leptospira interrogans serovar hardjo (type hardjoprajitno ) antibody and a control immunoglobulin.
• a diagnostic kit comprising, an anti- Leptospira interrogans serovar hardjo (type hardjoprajitno ) antibody and a control immunoglobulin.
• one of the foregoing compounds of the container can be detectably labeled.
• a kit can optionally further comprise in a container a predetermined amount of a Leptospira interrogans serovar hardjo (type hardjoprajitno ) recognized by the antibody of the kit, for use as a standard or control.
• compositions of the invention may also be administered in one, two or more doses, as well as, by other routes of administration.
• routes of administration include oral, intradermal, intranasal, subcutaneous, intracutaneous, intravenous, intraarterial, intraperitnoeal, intrathecal, intratracheal, intracardial, intralobal, intramedullar, intrapulmonary, and intravaginal.
• the compositions according to the invention may be administered once or several times, also intermittently, for instance on a daily basis for several days, weeks or months and in different dosages.
• BVDV Bovine Viral Diarrhea Virus
• IHC immunohistochemical
• mice were group housed in a 33,750 square feet (sq ft) dry lot with a 150 feet (ft) concrete fence-line bunk. Animals were moved as a group into a hoop barn approximately 4,080 sq ft in size prior to challenge.
• the hoop barn facility provided 100 ft of bunk line space with head-locks, as well as two automatic waterers. All animals were fed an age appropriate grain ration with grass hay and water provided ad libitum. Additionally, feed was utilized to entice the heifers into the head-locks on the days the animals were worked.
• Treatment Groups, Number of Animals, and Vaccine Dose Administered Treatment Number of Treatment/ Group Animals Administration Dose 1 21 Modified Live Combination 2 mL Product/Subcutaneous 2 21 Killed Virus Combination 5 mL Product/Subcutaneous 3 11 Placebo Controls/ 2 mL Subcutaneous
• Treatment Group 1 Vaccinates were administered a Modified Live Combination Product consisting of Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza 3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Campylobacter Fetus-Leptospira Canicola-Grippotyphosa-Hardjo-Icterohaemorrhagiae-Pomona Bacterin (a licensed commercially available combination product, Express FP® 5 VL5, Boehringer Ingelheim Vetmedica, Inc., St. Joseph, Mo.).
• Treatment Group 2 Vaccinates were administered a Killed Virus Combination Product consisting of Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza 3-Respiratory Syncytial Virus Vaccine, Killed Virus, Campylobacter Fetus-Haemophilus Somnus-Leptospira Canicola-Grippotyphosa-Hardjo-Icterohaemoffhagiae-Pomona Bacterin (an unlicensed experimental combination product, Boehringer Ingelheim Vetmedica, Inc., St. Joseph, Mo.).
• Treatment Group 3 The placebo vaccinated control group was administered a modified live virus consisting of Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza 3-Respiratory Syncytial Virus Vaccine (a licensed commercially available combination product, Express FP® 5, Boehringer Ingelheim Vetmedica, Inc., St. Joseph, Mo).
• the products used for vaccination of Treatment Groups 1 and 3 were fully released commercially available products.
• the product used for vaccination of Group 2 was an experimental serial of product prepared specifically for use in this study. All vaccinations were administered via the subcutaneous (SC) route.
• SC subcutaneous
• the test vaccines and placebo were administered as two doses, each 2 or 5 mL as indicated in Table 1, with a 21-day interval between the vaccinations.
• the test vaccines used were formulated to the minimum immunizing dose amount of organisms for the L. hardjo component. All remaining components were batched at or above the normal release dose level.
• Blood Sample Collection Blood samples were collected from all animals on PV days 0, 21, 35, 43, 105, 112, 119, 126, 133, 140, 147, 154 and 160 via jugular venipuncture. Tubes were labeled with the date and the animals' identification (ID) number and returned to the laboratory for processing. The samples were allowed to clot at room temperature, centrifuged at 800 ⁇ g for 15 minutes, then aliquoted.
• ID the dates and the animals' identification
• MAT Microagglutination Test
• Serum samples were processed as described above and an aliquot was submitted to South Dakota State University Animal Disease Research and Diagnostic Laboratory (SDSU ADRDL) for leptospira MAT testing to determine antibody response to Leptospira canicola, grippotyphosa, hardjo, icterohaemorrhagiae, bratislava and pomona .
• the test was performed by adding known live cultures of Leptospira to equal amounts of diluted serum and observing the mixture microscopically for agglutination at the end of the reaction time.
• the end-point titer was the highest serum dilution showing agglutination of at least 50% of the leptospires in the test well. Based on the SDSU ADRDL MAT procedure, a MAT endpoint titer >100 was considered to be positive.
• Strain LHP was used in the L. hardjo MAT.
• Urine Collection Two 50-mL conical vials of urine were taken from each heifer on PV days 0, 105, 112, 119, 126, 133, 140, 147, 154, and 160. Samples were collected during mid-stream urination. The samples were obtained after administering 500 mg furosemide (Furosemide, Vedco Inc., St. Joseph, Mo.) intravenously (IV) to each heifer. Following collection, the outside of each vial was disinfected, labeled with animals' ID numbers, and transported to the RTI laboratory for processing for Leptospira culture.
• furosemide Furosemide, Vedco Inc., St. Joseph, Mo.
• Urine Cultures The urine samples were used to detect Leptospires in the urine via culturing. Briefly, 1 mL of urine from each heifer was serially diluted 1:10 in transport medium to the 10 ⁇ 2 dilution. Sample volumes of 100 and 300 ⁇ L from each dilution were inoculated in Ellis (80/40) culture medium and incubated at 29° C. for up to two months. Cultures were observed microscopically for signs of Leptospira growth. Culture samples showing positive growth were confirmed to be Leptospira by dark-field microscopy. Cultures showing no growth after 2 months of observation were considered to be negative.
• Kidney Cultures Immediately following euthanasia, both kidneys were removed from each heifer. Tissue samples totaling approximately 1 cm 2 /l gram of tissue per each kidney were collected. If suspect areas of the kidney were noted, characterized by pale areas of depression on the surface of the kidney, tissue samples were obtained from those areas. If no suspect areas were seen, samples were taken at random from each kidney. Each kidney sample was homogenized, and the kidney homogenates were diluted in growth medium and incubated at 29° C. for up to two months. Cultures were observed microscopically for signs of leptospira growth. Culture samples showing positive growth were confirmed to be leptospira by dark-field microscopy. Cultures showing no growth after 2 months of observation were considered to be negative.
• the LHB strain 203 used for the challenge was originally obtained from the National Animal Disease Center, Ames, Iowa. This strain has been previously described. See Bolin, et. al., 1989(a); Bolin et al., 1989(b); and Bolin et al., 1991.
• the two passage heifers were challenged on PV study days 25, 26, and 27. Each heifer was challenged intraocularly with approximately 1.4 ⁇ 10 7 freshly grown LHB culture contained in 1.0 ml inoculum on each challenge day. The animals were restrained in a chute and the head secured with a halter. Animals were challenged intraocularly by pulling the lower eyelid down to expose the conjunctival sac. A volume of 0.5 mL of challenge material was dropped into each sac, one eye at a time, and each eyelid was held closed for 60 seconds following administration of the challenge material.
• Blood and urine samples were obtained from the two passage heifers on post-first challenge days 0, 15, 23, 28, 36, 42 and 51 to follow progress of the infection. Urine samples collected from both animals were tested for presence of the organism. The culture on Heifer #48 was positive for leptospire in the urine beginning the third week following challenge and continuing until necropsy. The urine cultures on Heifer #29 were positive for leptospire on the sixth and seventh week following challenge.
• animals #29 and #48 were humanely euthanized by IV administration of a barbiturate (Euthanasia 6 Grain, Vedco Inc., St. Joseph, Mo.) overdose.
• a barbiturate Esuthanasia 6 Grain, Vedco Inc., St. Joseph, Mo.
• kidneys were removed from the animals and transported to the RTI laboratory for processing and leptospira isolation. Suspect lesions from each kidney of Heifer #48 were removed, weighed, and homogenized before adding to the culture media. No suspect lesions were found on the kidneys from Heifer #29 thus random sections were removed, weighed, and homogenized before adding to the culture media. The kidney homogenates were diluted in growth medium and cultured. Kidney cultures were grown under the same conditions as the urine, as described herein.
• the kidney samples taken at the time of necropsy from Heifer #48 were culture positive, while those from Heifer #29 were negative.
• the positive kidney cultures were passaged into fresh growth medium to produce the challenge inoculum.
• the challenge inoculum was checked weekly to determine organism growth and motility. The challenge inoculum was considered ready when motility was high and sufficient culture was available for three challenges of all study animals with 1 ml inoculum containing approximately 10 6 organisms per mL.
• the identities of the cultures as Leptospira were confirmed by darkfield microscopy.
• the purpose of this study was to evaluate efficacy of the LHP component of a commercial pentavalent combination vaccine against a virulent challenge with LHB. Efficacy was based on 1) reduction of renal infection/colonization, and 2) reduction in urinary shedding of the challenge strain.
• the treatments include a modified live virus (MLV) and bacterin combination vaccine (a licensed commercially available combination product, Express FP® 3 VL5, Boehringer Ingelheim Vetmedica, Inc., St. Joseph) (Group 1), a killed virus bacterin combination vaccine (an unlicensed experimental combination product, Boehringer Ingelheim Vetmedica, Inc., St.
• Efficacy was determined by comparison of vaccinated and control heifers based on post-challenge organism recovery in urine and in kidney tissue at necropsy. Prevented fractions and corresponding 95% confidence limits were constructed for each variable.
• LHB strain 203 was grown in the RTI laboratory following the two-animal challenge passage phase as described above and was used for challenge. On PV days 105, 106, and 107, fresh material was counted on a hemocytometer and aliquoted into 3 mL syringes, each containing 1 mL of challenge material at approximately 10 6 leptospires per mL. Additionally, a post-challenge sample was returned to the RTI laboratory and counted on a hemocytometer. The aliquots were used to challenge the heifers in Groups 1, 2 and 3 intraocularly as described above. Briefly, the animals were restrained and challenged intraocularly by pulling the lower eyelid down to expose the conjunctival sac. A volume of 0.5 mL of challenge material was dropped into each sac, one eye at a time. Each eyelid was held closed for 60 seconds following administration of the challenge material.
• Blood and Urine Sample Collection Blood samples were collected via jugular venipuncture from all animals just prior to challenge, and weekly from 7 to 55 Days Post Challenge (DPC). The samples were processed as described above, and an aliquot was submitted to SDSU ADRDL for Leptospira MAT testing. Two 50 mL conical vials of urine were taken from each animal once weekly from 0 through 55 DPC. Samples were collected as described above. The urine samples were used to detect leptospires in the urine via culture as described above.
• the 53 animals were randomly assigned to treatment groups, with 21 heifers in both Group 1 and 2, and 11 animals in Group 3 (placebo control group).
• Urine samples were evaluated for organism recovery on PV day 0, PV day 105 (0 DPC), PV day 112 (7 DPC), PV day 119 (14 DPC), PV day 126 (21 DPC), PV day 133 (28 DPC), PV day 140 (35 DPC), PV day 147 (42 DPC), PV day 154 (49 DPC), and PV day 160 (55 DPC).
• Kidney tissue samples were evaluated for organism recovery following necropsy.
• Organism recovery for urine shedding was defined as the (1) presence of at least one positive urine culture during the study or (0) no positive urine cultures on any study day.
• Organism recovery for kidney tissue samples was defined as (1) a positive kidney culture or (0) a negative kidney culture.
• StatXact® 8.0 was used to compute the exact 95% confidence interval of the risk ratio based on the standardized statistic and inverting two 1-sided tests.
• the confidence limits for the prevented fraction are the compliment of the confidence limits for the risk ratio, or [1 ⁇ U, 1 ⁇ L].
• the corresponding two-sided value produced by StatXact® 8.0 was reported.
• the entire 95% confidence interval is greater than 0.0% when the prevented fraction is significantly different (p ⁇ 0.05) from 0.0%.
• Microaggluntination Test Results Blood samples were taken from all enrolled heifers in Groups 1, 2 and 3 on PV days 0, 21, 35 and 43 for MAT testing to determine antibody response to Leptopsira canicola, grippotyphosa, hardjo, icterohaemorrhagiae and pomona . Transient post-vaccination MAT serological responses were detected to the L. canicola, grippotyphosa, icterohaemorrhagiae and pomona serovars in 40 to 75 percent of the vaccinated heifers on 14 and 21 days after the second vaccination in both vaccination groups (data not shown). Transient positive MAT serological response to the L. hardjo were observed only on day 14 post second vaccination in less than 24 percent of the vaccinates. All unvaccinated controls remained negative to all serovars through the day of challenge.
• Post-challenge blood samples were taken from all enrolled heifers in Groups 1, 2 and 3 on 0, 7, 14, 21, 28, 35, 42, 49 and 55 DPC for MAT testing to determine antibody response to L. canicola, grippotyphosa, hardjo, icterohaemorrhagiae and pomona .
• Post-challenge MAT antibody responses remained negative for L. canicola, grippotyphosa, icterohaemorrhagiae and pomona in all animals through the end of the study.
• Post-challenge MAT results for the L. hardjo remained negative in all vaccinated heifers from Groups 1 and 2 through the end of the study.
• Urine Shedding Results All pre- and post-challenge urine cultures from all urine samples collected from the vaccinated heifers (Groups 1 and 2) were negative for growth of leptospires (Table 2). This is in contrast to placebo control heifers (Group 3) where 100% had positive urine cultures (Tables 2 and 3) with a minimum of two post-challenge samples (Table 3). The range was 2-6 positive cultures/heifer (Table 3). Urine shedding was first detected in Group 3 placebo control heifers at 21 DPC with the highest number of animals shedding at days 35 and 49 DPC (Table 3).
• Kidney Culture Results All the vaccinated heifers (Groups 1 and 2) kidney tissues were negative for leptospire isolations (Table 6), while 10 of 11 heifers in the control group had positive leptospire cultures from kidney tissue (Tables 3 and 6).
• the serological MAT results show transient seroconversion post-second vaccination in a portion of the vaccinated animals for all serovars. All animals in all groups were negative by MAT for all serovars at the time of challenge (data not shown). By three weeks post-challenge, all placebo control animals were MAT positive for L. hardjo as a response to challenge and resulting infection with the challenge organism. Challenge of the animals with the LHB did not elicit an anamnestic MAT serological response to L. hardjo in the vaccinated animals, whereas 100% (11 of 11) of the placebo controls showed positive MAT results after challenge. The challenge organism was recovered utilizing culture from urine samples taken at weekly intervals through day 56 post-challenge.
• Each of the placebo control animals had a minimum of two urine samples test culture positive, indicating shedding for at least 7 days.
• the duration of shedding in the placebo controls ranged from 7 days to 35 days.
• one of 11 heifers shed for two sampling days 4 of 11 shed for 4 days; 4 of 11 f shed or five sampling days; and 2 of 11 shed for six sampling days.
• vaccination with the L. hardjo bacterin completely prevented urine shedding of the challenge organism.
• Kidney samples taken at the time of necropsy were also cultured to determine challenge organism recovery. Kidney tissues from 10 of 11 (90.9%) of the placebo controls were positive for recovery of the challenge organism. There was no recovery of the challenge organism from any kidney tissues from any of the vaccinated heifers (Groups 1 and 2). Based upon culture results, vaccination with the L. hardjo bacterin completely prevented kidney infection/colonization with the challenge organism.
• Subtle differences in the serovar of hardjo used to prepare the vaccine may, in part, account for the level of protection provided by this vaccine. Such distinctions may include differences in the original isolate, as well as, differences induced based on methods of growth and passage.
• the level of protection provided by a vaccine will depend not only on the specifics of the serovar/strain of the organism contained in the vaccine, but also on the adjuvant, if any, used in the formulation of the vaccine.
• the vaccines used included an adjuvant(s). Growth and inactivation conditions utilized for production of the strain can also impact the efficacy provided by the vaccine. Serovar differences combined with adjuvant formulation and organism processing for the vaccine can effect the ability of the vaccine to induce a protective immune response.
• Vaccination with both the modified live viral/LHP bacterin combination and killed viral/LHP bacterin combination resulted in prevention of urine shedding as well as prevention of renal infection and colonization after challenge with LHB.
• the results of this study show that the L. hardjo component of the test vaccines is highly efficacious against challenge induced renal infection and colonization and associated urinary shedding due to LHB.
• compositions and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the following claims.

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