AU2002365922A1 - Methods of preventing and treating flavivirus infection in animals - Google Patents

Description

METHODS OF PREVENTING AND TREATING FLAVIVIRUS

INFECTION IN ANIMALS

Field of the Invention This invention relates to methods of preventing and treating flavivirus infection in animals.

Background of the Invention

Flaviviruses are small, enveloped, positive-strand RNA viruses that are of concern in many medical and veterinary settings throughout the world. West Nile (WN) virus, for example, which is a member of the flavivirus family, is the causative agent of WN encephalitis, an infectious, non-contagious, arthropod-borne viral disease (Monath et al., "Flaviviruses," In Virology, Fields (ed.), Raven-Lippincott, New York, 1996, pp. 961-1034). The virus has been found in Africa, western Asia, the Middle East, the Mediterranean region of Europe, and, recently, in the United States. Mosquitoes become infected with the virus after feeding on infected wild birds, and then transmit the virus through bites to humans, birds, and animals, such as horses, sheep, cattle, and pigs.

In 1999, twenty-five horses in New York with neurological symptoms were found to have WN virus infection. These horses presented with signs of ataxia, difficulty walking, knuckling over, head tilt, muscle tremors, and the inability to rise. Of these twenty-five horses, nine died or were euthanized, and virus, as well as virus- specific antibodies, were found in tissue samples from these horses. The sixteen surviving horses all recovered, and also developed WN virus antibody titers. Since then, increasing numbers of West Nile virus-infected horses have been confirmed.

Flavivirus proteins are produced by translation of a single, long open reading frame to generate a polyprotein, which undergoes a complex series of post-translational proteolytic cleavages by a combination of host and viral proteases to generate mature viral proteins (Amberg et al., J. Virol. 73:8083-8094, 1999; Rice, "Flaviviridae," In Virology, Fields (ed.), Raven-Lippincott, New York, 1995, Volume I, p. 937). The virus structural proteins are arranged in the polyprotein in the order C-prM-E, where "C" is capsid, "prM" is a precursor of the viral envelope-bound M (membrane) protein, and "E" is the envelope protein. These proteins are present in the N-terminal region of the polyprotein, while the non-structural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5) are located in the C-terminal region of the polyprotein.

Summary of the Invention The invention provides methods of preventing or treating flavivirus infection (e.g., West Nile virus infection) in non-human mammals (e.g., horses), which involve administering to the non-human mammals chimeric flaviviruses. The invention also provides the use of chimeric flaviviruses in the preparation of medicaments for use in such methods. The chimeric flaviviruses can include, for example, the capsid and non- structural proteins of a first flavivirus (e.g., a yellow fever virus, such as a yellow fever virus derived from the 17D strain) and the prM and envelope proteins of a second flavivirus (e.g., West Nile virus). The invention provides several advantages. For example, as is discussed below, horses treated using the methods of the invention do not present with adverse side effects due to the vaccination, and yet are protected against substantial virus challenge. Thus, the methods of the invention are highly effective at protecting horses against flavivirus, e.g., West Nile virus, infection. In addition, referring specifically to the yellow fever/West Nile virus chimera described herein, the host range of yellow fever virus is very specific, being limited to primates. Thus, the efficacy of the yellow fever/West Nile virus chimera in protecting horses against West Nile virus challenge was surprising, as horses, which are only distantly related to primates, are well outside of the natural host range of yellow fever virus. Further, because the vaccine viruses used in the invention are chimeric, consisting of material from more than one different virus, the chances of reversion to wild type virus are eliminated.

Other features and advantages of the invention will be apparent from the following detailed description and the claims.

Detailed Description

The invention provides methods of preventing and treating flavivirus (e.g., West Nile (WN) virus) infection in animals, such as horses. The methods of the invention involve vaccination of animals that are at risk of developing or have flavivirus infection with a live, attenuated chimeric flavivirus. These viruses consist of a flavivirus (i.e., a backbone flavivirus) in which a structural protein (or proteins) has been replaced with a corresponding structural protein (or proteins) of a second flavivirus, to which immunity is sought. Preferably, the chimeras consist of a backbone flavivirus in which the prM and E proteins have been replaced with the prM and E proteins of the second flavivirus. The chimeric viruses that are used in the invention can consist of any combination of viruses, provided that, as is mentioned above, the virus to which immunity is desired is the source of the inserted structural protein(s). For example, to vaccinate an animal, such as a horse, against West Nile virus infection, a chimeric flavivirus consisting of a flavivirus backbone, such as that of yellow fever (YF) virus, into which West Nile virus structural proteins (e.g., prM and E proteins) are inserted can be used. In this chimera, the YF prM and E proteins are replaced with those of WN. Similarly, if immunity against Japanese encephalitis (JE) virus is desired, then the prM and E proteins of JE virus can be inserted into a backbone flavivirus, such as a yellow fever virus, in place of the corresponding backbone proteins. Other flaviviruses that cause disease in horses, and for which chimeric viruses can be used for inducing protection, include Kunjin, Murray Valley encephalitis, and Louping ill viruses.

In addition to horses, animals that can be treated using the methods of the invention include, for example, pigs, sheep, cattle, domestic animals, such as cats and dogs, and domestic birds. As specific examples of non-horse vaccinations, sheep can be treated using a chimeric virus including structural insert proteins from Wesselsbron virus or Louping ill virus, and pigs can be treated using a chimeric virus including structural insert proteins from Japanese encephalitis virus.

Thus, examples of flaviviruses that can be used in the invention, as sources of backbone virus or structural protein inserts, include mosquito-borne flaviviruses, such as Japanese encephalitis, Dengue (serotypes 1-4), Yellow fever, Murray Valley encephalitis, St. Louis encephalitis, West Nile, Kunjin, Rocio encephalitis, Wesselsbron, and Ilheus viruses; tick-borne flaviviruses, such as Central European encephalitis, Siberian encephalitis, Russian Spring-Summer encephalitis, Kyasanur Forest Disease, Omsk Hemorrhagic fever, Louping ill, Powassan, Negishi, Absettarov, Hansalova, Apoi, and Hypr viruses; as well as viruses from the Hepacivirus genus (e.g., Hepatitis C virus). Additional viruses that can be used as the source of inserted structural proteins include viruses from the Pestivirus genus (e.g., Bovine diarrhea virus), and other viruses, such as Lassa, Ebola, and Marburg viruses. As is noted above, preferably, the virus consists of a yellow fever virus backbone containing a West Nile virus insert.

Details of making chimeric viruses that can be used in the invention are provided, for example, in U.S. patent application serial numbers 09/007,664, 09/121 ,587, and 09/452,638; International applications PCT/US98/03894 and

PCT/US00/32821; and Chambers et al., J. Virol. 73:3095-3101, 1999, which are each incorporated by reference herein in their entirety.

The vaccines of the invention can be administered in amounts, and by using methods, which can readily be determined by persons of ordinary skill in this art. The vaccines can be administered and formulated, for example, as a fluid harvested from cell cultures infected with the appropriate chimeric virus. The live, attenuated chimeric virus is formulated as a sterile aqueous solution containing between 10² and 10⁸, e.g., between 10⁶ and 10⁷, infectious units (e.g., plaque-forming units (pfu) or tissue culture infectious doses) in a dose volume of 0.1 to 1.0 ml, to be administered by, for example, subcutaneous, intramuscular, or intradermal routes. In addition, a mucosal route, such as an oral route, may be selected. Selection of an appropriate amount of chimera to administer can be determined by those of skill in this art, and this amount can vary due to numerous factors, e.g., the size, type, and general health of the animal to which the chimera is to be administered. As is noted above, the vaccines can be administered as primary prophylactic agents to an animal that is at risk of flavivirus infection. The vaccines can also be used as secondary agents for treating flavivirus-infected animals by stimulating an immune response against the infecting flavivirus. Also, although not required, adjuvants can be used to enhance the immunogenicity of the chimeric vaccines. Selection of appropriate adjuvants can readily be carried out by those of skill in this art.

Experimental Results

The safety and efficacy of ChimerVax-WN was evaluated in horses. Efficacy was defined in terms of humoral immune responses and protection from challenge. Animals

Eleven horses were used in this study, as summarized below in Table 1. The horses were housed in an ABSL3 containment building for the duration of the study, and were fed alfalfa hay and mixed grain.

Table 1. Summary of Animal Characteristics and Treatments

Immunization

Four horses (EQ1, EQ2, EQ3, and EQ4) were immunized by two injections, three weeks apart, of ChimeriVax-WN virus. At each immunization, a dose of 10⁷ plaque-forming units (pfu) of virus in 1 ml was inoculated subcutaneously over the left shoulder.

Viremia in the vaccinated horses was analyzed using a standard WN plaque assay. Samples were tested in duplicate, at neat and 1 :5 dilution. We found that, although the levels of viremia were very low from day 0 through 7, a peak of viremia was detectable on days 3 and 4.

Antibody levels were measured in samples taken from each horse after vaccination, as is indicated in Table 2, using a plaque reduction neutralization test (PRNT). In summary, two of the horses developed and 80% reduction titer of 10 within two weeks of primary immunization, and all four horses had a titer between 10 and 20 at four weeks (one week following the second immunization).

Validation of an equine challenge model Mosquito-borne challenge of horses with WNV usually results in viremia, but clinical disease is rare. Thus, to enable assessment of protective immunity to WNV, an appropriate challenge model was developed. The challenge virus used in these studies was WNV NY99 (4132), which was originally isolated from a crow and had been passaged once in Vero cells and once in C636 cells. Due to the hypersensitivity reactions observed following booster vaccine injections, we passaged the virus an additional time in BHK-21 cells, washed the FBS -containing inoculum off after adsorption, and prepared stocks using 20% WNV/SLE-seronegative horse serum. This FBS-free preparation was diluted in PBS and used for the challenges of horses EQ1, EQ2, EQ4, EQ8, EQ9, EQ10, and EQ11. Most of the horses were challenged by intrathecal inoculation. For this procedure, they were anesthetized with a combination of xylazine and ketamine and a cisternal tap was performed under asceptic conditions. Two ml of CSF were withdrawn, and 1.0 ml of virus was injected. In all cases, recovery from the procedure was uneventful. The results from challenge development studies are summarized as follows.

Horse EQ5

This horse was inoculated with 10⁴pfu of WNV by the intrathecal route. The horse appeared normal that day and the following, but was found recumbent and poorly responsive on the morning of day 2. She was euthanized and necropsied, and virus was not recovered from several areas of brain. This animal may have fallen during the previous night and seriously injured her spinal cord, which was not examined at necropsy. It appears clear that her death was not related to WNV infection.

Horse EQ6

This horse was inoculated with 10⁴pfu WNV subcutaneously; four days later, a cisternal puncture was performed with the idea of facilitating passage of virus across the blood brain barrier. On the morning of day 10, she was noticeably anxious and not normal, but by that evening, had returned to normalcy. No other clinical signs were observed during the 6 weeks following challenge. Serum samples collected twice daily for the first 13 days after inoculation were assayed for virus on Vero cells- no virus was recovered from any specimen. PRNT assays were performed using serum collected on the day of inoculation and 3 weeks later. The 80% (and 90%) neutralization titers on these samples were 10 (<10) and 40 (40) respectively. She had been tested as serologically negative prior to use, so the 1 :10 at 80% titer on the day of inoculation was surprising. This animal may have had a mild case of WN.

Horse EQ7

This horse was inoculated with 10⁴pfu WNV intrathecally; backtitration of the inoculum revealed the dose to be 6 x 10³ pfu. Clinical signs of disease were absent until day 20, when the animal was noticed to be anxious and nervous. Over the following 2 days, her condition worsened with increased anxiety, head and lip tremors, muscle fasiculation, and rear limb paresis. However, by the evening of day 23, she appeared to be recovering and clinical signs were considerably decreased in severity. She was euthanized on day 24 to allow confirmation that the disease was indeed due to WNV. Histopathological examination of brain revealed a diffuse, widespread encephalitis. Serum samples collected twice daily from day 1 to day 9 were assayed for virus by plaqueing on Vero cells; virus was not isolated from any of the samples. We also failed to isolate virus from CSF and from homogenates of cerebrum, cerebellum, and brainstem collected at necropsy (tissues assayed as 10% suspensions and -1 and -2 dilutions). PRNT titers (80 or 90%) of sera collected on day 0, 7, 14, and 23 were <10, <10, 160, and 160.

Horses EO8 and EQ9

These horses were challenged by intrathecal inoculation of 10⁵ pfu WNV; back titration revealed the dose administered to be 2 x 10⁵ pfu. Both animals remained clinically normal for 7 to 7.5 days, then developed progressively severe disease (clinical descriptions on individual animal records). The course of disease in the two horses was almost identical and both were euthanized and necropsied on day 9. Histopathologic examination revealed severe encephalitis in both horses. Sera collected twice daily following inoculation were assayed for plaque production on Vero cells. The viremia titers (logic pfu/ml) determined were:

Samples of CSF, cerebrum, cerebellum, brainstem, and cranial cervical cord collected at necropsy were assayed for virus on Vero cells. EQ8 had a trace (1.5 logio pfu/gram) of virus in brainstem, and EQ8 had a small amount of virus (1.3 logio pfu/gram) in cerebellum; all other samples were negative. Both animals had PRNT titers of <10 at the time of challenge. At the time of euthanasia, EQ8 and EQ9 had PRNT titers (90%) of 160 and <10, respectively.

Challenge of Vaccinated Horses and Controls

Vaccinated horses EQ1, EQ2, and EQ4 were challenged exactly 24 weeks after primary immunization. Two additional control horses were challenged simultaneously. All of these challenges consisted of intrathecal inoculation of 1.0 ml containing 10⁵ pfu WVN (FBS-free preparation diluted in PBS). Backtitration of the inoculum indicated that the horses received approximately 125,000 pfu of virus.

The two control horses (EQ10 and EQ11) developed severe clinical disease beginning 7 to 8 days after virus inoculation and were euthanized 8.5 and 10 days after challenge, respectively. At the time of euthanasia, their PRNT antibody titers were 1 :40 and <10, respectively. Serum collected at half day intervals between the time of challenge and euthanasia were assayed by plaque production on Vero cells; viremia titers (logio pfu/ml serum) are shown in the following tables (negative samples from EQ11 taken after day 8.0 not shown).

Samples of CSF, cerebrum, cerebellum, and brainstem collected at necropsy were also assayed by plaque production on Vero cells. Virus was not isolated from either CSF sample. Trace amounts of virus (1-2 plaques per well inoculated with 0.1 ml of 10% suspension) were isolated from all three areas of brain from horse EQ10, and from brainstem only from horse EQl 1. Histopathologic examination of the brains of EQ10 and EQl 1 revealed widespread encephalitis.

In marked contrast to the two control horses, the vaccinated horses EQl, EQ2, and EQ4 failed to show any evidence of clinical disease in the 4 weeks following challenge. Further, virus was not isolated from any of the serum samples collected twice daily from these animals during the first 10 days following challenge, nor from samples of cerebrum, cerebellum, brainstem, or CSF collected at necropsy on day 28. Histopathologic examination of their brains did not reveal lesions, other than a few incidental findings not associated with WNV infection.

Antibodies to WNV were assayed in CSF collected at the time of virus inoculation and the time of euthanasia (day 28 for EQl, EQ2, and EQ4; day 8.5 for

EQ10, and day 10 for EQl 1). Samples were assayed at dilutions of 1 :5, 10, and 20. The samples collected at necropsy from horse EQl showed an 87% reduction in plaque count at 1 :5, and postmortem sample from EQ4 showed a 98% reduction at 1 :5. All other samples had titers of <5 at 80% reduction.

Serological Responses to Vaccination

Serum samples were collected from the four immunized horses weekly for the duration of their tenure and stored in duplicate. Neutralizing antibody titers were determined on a subset of these samples, using a standard plaque-reduction neutralization test on Vero cells. Only some of the assays were conducted using 8% human serum in the virus inoculum, as indicated in Table 2.

* indicates with (+) or without (-) use of labile serum factor

What is claimed is:

Claims (8)

1. Use of a chimeric flavivirus in the preparation of a medicament for preventing or treating flavivirus infection in a non-human mammal.

2. The use of claim 1, wherein said non-human mammal is a horse.

3. The use of claim 1, wherein said flavivirus infection is West Nile virus infection.

4. The use of claim 1, wherein said chimeric flavivirus comprises the capsid and non-structural proteins of a first flavivirus and the prM and envelope proteins of a second flavivirus.

5. The use of claim 4, wherein said first flavivirus is a yellow fever virus.

6. The use of claim 5, wherein said yellow fever virus is derived from the 17D strain.

7. The use of claim 4, wherein said second flavivirus is a West Nile virus.

8. Use of a chimeric flavivirus comprising the capsid and non-structural proteins of a yellow fever virus and the prM and envelope proteins of a West Nile virus in the preparation of a medicament for preventing West Nile virus infection in a horse.