Patent Application
20110014220
The preset invention relates to a human respiratory syncytial virus (RSV) vaccine; in particular, a vaccine composition comprising a recombinant adenoviral construct carrying the nucleotide encoding a RSV protein.
Respiratory syncytial virus (RSV) is a single-stranded, negative sense RNA pleomorphic enveloped Pneumovirus of the Paramyxoviruidae family. Human RSV genome contains eight structural genes and two non-structural genes, wherein the major genes code for the attachment glycoprotein (G protein), the fusion protein (F protein), and a small hydrophobic envelope protein (SH protein), respectively.
The infection of RSV would lead to the induction of both humoral and cellular immune responses directed against the virus. It was proved in several studies in animal models that the RSV-specific neutralizing antibodies and cytotoxic lymphocytes (CTLs) contributed to a protection against RSV infection and/or diseases. For example, it was reported that RSV-specific antibodies played an important role in prevention from the RSV infection in terms of the protective efficacy of the passive transfer of immune sera containing RSV-specific antibodies of unvaccinated mice challenged by a live RSV (Graham et al., Immunoprophylaxis and immunotherapy of respiratory syncytial virus-infected mice with respiratory syncytial virus-specific immune serum; Pediatr Res 1993 August; 34(2):167-72). It was also reported that RSV-specific CTLs were detected more readily in adults who developed mild symptoms due to RSV infection exposure (Isaacs D., Viral subunit vaccines; Lancet 1991 May 18; 337(8751): 1223-4).
It was evidenced that F protein of RSV as target of vaccine antigen was better than G protein of RSV because the recombinant vaccinia virus expressing the G protein of RSV (vacvG) enhanced pulmonary eosinophilia upon RSV infection of mice (as reported in, for example, Openshaw et al., Pulmonary eosinophilic response to respiratory syncytial virus infection in mice sensitized to the major surface glycoprotein G; Int Immunol 1992 April; 4(4):493-500). However, it was also reported that Th-2 type response to RSV infection after F1-RSV-vaccination (a vaccination with the F1 subunit of F protein of RSV) played a role in an abnormal response, characterized by extensive eosinophils increasing in the blood, wheezing, and hyper reactive airways (Kim et al., Respiratory syncytial virus disease in infants despite prior administration of antigenic inactivated vaccine; Am J Epidemiol 1969 April; 89(4):422-34), and that the Th2-associated cytokines IL-4 and IL-13 both promoted the development of pulmonary eosinophilia (Johnson and Graham, Secreted respiratory syncytial virus G glycoprotein induces interleukin-5 (IL-5), IL-13, and eosinophilia by an IL-4-independent mechanism; J Virol 1999 October; 73(10):8485-95; and Johnson et al., IL-13 is sufficient for respiratory syncytial virus G glycoprotein-induced eosinophilia after respiratory syncytial virus challenge; J Immunol 2003 Feb. 15; 170(4):2037-45).
Given the above, it is still desired to develop a new vaccine for prevention against the RSV infection or the vaccine-enhanced diseases without undesired side effects, such as eosinophilia.
The present invention features a novel RSV DNA vaccine characterized by a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding F protein of RSV. It is unexpectedly discovered that the RSV vaccine of the present invention does not have undesired side effects, such as inflammation and eosinophila, present in the RSV vaccines known in the art.
In one aspect, the invention is to provide a vaccine composition comprising a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding a polypeptide of F protein of RSV or fragments thereof
In the other aspect, the invention is to provide a method of preventing RSV infection-related diseases comprising administering to a subject in need thereof a vaccine composition comprising a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding a polypeptide of F protein of RSV or fragments thereof.
The foregoing summary, as well as the following detailed description of the invention, will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating the invention, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the invention is not limited to the preferred embodiments shown.
In the drawings:
Unless defined otherwise, all technical and scientific terms used herein have the meaning commonly understood by a person skilled in the art to which this invention belongs. As used herein, the following terms have the meanings ascribed to them unless specified otherwise.
The articles “a” and “an” are used herein to refer to one or more than one (i.e., at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.
The term “encoding” refers to the inherent property of specific sequences of nucleotides in a polynucleotide (e.g., a gene, a cDNA, or an mRNA) to serve as templates for synthesis of other polymers and macromolecules in biological processes having either a defined sequence of nucleotides (i.e., rRNA, tRNA and mRNA) or a defined sequence of amino acids and the biological properties resulting therefrom. Therefore, a gene encodes a protein if transcription and translation of mRNA produced by that gene produces the protein in a cell or other biological system. It is understood by a skilled person that numerous different polynucleotides and nucleic acids can encode the same polypeptide as a result of the degeneracy of the genetic code. It is also understood that skilled persons may, using routine techniques, make nucleotide substitutions that do not affect the polypeptide sequence encoded by the polynucleotides described there to reflect the codon usage of any particular host organism in which the polypeptides are to be expressed. Therefore, unless otherwise specified, a “nucleotide sequence encoding an amino acid sequence” includes all nucleotide sequences that are degenerate versions of each other and that encode the same amino acid sequence. Nucleotide sequences that encode proteins and RNA may include introns.
The term “recombinant” is used to describe a polynucleotide or nucleic acid having sequences that are not naturally joined together. A recombinant nucleic acid may be present in the form of a construct. The term “construct” as used herein may contain a given nucleotide sequence of interest, and some sequence required for expression of the nucleotide sequence of interest, such as a regulatory sequence. Constructs may be used for expressing the given nucleotide sequence or maintaining the given nucleotide sequence for replicating it, manipulating it or transferring it between different locations (e.g., between different organisms). Constructs can be introduced into a suitable host cell for the above mentioned purposes.
Examples of constructs include, but are not limited to, plasmids, cosmids, phages, YACs or PACs. Typically, in a construct, the given nucleotide sequence is operatively linked to the regulatory sequence such that when the constructs are introduced into a host cell, the given nucleotide sequence can be expressed in the host cell under the control of the regulatory sequence. The regulatory sequence may comprises, for example and without limitation, a promoter sequence (e.g., the cytomegalovirus (CMV) promoter, simian virus 40 (SV40) early promoter, T7 promoter, and alcohol oxidase gene (AOX1) promoter),a start codon, a replication origin, enhancers, an operator sequence, a secretion signal sequence (e.g., —mating factor signal) and other control sequence (e.g., Shine-Dalgano sequences and termination sequences). Preferably, constructs may further contain a marker sequence (e.g., an antibiotic resistant marker sequence) for the subsequent screening procedure. More preferably, in constructs, the given nucleotide sequence of interest may be connected to another nucleotide sequence other than the above-mentioned regulatory sequence such that a fused polypeptide is produced and beneficial to the subsequent purification procedure. Said fused polypeptide includes, but is not limited to, a His-tag fused polypeptide and a GST fused polypeptide.
The term “fragment” as used herein refers to a peptide that has an amino-terminal and/or carboxy-terminal deletion, but where the remaining amino acid sequence is identical to the corresponding positions in the sequence of a major or target polypeptide or protein, for example, from a full-length sequence of a protein.
The term “vaccine” refers to an agent or composition containing an active component effective to induce a therapeutic degree of immunity in a subject against a certain pathogen or disease. Traditionally, the active component of a vaccine is a polypeptide derived from a pathogen which is the target of the vaccine. The term “DNA vaccine” refers to a vaccine wherein the active component is DNAs.
A “subject” in need of therapy is a human or non-human mammal. Non-human mammals include, but are not limited to, primates, ungulates, canines and felines.
The term “adenovirus” as referred to herein indicates over 47 adenoviral subtypes isolated from humans, and as many from other mammals and birds. See, Strauss, “Adenovirus infections in humans,” in The Adenoviruses, Ginsberg, ed., Plenum Press, New York, N.Y., pp. 451 596 (1984).
The present invention provides a vaccine composition comprising a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding a polypeptide of F protein of RSV or fragment thereof.
In one example of the invention, the vaccine composition comprises a replication-defective recombinant adenoviral construct transformed with a nucleotide sequence encoding F protein of RSV. As demonstrated in the examples below, the vaccine composition of the present invention effectively elicited both humoral and cellular immune responses. The vaccine composition of the present invention is further characterized in that it does not have undesired side effects, such as eosinophilia and inflammatory responses associated with interleukins, such as IL-17.
According to the invention, the F protein of RSV may be derived from any strains of naturally-occurring or recombinant RSV, preferably from human RSV strains, such as A2, long, or B strains. In one example of the invention, the RSV strain is RSV-B1 strain.
According to the invention, the F protein of RSV may be the full length of F protein of RSV or fragement thereof. In one embodiment of the invention, the nucleotide sequence encoding F protein of RSV encodes the full length of F protein of RSV (F0), such as the amino acid of SEQ ID NO: 2. In one example of the invention, the nucleotide sequence encoding F protein of RSV has the nucleotide sequence of SEQ ID NO: 1 (GenBank, NC—001803). The F protein of RSV may be any sequence that is at least about 75%, preferably more than about 85%, homologous to the nucleotide sequence of SEQ ID NO: 1.
In another embodiment of the invention, the nucleotide sequence may alternatively encode a fragment of F protein of RSV. The fragment may be resulted from either or both of amino-terminal and carboxy-terminal deletions. The extent of deletion may be determined by a person skilled in the art to, for example, achieve better yield of the recombinant adenovirus. In one example of the present invention, the fragment was the transmembrane coding region-truncated F protein of RSV (F0ΔTM), which was deleted from the full-length sequence of F protein. In one Embodiment of the invention, the nucleotide sequence is the transmembrane coding region-truncated F protein of RSV (F0ΔTM), such as the amino acid sequence of SEQ ID NO: 3. In one example of the invention, the transmembrane coding region-truncated F protein of RSV (F0ΔTM) has the nucleotide sequence of SEQ ID NO: 3. The fragments of F protein may also be F1 domain or F2 domain of F protein.
The adenoviral construct which serves as the backbone of the recombinant vaccine construct of the present invention is preferably a “first generation” adenoviral construct. This type of adenoviral constructs is known in the art, and is characterized by being replication-defective. These viruses typically have a deleted or inactivated E1 gene region, and preferably additionally have a deleted or inactivated E3 gene region. In one embodiment of the present invention, the first generation replication-defective adenovirus construct used is a serotype 5 adenovirus (Ad5) containing deletions in E1 (Ad5 base pairs 342-3523) and E3 (Ad5 base pairs 28133 to 30818). For adenovirus serotype 2 (Ad2), the E1 deletions are preferably bps 559-3503 and the E3 deletions are preferably bps 28812-29773. (Genbank gb:J01917). Those of skill in the art can easily determine the equivalent sequences for other serotypes, such as serotypes 4, 12, 6, 17, 24, 33, 42, 31, 16.
In one example of the invention, adenoviral serotypes 2 and 5, particularly 5, may be used. since at this point in time, more is known about these serotypes generally than other serotypes, and their complete DNA sequences are known. The prototype serotype 5 adenovirus has been completely sequenced (Chroboczek et al, 1992 J. Virology 186:280). They also belong to the subgroup C adenoviruses, which are not associated with human or rodent malignancies. However, it is envisioned that any adenovirus serotype can be used in this invention, including non-human ones, as deletion of E1 genes should render all adenoviruses non-tumorogenic. Also it may be advantageous to use a serotype which has less prevalence in the wild, as patients are less likely to have previous exposure (and less pre-existing antibodies) to a rarer serotype.
The recombinant adenoviruses according to the present invention can be prepared by any technique known to those of ordinary skill in the art (Levrero et al., Gene 101 (1991) 195, EP 185 573; Graham, EMBO J. 3 (1984) 2917). In particular, they can be prepared by homologous recombination between an adenovirus and a plasmid carrying, inter alia, the F protein-encoding DNA sequence. The homologous recombination occurs after co-transfection of the said adenoviruses and plasmid into an appropriate cell line. The cell line used should preferably (i) be transformable by the said elements and (ii) contain the sequences capable of complementing the defective adenovirus genome part, preferably in integrated form in order to avoid risks of recombination. As an example of a cell line, there may be mentioned the human embryonic kidney line 293 (Graham et al., J. Gen. Virol. 36 (1977) 59) which contains especially, integrated into its genome, the left-hand part of the genome of an Ad5 adenovirus (12%).
The vaccine composition of the present invention may further comprise one or more adjuvants. The term “adjuvant” as used herein refers to an agent that enhances the immunogenicity of an antigen but is not necessarily immunogenic. Adjuvants may act by retaining the antigen locally near the site of administration to produce a depot effect facilitating a slow, sustained release of antigen to cells of the immune system. Adjuvants can also attract cells of the immune system to an antigen depot and stimulate such cells to elicit immune responses.
In the other aspect, the present invention provides a method of preventing RSV infection or RSV infection-related diseases comprising administering to a subject in need thereof a vaccine composition comprising a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding a polypeptide of the F protein of RSV or fragments thereof.
RSV infection-related diseases include, but not limited to, otitis media, bronchilitis, eosinophilia, and pneumonia.
As demonstrated in the examples below, the vaccine composition of the present invention effectively elicits mucosal immune response when administered intranasally. Therefore, although the vaccine composition of the present invention may be administered via any traditional route such as subcutaneous, intradermal, intramuscular and intravenous injection, it is preferably administered transmucosally via, for example, the nasal or oral (intragastric) routes. In a preferred embodiment of the present invention, the vaccine composition is administered intranasally.
Other modes of administration including suppositories and oral formulations may also be desirable. Any suitable formulations for vaccines may be formulated by incorporating into the vaccine composition of the present invention pharmaceutically acceptable excipients, such as water, saline, glycerol, and ethanol, and substances such as wetting agents, emulsifying agents, or pH buffering agents.
The vaccine composition of the present invention may also be co-administered with antigens from other pathogens as a multivalent vaccine.
The present invention will now be described more specifically with reference to the following embodiments, which are provided for the purpose of demonstration rather than limitation.
Construction and Production of rAd-F0 and rAd-F0ΔTM
Human embryonic kidney cells (293A) [Invitrogen, CA, USA] were grown and maintained in DMEM medium (Hyclone, Cat No. SH300) supplemented with 10% fetal bovine serum (Biological), and 1% penicillin/streptomycin (Biological) in an incubator maintained at 37° C. and equilibrated with 5% CO2. RSV-B1 fusion (F) glycoprotein genes encoding the full length of F protein, F0 (SEQ ID NO: 1) and F0ΔTM (SEQ ID NO: 3, lacking the sequence coding for the transmembrane domain) were individually amplified by PCR and inserted into the shuttle vector, pENTRY4 (Invitrogen), to facilitate the subsequent recombination of inserted F gene into the ΔE1/ΔE3 (replication-incompetent) Ad5 vector, pAd/CMV/V5-DEST (Mizuguchi and Kay, Efficient construction of a recombinant adenovirus construct by an improved in vitro ligation method. Hum Gene; Ther 1998 Nov. 20; 9(17):2577-83; and Mizuguchi and Kay, A simple method for constructing E1- and E1/E4-deleted recombinant adenoviral vectors; Hum Gene Ther 1999 Aug. 10; 10(12):2013-7). The Recombinant plasmids pAd-F0, and pAd-F0ΔTM DNA were individually transfected into the packaging cell line, 293A, to produce the respective recombinant adenoviruses, designated as rAd-F0 and rAd-F0ΔTM, respectively (
Purification and concentration of the recombinant constructs were achieved by ultracentrifugation through a 15% sucrose/PBS gradient at 20,000 rpm for 60 min. The viruses were then resuspended in PBS, pH 7.2, and their titers determined by the modified standard plaque assay described. Briefly, varying dilutions of rAd-F0ΔTM rAd-F0 viruses were added to 293A cells plated in each well of a 6-well tissue culture plate. After overlaying the cultures with DMEM containing 0.75% methylcellulose, the cultures were incubated at 37° C. for 10 to 12 days and plaques were counted. The yield of rAd-F0 and rAd-F0ΔTM was usually around 1×109 pfu/mL.
Determination of RSV F Gene Expression in rAd-F0- and rAd-F0ΔTM-Infected 293A Cells
Protocol described for live RSV infection of 293A cells was used to determine the infectivity of rAd-F0 or rAd-F0ΔTM and assess the expression of their respective F genes. To this end, 2×106 293A cells were infected with 2×105 pfu of either rAd-F0 or rAd-F0ΔTM. Three days later, cells were collected by scraping and placed into a 50.0 mL sterile centrifuge tube (Corning). Harvested cells were divided into equal parts, and were washed twice, each time with 10.0 mL of ice-cold PBS, pH 7.2 to remove residual FBS. Total RNA was extracted from one part of the cell pellet using RNeasy Mini kit (Qiagen) according to the protocol provided by the supplier. cDNA was then generated using the SuperScript reverse™ II reverse transcriptase kit (Invitrogen). The forward and reverse primers: 5′-ACATCGACAAGCAGCTGCTGC-3′ (forward; SEQ ID NO: 5) and 5′-GAGGTGAACCTGTGCAACG-3′ (reverse; SEQ ID NO: 6) were used to amplify and detect the 593-1151 region of the full length of F1 mRNA transcribed from the F0 (of 1722 nucleotides, SEQ ID NO: 1) and F0ΔTM (of 1572 nucleotides, SEQ ID NO: 3) inserts. The molecular size of the PCR product obtained was expected to be 559 bps. The fragment covering the nucleotide sequence 13-390 was amplified by using the F2 primer pairs: 5′-ATCCTGAAGGCTAAGGCTATC-3′ (forward; SEQ ID NO: 7), and 5′-ACCAACGTGACCCTGTCCAA-3′ (reverse; SEQ ID NO: 8) to generate a PCR product was expected to be 378 bps. Using primers specific to β-actin as Internal control in the RT-PCR was included (Invitrogen, CA, USA). The PCR products were analyzed by agarose electronpheresis.
The PCR products were analyzed by agarose electrophoresis. The second cell pellet was lysed to release the intracellular proteins for immunoblot analysis. Cell lysis was performed by treating the cell pellet with a pH 8.0 lysis buffer (containing 50 mM Tris-HCl, 150 mM NaCl, 1% Triton X-100, and 1× protease inhibitor cocktail (Roche). Lysis was allowed to take place on ice for 30 minutes with occasional pipetting. Cell debris was removed by centrifugation at 14,000×g for 20 minutes at 4° C. The cell lysate was subjected to SDS-PAGE electrophoresis, and proteins were transferred onto a Hybond ECL nitrocellular membrane (Amersham). The membrane was blocked with 5% skim milk in Tris-buffer saline, pH 7.2, at room temperature for 1 hour, washed twice with PBS containing 0.05% Tween 20 (PBST) and incubated with a polyclonal human antiserum raised against RSV (a gift from Burney S. Graham, NIH, USA) at 4° C. overnight. The membrane was washed twice with PBST, and an anti-human horseradish peroxidase (HRP)-conjugated antibody (KPL Immunochemical) diluted at 1 in 5000 in PBS containing 5% skim milk was then added to the membrane for protein visualization. Alternatively, 1:500 diluted polyclonal sera from recombinant adenoviruses-immunized mice were used to be primary antibody to blot HIRSV-B1-transferred membrane. After washing, a 1:20000 diluted HRP-conjugated donkey anti-mouse polyclonal serum as secondary antibody was used (Jackson). After 1 hour incubation at room temperature, the membrane was washed twice with PBST before it was treated with SuperSignal West Pico chemiluminescent substrate (Pierce), and exposed onto an X-ray film.
Upon transfection into competent 293A cells which constitutively expressed the E1 protein, the recombinant adenoviruses were shown to express their respective F inserts, as judged by RT-PCR reaction. The result showed that the PCR products corresponding to 378 bps and 559 bps were obtained via amplification of the 13-390 and 593-1151 nucleotide region of RSV F0 (F2+F1) or RSV F0ΔTM (F2+F1ΔTM) cDNA with the F2 and F1 primer pairs, respectively, from 293A cells transfected with rAd-F0 or rAd-F0ΔTM (
Preparation of RSV-B1, -Long and -A2 Strain Stocks
Human larynx carcinoma cells (Hep-2) provided by Dr. Burney Graham of National Institute of Health, USA were grown and maintained in DMEM medium (Hyclone, Cat No. SH300) supplemented with 10% fetal bovine serum (Biological), and 1% penicillin/streptomycin (Biological) in an incubator maintained at 37° C. and equilibrated with 5% CO2.
The human RSV-B1 (VR-1580), -long (VR-26) and -A2 (VR-1540) strains (purchased from the American Type Culture Collection) were propagated in Hep-2 cells. Hep-2 cells were grown in 150 mm Petri dish (Corning) up to 80% confluency before they were inoculated at an m.o.i. (multiplicity of infection) of 0.2 of RSV-B1, -long or -A2 isolates. Infection was allowed to take place for 4 days before the infected cells were harvested by scraping. Virus-containing Hep-2 cells were collected into a sterile 50.0 mL centrifuge tube (Beckman), and pelleted by centrifugation for 5 min at 3000 rpm. The cell pellet was disrupted using a tissue grinder to release the virions. Cell debris were removed by centrifugation at 3,000 rpm for 10 min. Partial purification of the individual viruses was performed by centrifugation of cell supernatants through a 15% sucrose (in PBS) gradient for 2 hours at 30,000 rpm. The virus was collected and resuspended in PBS, pH 7.2. The titer of RSV was determined by a standard plaque assay. Briefly, 100.0 μL of varying dilutions of purified virus preparations were added to 5×105 Hep-2 cells cultured in a 12-well plate (Corning). Each of the cultures was then overlaid with DMEM containing 1.5% methylcellulose (Sigma-Aldrich) and incubated for 5 to 6 days for the plaques to develop. Cells were stained with hematoxylin and eosin plaques were counted under a light microscope. The concentration of the individual virus is expressed as plaque-forming units per mL (pfu/mL).
Immunization and Live RSV Challenge of Mice
Six to eight week-old female BALB/c mice were purchased from the National Laboratory Animal Center, Taiwan. Mice were maintained in pathogen-free cages at the Animal Care Center of National Health Research Institutes throughout the animal study.
The four groups of BALB/c mice were anesthetized with isoflurane and primed with 1×107 pfu/50 μL of rAd-F0ΔTM, rAd-F0, rAd-LacZ and heat-inactivated RSV (HIRSV-B1) via the intranasal (i.n.) route. Twenty (20) days later, animals were boosted at an interval of 20 days apart either i.n., subcutaneously (s.c.), or intraperitoneally (i.p.) with the same dose of the respective immunogens. Mice were bled 14 days after priming or 10 days after booster immunization, serum samples were individually analyzed against HIRSV-Blor Ad5 in ELISA, and virus-specific neutralizing activity. For challenge studies, 1×106 pfu of live RSV-B1 was administered intranasally thirty days after the second immunization.
Individual BALB/c mice (H-2d) was intranasally administered with 1×107 pfu rAd-F0, rAd-F0ΔTM or, rAd-LacZ as control. Animals of a separate group were give the same pfu equivalent of HIRSV-B1 via the same immunization route to evaluate the virus-specific immune responses elicited as compared to those by the recombinant adenoviruses. The results of the ELISA assays obtained from two independent experiments are summarized in Table 1.
It was found that serum samples collected from mice post intranasally primed with rAd-F0ΔTM and rAd-F0 gave mean HIRSV-B1-specific titers corresponding to 104 and 44, and, 88 and 38, respectively, in the two studies. The mean titer of the serum antibodies measured against immobilized HIRSV-B1 in the HIRSV-B1 immunized animals was 136 in experiment 1, and 112 in experiment 2. In contrast, no HIRSV-B1 reactivity was detected in the serum samples of mice primed with the empty vector, rAd-LacZ. rAd-LacZ component of the recombinant adenoviruses was immunogenic as evident from the low anti-rAd-LacZ (Ad5) IgG titers (mean) corresponding to 52 and 60 of mice intranasally administered once with rAd-F0ΔTM and rAd-F0, respectively; and 42 for animals administered with rAd-LacZ. In the second experiment, mean anti-AdS-specific titers measured in the immune sera of animals were 76 for rAd-F0ΔTM, 96 for rAd-F0 and, 92 for rAd-LacZ that was administered. Following booster immunization with the respective immunogen via intranasal, subcutaneous (s.c) or intraperitoneal (i.p.) route, HIRSV-B1 reactive titers assayed in the serum samples of the experimental groups of mice were found to be substantially increased. In experiment 1, the IgG antibody titers were in the range of 2560 and 5120 (mean=4608) for the animals administered i.n. twice with HIRSV-B1; and 2560 and 10240 (mean=6144), and 1280 and 10240 (mean=6400) for mice primed intranasally and boosted s.c. and i.p. with HIRSV-B1, respectively. In experiment 2, mean HIRSV-B1-binding antibody titers obtained from mice following booster inoculation with HIRSV-B1 were: 2816 via i.n., 10240 via s.c. and 12288 via i.p. routes. In both studies, serum anti-RSV-B1-specific IgG antibodies were not detected in mice given 1×107 pfu of rAd-LacZ under the three immunization routes tested. However, high titers of HIRSV-B1 IgG binding antibodies in the range of 2560 and 10240 (mean=6656), and, 2560 and 5120 (mean=3584) were detected in the sera of animals immunized intranasally with the same dose of rAd-F0ΔTM in experiments 1 and 2, respectively. These antibody levels were not markedly different from those detected in animals inoculated intranasally, followed by boosting either s.c. or i.p. with rAd-F0ΔTM. Compared to rAd-F0ΔTM, rAd-F0 was found to be slightly less immunogenic under the three immunization protocols tested. Serum HIRSV-B1-specific antibody titers were between 640 and 5120 (mean=2432), and 1280 and 5120 (mean=2304) in animals vaccinated intranasally with rAdF0 in experiments 1 and 2. For mice in experiment 1 that were primed intranasally and boosted either s.c. or i.p. with rAd-F0, HIRSV-B1 binding IgG antibody titers were within the range of 1280 and 10240 (mean=6400), and 160 and 10240 (mean=4128), respectively. Comparable HIRSV-B1-binding titers were detected in the immune sera of animals in experiment 2 boosted with rAd-F0 via the two immunization routes. Given the fact that rAd-LacZ immunization did not lead to the production of anti-HIRSV-B1 antibody responses, the specificity of the IgG antibodies in the immune sera of rAd-F0ΔTM and rAd-F0 vaccinated animals either after priming or booster immunization would be directed against the viral F protein. However, there is no difference of F-specific antibody responses in the three different administrative routes after statistical analysis. As intranasal vaccination is effective, we chose this route of immunization to further investigate the nature of the humoral as well as cellular responses elicited by rAd-F0ΔTM, and the less immunogenic rAd-F0 construct.
Determination of Serum and Bronchoalveolar Lavage (BAL) IgA and IgG Levels
Virus-specific IgG and IgA antibodies in immune sera and bronchoalveolar lavages (BALs) of the individual animals were determined by ELISA using HIRSV-B1 as target antigen. BAL fluids were collected by performing 2 consecutive washes of the airspace of the lungs of individual experimental mice, each time with 1.0 mL of sterile PBS containing 1× protease inhibitor coattail (Roche), pH 7.4. The samples obtained were stored in a −80° C. freezer until tested for their contents of RSV-specific IgA and IgG antibodies.
For ELISA, blood samples collected by tail vein puncture of the individual experiments mice 14 days after intranasal priming, and 10 days after the booster immunization were clotted at room temperature, then centrifuged at 12,000 rpm for 20 min. Sera were pipetted out and inactivated at 56° C. for 30 min. ELISA for the detection of RSV-specific IgG and IgA antibodies entailed coating wells of a 96-well Immulon 2B plate (Corning Life Sciences, USA) with 2.5×10 pfu of cesium chloride gradient-purified, heat-inactivated (75° C. for 1 hr) RSV-B1 virus in 100 uL of sterile sodium carbonate buffer (8.4 g/L NaHCO3, and 3.5 g/L Na2CO3, pH 9.5) at 37° C. overnight. The Sera of the individual mice collected from tail sample bleeds on day 14 following intranasal priming with rAdF0ΔTM, rAd-F0 or, the empty vector, rAd-LacZ, were also assayed against rAd-LacZ immobilized on ELISA wells (2.5×104 pfu of the virus per well) using the same coating condition to determine their contents of anti-adenovirus antibodies. All the antigen-coated ELISA wells were then blocked with 5% skim milk in PBS at room temperature for 1 hour and washed three times with 200 μL of PBS containing 0.05% Tween 20. Individual sera were 2-times serially diluted (80 to 163840) and 100 uL were added to virus-coated well for 2 hours at room temperature, and the reaction was allowed to take place at room temperature for 2 hours. Wells were washed three times with 200 μL of wash buffer (PBS containing 0.5% Tween 20). One hundred μL of either horseradish peroxidase (HRP)-conjugated donkey anti-mouse IgG antibodies (Jackson), or anti-mouse IgA antibodies (ZYMED) were then added to detect the binding of anti-RSV binding antibodies. After another one-hour incubation at room temperature, the plates were washed four times with the wash buffer, and 70.0 μL of SureBlue™ TMB peroxidase substrate solution (Kirkegaard & Perry Laboratories) were added to the wells. Following 15 min incubation in the dark, absorbance at wavelength 450 nm was recorded in an ELISA reader (SPECTRA NAX M2, Molecular Devices).
The same ELISA protocol was also used to determine IgA levels in the BALs.
The results were summarized below. Mice primed intranasally (i.n.) with 1×107 pfuof the recombinant adenoviruses of the invention, or HIRSV-B1 and boosted either i.n., subcutaneously (s.c) or intraperitoneally (i.p.) with the priming dose of immunogen were found to mount comparable levels of anti-viral antibody responses. The IgG antibody titers measured against immobilized HIRSV-B1 were in the range of 2560 and 5120 (mean=4608) for the animals administered i.n. twice with HIRSV-B1, and 2560 and 10240 (mean=6144), and 1280 and 10240 (mean=6400) for mice primed intranasally and boosted s.c. and i.p. with HIRSV-B1, respectively. Serum anti-RSV-B1-specific IgG antibodies were not detected in mice given 1×107 pfu of rAd-lacZ under the three immunization routes tested. However, high titers of HIRSV-B1 IgG binding antibodies in the range of 2560 and 10240 (mean=6656) were detected in the sera of animals immunized intranasally with the same dose of rAd-F0ΔTM. These antibody levels were comparable to those detected in animals inoculated intranasally, followed by boosting either s.c. or i.p. with rAd-F0ΔTM. Compared to rAd-F0ΔTM, rAd-F0 was found to be less immunogenic regardless of the immunization schedule. Serum HIRSV-B1-specific antibody titers were between 640 and 5120 (mean=2432) in animals vaccinated intranasally with rAd-F0. For mice primed intranasally and boosted either s.c. or i.p. with rAd-F0, HIRSV-B1 binding IgG antibody titers were within the range of 1280 and 10240 (mean=6400), and 160 and 10240 (mean=4128), respectively (
Intranasal administration with either rAd-F0ΔTM or rAd-F0 also led to the production of F protein-specific IgA antibodies. IgA antibody titers in sera and BALs of mice immunized with rAd-F0ΔTM were found to be slightly lower than those in the samples from animals given HIRSV-B1, but significantly higher than the levels measured in the samples from mice vaccinated with rAd-F0 (
Anti-RSV-B1 antibodies generated by the mice immunized via the intranasal route with rAd-F0ΔTM and rAd-F0 also cross-reacted with RSV-long and -A2 strains. The serum samples were collected from individual BABL/c mice administered twice with 107 pfu of rAd-F0, rAd-F0ΔTM, rAd-LacZ, or HIRSV-B1, 10 days after the booster administration, and the titles were assayed against the heat-inactivated RSV-B1 (B1 strain pf RSV), RSV-long (Long strain of RSV) and RSV-A2 (A2 strain of RSV) immobilized on ELISA plate wells. As shown in the results in
Virus Neutralization Assay and Viral Load Determination
The RSV-specific neutralizing activity of immune sera was determined by mixing 50 μL of serially diluted sera (reconstituted with pre-immunized normal mouse sera to equal amount of sera) with 50.0 μL (103 pfu) of live RSV-B1, -long, or -A2 and incubated for 1 hour at 37° C. The mixture was then added to 2×105 Hep-2 cells in a 6-well plate. One hour later, wells were overlaid with a 1.5% (w/v) semi-solid methylcellulose. Hep-2 cell cultures treated with the same dose of virus were used as positive control. RSV induced syncytia-formation was assessed by light microscopy 5 days later, and syncytia reduction was calculated by regression analysis to obtain a 60% syncytia reduction titer (giving 60% inhibition of plaque-formation). A second similar set of experimental cultures were fixed with 3.7% formaldehyde and stained with 1% hematoxylin and eosin to develop plaques that were counted under a light microscope.
As shown in
IgA antibodies in BAL samples of mice immunized with the recombinant adenoviruses at varying dilutions, 4×, 8×, 16×, 32×, 64× and 128×, respectively, as scored after 4 days of culture. As shown in
In this example, an investigation regarding the F protein-specific CD4+ lymphocyte response profile elicited in mice immunized with the rAd-F0ΔTM and rAd-F0 was conducted because it was known that an immunological help provided by CD4+ helper T cells from the Th1 and Th2 phenotypes regulated antigen-specific humoral and cytotoxic T-cells (CTLs) responses.
Splenocyte suspensions were prepared from the spleens of individual experimental mice. After cell sedimentation, 5.0 mL of ice-cold red blood cell (RBC) lysing buffer (Gibco) was added to cell pellets. RBC lysis was facilitated by continuous gentle pipetting for 1 min. Lysis was stopped by adding 5.0 mL of culture medium (CM: DMEM (Gibco) supplemented with 10.0% fetal bovine serum, and 100 μg/mL of penicillin/streptomycin mix). Lymphocytes were pelleted by centrifugation at 2,000 rpm for 5 min, and washed one more time with 10.0 mL of CM. Splenocytes (2×106) were then cultured in a 24-well tissue culture plate (Corning) in the presence or absence of 103 pfu of HI-RSB-B1. Cultures were kept in a 5.0% CO2 incubator at 37° C. Culture supernatants were collected 48 hr later, and stored at −80° C. until tested. Th1 (IFN-γ) and Th2 (IL-4, IL-5, IL-10 and IL-13) cytokines as well as IL-17 present in culture supernatants were quantitated by using the respective antibody-pairs purchased from eBiosceince (IL-13-Cat. No. 88-7137-88; IL-17-Cat No 88-7371-88; IL-4-Cat. No. BMS609MST; IL-5-Cat. No. BMS610MST; IL-10-Cat. No. BMS614MST). Recombinant IFN-γ and IL-13 used as standards were from eBioscience and recombinant IL-4, IL-5 and IL-10 were purchased from Bender MedSystems, Inc.
Following in vitro restimulation with HIRSV-B1, lymphocytes of mice immunized with the control construct, rAd-LacZ, produced a background level of IFN-γ corresponding to 582±138 pg/mL (mean). In contrast, significantly higher IFN-γ levels of 1709±433 pg/mL and 1988±429 pg/mL were measured in the supernatants of HIRSV-B1-stimulated splenocyte cultures of mice administered with rAd-F0ΔTM and rAd-F0, respectively (
In this example, the effect on immunization with rAd-F0ΔTM and rAd-F0 constructs leading to the induction of F-specific CTLs was investigated in order to detect the apoptotic death of target infected cells. A granzyme B ELISPOT assay was used to measure the frequencies of CTLs directed against a F85-93 peptide, KL-9 (KYKNAVTEL). KL-9 was known as a peptide containing an immunodominant H-2Kd-resticted epitope of the RSV F protein in the spleens of immune animals, and to comprise a dominant Kd-restricted CTL epitope from RSV F protein in the presence of 10 U/mL of recombinant IL-2 at 37° C. for 5 days (Chang J, Srikiatkhachorn A, Braciale T J. Visualization and characterization of respiratory syncytial virus F-specific CD8(+) T cells during experimental virus infection. J Immunol 2001 Oct. 15; 167(8):4254-60).
Granzyme B release ELISPOT assay previously described to determine the effector function of antigen-specific CTLs (Shafer-Weaver K, Sayers T, Strobl S, Derby E, Ulderich T, Baseler M, et al. The Granzyme B ELISPOT assay: an alternative to the 51Cr-release assay for monitoring cell-mediated cytotoxicity. J Transl Med 2003 Dec. 29; 1(1):14) was used to assess the presence of RSV F protein-specific CTLs in the spleens of the immunized animals. The assay entailed culturing 5×106 splenocytes with 2.0 μg per mL of a KL-9 peptide. Target cells (p815 cells) were supplemented with 2.0 μg per mL of a KL-9 peptide at a ratio of 30:1, 10:1, and 1;1 in anti-granzyme B capture antibody coated well for 2 days at 37° C. prior use in assay. Unpulsed p815 cells served as negative control. 104 target cells per well (100 μL) were added to wells of a 96-well plate pre-coated with capture monoclonal antibodies (0.1 μg per well) (R&D) specific for murine granzyme B following the appropriate number of in vitro restimulated splenocytes culture (as effectors cells). The defined effector:target (E:T) ratios were plated in triplicate. Two days later, the cells were damped off and the plates were washed three times with wash buffer before adding 100 μL of PBS-Tween 20 containing 0.25 μg of the detection monoclonal antibody specific for mouse granzyme B. The plates were left at 4° C. for overnight, washed four times with wash buffer, 100 μL of streptavidin-alkaline phosphatase were added and the plates were incubated at room temperature for 2 hr. The wells were washed again four times before 100 μL of substrate (BCIP/NBT) were added to develop the immunospots. After 30 min incubation in the dark, the plates were washed with water, left to dry, and the number of immunospots was scored using the ELISPOT reader (C.T.L. IMMUNOSPOT, CELLULAR TECHNOLOGY LTD).
Following co-culturing of splenocytes (effector) from rAd-LacZ-immunized mice with 104 P815 (target) cells loaded with the KL-9 peptide at effector/target ratios of 30:1, 10:1, and 1:1, a mean background number of granzyme B-secreting effector splenocytes cells was scored. In contrast, rAd-F0ΔTM immunized mice mounted a significantly more vigorous KL-9-restricted response than animals administered with rAd-F0. No KL-9-restricted CTL response was detected in mice immunized with HIRSV-B1 (
The anti-viral humoral and cellular responses elicited via intranasal immunization with rAd-F0ΔTM and rAd-F0 were assessed in parallel to those generated by HIRSV-B1 vaccination for their immunprotective ability against live RSV challenge. The parameters selected to assess protection included measurement of viremia in the lungs, recovery from initial weight loss, and blood eosinophilia.
Lung Viral Load Determination
Mice were individually immunized via the intranasal route twice with relevant immunogens before they were intranasally challenged with 106 pfu of live RSV-B1. Viral plaques in the lungs of individual mouse was determined 5 days after challenge using the plaque-forming assay. Whole lungs from individual experimental mice were removed, and homogenized. The homogenized tissues were centrifuged at 3,000 rpm for 10 min at 4° C. to sediment cell debris. Supernatants were collected, serially diluted, and tested for their ability to infect Hep-2 cells in the plaque formation assay. In
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Body Weight Loss
Progressive body weight was determined for each of the mice challenged with live RSV-B1 regardless of whether they were immunized with rAd-F0ΔTM, rAd-F0, rAd-LacZ or HIRSV-B1, in addition to an untreated group in the study. Each animal was then intranasally inoculated with 106 pfu of live RSV B1. The body weight of each mouse was recorded daily. The results in
Blood Eosinophilia Determination
The mice were individually immunized via the intranasal route twice with the immunogen before they were intranasally challenged with 106 pfu of live RSV-B1. Peripheral blood samples obtained by tail vein puncture 7 days post-live RSV challenge were collected in sterile Eppendorf vial (Corning) containing 5.0 μL of 3% EDTA. Five μL of blood were smeared onto a glass slip. The blood sample was dried at room temperature, and then stained with 1.0-2.0 mL of Wright-Giemsa stain solution (Sigma-Aldrich) for 1.5 min at room temperature. Excess stain was washed by rinsing the glass slips twice with deionized water. After air-drying, eosinophils identified as red/pink cells were counted under an oil immersion microscope, and their numbers were scored as percentage of total leukocytes.
As shown in
The above examples showed that the F0 and F0ΔTM proteins expressed in mice vaccinated with the respective recombinant adenoviruses are immunogenic as judged by the induction of F protein-specific humoral and cellular immune responses. F protein-specific antibodies present in sera and BALs of mice primed and boosted with rAd-F0ΔTM and rAd-F0 using either i.n./i.n., i.n./s.c., or i.n./i.p. routes are virus neutralizing. It is further demonstrated that serum antibodies elicited by adenovirus constructs cross-react with the F proteins of the RSV-long and A2 strains. A notable finding in the present invention is the effectiveness of the intranasal delivery of the recombinant adenoviruses at inducing F-specific IgA antibodies in bronchoalveolar lavages of immune mice. Intranasal immunization with rAd-F0ΔTM and rAd-F0 also allowed for the correct processing of the RSV F protein to generate MHC class 1-restricted CTLs.
The anti-viral immunity elicited by rAd-F0 and rAd-F0ΔTM constructs confers protection against live RSV-B1 virus challenge. This is evident from the significantly lower viral load recovered from the lungs of animals immunized intranasally with the recombinant adenoviruses, but not with the rAd-LacZ control construct. Vaccination with rAd-F0 or rAd-F0ΔTM constructs allows for an accelerated recovery from initial body weight lost following live RSV challenge, faster than that observed in mice given rAd-LacZ. Protection studies showed that resistance to RSV challenge is greater in mice administered with rAd-F0ΔTM that mount stronger virus-neutralizing antibody and CTL responses than animals immunized with the less immunogenic rAd-F0 construct.
Since there is no current RSV vaccine available, a heat-inactivated RSV preparation is used in the present invention to compare the anti-viral humoral responses contributing to protection against RSV infection. Indeed, mice immunized with HIRSV-B1 produced virus-specific binding and neutralizing antibodies at significantly higher levels than those administered with either rAd-F0 or rAd-F0ΔTM, and were found to be at least equally protected from live RSV challenge. In summary, HIRSV-B1-immunized mice did not mount CTL responses, which anti-viral immunity could be attributed to neutralizing antibodies generated against the F protein, and the G antigen that also contained virus-neutralization epitopes. However, as observed in the vaccinated mice with the recombinant adenovirus construct of the invention followed by a live RSV post challenge, the level of eosinophilia was significantly lower than that in the mice pre-immunized with HIRSV-B1 followed by a live RSV post challenge. Accordingly, it was concluded that the immunization with HIRSV-B1, instead of the F protein-expressing adenovirus construct of the invention, leaded to the generation of T cells that secreted an enhanced level of Th2 cytokines
It is also observed here that Splenocytes from mice immunized with HIRSV-B1, produced markedly higher level of IL-17 as compared to those from the mice vaccinated with the recombinant adenovirus construct of the invention, rAd-F0. Unexpectedly, Th17 cells producing IL-17 (associated with inflammation) were not detected in the spleens of the mice vaccinated with the vaccine of the invention, Ad-F0ΔTM. The above findings suggested that the presentation of the G glycoprotein, and the transmembrane portion of the F protein might drive the differential development of CD4+ cells to acquire the Th17 phenotype in addition to the Th1 and Th2 phenotypes. Because Th17 cells was found to be substantially associated with various aspects of inflammation (Annunziato et al, The phenotype of human Th17 cells and their precursors, the cytokines that mediate their differentiation and the role of Th17 cells in inflammation; Int Immunol 2008 November; 20(11):1361-8.), the recombinant adenovirus vaccines of the present invention utilizing the F protein of RSV (in place of the glycoprotein) could avoid such undesired side effect, inflammation, while maintaining great immunizing effect.
All publications and patent documents cited in this application are incorporated by reference in their entirety for all purposes to the same extent as if each individual publication or patent document were so individually denoted.
