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Article ; Online: Co-formulation of the rF1V plague vaccine with depot-formulated cytokines enhances immunogenicity and efficacy to elicit protective responses against aerosol challenge in mice.

Galloway, Darrell R / Li, Jiahui / Nguyen, Nguyen X / Falkenberg, Frank W / Henning, Lisa / Krile, Robert / Chou, Ying-Liang / Herron, James N / Hale, J Scott / Williamson, E Diane

Frontiers in immunology

2024 Volume 15, Page(s) 1277526

Abstract: This study evaluated a depot-formulated cytokine-based adjuvant to improve the efficacy of the recombinant F1V (rF1V) plague vaccine and examined the protective response following aerosol challenge in a murine model. The results of this study showed that ...

Abstract	This study evaluated a depot-formulated cytokine-based adjuvant to improve the efficacy of the recombinant F1V (rF1V) plague vaccine and examined the protective response following aerosol challenge in a murine model. The results of this study showed that co-formulation of the Alhydrogel-adsorbed rF1V plague fusion vaccine with the depot-formulated cytokines recombinant human interleukin 2 (rhuIL-2) and/or recombinant murine granulocyte macrophage colony-stimulating factor (rmGM-CSF) significantly enhances immunogenicity and significant protection at lower antigen doses against a lethal aerosol challenge. These results provide additional support for the co-application of the depot-formulated IL-2 and/or GM-CSF cytokines to enhance vaccine efficacy.
MeSH term(s)	Humans ; Animals ; Mice ; Plague Vaccine ; Cytokines ; Yersinia pestis ; Antigens, Bacterial ; Vaccines, Synthetic ; Aerosols
Chemical Substances	Plague Vaccine ; Cytokines ; Antigens, Bacterial ; Vaccines, Synthetic ; Aerosols
Language	English
Publishing date	2024-03-28
Publishing country	Switzerland
Document type	Journal Article ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	2606827-8
ISSN	1664-3224 ; 1664-3224
ISSN (online)	1664-3224
ISSN	1664-3224
DOI	10.3389/fimmu.2024.1277526
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Article: Predictors of Survival after Vaccination in a Pneumonic Plague Model.

Moore, Barry D / Macleod, Clair / Henning, Lisa / Krile, Robert / Chou, Ying-Liang / Laws, Thomas R / Butcher, Wendy A / Moore, Kristoffer M / Walker, Nicola J / Williamson, Ethel Diane / Galloway, Darrell R

Vaccines

2022 Volume 10, Issue 2

Abstract: Background: ...

Abstract	Background:
Language	English
Publishing date	2022-01-19
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2703319-3
ISSN	2076-393X
ISSN	2076-393X
DOI	10.3390/vaccines10020145
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Article ; Online: The magnitude of the germinal center B cell and T follicular helper cell response predicts long-lasting antibody titers to plague vaccination.

Galloway, Darrell R / Nguyen, Nguyen X / Li, Jiahui / Houston, Nicholas / Gregersen, Gage / Williamson, E Diane / Falkenberg, Frank W / Herron, James N / Hale, J Scott

Frontiers in immunology

2022 Volume 13, Page(s) 1017385

Abstract: The development of a safe and effective vaccine ... ...

Abstract	The development of a safe and effective vaccine against
MeSH term(s)	Mice ; Animals ; Aluminum Hydroxide ; Germinal Center ; T Follicular Helper Cells ; Vaccination ; Adjuvants, Immunologic/pharmacology ; Vaccines, Subunit ; Immunization, Secondary ; Vaccines, Synthetic
Chemical Substances	Aluminum Hydroxide (5QB0T2IUN0) ; Adjuvants, Immunologic ; Vaccines, Subunit ; Vaccines, Synthetic
Language	English
Publishing date	2022-10-28
Publishing country	Switzerland
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	2606827-8
ISSN	1664-3224 ; 1664-3224
ISSN (online)	1664-3224
ISSN	1664-3224
DOI	10.3389/fimmu.2022.1017385
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Article ; Online: DNA vaccines against anthrax.

Galloway, Darrell R / Baillie, Les

Expert opinion on biological therapy

2003 Volume 4, Issue 10, Page(s) 1661–1667

Abstract: DNA vaccination is vaccination at its simplest. Due to renewed interest in vaccination against anthrax and other biothreat agents, a genetic immunisation approach offers attractive possibilities for rapid, responsive vaccine development. DNA vaccination ... ...

Abstract	DNA vaccination is vaccination at its simplest. Due to renewed interest in vaccination against anthrax and other biothreat agents, a genetic immunisation approach offers attractive possibilities for rapid, responsive vaccine development. DNA vaccination against anthrax is an active area of research showing promising results at present, which in the short-term and in the future could form the basis for new advances in multi-agent vaccine development. The anthrax 'model' constitutes an important experimental system for genetic immunisation technology development.
MeSH term(s)	Animals ; Anthrax/prevention & control ; Anthrax Vaccines/immunology ; Bacillus anthracis/genetics ; Bacillus anthracis/immunology ; Bioterrorism ; Cattle ; Cattle Diseases/transmission ; DNA, Bacterial/immunology ; Drug Evaluation, Preclinical ; Female ; Humans ; Macaca mulatta ; Male ; Mice ; Plasmids/administration & dosage ; Plasmids/genetics ; Rabbits ; Vaccination ; Vaccines, DNA/immunology
Chemical Substances	Anthrax Vaccines ; DNA, Bacterial ; Vaccines, DNA
Language	English
Publishing date	2003-06-09
Publishing country	England
Document type	Journal Article ; Review
ZDB-ID	2052501-1
ISSN	1744-7682 ; 1471-2598
ISSN (online)	1744-7682
ISSN	1471-2598
DOI	10.1517/14712598.4.10.1661
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Zs.A 6094: Show issues

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Article: Synthesis and assembly of anthrax lethal factor-cholera toxin B-subunit fusion protein in transgenic potato.

Kim, Tae-Geum / Galloway, Darrell R / Langridge, William H R

Molecular biotechnology

2004 Volume 28, Issue 3, Page(s) 175–183

Abstract: A DNA encoding the 27-kDa domain I of anthrax lethal factor protein (LF), was linked to the carboxyl terminus of the cholera toxin B-subunit (CTB-LF). The CTB-LF fusion gene was transferred into Solanum tuberosum cells by Agrobacterium tumefaciens- ... ...

Abstract	A DNA encoding the 27-kDa domain I of anthrax lethal factor protein (LF), was linked to the carboxyl terminus of the cholera toxin B-subunit (CTB-LF). The CTB-LF fusion gene was transferred into Solanum tuberosum cells by Agrobacterium tumefaciens-mediated in vivo transformation methods and antibiotic-resistant plants were regenerated. The CTB-LF fusion gene was detected in transformed potato leaf genomic DNA by polymerase chain reaction (PCR)-mediated DNA amplification. Immunoblot analysis with anti-CTB and anti-LF primary antibodies verified the synthesis and assembly of biologically active CTB-LF fusion protein oligomers in transformed plant tuber tissues. Furthermore, the binding of CTB-LF fusion protein pentamers to intestinal epithelial cell membrane receptors measured by GM1-ganglioside enzyme-linked immunosorbent assay (GM1-ELISA) indicated that the CTB-LF fusion protein made up approx 0.002% of the total soluble tuber protein. Synthesis of CTB-LF monomers and their assembly into biologically active CTB-LF fusion protein pentamers in potato tuber tissues demonstrates the feasibility of using edible plants for production and delivery of adjuvanted LF protein for CTB-mediated immunostimulation of mucosal immune responses against anthrax toxin.
MeSH term(s)	Antigens, Bacterial/genetics ; Bacterial Toxins/genetics ; Base Sequence ; Cholera Toxin/genetics ; DNA Primers ; Enzyme-Linked Immunosorbent Assay ; Plants, Genetically Modified ; Polymerase Chain Reaction ; Recombinant Fusion Proteins/chemical synthesis ; Recombinant Fusion Proteins/genetics
Chemical Substances	Antigens, Bacterial ; Bacterial Toxins ; DNA Primers ; Recombinant Fusion Proteins ; anthrax toxin ; Cholera Toxin (9012-63-9)
Language	English
Publishing date	2004-11
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	1193057-3
ISSN	1559-0305 ; 1073-6085
ISSN (online)	1559-0305
ISSN	1073-6085
DOI	10.1385/MB:28:3:175
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Zs.A 4031: Show issues

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Article ; Online: The early humoral immune response to Bacillus anthracis toxins in patients infected with cutaneous anthrax.

Brenneman, Karen E / Doganay, Mehmet / Akmal, Arya / Goldman, Stanley / Galloway, Darrell R / Mateczun, Alfred J / Cross, Alan S / Baillie, Leslie W

FEMS immunology and medical microbiology

2011 Volume 62, Issue 2, Page(s) 164–172

Abstract: Bacillus anthracis, the causative agent of anthrax, produces a tripartite toxin composed of two enzymatically active subunits, lethal factor (LF) and edema factor (EF), which, when associated with a cell-binding component, protective antigen (PA), form ... ...

Abstract	Bacillus anthracis, the causative agent of anthrax, produces a tripartite toxin composed of two enzymatically active subunits, lethal factor (LF) and edema factor (EF), which, when associated with a cell-binding component, protective antigen (PA), form lethal toxin and edema toxin, respectively. In this preliminary study, we characterized the toxin-specific antibody responses observed in 17 individuals infected with cutaneous anthrax. The majority of the toxin-specific antibody responses observed following infection were directed against LF, with immunoglobulin G (IgG) detected as early as 4 days after the onset of symptoms in contrast to the later and lower EF- and PA-specific IgG responses. Unlike the case with infection, the predominant toxin-specific antibody response of those immunized with the US anthrax vaccine absorbed and UK anthrax vaccine precipitated licensed anthrax vaccines was directed against PA. We observed that the LF-specific human antibodies were, like anti-PA antibodies, able to neutralize toxin activity, suggesting the possibility that they may contribute to protection. We conclude that an antibody response to LF might be a more sensitive diagnostic marker of anthrax than to PA. The ability of human LF-specific antibodies to neutralize toxin activity supports the possible inclusion of LF in future anthrax vaccines.
MeSH term(s)	Anthrax/immunology ; Antibodies, Bacterial/blood ; Antibodies, Neutralizing/blood ; Antigens, Bacterial/immunology ; Antitoxins/blood ; Bacillus anthracis/immunology ; Bacillus anthracis/pathogenicity ; Bacterial Toxins/immunology ; Humans ; Immunity, Humoral ; Immunoglobulin G/blood ; Skin Diseases, Bacterial
Chemical Substances	Antibodies, Bacterial ; Antibodies, Neutralizing ; Antigens, Bacterial ; Antitoxins ; Bacterial Toxins ; Immunoglobulin G ; anthrax toxin
Language	English
Publishing date	2011-04-15
Publishing country	England
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	1143208-1
ISSN	1574-695X ; 0928-8244
ISSN (online)	1574-695X
ISSN	0928-8244
DOI	10.1111/j.1574-695X.2011.00800.x
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Article: Analysis of peptide mimotopes of Burkholderia pseudomallei exopolysaccharide.

Legutki, Joseph B / Nelson, Michelle / Titball, Richard / Galloway, Darrell R / Mateczun, Alfred / Baillie, Leslie W

Vaccine

2007 Volume 25, Issue 45, Page(s) 7796–7805

Abstract: Previously two capsule-specific monoclonal antibodies (4VA5 and 3VIE5) were identified as protective against Burkholderia pseudomallei in passive transfer experiments. Panning these antibodies against evolutionary phage libraries identified reactive ... ...

Abstract	Previously two capsule-specific monoclonal antibodies (4VA5 and 3VIE5) were identified as protective against Burkholderia pseudomallei in passive transfer experiments. Panning these antibodies against evolutionary phage libraries identified reactive peptides capable of inhibiting its parent monoclonal from binding to B. pseudomallei. Mice immunized with peptide conjugated to thyroglobulin developed serum antibodies capable of recognizing the immunizing peptide of which a subset recognized exopolysaccharide in the context of whole B. pseudomallei cells. These serum antibodies recognized protease treated B. pseudomallei but not B. thailandensis suggesting that these peptides are mimotopes of the B. pseudomallei capsular exopolysaccharide. In a murine model of acute melioidosis, immunization with the mimotope of the 4VA5 binding site extended the mean time to death to 8.00 days over the 2.18 days afforded by immunization with thyroglobulin alone. This mimotope may be of use in developing an antibody response against B. pseudomallei exopolysaccharide.
MeSH term(s)	Animals ; Antibodies, Bacterial/blood ; Antibodies, Bacterial/immunology ; Antibodies, Monoclonal/immunology ; Antigens, Bacterial/immunology ; Bacterial Vaccines/immunology ; Burkholderia pseudomallei/chemistry ; Burkholderia pseudomallei/immunology ; Epitopes/immunology ; Melioidosis/immunology ; Mice ; Mice, Inbred BALB C ; Models, Animal ; Peptides/immunology ; Polysaccharides, Bacterial/immunology
Chemical Substances	Antibodies, Bacterial ; Antibodies, Monoclonal ; Antigens, Bacterial ; Bacterial Vaccines ; Epitopes ; Peptides ; Polysaccharides, Bacterial
Language	English
Publishing date	2007-11-07
Publishing country	Netherlands
Document type	Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	605674-x
ISSN	1873-2518 ; 0264-410X
ISSN (online)	1873-2518
ISSN	0264-410X
DOI	10.1016/j.vaccine.2007.08.045
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Zs.A 1930: Show issues			Location: Je nach Verfügbarkeit (siehe Angabe bei Bestand) bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular Jg. 1995 - 2021: Lesesall (1.OG) ab Jg. 2022: Lesesaal (EG)
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Article ; Online: Microarray-based resequencing of multiple Bacillus anthracis isolates.

Zwick, Michael E / Mcafee, Farrell / Cutler, David J / Read, Timothy D / Ravel, Jacques / Bowman, Gregory R / Galloway, Darrell R / Mateczun, Alfred

Genome biology

2005 Volume 6, Issue 1, Page(s) R10

Abstract: We used custom-designed resequencing arrays to generate 3.1 Mb of genomic sequence from a panel of 56 Bacillus anthracis strains. Sequence quality was shown to be very high by replication (discrepancy rate of 7.4 x 10(-7)) and by comparison to ... ...

Abstract	We used custom-designed resequencing arrays to generate 3.1 Mb of genomic sequence from a panel of 56 Bacillus anthracis strains. Sequence quality was shown to be very high by replication (discrepancy rate of 7.4 x 10(-7)) and by comparison to independently generated shotgun sequence (discrepancy rate < 2.5 x 10(-6)). Population genomics studies of microbial pathogens using rapid resequencing technologies such as resequencing arrays are critical for recognizing newly emerging or genetically engineered strains.
MeSH term(s)	Bacillus anthracis/classification ; Bacillus anthracis/genetics ; Bacillus anthracis/isolation & purification ; Bacillus anthracis/pathogenicity ; Chromosomes, Bacterial/genetics ; Genetic Variation/genetics ; Genome, Bacterial ; Molecular Sequence Data ; Oligonucleotide Array Sequence Analysis ; Recombination, Genetic/genetics ; Reproducibility of Results ; Sequence Analysis, DNA/economics ; Sequence Analysis, DNA/methods ; Sequence Analysis, DNA/standards ; Time Factors
Language	English
Publishing date	2005
Publishing country	England
Document type	Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	2040529-7
ISSN	1474-760X ; 1465-6914 ; 1465-6906
ISSN (online)	1474-760X ; 1465-6914
ISSN	1465-6906
DOI	10.1186/gb-2004-6-1-r10
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Article ; Online: The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages

Sozhamannan Shanmuga / Chute Michael D / McAfee Farrell D / Fouts Derrick E / Akmal Arya / Galloway Darrell R / Mateczun Alfred / Baillie Leslie W / Read Timothy D

BMC Microbiology, Vol 6, Iss 1, p

2006 Volume 34

Abstract: Abstract Background Bacillus anthracis is considered to be a recently emerged clone within the Bacillus cereus sensu lato group. The B. anthracis genome sequence contains four putative lambdoid prophages. We undertook this study in order to understand ... ...

Abstract	Abstract Background Bacillus anthracis is considered to be a recently emerged clone within the Bacillus cereus sensu lato group. The B. anthracis genome sequence contains four putative lambdoid prophages. We undertook this study in order to understand whether the four prophages are unique to B. anthracis and whether they produce active phages. Results More than 300 geographically and temporally divergent isolates of B. anthracis and its near neighbors were screened by PCR for the presence of specific DNA sequences from each prophage region. Every isolate of B. anthracis screened by PCR was found to produce all four phage-specific amplicons whereas none of the non- B. anthracis isolates, produced more than one phage-specific amplicon. Excision of prophages could be detected by a PCR based assay for attP sites on extra-chromosomal phage circles and for attB sites on phage-excised chromosomes. SYBR-green real-time PCR assays indicated that prophage excision occurs at very low frequencies (2 × 10 -5 - 8 × 10 -8 /cell). Induction with mitomycin C increased the frequency of excision of one of the prophages by approximately 250 fold. All four prophages appear to be defective since, mitomycin C induced culture did not release any viable phage particle or lyse the cells or reveal any phage particle under electron microscopic examination. Conclusion The retention of all four putative prophage regions across all tested strains of B. anthracis is further evidence of the very recent emergence of this lineage and the prophage regions may be useful for differentiating the B. anthracis chromosome from that of its neighbors. All four prophages can excise at low frequencies, but are apparently defective in phage production.
Keywords	Microbiology ; QR1-502 ; Science ; Q ; DOAJ:Microbiology ; DOAJ:Biology ; DOAJ:Biology and Life Sciences
Subject code	500
Language	English
Publishing date	2006-04-01T00:00:00Z
Publisher	BioMed Central
Document type	Article ; Online
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Article: Enhancement of the protective efficacy of an oprF DNA vaccine against Pseudomonas aeruginosa.

Price, Brian M / Barten Legutki, J / Galloway, Darrell R / von Specht, Bernd Ulrich / Gilleland, Linda B / Gilleland, Harry E / Staczek, John

FEMS immunology and medical microbiology

2002 Volume 33, Issue 2, Page(s) 89–99

Abstract: The outer membrane protein F gene (oprF) of Pseudomonas aeruginosa was recently shown by us to protect mice from P. aeruginosa chronic pulmonary infection when used as a DNA vaccine administered by three biolistic (gene gun) intradermal inoculations ... ...

Abstract	The outer membrane protein F gene (oprF) of Pseudomonas aeruginosa was recently shown by us to protect mice from P. aeruginosa chronic pulmonary infection when used as a DNA vaccine administered by three biolistic (gene gun) intradermal inoculations given at 2-week intervals. In the present study, we used two different strategies to improve the protective efficacy of the DNA vaccine. In the first strategy, mice were primed with two biolistic intradermal inoculations with the oprF vaccine and then were given a final intramuscular booster immunization containing either a synthetic peptide-keyhole limpet hemocyanin (KLH) conjugate or a chimeric influenza virus. Both the synthetic peptide conjugate and the chimeric virus contained peptide 10, a previously identified immunoprotective epitope of protein F. The second strategy involved the addition of a second outer membrane protein to the vaccine. DNA encoding a fusion protein comprised of the C-terminal half of protein F fused to OprI was administered by three biolistic intradermal inoculations. Challenge with P. aeruginosa in a chronic pulmonary infection model demonstrated that boosting with the chimeric virus (but not with peptide-KLH) or adding oprI to the DNA vaccine significantly enhanced protection as compared to that afforded by the oprF vaccine given alone. Thus, both strategies appear to augment the protection afforded by an oprF-only DNA vaccine.
MeSH term(s)	Animals ; Antibodies, Bacterial/blood ; Bacterial Vaccines/administration & dosage ; Bacterial Vaccines/immunology ; Chronic Disease ; Disease Models, Animal ; Female ; Hemocyanins/genetics ; Hemocyanins/immunology ; Humans ; Immunization Schedule ; Immunization, Secondary ; Lung Diseases/microbiology ; Lung Diseases/prevention & control ; Mice ; Mice, Inbred BALB C ; Opsonin Proteins/metabolism ; Orthomyxoviridae/genetics ; Orthomyxoviridae/immunology ; Orthomyxoviridae/metabolism ; Peptides/chemical synthesis ; Peptides/genetics ; Peptides/immunology ; Porins/chemistry ; Porins/genetics ; Porins/immunology ; Porins/metabolism ; Pseudomonas Infections/microbiology ; Pseudomonas Infections/prevention & control ; Pseudomonas aeruginosa/genetics ; Pseudomonas aeruginosa/immunology ; Recombinant Fusion Proteins/immunology ; Vaccines, DNA/administration & dosage ; Vaccines, DNA/immunology
Chemical Substances	Antibodies, Bacterial ; Bacterial Vaccines ; Opsonin Proteins ; Peptides ; Porins ; Recombinant Fusion Proteins ; Vaccines, DNA ; Hemocyanins (9013-72-3) ; keyhole-limpet hemocyanin (FV4Y0JO2CX)
Language	English
Publishing date	2002-06-03
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	1143208-1
ISSN	1574-695X ; 0928-8244
ISSN (online)	1574-695X
ISSN	0928-8244
DOI	10.1111/j.1574-695X.2002.tb00577.x
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