RESUMO
As most pathogens enter through the mucosa, it is important to develop vaccines that induce mucosal immunity. To this end, we generated a novel adenovirus (Ad) vaccine that displays the σ1 protein from reovirus to target junctional adhesion molecule 1 and sialic acid. Replication-defective Ad5 vectors were modified by replacement of the Ad fiber protein with σ1 (T3Dσ1) protein of reovirus T3D in previous work. Ad5 and Ad5-σ1 were compared in mouse models for gene delivery and vaccination to monitor cytokine, antibody, and T-cell responses. The viruses were also tested for the ability to transduce and mature dendritic cells. Ad5-σ1 was 40-fold less efficient at gene delivery in vivo, yet it was capable of inducing equal or greater cellular immune responses and systemic interferon-γ levels than Ad5 after intranasal administration. Despite weaker gross transduction, intranasal administration of Ad5-σ1 produced more green fluorescent protein-positive (GFP+) major histocompatibility complex class II (MHC II) cells in the draining lymph nodes, less GFP+/MHC II+ cells in the lungs, and mediated modestly better maturation of dendritic cells in vitro. These data suggest that targeting gene-based vaccination via the σ1 protein may enhance the T-cell immune response, perhaps by skewing immune responses to encoded antigens.
Assuntos
Infecções por Adenoviridae/imunologia , Adenoviridae/fisiologia , Proteínas do Capsídeo/metabolismo , Reoviridae/fisiologia , Mucosa Respiratória/metabolismo , Linfócitos T/imunologia , Infecções por Adenoviridae/virologia , Animais , Proteínas do Capsídeo/genética , Proteínas do Capsídeo/imunologia , Diferenciação Celular , Células Cultivadas , Apresentação Cruzada/genética , Células Dendríticas/imunologia , Engenharia Genética , Vetores Genéticos/imunologia , Imunidade Celular/genética , Interferon gama/metabolismo , Camundongos , Camundongos Endogâmicos BALB C , Mucosa Respiratória/imunologia , Mucosa Respiratória/virologiaRESUMO
Although there are 55 serotypes of adenovirus (Ad) that infect humans, Ad serotype 5 (Ad5) is the most widely studied because of the availability of commercial kits for its genetic manipulation. In fact, engineered Ad 5 is currently being used in all of the 87 global clinical trials utilizing Ad for the treatment of cancer. Unfortunately, Ad5 is one of the most seroprevalent serotypes, meaning that this virus has to confront additional immunological barriers to be effective in Ad5-immune patients. In this work, we compare Ad5 to 13 other adenoviral serotypes from species B, C, D and E for oncolytic potential in both immunodeficient mouse and immunocompetent hamster models. Our results indicate that species D Ads are not effective oncolytics against most solid tumors. Conversely, lower seroprevalent Ad6 and Ad11 had anti-cancer activity comparable to Ad5. This work strongly supports the consideration of Ad6-based oncolytic therapies for the treatment of breast, ovarian, kidney and liver tumors.
Assuntos
Adenovírus Humanos/imunologia , Neoplasias/imunologia , Terapia Viral Oncolítica , Vírus Oncolíticos/imunologia , Adenovírus Humanos/classificação , Adenovírus Humanos/genética , Animais , Células CHO , Linhagem Celular Tumoral , Sobrevivência Celular , Cricetinae , Efeito Citopatogênico Viral , Feminino , Células HEK293 , Humanos , Camundongos , Camundongos Nus , Neoplasias/metabolismo , Neoplasias/terapia , Vírus Oncolíticos/classificação , Vírus Oncolíticos/genética , Filogenia , Ensaios Antitumorais Modelo de XenoenxertoRESUMO
Consensus HIV-1 genes can decrease the genetic distances between candidate immunogens and field virus strains. To ensure the functionality and optimal presentation of immunologic epitopes, we generated two group-M consensus env genes that contain variable regions either from a wild-type B/C recombinant virus isolate (CON6) or minimal consensus elements (CON-S) in the V1, V2, V4, and V5 regions. C57BL/6 and BALB/c mice were primed twice with CON6, CON-S, and subtype control (92UG37_A and HXB2/Bal_B) DNA and boosted with recombinant vaccinia virus (rVV). Mean antibody titers against 92UG37_A, 89.6_B, 96ZM651_C, CON6, and CON-S Env protein were determined. Both CON6 and CON-S induced higher mean antibody titers against several of the proteins, as compared with the subtype controls. However, no significant differences were found in mean antibody titers in animals immunized with CON6 or CON-S. Cellular immune responses were measured by using five complete Env overlapping peptide sets: subtype A (92UG37_A), subtype B (MN_B, 89.6_B and SF162_B), and subtype C (Chn19_C). The intensity of the induced cellular responses was measured by using pooled Env peptides; T-cell epitopes were identified by using matrix peptide pools and individual peptides. No significant differences in T-cell immune-response intensities were noted between CON6 and CON-S immunized BALB/c and C57BL/6 mice. In BALB/c mice, 10 and eight nonoverlapping T-cell epitopes were identified in CON6 and CON-S, whereas eight epitopes were identified in 92UG37_A and HXB2/BAL_B. In C57BL/6 mice, nine and six nonoverlapping T-cell epitopes were identified after immunization with CON6 and CON-S, respectively, whereas only four and three were identified in 92UG37_A and HXB2/BAL_B, respectively. When combined together from both mouse strains, 18 epitopes were identified. The group M artificial consensus env genes, CON6 and CON-S, were equally immunogenic in breadth and intensity for inducing humoral and cellular immune responses.
Assuntos
Vacinas contra a AIDS/imunologia , Sequência Consenso/imunologia , HIV-1/imunologia , Linfócitos T/imunologia , Vacinas de DNA/imunologia , Produtos do Gene env do Vírus da Imunodeficiência Humana/imunologia , Vacinas contra a AIDS/genética , Sequência de Aminoácidos , Animais , Sequência Consenso/genética , Epitopos de Linfócito T/genética , Epitopos de Linfócito T/imunologia , Feminino , Anticorpos Anti-HIV/sangue , Infecções por HIV/imunologia , Infecções por HIV/prevenção & controle , HIV-1/classificação , HIV-1/genética , Imunização , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Dados de Sequência Molecular , Vacinas de DNA/genética , Vaccinia virus/genética , Vaccinia virus/imunologia , Produtos do Gene env do Vírus da Imunodeficiência Humana/química , Produtos do Gene env do Vírus da Imunodeficiência Humana/genéticaRESUMO
Biofilm formation and function was studied in mixed culture using 20 bacterial strains isolated from a karst aquifer. When co-cultured in a glucose-limited chemostat, Vogesella indigofera and Pseudomonas putida were the dominant planktonic and biofilm organisms respectively. Biofilm formation and resistance to the iodine disinfectant betadine were then studied with monoculture and binary cultures of V. indigofera and P. putida and a 20-strain community. Biofilm population size [measured as colony-forming units (CFU) cm(-2)] increased with increasing species diversity. Significantly larger populations formed at dilution rates (DRs) of 0.0083 h(-1) than at 0.033 h(-1). P. putida populations were higher and V. indigofera lower in binary than in monoculture biofilms, suggesting that P. putida outcompeted V. indigofera. In binary biofilms, V. indigofera, a betadine-resistant organism, enhanced the survival of P. putida, a betadine-susceptible organism. In the 20-strain biofilms, this protective effect was not observed because of low concentrations of V. indigofera (< 1% of the total population), suggesting that resistant organisms contribute to overall biofilm disinfectant resistance. Growth at 0.033 h(-1) enhanced survival of V. indigofera biofilms against betadine. Although DR did influence survival of the other communities, its effects were neither consistent nor significant. All told, biofilm formation and betadine resistance are complex phenomena, influenced by community composition, growth rate and betadine concentration.
Assuntos
Betaproteobacteria/crescimento & desenvolvimento , Biofilmes/crescimento & desenvolvimento , Desinfetantes/farmacologia , Ecossistema , Povidona-Iodo/farmacologia , Pseudomonas putida/crescimento & desenvolvimento , Técnicas Bacteriológicas , Betaproteobacteria/isolamento & purificação , Contagem de Colônia Microbiana , Meios de Cultura , Água Doce/microbiologia , Pseudomonas putida/isolamento & purificaçãoRESUMO
ATFIM1 is a widely expressed gene in Arabidopsis thaliana that encodes a putative actin filament-crosslinking protein, AtFim1, belonging to the fimbrin/plastin class of actin-binding proteins. In this report we have used bacterially expressed AtFim1 and actin isolated from Zea mays pollen to demonstrate that AtFim1 functions as an actin filament-crosslinking protein. AtFim1 binds pollen actin filaments (F-actin) in a calcium-independent manner, with an average dissociation constant (Kd) of 0.55+/-0.21 microM and with a stoichiometry at saturation of 1:4 (mol AtFim1 : mol actin monomer). AtFim1 also crosslinks pollen F-actin by a calcium-independent mechanism, in contrast to crosslinking of plant actin by human T-plastin, a known calcium-sensitive actin-crosslinking protein. When micro-injected at high concentration into living Tradescantia virginiana stamen hair cells, AtFim1 caused cessation of both cytoplasmic streaming and transvacuolar strand dynamics within 2-4 min. Using the 'nuclear displacement assay' as a measure of the integrity of the actin cytoskeleton in living stamen hair cells, we demonstrated that AtFim1 protects actin filaments in these cells from Z. mays profilin (ZmPRO5)-induced depolymerization, in a dose-dependent manner. The apparent ability of AtFim1 to protect actin filaments in vivo from profilin-mediated depolymerization was confirmed by in vitro sedimentation assays. Our results indicate that AtFim1 is a calcium-independent, actin filament-crosslinking protein that interacts with the actin cytoskeleton in living plant cells.
Assuntos
Proteínas de Arabidopsis , Arabidopsis/metabolismo , Proteínas dos Microfilamentos/metabolismo , Proteínas de Plantas/metabolismo , Actinas/metabolismo , Arabidopsis/genética , Ligação Competitiva , Cálcio/farmacologia , Reagentes de Ligações Cruzadas , DNA Recombinante , Células Vegetais , Proteínas de Plantas/genética , Proteínas de Plantas/farmacologia , Plantas/efeitos dos fármacos , Plantas/metabolismo , Pólen/química , Ligação Proteica/efeitos dos fármacosRESUMO
Ochratoxin A (OA) was incorporated in the diets of growing gilts (mean body weight, 20.1 kg) at a concentration of 2.5 mg of OA/kg of feed and was fed continuously for 35 days. Humoral and cell-mediated immunologic measurements were evaluated to determine the effects of OA on immune function in swine. Cutaneous basophil hypersensitivity to phytohemagglutinin (PHA), delayed hypersensitivity to tuberculin, PHA-induced lymphocyte blastogenesis, interleukin-2 production, total and isotype immunoglobulin concentrations, antibody response to chicken RBC, and macrophage activation were used to evaluate immune function. Gilts treated with OA had reduced cutaneous basophil hypersensitivity response to PHA, reduced delayed hypersensitivity to tuberculin, decreased stimulation index for lymphoblastogenesis, decreased interleukin-2 production when lymphocytes were stimulated with concanavalin A, and decreased number and phagocytic activity of macrophages. Differences were not observed for total and isotype immunoglobulin concentrations, or humoral hemagglutination (chicken RBC) titer. These data indicate that OA may suppress cell-mediated immune response in growing swine.
Assuntos
Imunidade/efeitos dos fármacos , Ocratoxinas/toxicidade , Suínos/imunologia , Animais , Peso Corporal/efeitos dos fármacos , Feminino , Tamanho do Órgão/efeitos dos fármacos , Suínos/crescimento & desenvolvimentoRESUMO
The E-sigma 37-transcribed gene ctc was inactivated by a site-specific insertion into the Bacillus subtilis chromosome. The resulting mutation inhibited sporulation by 95% at elevated temperatures (48 degrees C). If the ctc- mutation is placed in a strain that carries a mutation in the closely linked but distinct spoVC gene, ctc now affects both growth and sporulation at elevated temperatures. Growth of the ctc- spoVC285 strain was transiently inhibited when exponentially growing cultures were shifted from 37 degrees C to 48 degrees C. A similar, but less pronounced "growth lag", was also seen in a B. subtilis strain carrying only the spoVC-285 mutation. This finding suggests that both the ctc and spoVC products function in vegetatively growing B. subtilis.
Assuntos
Bacillus subtilis/genética , RNA Polimerases Dirigidas por DNA/metabolismo , Mutação , Transcrição Gênica , Bacillus subtilis/crescimento & desenvolvimento , Bacillus subtilis/fisiologia , Cruzamentos Genéticos , Enzimas de Restrição do DNA , Escherichia coli/genética , Plasmídeos , Esporos Bacterianos , TemperaturaRESUMO
A sporulation-specific sigma factor of Bacillus subtilis (sigma E) is formed by a proteolytic activation of a precursor protein (P31). Synthesis of the precursor protein is shown to be abolished in B. subtilis mutants with plasmid insertions as far as 940 base pairs upstream of the P31 structural gene (sigE), and processing of P31 to sigma E is blocked by a deletion in this upstream region. These results substantiate the view that sigE is the distal member of a 2-gene operon and demonstrate that the upstream gene (spoIIGA) is necessary for sigma E formation.
Assuntos
Bacillus subtilis/genética , Regulação da Expressão Gênica , Óperon , Precursores de Proteínas/genética , Fator sigma/genética , Fatores de Transcrição/genética , Alelos , Bacillus subtilis/metabolismo , Bacillus subtilis/fisiologia , Genes , Genes Bacterianos , Mutação , Hibridização de Ácido Nucleico , Plasmídeos , Regiões Promotoras Genéticas , Precursores de Proteínas/biossíntese , Processamento de Proteína Pós-Traducional , RNA Bacteriano/genética , Fator sigma/biossíntese , Esporos Bacterianos , Transcrição Gênica , Transformação BacterianaRESUMO
Some of the requirements for release of immunoglobulin A (IgA) from human milk leukocytes during phagocytosis were investigated. The role of particle adherence in IgA release was studied by using an in vitro model of frustrated phagocytosis in which human milk leukocytes were incubated with latex particles too large to ingest. Release of IgA was significantly increased from control values within 30 min in these leukocytes. A similar increment in IgA release also occurred when human milk leukocytes were incubated with other surface membrane stimuli, e.g., NFMP and phorbol. No increase in IgA release was found, however, in cells incubated with zymosan-activated serum. In addition, the release of IgA was blocked by inhibitors of actin filaments (cytochalasin B) and microtubules (colchicine). Thus, IgA is released from human milk leukocytes by secretory mechanisms that are initiated by certain membrane stimuli, some of which are shared by peripheral blood neutrophils and monocytes. Because human milk leukocytes appear to be refractory to C5a or other activated complement components and are blocked by cytochalasin B, it appears that these unusual cells may be uniquely adapted to play a role in the immunologic protection of the neonate.
Assuntos
Imunoglobulina A Secretora/biossíntese , Leucócitos/imunologia , Leite Humano/imunologia , Fagocitose , Adolescente , Adulto , Membrana Celular/efeitos dos fármacos , Membrana Celular/imunologia , Colchicina/farmacologia , Colostro/citologia , Colostro/imunologia , Ativação do Complemento , Citocalasina B/farmacologia , Dipeptídeos/farmacologia , Feminino , Humanos , Leite Humano/citologia , Fagocitose/efeitos dos fármacos , Acetato de Tetradecanoilforbol/farmacologiaRESUMO
Macrophages and neutrophils that contain mainly secretory immunoglobulin A (IgA) comprise the majority of cells in human colostrum. These cell populations were separated and analyzed for their ability to release total IgA and secretory IgA when stimulated to phagocytose. Colostral macrophages phagocytosed opsonized bacteria and nonopsonized latex particles; at the same time, IgA was released. Neutrophils poorly phagocytosed opsonized bacteria but actively phagocytosed latex particles. In contrast to the macrophages, the neutrophils did not release IgA, even after active phagocytosis of latex. Consequently, colostral macrophages are the main source of IgA released from colostral leukocytes when these cells are exposed to organisms or particles that are phagocytosed. A function for colostral neutrophils which sequester IgA is proposed.
Assuntos
Colostro/citologia , Imunoglobulina A/metabolismo , Macrófagos/imunologia , Adolescente , Adulto , Separação Celular , Escherichia coli/imunologia , Feminino , Humanos , Imunoglobulina A Secretora/metabolismo , Microesferas , Neutrófilos/imunologiaRESUMO
Immunoglobulin A antibodies with binding specificity for purified Klebsiella pneumoniae type 1 pili were detected by an enzyme-linked immunosorbent assay in 20 of 21 human samples (95%). The concentrations of secretory immunoglobulin A antibody in colostrum directed against the pili were calculated by comparison of experimental enzyme-linked immunosorbent assay values with values obtained from known secretory immunoglobulin A concentrations. The presence of antibodies to K. pneumoniae type 1 pili was confirmed by double diffusion-gel studies with selected specimens of colostrum. This study shows that in the majority of human colostral samples examined, secretory immunoglobulin A antibodies with specificity for K. pneumoniae type 1 pili can be commonly found in variable, but frequently high, concentrations.
Assuntos
Colostro/imunologia , Fímbrias Bacterianas/imunologia , Imunoglobulina A Secretora/análise , Imunoglobulina A/análise , Klebsiella pneumoniae/imunologia , Adolescente , Adulto , Anticorpos Antibacterianos/análise , Fracionamento Celular , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Imunodifusão , Klebsiella pneumoniae/ultraestruturaRESUMO
Human colostral leukocytes were investigated for their ability to release immunoglobulin A during phagocytosis of latex particles, heat-killed Candida albicans, or live Escherichia coli. Leukocytes readily phagocytosed latex or serum-opsonized candida or the E. coli. Colostral fluid was also opsonic for yeast and bacteria. Immunoglobulin release, which consisted mainly of secretory immunoglobulin A, began during the first 15 min of incubation with latex, opsonized yeast, or opsonized bacteria. Release was significantly increased from control levels by 30 or 60 min. The release of immunoglobulin A could be inhibited by incubating leukocytes at 4 degrees C. We conclude that phagocytosis and immunoglobulin A release by human colostral leukocytes are related. The data support the hypothesis that colostral leukocytes may play an active role in protecting infants from pathogenic microorganisms.
Assuntos
Colostro/imunologia , Imunoglobulina A Secretora/metabolismo , Imunoglobulina A/metabolismo , Leucócitos/imunologia , Fagocitose , Candida albicans/imunologia , Colostro/citologia , Escherichia coli/imunologia , Humanos , Proteínas OpsonizantesRESUMO
Morphometric evaluation of intestinal capillary basement membranes demonstrated a significant thickening in those of ketonuric diabetic Chinese hamsters compared to age-matched nondiabetic controls. A highly significant correlation was found between increased capillary basement membrane thickness and progression of ketonuria. Age was also positively related to elevation in capillary basement membrane thickness of control and diabetic hamsters. Capillary basement membrane thickness of diabetic animals was not significantly related to a combination of progredient ketonuria and advance in age.