RESUMO
Measles remains a principal cause of worldwide mortality, in part because young infants cannot be immunized effectively. Development of new vaccines has been hindered by previous experience with a formalin-inactivated vaccine that predisposed to a severe form of disease (atypical measles). Here we have developed and tested potential DNA vaccines for immunogenicity, efficacy and safety in a rhesus macaque model of measles. DNA protected from challenge with wild-type measles virus. Protection correlated with levels of neutralizing antibody and not with cytotoxic T lymphocyte activity. There was no evidence in any group, including those receiving hemagglutinin-encoding DNA alone, of 'priming' for atypical measles.
Assuntos
Hemaglutininas Virais/uso terapêutico , Vacina contra Sarampo/uso terapêutico , Sarampo/prevenção & controle , Vacinação , Vacinas de DNA/uso terapêutico , Proteínas Virais de Fusão/uso terapêutico , Animais , Anticorpos Antivirais/sangue , Vias de Administração de Medicamentos , Exantema , Hemaglutininas Virais/genética , Imunização Secundária , Macaca mulatta , Testes de Neutralização , Pneumonia , Pele/patologia , Vacinas Atenuadas/uso terapêutico , Proteínas Virais de Fusão/genéticaRESUMO
The severe disease atypical measles occurred when individuals immunized with a poorly protective inactivated vaccine contracted measles, and was postulated to be due to a lack of fusion-inhibiting antibodies. Here, rhesus macaques immunized with formalin-inactivated measles vaccine developed transient neutralizing and fusion-inhibiting antibodies, but no cytotoxic T-cell response. Subsequent infection with measles virus caused an atypical rash and pneumonitis, accompanied by immune complex deposition and an increase in eosinophils. Fusion-inhibiting antibody appeared earlier in these monkeys than in non-immunized monkeys. These data indicate that atypical measles results from previous priming for a nonprotective type 2 CD4 T-cell response rather than from lack of functional antibody against the fusion protein.
Assuntos
Anticorpos Antivirais/imunologia , Eosinófilos/imunologia , Vacina contra Sarampo/imunologia , Sarampo/imunologia , Animais , Linfócitos T CD4-Positivos/metabolismo , Linfócitos T CD8-Positivos/metabolismo , Eosinofilia/imunologia , Feminino , Imunoglobulina A/metabolismo , Macaca mulatta , Masculino , Sarampo/patologia , Sarampo/terapia , Vacina contra Sarampo/farmacologia , Pele/patologia , Vacinas de Produtos Inativados/imunologiaRESUMO
The mononuclear cells of the central nervous system (CNS) inflammatory response were characterized in cerebrospinal fluid (CSF), meningeal exudate, and brain parenchyma of mice 3-14 d after infection with Sindbis virus. The inflammatory infiltrate in CSF peaked and resolved before that of the parenchyma or meningeal exudate. Immunoperoxidase staining with monoclonal antibodies identified CSF inflammatory cells to be almost exclusively T cells, while inflammatory cells in the brain parenchymal perivascular cuffs and the meninges were a mixture of T cells, B cells, and macrophages. The percentage of B cells and macrophages increased at the later time points. Approximately 20% of CSF and 50% of the cells present early in the perivascular cuffs were not identified, suggesting that another subset of inflammatory cells may be present. We concluded that significant differences exist in the time course and cellular composition of the inflammatory responses in different compartments of the CNS during an acute viral infection.
Assuntos
Linfócitos/imunologia , Macrófagos/imunologia , Meningoencefalite/imunologia , Doença Aguda , Animais , Encéfalo/imunologia , Encéfalo/patologia , Líquido Cefalorraquidiano/imunologia , Líquido Cefalorraquidiano/patologia , Histocitoquímica , Técnicas Imunoenzimáticas , Isoanticorpos/análise , Linfócitos/classificação , Linfócitos/patologia , Macrófagos/patologia , Meninges/imunologia , Meninges/patologia , Meningoencefalite/patologia , Camundongos , Camundongos Endogâmicos BALB C , Fenótipo , Linfócitos T/classificação , Linfócitos T/imunologiaRESUMO
The viral-induced perivascular inflammatory response in Sindbis virus encephalitis of mice was shown to be immunologically specific. Mice were inoculated intracerebrally with Sindbis virus, and 24 hr later a single dose of cyclophosphamide was given which ablated the inflammatory response. 3 days after virus inoculation, cells and/or sera from specifically and nonspecifically sensitized donor mice were given, and the inflammatory reactions, virus content, and antibody response of recipients were examined 5 days later. Reconstitution of the viral inflammatory response required virus-specific sensitized lymph node cells and was enhanced when these lymph node cells were combined with bone marrow cells. Reconstitution was not achieved with Sindbis virus immune serum even when combined with nonspecifically sensitized cells. Combination of immune serum with Sindbis virus-sensitized cells did not produce an accentuation of the reaction. In distinction, reconstitution of the inflammatory reaction surrounding the stab wound was reconstituted with bone marrow cells from mice inoculated with Sindbis virus or control antigens. Reconstitution of the perivascular reaction was associated with a reduction in brain virus content. Although the transfer of Sindbis virus-sensitized lymph node cells and bone marrow cells resulted in the limited production of neutralizing antibody in the immunosuppressed recipient, the reduction in virus was significantly greater with the transfers of Sindbis virus-sensitized lymph node cells than with the passive transfer of immune serum alone.
Assuntos
Encefalite/imunologia , Imunidade Materno-Adquirida , Inflamação/imunologia , Animais , Encéfalo/microbiologia , Embrião de Galinha/citologia , Ciclofosfamida/uso terapêutico , Encefalite/patologia , Fibroblastos/microbiologia , Imunização Passiva , Inflamação/tratamento farmacológico , Linfonodos/imunologia , Camundongos , Camundongos Endogâmicos , Sindbis virus/imunologia , Sindbis virus/patogenicidade , Replicação ViralRESUMO
Isolation of measles virus in tissue culture by Enders and colleagues in the 1960s led to the development of the first measles vaccines. An inactivated vaccine provided only short-term protection and induced poor T cell responses and antibody that did not undergo affinity maturation. The response to this vaccine primed for atypical measles, a more severe form of measles, and was withdrawn. A live attenuated virus vaccine has been highly successful in protection from measles and in elimination of endemic measles virus transmission with the use of two doses. This vaccine is administered by injection between 9 and 15 months of age. Measles control would be facilitated if infants could be immunized at a younger age, if the vaccine were thermostable, and if delivery did not require a needle and syringe. To these ends, new vaccines are under development using macaques as an animal model and various combinations of the H, F, and N viral proteins. Promising studies have been reported using DNA vaccines, subunit vaccines, and virus-vectored vaccines.
Assuntos
Vacina contra Sarampo/administração & dosagem , Sarampo/imunologia , Vacinas Atenuadas/administração & dosagem , Vacinas de Produtos Inativados/administração & dosagem , Animais , Feminino , Interações Hospedeiro-Patógeno , Humanos , Imunidade , Imunização , Lactente , Masculino , Sarampo/virologia , Vacina contra Sarampo/imunologia , Vírus do Sarampo/imunologia , Vacinas Atenuadas/imunologia , Vacinas de DNA/administração & dosagem , Vacinas de DNA/imunologia , Vacinas de Produtos Inativados/imunologiaRESUMO
Recovery from viral encephalomyelitis requires immune-mediated noncytolytic clearance from neurons by mechanisms assumed to be the same for all neurons. In alphavirus encephalomyelitis, antibody clears infectious virus from neurons in all regions of the central nervous system (CNS), but CD8 T cells contribute to elimination of viral RNA. To understand the role of T cells in clearance, we infected antibody knockout mice with Sindbis virus. Virus was cleared from spinal cord and brain stem neurons, but not from cortical neurons, and required both CD4 and CD8 T cells. Infection with cytokine-expressing recombinant viruses suggested that T cells used interferon-gamma, but not tumor necrosis factor alpha, in clearing virus and that populations of neurons differ in responsiveness to this effector pathway.
Assuntos
Infecções por Alphavirus/imunologia , Sistema Nervoso Central/virologia , Encefalite Viral/imunologia , Interferon gama/fisiologia , Neurônios/virologia , Sindbis virus/imunologia , Linfócitos T/imunologia , Animais , Encéfalo/imunologia , Encéfalo/virologia , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD8-Positivos/imunologia , Sistema Nervoso Central/imunologia , Encefalite Viral/virologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Camundongos SCID , Medula Espinal/imunologia , Medula Espinal/virologia , Linfócitos T Citotóxicos/imunologia , Fator de Necrose Tumoral alfa/imunologia , Replicação ViralRESUMO
Visna viruses isolated from persistently infected sheep were antigenically distinct from the plaque-purified virus used for inoculation. The selection of antigenic variants under antibody pressure, thought to occur in vivo, was reproduced in sheep cell cultures inoculated with plaque-purified visna virus and maintained in antibody. Antigenic shift may be a mechanism for persistence of virus in slow or recurrent viral infections.
Assuntos
Antígenos Virais/análise , Adenomatose Pulmonar Ovina/imunologia , Vírus de RNA/imunologia , Vírus Visna-Maedi/imunologia , Animais , Leucócitos/imunologia , Leucócitos/microbiologia , OvinosRESUMO
Humoral immunity is important for protection against viral infection and neutralization of extracellular virus, but clearance of virus from infected tissues is thought to be mediated solely by cellular immunity. However, in a SCID mouse model of persistent alphavirus encephalomyelitis, adoptive transfer of hyperimmune serum resulted in clearance of infectious virus and viral RNA from the nervous system, whereas adoptive transfer of sensitized T lymphocytes had no effect on viral replication. Three monoclonal antibodies to two different epitopes on the E2 envelope glycoprotein mediated viral clearance. Treatment of alphavirus-infected primary cultured rat neurons with these monoclonal antibodies to E2 resulted in decreased viral protein synthesis, followed by gradual termination of mature infectious virion production. Thus, antibody can mediate clearance of alphavirus infection from neurons by restricting viral gene expression.
Assuntos
Alphavirus/fisiologia , Anticorpos Monoclonais/uso terapêutico , Sistema Nervoso Central/microbiologia , Encefalomielite/imunologia , Imunoterapia Adotiva , Neurônios/microbiologia , Linfócitos T/imunologia , Infecções por Togaviridae/imunologia , Alphavirus/imunologia , Alphavirus/isolamento & purificação , Animais , Sistema Nervoso Central/imunologia , Encefalomielite/microbiologia , Encefalomielite/terapia , Camundongos , Camundongos Endogâmicos , Camundongos SCID , Neurônios/imunologia , RNA Viral/isolamento & purificação , Infecções por Togaviridae/terapia , Replicação ViralRESUMO
A genetically determined deficiency of the third component of complement (C3) has been identified in a colony of Brittany spaniels. Immunochemical methods show no detectable C3 in the serum of the affected dogs, and there is no evidence of an inhibitor of C3 in the serum. The C3 deficiency appears to be transmitted as an autosomal recessive trait.
Assuntos
Complemento C3/genética , Animais , Complemento C3/deficiência , Doenças do Cão/genética , Cães , Feminino , Genes Recessivos , Triagem de Portadores Genéticos , Homozigoto , Masculino , Atrofia Muscular/genética , Atrofia Muscular/veterinária , LinhagemRESUMO
The mechanisms underlying the profound suppression of cell-mediated immunity (CMI) accompanying measles are unclear. Interleukin-12 (IL-12), derived principally from monocytes and macrophages, is critical for the generation of CMI. Measles virus (MV) infection of primary human monocytes specifically down-regulated IL-12 production. Cross-linking of CD46, a complement regulatory protein that is the cellular receptor for MV, with antibody or with the complement activation product C3b similarly inhibited monocyte IL-12 production, providing a plausible mechanism for MV-induced immunosuppression. CD46 provides a regulatory link between the complement system and cellular immune responses.
Assuntos
Antígenos CD/fisiologia , Tolerância Imunológica , Interleucina-12/biossíntese , Vírus do Sarampo/imunologia , Glicoproteínas de Membrana/fisiologia , Monócitos/imunologia , Monócitos/virologia , Receptores Virais/fisiologia , Anticorpos Monoclonais , Antígenos CD/imunologia , Sítios de Ligação , Células Cultivadas , Quimiocinas/biossíntese , Complemento C3b/imunologia , Complemento C3b/fisiologia , Citocinas/biossíntese , Regulação para Baixo , Humanos , Interleucina-10/fisiologia , Vírus do Sarampo/metabolismo , Proteína Cofatora de Membrana , Glicoproteínas de Membrana/imunologia , Receptores Virais/imunologiaRESUMO
Entry of proteins into the cerebrospinal (CSF) from the blood is partially determined by the size of the protein. To determine whether other characteristics of proteins influence CSF entry, proteins or protein fragments were iodinated, inoculated intravenously, and serum and CSF were sampled at later times. The Fc fragment of immunoglobulin G (IgG) did not enter the CSF significantly better than the Fab fragment suggesting that choroidal Fc receptors are not of importance for selective immunoglobulin entry. To determine the role of protein charge on entry, bovine serum albumin [isoelectric point (pI) = 3.9] was chemically altered to provide an albumin with an average pI of 6 (A-6) and another with a pI of 8.5 (A-8). All albumins were of the same size on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. A-8 entered the CSF approximately 10-fold better than the native albumin. A-6 was intermediate, entering approximately twofold better. At the time of increased CSF protein concentration during an acute viral encephalitis these differences were narrowed but not eliminated. It is concluded that charge is an important determinant of protein entry into the CSF.
Assuntos
Proteínas do Líquido Cefalorraquidiano/metabolismo , Encefalite/líquido cefalorraquidiano , Animais , Eletroforese em Gel de Poliacrilamida , Fragmentos Fab das Imunoglobulinas/líquido cefalorraquidiano , Fragmentos Fc das Imunoglobulinas/líquido cefalorraquidiano , Ponto Isoelétrico , Camundongos , Camundongos Endogâmicos BALB C , Albumina Sérica/metabolismo , Soroalbumina Bovina/líquido cefalorraquidiano , Fatores de TempoRESUMO
Neurologic diseases are important complications of measles. The role of virus infection of the central nervous system as well as the route of virus entry has been unclear. Five autopsied cases of individuals who died with severe acute measles 3-10 d after the onset of the rash were studied for evidence of viral involvement of the central nervous system. In all cases, in situ hybridization and RT-PCR in situ hybridization techniques showed endothelial cell infection. Immunoperoxidase staining with an anti-ferritin antibody revealed a reactive microgliosis. These data suggest that endothelial cells in the brain are frequently infected during acute fatal measles. This site of infection may provide a portal of entry for virus in individuals who subsequently develop subacute sclerosing panencephalitis or measles inclusion body encephalitis and a target for immunologic reactions in post-measles encephalomyelitis.
Assuntos
Encéfalo/virologia , Sarampo/virologia , Morbillivirus/isolamento & purificação , Sequência de Bases , Pré-Escolar , Endotélio/virologia , Evolução Fatal , Humanos , Hibridização In Situ , Lactente , Dados de Sequência MolecularRESUMO
Alphaviruses are mosquito-borne, enveloped, plus-strand RNA viruses that cause a spectrum of diseases in humans that include fever, rash, arthritis, meningitis, and encephalomyelitis. Sindbis virus (SINV) is the prototype alphavirus, causes encephalomyelitis in mice, and provides a model system for studying the pathogenesis of alphavirus-induced neurological disease. Major target cells for SINV infection in the central nervous system (CNS) are neurons, and both host and viral factors determine the fate of infected neurons. Young animals are most susceptible to fatal disease. This correlates with the ability of SINV to induce apoptosis in immature neurons. In vitro, apoptotic death of neuroblastoma cells can be induced by fusion of the virus envelope with the endosomal membrane and does not require infectious virus. This fusion process activates acid sphingomyelinase that cleaves sphingomyelin to release ceramide, an initiator of apoptosis. Within an hour, poly(ADP-ribose) polymerase is activated, and this is followed by release of cytochrome c and activation of effector caspases. SINV-induced cell death can be delayed or prevented by treatment with antioxidants or caspase inhibitors and by intracellular expression of Bcl-2, Beclin-1, or protease inhibitors. Older animals survive infection unless infected with a neurovirulent strain of SINV. In these mice, anterior horn motor neurons die by a primarily necrotic process that is influenced by excitotoxic amino acids and inflammation, whereas hippocampal neurons can be either apoptotic or necrotic. Death also occurs in uninfected neurons in the vicinity of infected neurons and can be delayed or prevented by treatment with glutamate receptor antagonists.
Assuntos
Infecções por Alphavirus/patologia , Apoptose/fisiologia , Encefalomielite/patologia , Neurônios/patologia , Sindbis virus/fisiologia , Infecções por Alphavirus/virologia , Animais , Encefalomielite/virologia , Humanos , Neurônios/virologiaRESUMO
Neuronotropic viruses induce apoptosis in neurons, and Bcl-2-related anti-apoptotic proteins and caspase inhibitors decrease mortality from acute viral encephalitis. Infected neurons develop cytoplasmic blebbing characteristic of apoptosis, but a paucity of apoptotic nuclear changes potentially indicates unique aspects of virus-induced neuronal apoptosis that remain to be discovered.
Assuntos
Apoptose , Infecções do Sistema Nervoso Central/virologia , Neurônios/citologia , Neurônios/virologia , Viroses/fisiopatologia , Animais , Apoptose/fisiologia , Morte Celular/fisiologia , Infecções do Sistema Nervoso Central/patologia , Infecções do Sistema Nervoso Central/fisiopatologia , Neurônios/fisiologia , Transdução de Sinais , Viroses/patologiaRESUMO
Alphaviruses are a group of arthropod-borne, positive-strand RNA viruses that cause acute encephalitis or arthritis. These viruses were previously thought to cause only acute infections in vertebrates, but recent evidence suggests that host immunological and tissue-specific factors may act together to promote the persistence of alphavirus genomes in vivo.
Assuntos
Infecções por Alphavirus/microbiologia , Alphavirus/isolamento & purificação , Alphavirus/imunologia , Alphavirus/fisiologia , Infecções por Alphavirus/etiologia , Infecções por Alphavirus/imunologia , Animais , Humanos , Imunidade Celular , Camundongos , Replicação ViralRESUMO
The characteristic disease features of measles--fever and rash--are associated with the immune response to infection and are coincident with virus clearance. MV-specific antibody and CD4 and CD8 T cell responses are generated and contribute to virus clearance and protection from reinfection. During this same phase of immune activation immunologic abnormalities are also apparent. There is a generalized suppression of cellular immune responses that may contribute to increased susceptibility to other infections. Autoimmune disease may appear in the form of acute disseminated encephalomyelitis. If virus-specific immune responses are inadequate infection may progress with pulmonary or CNS manifestations, but without a rash. The pathogenesis of the rare disease SSPE, that occurs many years after primary infection is not clear, but immune responses show increased antibody to measles and cellular immune responses similar to those seen after uncomplicated infection.
Assuntos
Sarampo/imunologia , Animais , Anticorpos Antivirais/imunologia , Humanos , Imunidade Celular , Vacina contra Sarampo/imunologia , Latência Viral/imunologiaRESUMO
Epidemiological evidence has suggested an association between diets rich in antioxidants and diminished risks of various types of cancer. Proposed mechanisms for protective effects of antioxidants have involved inhibition of free radical-mediated DNA damage. Recent data suggest that antioxidants may prevent or eliminate cancerous cells through their ability to inhibit proliferation or to induce programmed cell death (PCD). To begin to identify cell cycle and cell death regulatory factors involved in antioxidant-induced growth arrest and PCD, we have studied colorectal carcinoma cells (CRCs) that differ in expression of the tumor suppressor protein p53, and of the cyclin-dependent kinase (CDK) inhibitor p21(Waf1/Cip1). The antioxidants, N-acetylcysteine (NAC) and vitamin E either inhibited proliferation in a p53-independent manner without affecting cell viability or induced cell death. Growth arrest was not associated with upregulation of the CDK inhibitors p21(Waf1/Cip1), p18(ink4c) or p16(ink4a), but was associated with a decrease in reactive oxygen species (ROS). In contrast to previous observations, the absence of p21(Waf1/Cip1) increased susceptibility of CRCs to antioxidant-induced PCD. NAC decreased levels of retinoblastoma protein (Rb) phosphorylation in all cells tested, but Rb was cleaved only in cells which underwent NAC-induced death. Although NAC decreased ROS in all cells studied, cell lines in which PCD occurred had higher baseline levels of ROS than cell lines in which proliferation was blocked. These observations suggest that expression of p21(Waf1/Cip1) and basal levels of ROS are important determinants of outcome after antioxidant treatment.
Assuntos
Acetilcisteína/farmacologia , Antioxidantes/farmacologia , Apoptose/efeitos dos fármacos , Ciclinas/fisiologia , Proteína Supressora de Tumor p53/fisiologia , Vitamina E/farmacologia , Divisão Celular/efeitos dos fármacos , Células Cultivadas , Inibidor de Quinase Dependente de Ciclina p21 , Humanos , Fosforilação , Espécies Reativas de Oxigênio/metabolismo , Proteína do Retinoblastoma/metabolismoRESUMO
To characterize the expression of Ia systemically and locally on mononuclear cells during acute viral encephalitis, weanling mice were inoculated intracerebrally with Sindbis virus (SV), an alphavirus. Peripheral blood mononuclear cells, splenocytes and perivascular inflammatory cells in frozen brain sections were examined immunocytochemically for the presence of Ia. Ia expression increased in the spleen, blood and brain during SV encephalitis. The majority of the cells in the central nervous system (CNS) expressing Ia were perivascular mononuclear cells but Ia was also found on stellate parenchymal cells. Using one micrometer cryopreserved serial sections we identified these parenchymal cells as macrophages and microglia but not astrocytes. We also identified rare Ia-positive cells resembling endothelial cells. Frozen brain sections of SV-infected T cell-deficient nu/nu mice were also examined for Ia expression. The number and percentage of Ia-positive cells in perivascular inflammatory cells were markedly decreased compared to normal mice and Ia-positive stellate parenchymal cells were less numerous. This suggests that immunocompetent T cells are necessary for "normal" infiltration of inflammatory cells and for Ia expression in the CNS during SV encephalitis.
Assuntos
Encefalite/imunologia , Antígenos de Histocompatibilidade Classe II/análise , Infecções por Togaviridae/imunologia , Animais , Encéfalo/citologia , Encéfalo/imunologia , Imuno-Histoquímica , Camundongos , Camundongos Nus , Monócitos/imunologia , Sindbis virus/imunologia , Baço/citologia , Baço/imunologia , Fatores de TempoRESUMO
Alphaviruses are important causes of mosquito-borne viral encephalitis. The prototype alphavirus, Sindbis virus, causes encephalomyelitis in mice. The primary target cell for nervous system infection is the neuron. Thus, Sindbis virus infection of mice provides a model system for studying virus-neuron interactions. The outcome of infection is dependent on the maturity of the targeted neurons and on the strain of Sindbis virus used for infection. Most Sindbis virus strains can induce programmed cell death or apoptosis in cultured lines of mammalian cells and in immature postmitotic neurons both in vitro and in vivo. As neurons mature they become increasingly resistant to Sindbis virus-induced apoptosis presumably due to increased expression with differentiation of cellular antiapoptotic proteins. Therefore, in the absence of an effective immune response, these relatively avirulent strains of Sindbis virus establish persistent nonfatal infection in mature neurons. More virulent strains of Sindbis virus can overcome this intrinsic resistance of mature neurons to apoptosis and cause neuronal death. Amino acid changes in the virion glycoproteins are the main determinants of neurovirulence and knowledge of the effects of specific changes allows the investigator to design Sindbis viruses of specified neurovirulence for animals of different ages.
Assuntos
Infecções por Alphavirus/virologia , Alphavirus/fisiologia , Alphavirus/patogenicidade , Neurônios/virologia , Replicação Viral , Infecções por Alphavirus/patologia , Animais , HumanosRESUMO
Four-week-old BALB/c mice inoculated intracerebrally with the JHM strain of mouse hepatitis virus developed an acute demyelinating disease followed by apparent recovery with remyelination. When surviving mice were examined 16 months later, small areas of active demyelination were still present. This is the first reported example, to our knowledge, of an experimental viral infection in which acute demyelination with recovery is followed by persisting or recurring demyelination.