RESUMEN
HLA-G is a nonclassical class I human leukocyte antigen (HLA) involved in mechanisms of immune tolerance. The objective of this study was to determine whether N-(3-oxododecanoyl)-l-homoserine lactone (3O-C12-HSL), a quorum sensing molecule produced by Pseudomonas aeruginosa, could modify HLA-G expression to control the host immune response. We evaluated the ability of 3O-C12-HSL to induce HLA-G expression in primary immune cells, monocytes (U937 and THP1), and T-cell lines (Jurkat) in vitro and analyzed the cellular pathway responsible for HLA-G expression. We studied the HLA-G promoter with a luciferase assay and interleukin-10 (IL-10) and p38/CREB signaling with enzyme-linked immunosorbent assay and immunofluorescence, respectively. We observed that 3O-C12-HSL is able to induce HLA-G expression in human monocytes and T cells. We showed that the induction of HLA-G by 3O-C12-HSL is p38/CREB and IL-10 dependent. 3O-C12-HSL treatment is able to arrest only the U937 cell cycle, possibly due to the peculiar expression of the ILT2 receptor in the U937 cell line. Our observations suggest HLA-G as a mechanism to create a protected niche for the bacterial reservoir, similar to the role of HLA-G molecules during viral infections.
Asunto(s)
4-Butirolactona/análogos & derivados , Antígenos HLA-G/genética , Homoserina/análogos & derivados , Infecciones por Pseudomonas/inmunología , Pseudomonas aeruginosa/fisiología , Percepción de Quorum , Regulación hacia Arriba , 4-Butirolactona/inmunología , 4-Butirolactona/metabolismo , Antígenos HLA-G/inmunología , Homoserina/inmunología , Homoserina/metabolismo , Humanos , Interleucina-10/genética , Interleucina-10/inmunología , Monocitos/inmunología , Infecciones por Pseudomonas/genética , Infecciones por Pseudomonas/microbiología , Pseudomonas aeruginosa/genética , Pseudomonas aeruginosa/inmunología , Linfocitos T/inmunología , Células U937RESUMEN
The detection of bacterial signaling molecules in liquid or gaseous environments has been occurring in nature for billions of years. More recently, man-made materials and systems has also allowed for the detection of small molecules in liquid or gaseous environments. This chapter will outline some examples of these man-made detection systems by detailing several acoustic-wave sensor systems applicable to quorum sensing. More importantly though, a comparison will be made between existing bacterial quorum sensing signaling systems, such as the Vibrio harveyi two-component system and that of man-made detection systems, such as acoustic-wave sensor systems and digital communication receivers similar to those used in simple cell phone technology. It will be demonstrated that the system block diagrams for either bacterial quorum sensing systems or man-made detection systems are all very similar, and that the established modeling techniques for digital communications and acoustic-wave sensors can also be transformed to quorum sensing systems.
Asunto(s)
Gases , Percepción de Quorum , Vibrio/citología , Acústica , Proteínas Bacterianas/metabolismo , Técnicas Biosensibles , Reacciones Cruzadas , Homoserina/análogos & derivados , Homoserina/inmunología , Homoserina/metabolismo , Lactonas/inmunología , Lactonas/metabolismo , Redes Neurales de la Computación , Fosfotransferasas/metabolismo , Proteínas Quinasas/metabolismo , Dispositivo de Identificación por Radiofrecuencia , Factores de Transcripción/metabolismo , Vibrio/metabolismoRESUMEN
Quorum sensing system is a cell-to-cell communication system that plays a pivotal role in virulence expression in bacteria. Recent advances have demonstrated that the Pseudomonas aeruginosa quorum sensing molecule, N-3-oxododecanoyl homoserine lactone (3OC(12)-HSL), exerts effects on mammalian cells and modulates host immune response. Mast cells (MCs) are strategically located in the tissues that are constantly exposed to external stimulus. Therefore, it is very much possible that 3OC(12)-HSL may interact with MCs. Little is known, however, about specific effects of 3OC(12)-HSL on MCs. To address this, we investigated the influence of 3OC(12)-HSL on cell viability, apoptosis, intracellular calcium and cytokine release in MCs. We found that at high concentrations (100 microM), 3OC(12)-HSL inhibited proliferation and induced apoptosis in P815. The 3OC(12)-HSL treatment significantly increased intracellular calcium release in both P815 and HMC-1. We also observed that 3OC(12)-HSL-induced histamine release and degranulation in HMC-1 cells. Furthermore, 3OC(12)-HSL-induced IL-6 production at lower concentrations (6.25-12.5 microM) but steadily reduced IL-6 production at high concentration (50-100 muM). These data demonstrate that P. aeruginosa 3OC(12)-HSL affects MCs function.
Asunto(s)
4-Butirolactona/análogos & derivados , Homoserina/análogos & derivados , Mastocitos/inmunología , Pseudomonas aeruginosa/metabolismo , Percepción de Quorum , 4-Butirolactona/inmunología , 4-Butirolactona/farmacología , Animales , Apoptosis , Calcio/metabolismo , Degranulación de la Célula , Línea Celular , Proliferación Celular , Supervivencia Celular , Histamina/metabolismo , Homoserina/inmunología , Homoserina/farmacología , Interleucina-6/biosíntesis , Interleucina-6/inmunología , Mastocitos/efectos de los fármacos , Mastocitos/microbiología , Mastocitos/fisiología , Ratones , Infecciones por Pseudomonas/inmunología , Pseudomonas aeruginosa/inmunología , Pseudomonas aeruginosa/patogenicidad , VirulenciaRESUMEN
BACKGROUND: Cell-to-cell communication via exchange of small molecules, 'autoinducers', is a widespread phenomenon among Gram-negative and -positive bacteria. This intercellular signaling that synchronizes population-wide gene expression in a cell-density-dependent manner is termed 'quorum sensing' (QS). The discovery that Gram-negative bacteria employ non-peptide structures, N-acyl homoserine lactones, to globally regulate production of secondary metabolites and proteins, initiated a new area of research. Subsequently, other quorum-sensing systems and small signaling molecules were identified. With the emergence of antibiotic-resistant bacteria, most prominently methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa, new approaches for combating infections are needed. Inhibition of QS results in attenuation of virulence rather than direct killing of microbes. OBJECTIVE: We highlight current trends in preventing bacterial infections using quorum-quenching strategies. METHODS: We mainly focus on P. aeruginosa and S. aureus and their QS systems as targets for intervention. RESULTS/CONCLUSION: New research strongly suggests that QS systems represent attractive targets for discovery of novel anti-infective agents, including immunotherapeutic strategies.
Asunto(s)
Antibacterianos/farmacología , Anticuerpos Antibacterianos/uso terapéutico , Anticuerpos Monoclonales/uso terapéutico , Infecciones Bacterianas/terapia , Inmunoterapia/métodos , Percepción de Quorum/fisiología , 4-Butirolactona/análogos & derivados , 4-Butirolactona/antagonistas & inhibidores , 4-Butirolactona/inmunología , 4-Butirolactona/fisiología , Animales , Antibacterianos/uso terapéutico , Anticuerpos Antibacterianos/inmunología , Anticuerpos Monoclonales/inmunología , Especificidad de Anticuerpos , Bacterias/efectos de los fármacos , Bacterias/inmunología , Infecciones Bacterianas/tratamiento farmacológico , Infecciones Bacterianas/veterinaria , Proteínas Bacterianas/farmacología , Proteínas Bacterianas/fisiología , Proteínas Bacterianas/uso terapéutico , Vacunas Bacterianas/uso terapéutico , Diseño de Fármacos , Farmacorresistencia Bacteriana , Regulación Bacteriana de la Expresión Génica/fisiología , Homoserina/análogos & derivados , Homoserina/antagonistas & inhibidores , Homoserina/inmunología , Homoserina/fisiología , Humanos , Inmunización Pasiva , Inmunoterapia Activa/veterinaria , Péptidos Cíclicos/antagonistas & inhibidores , Péptidos Cíclicos/fisiología , Percepción de Quorum/efectos de los fármacos , VirulenciaRESUMEN
Pathogenic bacteria use quorum-sensing signal molecules to co-ordinate the expression of virulence genes. Animal-based studies have demonstrated the immunomodulatory effects of quorum-sensing signal molecules. In the present study, we have examined the impact of these molecules on normal human immune function in vitro and compared this with immune changes in patients with sepsis where quorum-sensing signal molecules were detected in the sera of patients. Quorum-sensing signal molecules inhibited normal dendritic cell and T-cell activation and proliferation, and down-regulated the expression of co-stimulatory molecules on dendritic cells; in MLDCRs (mixed lymphocyte dendritic cell reactions), secretion of IL (interleukin)-4 and IL-10 was enhanced, but TNF-alpha (tumour necrosis factor-alpha), IFN-gamma (interferon-gamma) and IL-6 was reduced. Quorum-sensing signal molecules induced apoptosis in dendritic cells and CD4(+) cells, but not CD8(+) cells. Dendritic cells from patients with sepsis were depleted and ex vivo showed defective expression of co-stimulatory molecules and dysfunctional stimulation of allogeneic T-lymphocytes. Enhanced apoptosis of dendritic cells and differential CD4(+) Th1/Th2 (T-helper 1/2) cell apoptotic rate, and modified Th1/Th2 cell cytokine profiles in MLDCRs were also demonstrated in patients with sepsis. The pattern of immunological changes in patients with sepsis mirrors the effects of quorum-sensing signal molecules on responses of immune cells from normal individuals in vitro, suggesting that quorum-sensing signal molecules should be investigated further as a cause of immune dysfunction in sepsis.
Asunto(s)
4-Butirolactona/análogos & derivados , Homoserina/análogos & derivados , Infecciones por Pseudomonas/inmunología , Pseudomonas aeruginosa/inmunología , Percepción de Quorum/inmunología , Sepsis/inmunología , 4-Butirolactona/inmunología , Apoptosis/inmunología , Antígeno B7-2/sangre , Proteínas Bacterianas/inmunología , Células Cultivadas , Técnicas de Cocultivo , Citocinas/metabolismo , Células Dendríticas/inmunología , Homoserina/inmunología , Humanos , Tolerancia Inmunológica/inmunología , Activación de Linfocitos/inmunología , Sepsis/microbiología , Subgrupos de Linfocitos T/inmunología , Células Th2/inmunologíaRESUMEN
The Gram-negative bacterium Pseudomonas aeruginosa, an opportunistic human pathogen, uses acyl-homoserine lactone-based quorum sensing systems to control its pathogenicity. One of its quorum sensing factors, N-3-oxo-dodecanoyl-homoserine lactone, has been shown not only to mediate bacterial quorum sensing but also to exert cytotoxic effects on mammalian cells. The monoclonal antibody RS2-1G9 generated against a 3-oxo-dodecanoyl-homoserine lactone analogue hapten was able to protect murine bone marrow-derived macrophages from the cytotoxic effects and also prevented the activation of the mitogen-activated protein kinase p38. These data demonstrate that an immunopharmacotherapeutic approach to combat P. aeruginosa infections might be a viable therapeutic option as the monoclonal antibody RS2-1G9 can readily sequester bacterial N-3-oxo-dodecanoyl-homoserine lactone molecules, thus interfering with their biological effects in prokaryotic and eukaryotic systems.
Asunto(s)
4-Butirolactona/análogos & derivados , Anticuerpos Monoclonales/inmunología , Homoserina/análogos & derivados , Macrófagos/inmunología , Pseudomonas aeruginosa/fisiología , Percepción de Quorum/fisiología , 4-Butirolactona/inmunología , 4-Butirolactona/metabolismo , Animales , Línea Celular , Células Cultivadas , Activación Enzimática , Haptenos/inmunología , Homoserina/inmunología , Homoserina/metabolismo , Macrófagos/citología , Macrófagos/metabolismo , Ratones , Poli(ADP-Ribosa) Polimerasa-1 , Poli(ADP-Ribosa) Polimerasas/metabolismo , Pseudomonas aeruginosa/inmunología , Proteínas Quinasas p38 Activadas por Mitógenos/metabolismoRESUMEN
The Pseudomonas aeruginosa quorum-sensing signal molecule N-3-oxododecanoyl)-L-homoserine lactone (OdDHL) has been reported to affect the function of a wide range of mammalian cell types, including cells of the immune system. In T cells, it has been reported to inhibit the production of most cytokines, and it has been reported to inhibit the function of antigen-presenting cells. The intracellular target of OdDHL in these cells remains to be identified, although the lipophilic nature of the molecule suggested that the target could be membrane associated. We explored the association of radiolabelled OdDHL with the membrane and cytoplasm of Jurkat T-cell lines and of primary murine T cells and dendritic cells. We found that not only did 3H-OdDHL enter the cytoplasm of Jurkat cells without disproportionate association with the cell membrane, it also reached maximum levels in the cytoplasm very quickly, and that the intracellular concentration was proportional to the extracellular concentration. Similar results were obtained when 3H-OdDHL was incubated with primary murine T cells or cultured dendritic cells. In addition, we show that the cellular distribution of OdDHL does not significantly alter after stimulation of Jurkat cells or primary murine CD4 T cells with immobilized anti-CD3, with little activity being associated with nuclear fractions. Together, these data strongly suggest that OdDHL enters mammalian cells by passive mechanisms, and that it does not preferentially associate with the membrane or nucleus upon T-cell receptor ligation.
Asunto(s)
4-Butirolactona/análogos & derivados , Homoserina/análogos & derivados , Factores Inmunológicos/inmunología , Pseudomonas aeruginosa/inmunología , 4-Butirolactona/inmunología , 4-Butirolactona/farmacología , Animales , Transporte Biológico , Citocinas/biosíntesis , Citoplasma/metabolismo , Homoserina/inmunología , Homoserina/farmacología , Humanos , Factores Inmunológicos/farmacología , Interferón gamma/biosíntesis , Células Jurkat , Activación de Linfocitos/inmunología , Ratones , Muromonab-CD3 , Transducción de Señal , Bazo/citología , Fracciones Subcelulares , Linfocitos T/inmunología , TritioRESUMEN
The P. aeruginosa quorum-sensing molecule N-3-oxododecanoyl homoserine lactone (3OC12-HSL) interacts not only with bacteria, but also with mammalian cells, among others with those of the immune defence system. We focussed on the possible interaction of 3OC12-HSL with human polymorphonuclear neutrophils (PMN), because these cells are the first to enter an infected site. We found that 3OC12-HSL attracts PMN, and up-regulates expression of receptors known to be involved in host defence, including the adhesion proteins CD11b/CD18 and the immunoglobulin receptors CD16 and CD64. Furthermore, the uptake of bacteria (phagocytosis), which is crucial for an efficient defence against infection, was enhanced. Thus, recognising and responding to 3OC12-HSL not only attracts the PMN to the site of a developing biofilm, but also reinforces their defence mechanisms, and hence could be a means to control the infection in an early stage and to prevent biofilm formation.
Asunto(s)
4-Butirolactona/análogos & derivados , Bacterias/inmunología , Homoserina/análogos & derivados , Inmunidad , Activación Neutrófila/inmunología , Percepción de Quorum , 4-Butirolactona/inmunología , 4-Butirolactona/farmacología , Bacterias/química , Bacterias/patogenicidad , Biopelículas , Comunicación Celular/inmunología , Células Cultivadas , Quimiotaxis de Leucocito/efectos de los fármacos , Quimiotaxis de Leucocito/inmunología , Homoserina/inmunología , Homoserina/farmacología , Humanos , Inmunidad/efectos de los fármacos , Fagocitosis , Pseudomonas aeruginosa/inmunología , Pseudomonas aeruginosa/patogenicidad , Receptores Inmunológicos/genética , Regulación hacia Arriba/genética , Regulación hacia Arriba/inmunologíaRESUMEN
Quorum-sensing systems have been reported to play a critical role in the pathogenesis of several bacterial infections. Recent data have demonstrated that Pseudomonas N-3-oxododecanoyl-L-homoserine lactone (3-oxo-C12-homoserine lactone, 3-oxo-C12-HSL), but not N-butanoyl-L-homoserine lactone (C4-HSL), induces apoptosis in macrophages and neutrophils. In the present study, the effects of active immunization with 3-oxo-C12-HSL-carrier protein conjugate on acute P. aeruginosa lung infection in mice were investigated. Immunization with 3-oxo-C12-HSL-BSA conjugate (subcutaneous, four times, at 2-week intervals) elaborated significant amounts of specific antibody in serum. Control and immunized mice were intranasally challenged with approximately 3 x 10(6) c.f.u. P. aeruginosa PAO1, and survival was then compared. All control mice died by day 2 post bacterial challenge, while 36 % of immunized mice survived to day 4 (P<0.05). Interestingly, bacterial numbers in the lungs did not differ between control and immunized groups, whereas the levels of pulmonary tumour necrosis factor (TNF)-alpha in the immunized mice were significantly lower than those of control mice (P<0.05). Furthermore, the extractable 3-oxo-C12-HSL levels in serum and lung homogenate were also significantly diminished in the immunized mice. Immune serum completely rescued reduction of cell viability by 3-oxo-C12-HSL-mediated apoptosis in macrophages in vitro. These results demonstrated that specific antibody to 3-oxo-C12-HSL plays a protective role in acute P. aeruginosa infection, probably through blocking of host inflammatory responses, without altering lung bacterial burden. The present data identify a promising potential vaccine strategy targeting bacterial quorum-sensing molecules, including autoinducers.
Asunto(s)
4-Butirolactona/análogos & derivados , Homoserina/análogos & derivados , Neumonía Bacteriana/prevención & control , Infecciones por Pseudomonas/prevención & control , Pseudomonas aeruginosa , Albúmina Sérica Bovina/administración & dosificación , Vacunación , 4-Butirolactona/administración & dosificación , 4-Butirolactona/análisis , 4-Butirolactona/inmunología , Animales , Anticuerpos Antibacterianos/sangre , Anticuerpos Antibacterianos/farmacología , Apoptosis/efectos de los fármacos , Línea Celular , Recuento de Colonia Microbiana , Homoserina/administración & dosificación , Homoserina/análisis , Homoserina/inmunología , Sueros Inmunes/farmacología , Inyecciones Subcutáneas , Pulmón/metabolismo , Pulmón/microbiología , Macrófagos/efectos de los fármacos , Macrófagos/patología , Ratones , Ratones Endogámicos BALB C , Neumonía Bacteriana/sangre , Neumonía Bacteriana/metabolismo , Infecciones por Pseudomonas/sangre , Infecciones por Pseudomonas/metabolismo , Pseudomonas aeruginosa/inmunología , Pseudomonas aeruginosa/aislamiento & purificación , Factor de Necrosis Tumoral alfa/análisis , Factor de Necrosis Tumoral alfa/metabolismo , Vacunas Conjugadas/administración & dosificación , Vacunas SintéticasRESUMEN
To gain insight into the role of luxSHi in disease pathogenesis, we inactivated that gene in several non-typeable Haemophilus influenzae isolates with an antibiotic resistance cassette. Gene inactivation was confirmed by PCR and by Southern blot analysis in each strain. Culture filtrates from luxSHi mutants contained a decreased amount of autoinducer-2 (AI-2) activity in comparison to the wild-type isolates using the Vibrio harveyi BB170 bioassay. Culture filtrates from Escherichia coli strain DH5alpha expressing a cloned luxSHi contained 350-fold more AI-2 activity per cell than E. coli DH5alpha containing the vector alone. The growth rate in several liquid media, and the cell density after overnight growth were not significantly different between the parents and the luxSHi mutants. Two clinical H. influenzae and their luxSHi mutants produced an identical biofilm in a flow system. Invasion of human cells by the luxSHi mutants, in comparison to the wild-type parents was strain-dependent, and cell type-dependent, but the luxSHi mutants tended to be more invasive. The luxSHi mutant of an otitis media isolate, strain R3157 appeared more virulent in the chinchilla model of otitis media: there were more bacteria in the middle ear, a greater inflammatory response and more goblet cell hyperplasia 10 days after the inoculation. We conclude that the H. influenzae homologue of luxS modulates certain virulence traits.
Asunto(s)
Proteínas Bacterianas/genética , Biopelículas/crecimiento & desarrollo , Infecciones por Haemophilus/microbiología , Haemophilus influenzae/patogenicidad , Animales , Liasas de Carbono-Azufre , Línea Celular Tumoral , Chinchilla , ADN Bacteriano/química , ADN Bacteriano/genética , Femenino , Haemophilus influenzae/genética , Haemophilus influenzae/crecimiento & desarrollo , Haemophilus influenzae/ultraestructura , Homoserina/análogos & derivados , Homoserina/genética , Homoserina/inmunología , Humanos , Lactonas/inmunología , Microscopía Electrónica de Rastreo , Mutagénesis Insercional , Otitis Media/microbiología , VirulenciaRESUMEN
Pseudomonas aeruginosa has two well-characterized quorum-sensing systems, Las and Rhl. These systems are composed of LuxR-type proteins, LasR and RhlR, and two acyl homoserine lactone (AHL) synthases, LasI and RhlI. LasI catalyzes the synthesis of N-(3-oxododecanoyl)homoserine lactone (3O-C12-HSL), whereas RhlI catalyzes the synthesis of N-butyryl-homoserine lactone. There is little known about the importance of AHLs in vivo and what effects these molecules have on eukaryotic cells. In order to understand the role of AHLs in vivo, we first tested the effects that deletions of the synthase genes in P. aeruginosa had on colonization of the lung. We demonstrate that in an adult mouse acute-pneumonia model, deletion of the lasI gene or both the lasI and rhlI genes greatly diminished the ability of P. aeruginosa to colonize the lung. To determine whether AHLs have a direct effect on the host, we examined the effects of 3O-C12-HSL injected into the skin of mice. In this model, 3O-C(12)-HSL stimulated a significant induction of mRNAs for the cytokines interleukin-1alpha (IL-1alpha) and IL-6 and the chemokines macrophage inflammatory protein 2 (MIP-2), monocyte chemotactic protein 1, MIP-1beta, inducible protein 10, and T-cell activation gene 3. Additionally, dermal injections of 3O-C12-HSL also induced cyclooxygenase 2 (Cox-2) expression. The Cox-2 enzyme is important for the conversion of arachidonic acid to prostaglandins and is associated with edema, inflammatory infiltrate, fever, and pain. We also demonstrate that 3O-C12-HSL activates T cells to produce the inflammatory cytokine gamma interferon and therefore potentially promotes a Th1 environment. Induction of these inflammatory mediators in vivo is potentially responsible for the significant influx of white blood cells and subsequent tissue destruction associated with 3O-C12-HSL dermal injections. Therefore, the quorum-sensing systems of P. aeruginosa contribute to its pathogenesis both by regulating expression of virulence factors (exoenzymes and toxins) and by inducing inflammation.
Asunto(s)
4-Butirolactona/análogos & derivados , 4-Butirolactona/inmunología , Homoserina/análogos & derivados , Homoserina/inmunología , Pseudomonas aeruginosa/inmunología , 4-Butirolactona/administración & dosificación , 4-Butirolactona/biosíntesis , 4-Butirolactona/fisiología , Animales , Células Cultivadas , Quimiocinas/biosíntesis , Ciclooxigenasa 2 , Citocinas/biosíntesis , Homoserina/administración & dosificación , Homoserina/biosíntesis , Homoserina/fisiología , Inmunofenotipificación , Isoenzimas/biosíntesis , Isoenzimas/genética , Queratinocitos/citología , Queratinocitos/inmunología , Pulmón/microbiología , Ratones , Ratones Endogámicos C57BL , FN-kappa B/inmunología , Prostaglandina-Endoperóxido Sintasas/biosíntesis , Prostaglandina-Endoperóxido Sintasas/genética , Pseudomonas aeruginosa/crecimiento & desarrollo , Pseudomonas aeruginosa/patogenicidad , Piel/inmunología , Linfocitos T/inmunología , Células TH1/inmunología , VirulenciaRESUMEN
Diverse gram-negative bacterial cells communicate with each other by using diffusible N-acyl homoserine lactone (AHL) signal molecules to coordinate gene expression with cell population density. Accumulation of AHLs above a threshold concentration renders the population "quorate," and the appropriate target gene is activated. In pathogenic bacteria, such as Pseudomonas aeruginosa, AHL-mediated quorum sensing is involved in the regulation of multiple virulence determinants. We therefore sought to determine whether the immune system is capable of responding to these bacterial signal molecules. Consequently the immunomodulatory properties of the AHLs N-(3-oxododecanoyl)-L-homoserine lactone (OdDHL) and N-(3-oxohexanoyl)-L-homoserine lactone (OHHL) were evaluated in murine and human leukocyte immunoassays in vitro. OdDHL, but not OHHL, inhibited lymphocyte proliferation and tumor necrosis factor alpha production by lipopolysaccharide-stimulated macrophages. Furthermore, OdDHL simultaneously and potently down-regulated the production of IL-12, a Th-1-supportive cytokine. At high concentrations (>7 x 10(-5) M) OdDHL inhibited antibody production by keyhole limpet hemocyanin-stimulated spleen cells, but at lower concentrations (<7 x 10(-5) M), antibody production was stimulated, apparently by increasing the proportion of the immunoglobulin G1 (IgG1) isotype. OdDHL also promoted IgE production by interleukin-4-stimulated human peripheral blood mononuclear cells. These data indicate that OdDHL may influence the Th-1-Th-2 balance in the infected host and suggest that, in addition to regulating the expression of virulence determinants, OdDHL may contribute to the pathogenesis of P. aeruginosa infections by functioning as a virulence determinant per se.