concanavalin-a and Hypersensitivity

Topics: Agammaglobulinemia; alpha-Fetoproteins; Antibodies; Antibody Formation; Autoimmune Diseases; B-Lymphocytes; Concanavalin A; DNA; Epitopes; Genes, MHC Class II; Growth Inhibitors; Hybrid Cells; Hypersensitivity; Immune Tolerance; Immunity, Cellular; Immunoglobulins; Immunotherapy; Interferons; Lymphocyte Culture Test, Mixed; Multiple Myeloma; Nucleotides, Cyclic; Prostaglandins; T-Lymphocytes; T-Lymphocytes, Regulatory; Terminology as Topic; Thymus Hormones

Liver function abnormalities are common in patients with inflammatory arthritis. However, the precise mechanism is still unclear. In this study, inflammatory arthritis was established in mice by subcutaneous injection of complete Freund's adjuvant, and the intravenous injection of concanavalin A (Con A) was employed to induce acute immune-mediated hepatitis in mice. The result showed that the arthritis mice were more susceptible to ConA-induced hepatitis than the control mice, as evidenced by increased hepatic necrosis, elevated serum alanine aminotransferase activity, and raised inflammatory cytokines. Besides, the in vitro assay demonstrated that the T cells from arthritis mice were more sensitive to the Con A stimulation than those from control mice. Moreover, we determined that the level of leptin, a kind of adipokine, was significantly increased in the serum and hepatic T cells of arthritis mice. Interestingly, the data indicated that the enhanced expression of leptin in hepatic T cells is responsible for the hypersensitivity of arthritis mice-derived T cells to Con A challenge. Collectively, our findings demonstrate an unexpected role of leptin in the connection between inflammatory arthritis and acute immune-mediated hepatitis, thus providing new insight into the clinical therapy of arthritis-related liver dysfunction.

Topics: Acute Disease; Animals; Arthritis; Concanavalin A; Cytokines; Disease Susceptibility; Hepatitis; Hypersensitivity; Inflammation; Inflammation Mediators; Leptin; Liver; Lymphocyte Activation; Mice, Inbred C57BL; Signal Transduction; T-Lymphocytes

House dust mites are important allergen sources and some of these allergenic proteins may contain carbohydrate moieties, which are able to be isolated using lectins, as Concanavalin A (ConA). This study aimed to investigate allergenicity (IgE) and antigenicity (IgG1 and IgG4) of ConA-unbound and ConA-bound. We obtained mannose-enriched and mannose-depleted fractions from Dpt by ConA affinity chromatography. Both ConA-bound and ConA-unbound fractions were evaluated by ELISA and Western Blotting for specific IgE, IgG1, and IgG4 reactivity with sera obtained from 95 mite-allergic patients (DP+) and 92 nonallergic (NA) subjects. Inhibition ELISA was used to assess cross-reactivity between Dpt extract and its fractions.. Among the DP+ patients, no difference was found between ConA-unbound and ConA-bound fractions regarding the levels of specific IgE, IgG1, and IgG4. Nonallergic subjects had the same levels of specific IgG1 to both ConA-unbound and ConA-bound fractions, although for specific IgG4, values were higher for ConA-bound. A positive correlation was found among specific IgE, IgG1, and IgG4 levels when Dpt was compared to ConA-unbound and ConA-bound fractions. Recognition of crude Dpt by IgE, IgG1, and IgG4 was highly inhibited by ConA-unbound and ConA-bound fractions. Western Blotting revealed a broad spectrum of bands ranging from 14 to 116 kDa recognized by specific IgE and IgG4. However, IgG1 reached higher frequency values on high molecular weight polypeptides.

Topics: Adult; Allergens; Animals; Concanavalin A; Dermatophagoides pteronyssinus; Enzyme-Linked Immunosorbent Assay; Female; Glycosylation; Healthy Volunteers; Humans; Hypersensitivity; Immunoglobulin E; Immunoglobulin G; Male; Middle Aged; Plant Extracts; Pyroglyphidae

Topics: Biosensing Techniques; Concanavalin A; Electrochemical Techniques; Energy Transfer; Hypersensitivity; Limit of Detection; Luminescent Measurements; Manganese Compounds; Nanoparticles; Nanotubes, Carbon

We evaluated the immunomodulatory activity of type-4 resistant starch (RS) in mesenteric lymph nodes (MLNs) using a rat model. Sixteen male Sprague-Dawley rats were fed either a cellulose diet or an RS diet (RSD) for 4 weeks. Serum immunoglobulin A levels, as well as the CD4(+) T cell population and the ratio of CD4(+)/CD8(+) T cells in the MLNs of rats, were significantly elevated by replacing cellulose with RS in the diet. The survival rate of concanavalin A (Con A)-stimulated MLN lymphocytes and interleukin-4 secretion from the Con A-stimulated MLN lymphocytes were significantly increased in rats fed RSD. These results indicate that type-4 RS might ameliorate allergic inflammation in the MLNs of rats through an increased CD4(+) T cell population and enhanced differentiation of MLN lymphocytes into type-2 T cells.

Topics: Animals; CD4-CD8 Ratio; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Cell Differentiation; Cell Survival; Cellulose; Concanavalin A; Dietary Carbohydrates; Hypersensitivity; Immunoglobulin A; Immunologic Factors; Inflammation; Interleukin-4; Lymph Nodes; Lymphocytes; Male; Mesentery; Rats; Rats, Sprague-Dawley; Starch; Th2 Cells

The edeines analogs were tested in several in vitro and in vivo assays using the mouse model, with edeine B (peptide W1) and cyclosporine A as reference compounds. The peptides displayed moderate, stimulatory effects on concanavalin A-induced (ConA-induced) splenocyte proliferation, whereas their effects on pokeweed mitogen-induced (PWM-induced) splenocyte proliferation were inhibitory. The peptides inhibited lipopolysacharide-induced (LPS-induced) tumor necrosis factor alpha production but had little effect on interleukin 6 production. In the model of the humoral immune response in vitro to sheep red blood cells, peptide 1 was distinctly stimulatory in the investigated concentrations (1-100 microg/ml), whereas peptides 3 and 4 only stimulated the number of antibody-forming cells at the highest concentration (100 microg/ml). In the model of the delayed type hypersensitivity in vivo to ovalbumin, the peptides were moderately suppressive (3 being the most active). The reference peptide W1 stimulated ConA-induced cell proliferation at 1-10 microg/ml but was inhibitory at 100 microg/ml. It also inhibited PWM-induced cell proliferation in a dose-dependent manner. This peptide had no effect on the humoral immune response in vitro or on cytokine production, but inhibited DTH reaction in vivo. The relationship between structure and activity, and a possible mode of action of the peptides, is discussed in this paper.

Topics: Animals; Cell Proliferation; Concanavalin A; Edeine; Hypersensitivity; Immunity; Interleukin-6; Lipopolysaccharides; Mice; Ovalbumin; Pokeweed Mitogens; Sheep; Spleen; Tumor Necrosis Factor-alpha

To identify potent and selective calcium-release-activated calcium (CRAC) channel inhibitors, we examined the structure-activity relationships of the pyrazole and thiophene moieties in compound 4. Compound 25b was found to exhibit highly potent and selective inhibitory activity for CRAC channels and further modifications of the pyrazole and benzoyl moieties of compound 25b produced compound 29. These compounds were potent inhibitors of IL-2 production in vitro and also acted as inhibitors in pharmacological models of diseases resulting from T-lymphocyte activation, after oral administration.

Topics: Animals; Calcium; Calcium Channel Blockers; Calcium Channels; Cell Line, Tumor; Chemical and Drug Induced Liver Injury; Concanavalin A; Crystallography, X-Ray; Disease Models, Animal; Drug Evaluation, Preclinical; Female; Humans; Hypersensitivity; Jurkat Cells; Male; Mice; Mice, Inbred BALB C; Models, Molecular; Molecular Structure; Picryl Chloride; Pyrazoles; Stereoisomerism; Structure-Activity Relationship

Nigella sativa Linn. (Ranunculaceae) is known to have beneficial effects on a wide range of diseases including asthma. However, the mechanism of action in asthma and other allergic diseases is not entirely clear. The present study was planned to evaluate the effects of Nigella sativa on cytokine production of splenic mononuclear cells in ova-sensitized mice. Nineteen two-month-old BALB/c mice were given 0.3 mL of Nigella sativa oil by oro-eosophageal cannula once a day for a month. The control group consisting of 10 mice took 0.3 mL of 0.9% saline solution by the same route for the same period. In the third week of the study, all mice were sensitized by means of intraperitoneal injections of 20 microg of ovalbumin (OVA-Grade VI, Sigma). Ova injections were repeated three times with 7-day intervals. After another week, all mice were sacrificed by means of cervical dislocation. Then the splenic mononuclear cells (MNCs) of mice were cultured with OVA or Concavalin A (Con-A). From the culture supernatants, IL-4, IL-10 and IFN-gamma were assessed by means of ELISA. The cytokine production of splenic MNCs of mice that were given Nigella sativa for 30 days was not significantly different than those who took saline solution instead. In conclusion, Nigella sativa oil seems not to have an immunomodulatory effect on Th1 and Th2 cell responsiveness to allergen stimulation.

Topics: Allergens; Animals; Concanavalin A; Hypersensitivity; Immunologic Factors; Mice; Mice, Inbred BALB C; Monocytes; Nigella; Ovalbumin; Plant Oils; Spleen; Th1 Cells; Th2 Cells; Thymidine

The local lymph node assay (LLNA) is used to identify allergens by means of dermal exposure. For hazard identification, besides identification also the distinction between contact and respiratory allergens is of importance. We have previously shown that a modified LLNA can be used to identify respiratory allergens, on the basis of Con A induced IL-4 production. Here we show a good qualitative correlation between mRNA expression and production of IFN-gamma and IL-4. This suggests that distinction between contact and respiratory allergens may also be studied at the mRNA expression level. Secondly, another assay, similar to the modified LLNA but differing in the duration and the number of allergen applications as well as in the ex vivo culture conditions, here denoted as 'longer' assay, has been reported to be able to identify contact allergens, on the basis of (spontaneous) IFN-gamma production. In the present study we have compared these assays. Similar to our previous findings, in the modified LLNA exposure to the respiratory allergen trimellitic anhydride (TMA) resulted in a approximately 10-fold higher Con A induced IL-4 production compared with the contact allergen dinitrochlorobenzene (DNCB), while exposure to both allergens resulted in a similar Con A induced IFN-gamma production. In the 'longer' assay, TMA exposure resulted in Con A induced IL-4 production whereas DNCB exposure did not. Importantly, only a 2-fold higher spontaneous IFN-gamma production was induced by DNCB compared with TMA, the difference being not statistically significant. Thus, although the 'longer' assay indeed showed a somewhat higher IFN-gamma induction by DNCB compared with TMA, the magnitude and robustness of this effect question its applicability. These results favor the modified LLNA since it is shorter, and combines identification of allergens (by cell proliferation) with identification of respiratory allergens (by IL-4 production). Compounds that induce cell proliferation with a low concomitant IL-4 production may thus be identified as contact allergens, although the need to positively identity such allergens remain.

Topics: Allergens; Animals; Concanavalin A; Dinitrochlorobenzene; Enzyme-Linked Immunosorbent Assay; Female; Hypersensitivity; Interferon-gamma; Interleukin-4; Local Lymph Node Assay; Lymph Nodes; Lymphocyte Activation; Male; Mice; Mice, Inbred BALB C; Phthalic Anhydrides; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger

In the present study we compared the immunological reactions between Rhipicephalus sanguineus tick-infested susceptible (dogs and mice) and tick-resistant hosts (guinea pigs), elucidating some of the components of efficient protective responses against ticks. We found that T-cells from guinea pigs infested with adult ticks proliferate vigorously in the presence of concanavalin A (ConA), whereas ConA-induced cell proliferation of tick-infested mice and dogs was significantly decreased at 43.1 and 94.0%, respectively, compared to non-infested controls. Moreover, cells from mice and dogs submitted to one or three successive infestations did not exhibit a T-cell proliferative response to tick antigens, whilst cells from thrice tick-infested guinea pigs, when cultured with either a tick extract or tick saliva, displayed a significant increase in cell proliferation. Also, we evaluated the response of tick-infested mice to a cutaneous hypersensitivity test induced by a tick extract. Tick-infested mice developed a significant immediate reaction, whereby a 29.9% increase in the footpad thickness was observed. No delayed-type hypersensitivity (DTH) reaction was detected. Finally, the differential cell count at the tick attachment site in repeatedly infested mice exhibited a 6.6- and 4.1-fold increase in the percentage of eosinophils and neutrophils, respectively, compared to non-infested animals, while a decrease of 77.0-40.9 in the percentage of mononuclear cells was observed. The results of the cutaneous hypersensitivity test and the cellular counts at the tick feeding site for mice support the view that tick-infested mice develop an immune response to R. sanguineus ticks very similar to dogs, the natural host of this species of tick, but very different from guinea pigs (resistant host), which develop a DTH reaction in addition to a basophil and mononuclear cell infiltration at the tick-attachment site. In conclusion, saliva introduced during tick infestations reduces the ability of a susceptible animal host to respond to tick antigens that could stimulate a protective immune response. As a consequence, the animals present a lack of DTH response and disturbed cellular migration to tick feeding site, which can represent a deficient response against ticks.

Topics: Animals; Antigens; Cell Division; Concanavalin A; Disease Susceptibility; Dog Diseases; Dogs; Female; Guinea Pigs; Host-Parasite Interactions; Hypersensitivity; Ixodidae; Male; Mice; Mice, Inbred C3H; Saliva; Skin; T-Lymphocytes; Tick Infestations

Dysregulated expression of the T helper 2 cytokine interleukin (IL)-4 is thought to play a fundamental role in the pathogenesis of allergic asthma. The molecular basis for dysregulated IL-4 production is not well understood. We analyzed in detail the molecular factors involved in regulating IL-4 transcription in a well-characterized mouse model. In this model, A/J mice developed allergen-induced IL-4 cytokine gene expression, airway inflammation, and hyperresponsiveness, whereas C3H/HeJ (C3H) mice did not. Here we report that isolated splenocytes from A/J and C3H mice stimulated ex vivo with concanavalin A reproduced the cytokine phenotype observed in the airway after antigen challenge. We hypothesized that differences in splenocyte IL-4 production involved either polymorphisms in regulatory IL-4 promoter regions, or the expression and activation of transcription factors necessary for promoter transactivation in a strain-dependent manner. To address these questions, we first sequenced ~ 700 base pairs containing well-characterized IL-4 promoter regulatory elements using genomic DNA obtained from C3H and A/J mice. Next, we used electrophoretic mobility shift assays with relevant IL-4 promoter sequences to screen nuclear extracts isolated from A/J and C3H splenocytes for functional transcriptional factor complexes. Here we show that susceptibility to antigen-induced airway hyperresponsiveness is not due to polymorphisms in the IL-4 promoter, but is associated with preferential expression of nuclear factor of activated T cells c in splenocyte nuclear extracts obtained from A/J mice. In conclusion, our data link dysregulated activation of a specific transcription factor with susceptibility to allergic airway inflammation.

Topics: Animals; Cell Nucleus; Cells, Cultured; Concanavalin A; DNA-Binding Proteins; Gene Expression Regulation; Hypersensitivity; Immunophenotyping; Interleukin-4; Macromolecular Substances; Male; Mice; Mice, Inbred A; Mice, Inbred C3H; NFATC Transcription Factors; Nuclear Proteins; Promoter Regions, Genetic; Sequence Analysis, DNA; Species Specificity; Spleen; Stimulation, Chemical; T-Lymphocytes; Transcription Factors; Transcription, Genetic

p59fynT is a protein tyrosine kinase in the src family that has been associated with and believed to function in the signaling of many receptors, including the T-cell receptor. A role for the kinase in antigen-driven pulmonary inflammation was examined using mice whose p59fynT gene had been genetically ablated. FynKO mice that were sensitized to ovalbumin exhibited a marked increase in bronchoalveolar lavage eosinophils and cytokines, including interleukin (IL)-4 and IL-5, relative to wild-type mice in response to antigen aerosol exposure. Ovalbumin-stimulated IL-5 production was also increased in cultured splenocytes derived from fynKO mice relative to wild-type mice, whereas interferon-gamma levels were unchanged. Diminished concanavalin A--stimulated IL-4 levels from fynKO splenocytes were consistent with reduced serum immunoglobulin (Ig)E levels observed in sensitized/saline aerosol-challenged animals and may reflect defective natural killer 1.1(+) T cell development. Normalization of IgE levels in sensitized fynKO mice relative to wild-type mice occurred after repeat antigen challenge, which suggests a secondary source of IL-4. Overall, these data demonstrate fyn is a negative regulator of allergic airway inflammation in mice because its absence promotes a shift to a T helper-2 phenotype that may reflect the kinase's role in T-cell receptor signaling.

Topics: Animals; Antigens; Bronchoalveolar Lavage Fluid; Concanavalin A; Disease Models, Animal; Eosinophils; Hypersensitivity; Immunoglobulin E; Interleukin-4; Interleukin-5; Mice; Mice, Inbred C57BL; Mice, Knockout; Ovalbumin; Pneumonia; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-fyn; Spleen; src-Family Kinases; Th2 Cells

IL-5 plays a central role in allergic diseases associated with eosinophilic inflammation. We have previously reported that IL-5 production by peripheral blood mononuclear cells (PBMC) is greatly enhanced in both atopic and nonatopic asthmatics compared to control subjects.. Concanavalin A (Con A) blast lymphocytes were derived from PBMC of allergic and control subjects. Transcriptional regulation of the IL-5 gene was investigated by transient transfection assay.. A significant amount of IL-5 was produced by Con A blast lymphocytes derived from allergic subjects upon stimulation with phorbol ester and Ca(2+) ionophore, whereas the cells derived from control subjects did not produce a detectable amount of IL-5. Production of IL-2 and IL-4 was not significantly different between the two groups. A luciferase reporter plasmid containing the human IL-5 promoter/enhancer region was transcribed by Con A blast lymphocytes derived from allergic subjects, but not by the cells from control subjects, upon activation.. IL-5 synthesis by nontransformed T cells of allergic subjects is enhanced at the level of gene transcription. Elucidation of the molecular mechanism of IL-5 gene transcription by allergic T cells may delineate the pathogenesis of allergic disease for the future therapeutic intervention.

Topics: Adult; Concanavalin A; Humans; Hypersensitivity; Interleukin-5; Middle Aged; T-Lymphocytes; Transcription, Genetic

Immunity to Candida albicans (Candida) is characterized by a Th-1 type pattern of reactivity. Candida is rarely a cause antigen for bronchial asthma. Beta agonists have been found to inhibit secretion of IL-2 from T cells through intracellular cAMP elevation. We examined effects of isoproterenol (ISO) on Candida-stimulated T cells. Peripheral T cells obtained from six Candida-sensitive asthmatics, six Candida-sensitive non-asthmatic subjects, and six normal donors by Ficoll-Hypaque gradient centrifugation and nylon-wool column chromatography were incubated with Candida antigen or concanavalin A (Con A) in the absence or presence of ISO. Secretion of IL-2 and intracellular accumulation of cAMP were assayed by ELISA. Con A induced secretion of IL-2 in each of the three groups. Candida antigen induced IL-2 secretion in the normal and the non-asthmatic subjects, but not in the asthmatics. ISO, which reduced Con A-induced secretion of IL-2 in a dose-dependent manner, had no effect on Candida-induced secretion of IL-2. Although ISO increased the intracellular concentration of cAMP in untreated and Con A-treated T cells from all donors, cells from the normal and the non-asthmatic subjects, but not from the asthmatics, that were co-incubated with ISO and Candida had lower levels of cAMP than those treated with ISO alone. It is suggested that Candida antigen induces secretion of IL-2 and reduces ISO-inducible accumulation of cAMP in Candida-responsive IL-2 secreting cells, which may make Candida-induced secretion of IL-2 insensitive to ISO.

Topics: Asthma; Candida; Case-Control Studies; Concanavalin A; Cyclic AMP; Dose-Response Relationship, Drug; Humans; Hypersensitivity; In Vitro Techniques; Interleukin-2; Isoproterenol; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; T-Lymphocyte Subsets

Selection of poultry for fast growth rate is often accompanied by a reduction in specific immune responses or increased disease susceptibility. In this study, 17-wk-old male turkeys from each of four closed genetic lines, a randombred control (RBC) line and its subline (F) selected for increased 16-wk BW, and another RBC and its subline (E) selected for increased egg production, were tested for in vivo response to toe web inoculation with phytohemagglutinin-P (PHA-P), in vitro response of lymphocytes in whole blood to PHA-P and concanavalin A (Con A), hemolytic complement activity, differential white blood cell counts, hematology, and serum chemistry values. Fifteen male turkeys from each of two commercial lines, Com A and Com B, were also tested. The large-bodied F line birds had a lower toe web response to PHA-P, lower lymphocyte counts, and lower relative spleen weights than their smaller parent line. Body weights, total erythrocyte counts, blood urea nitrogen (BUN) levels, and in vitro mitogenic response to PHA-P and Con A were higher in the F line birds. Line E had lower hemolytic complement levels, lower relative spleen and relative bursal weights, and a higher in vitro mitogenic response to PHA-P than its parent line. The Com B line had a lower toe web response to PHA-P, and lower serum levels of gamma-glutamyltransferase and bilirubin than Com A. Line Com B had higher total RBC counts and higher levels of alanine aminotransferase (ALT) than Com A. These results support the concept that some changes in the cell-mediated immune response, as well as other physiological changes that may potentially affect immune response, appear to accompany selection for faster growth.

Topics: Alanine Transaminase; Alkaline Phosphatase; Animals; Aspartate Aminotransferases; Blood Urea Nitrogen; Body Weight; Breeding; Cells, Cultured; Complement System Proteins; Concanavalin A; Eggs; Erythrocyte Count; Female; gamma-Glutamyltransferase; Growth; Hemolysis; Hypersensitivity; Leukocyte Count; Lymphocyte Activation; Lymphocyte Count; Lymphocytes; Male; Organ Size; Oviposition; Phytohemagglutinins; Spleen; Turkeys

Candida albicans crossreacts with Saccharomyces cerevisiae or Pityrosporum ovale at the IgE level. However, the extent of crossreactivity of C. albicans with other yeast species is not known.. The crossreactivity at the immunoglobulin E (IgE) level of Candida albicans with other pathogenic Candida species and to the airborne yeast species Cryptococcus and Rhodotorula was studied by immunoblot analysis.. Crude antigens, designated as heat extract, were prepared from 13 different yeast species and a dot blot test was performed to detect IgE antibodies against each of the heat extracts in 349 patients with allergies who were positive for IgE antibodies against C. albicans in a CAP system.. In the dot blot test, most of the sera reacted with the heat extracts of not only C. albicans but also those prepared from the other yeast species. The sera of 41 of the 349 patients (11.7%) reacted with the heat extracts of all 13 yeast species. The extent of the binding of IgE antibodies to multiple yeast species correlated with both the fluorescence intensities measured in the CAP system and the intensities of dots generated by the heat extract of C. albicans in the dot blot test. In an inhibition dot blot test, mannoproteins, but not proteins, of C. albicans strongly inhibited the subsequent binding of IgE antibodies to all yeast species.. Our data suggest that the C. albicans mannoproteins are responsible for the crossreactivity among these yeast species at the IgE level.

Topics: Air Microbiology; Air Pollutants; Allergens; Antibodies, Fungal; Antibody Specificity; Antigens, Fungal; Candida; Candida albicans; Cell Extracts; Cell Wall; Concanavalin A; Cross Reactions; Cryptococcus; Hot Temperature; Humans; Hypersensitivity; Immunoblotting; Immunoglobulin E; Membrane Glycoproteins; Protein Binding; Rhodotorula; Rosaniline Dyes; Species Specificity; Staining and Labeling; Yeasts

In atopic patients, allergen-sensitized T lymphocytes specifically proliferate in the presence of T cell-growth factor, interleukin 2 (IL-2). Lecithin-bound iodine (LBI), which has been used as a therapeutic modality for patients with bronchial asthma (BA), effectively inhibited Dermatophagoides farinae (Df) mite antigen-induced IL-2 responsiveness in concentrations comparable to LBI concentrations in blood. IL-2-responding T cells were more sensitive to LBI than antigen-presenting cells, whereas LBI suppressed the release of interleukin 1 (IL-1) elicited by Df antigen. In addition, ovalbumin (OVA)-induced IL-2 responsiveness in egg sensitive patients and purified protein-derivative (PPD)-induced IL-2 responsiveness were similarly inhibited by LBI. The IL-2 responsiveness induced by concanavalin A (Con A), however, was not changed. On the basis of these results, LBI may act as a slight immunosuppressant to inhibit the induction of allergen-specific lymphocytes and to improve the clinical status in allergic diseases.

Topics: Adult; Allergens; alpha-Linolenic Acid; Antigens, Dermatophagoides; Asthma; Child, Preschool; Concanavalin A; Dermatitis, Atopic; Epitopes; Glycoproteins; Humans; Hypersensitivity; Infant; Interleukin-1; Interleukin-2; Iodine; Lymphocyte Activation; Ovalbumin; Phosphatidylcholines; T-Lymphocytes; Tuberculin

The effect of a thromboxane A2 (TXA2) receptor antagonist, ON-579, on experimental allergic skin and airway reactions was studied in vivo. ON-579 at doses of 1 and 20 mg/kg clearly inhibited U-46619-induced increases in respiratory resistance (Rrs) in guinea pigs. ON-579 at doses of 1, 20 and 50 mg/kg inhibited the aerosolized antigen-induced biphasic increase in Rrs in guinea pigs. Moreover, ON-579 clearly inhibited repeated aeroantigen-induced airway hyperreactivity in guinea pigs. ON-579, however, did not have any significant effects on allergic cutaneous reactions in rats. These results suggest that ON-579 is a relatively selective TXA2 antagonist, especially in the airways, and indicate the efficacy of ON-579 on antigen-induced increase in airway resistance and antigen-induced airway hyperreactivity in guinea pigs.

Topics: Aerosols; Airway Resistance; Animals; Antigens; Arthus Reaction; Bronchoalveolar Lavage Fluid; Concanavalin A; Dinitrophenols; Guinea Pigs; Histamine; Hypersensitivity; Ketotifen; Leukocyte Count; Male; Mice; Ovalbumin; Passive Cutaneous Anaphylaxis; Phenoxyacetates; Rats; Receptors, Thromboxane; Respiratory Tract Diseases; Serum Albumin, Bovine; Skin Diseases; Sulfonamides

Topics: Binding Sites; Carbohydrates; Concanavalin A; Glycosylation; Humans; Hypersensitivity; Immunoglobulin E; Lectins; Molecular Structure; Myeloma Proteins; Precipitin Tests

The effects of IL-2, IL-3, and IL-4 activities on occurrence of allergic asthma induced by spores of mushroom have been studied by measuring the IL-2, IL-3, and IL-4 activities in culture supernatants of spleen lymphocytes from guinea pigs being stimulated with Con A. The IL-4 activity (14.9 +/- 0.18 u) in the culture supernatant was higher than control group (6.7 +/- 1.5 u). The IL-2 and IL-3 activities were all similar to that of the control group. The IL-4 synthesis was similarly raised as the IL-4 activity. These results indicated that there is a relationship between the occurrence of allergic asthma and the increase of IL-4.

Topics: Animals; Asthma; Cells, Cultured; Concanavalin A; Guinea Pigs; Hypersensitivity; Interleukin-2; Interleukin-3; Interleukin-4; Lymphocytes; Mice; Polyporaceae; Reference Values; Spleen; Spores, Fungal; Tumor Cells, Cultured

Cloned human CD4+ T cell lines specific for the house dust mite Dermatophagoides pteronyssinus were used to map minimal T cell activation-inducing epitopes on the Group I allergen in D. pteronyssinus extracts (Der p I) molecule. Most of these Der p I-specific T cell clones expressed different TCR V alpha and V beta gene products. Using recombinant deletion proteins, three T cell epitopes were identified on the Der p I molecule; p45-67 and p117-143 were recognized by HLA-DR7-restricted T cells, whereas p94-104 was recognized in the context of HLA-DR2, DRw11 (DR5), and -DR8 molecules. This degenerate class II MHC restriction appears to be due to shared Phe and Asp residues at positions 67 and 70, respectively, in the third variable domain of the HLA-DR beta chain. All three T cell epitopes induced Th2-like cytokine production profiles by the Der p I-specific T cell clones, which were characterized by the production of very high levels of IL-4 and IL-5, as compared with those secreted by tetanus toxin-specific T cell clones derived from the same patients, but no or low amounts of IL-2 and IFN-gamma. This Th2-like production profile was, however, not an intrinsic property of the Der p I-specific T cells, but was dependent upon their mode of activation. Stimulation with Con A also induced very low or no measurable levels of IL-2 and IFN-gamma, whereas activation with TPA and the calcium ionophore A23187 resulted in the production of high levels of IL-4, IL-5, IL-2, and IFN-gamma. These results indicate that Der p I-specific T cell clones are not defective in their capacity to produce high levels of Th1 cytokines.

Topics: Allergens; Amino Acid Sequence; Animals; Antigens, Dermatophagoides; CD4-Positive T-Lymphocytes; Clone Cells; Concanavalin A; Cytokines; DNA Mutational Analysis; Epitopes; Genes; Humans; Hypersensitivity; Interferon-gamma; Interleukin-2; Lymphocyte Activation; Mites; Molecular Sequence Data; Receptors, Antigen, T-Cell, alpha-beta; Recombinant Proteins; Structure-Activity Relationship; T-Lymphocytes, Helper-Inducer

In an allergic inflammation model of air pouch type in rats, histamine level in the pouch fluid and histidine decarboxylase activity of pouch wall tissues in the postanaphylaxis phase were increased. Although treatment with dexamethasone failed to inhibit histamine release from mast cells in the anaphylaxis phase, histamine production in the postanaphylaxis phase was inhibited dose dependently. Histamine production-increasing activity in the pouch fluid collected 8 h after the Ag challenge, which was estimated by an activity to stimulate histamine production by bone marrow cells, was decreased by the administration of dexamethasone at the time of the Ag challenge. The addition of steroidal antiinflammatory drugs, dexamethasone, prednisolone, or hydrocortisone, into the incubation medium inhibited the pouch fluid-induced histamine production by bone marrow cells. Hydrocortisone mesylate antagonized the inhibitory effect of dexamethasone on histamine production by bone marrow cells. However, hydrocortisone mesylate failed to recover the decrease in histamine production-increasing activity of the pouch fluid collected from dexamethasone-treated rats. In addition, the dialyzed sample of pouch fluid obtained from dexamethasone-treated nonsensitized rats did not reduce the stimulated histamine production by the pouch fluid sample obtained from the sensitized rats. However, increase in histamine production of bone marrow cells stimulated by the pouch fluid was not inhibited by cyclosporin A that inhibited histamine production induced by Con A. This observation indicates that the pouch fluid has no effect to induce production of the histamine production-increasing factor by bone marrow cells. Consequently, it is suggested that dexamethasone inhibits not only the production of histamine production-increasing factor but also the response of histamine-producing cells to this factor.

Topics: Animals; Bone Marrow Cells; Concanavalin A; Cyclosporins; Cytokines; Dexamethasone; Histamine Release; Histidine Decarboxylase; Hydrocortisone; Hypersensitivity; Inflammation; Mast Cells; Rats; Time Factors

The histamine release (HR) after challenge with anti-IgE, concanavalin A, N-formyl-met-leu-phe and the calcium ionophore A23187 from 97 cord blood samples was determined by a microfiber-based assay. Maximum HR with anti-IgE showed great inter-individual variation (median: 20.5; range: 1-104 ng/ml blood), but was not significantly different from the results obtained in identically treated blood samples from 50 adults (median: 23; range: 1-93 ng/ml blood). Both the maximum HR and the sensitivity to anti-IgE were dependent on total plasma IgE content. Blood samples with plasma IgE greater than or equal to 0.5 IU/ml (n = 15) had significantly higher maximum HR than those with plasma IgE less than 0.5 IU/ml (n = 82; median: 32 vs. 18 ng/ml blood; p less than 0.01). Passive sensitization with IgE-rich atopic plasma increased the maximum HR with anti-IgE only in samples with a plasma IgE content of less than 0.5 IU/ml, although sensitivity to anti-IgE was universally increased. Preincubation with pharmacologic agents modulating the IgE-mediated HR produced effects generally similar to previous findings in adult blood. However, the effects of inhibiting the cyclooxygenase pathway in cord blood differed from our observations in adult blood, and may represent a maturational phenomenon. The family history of allergy was obtained by a questionnaire, and clinical observations were gathered from patient records. None of these parameters were found to influence HR with any secretagogue. However, HR stimulated by the calcium ionophore A 23187 was found to be highly dependent on the storage time of the EDTA-anticoagulated blood samples, which should be carefully controlled.

Topics: Basophils; Blood Preservation; Calcimycin; Concanavalin A; Female; Fetal Blood; Fluorometry; Histamine Release; Humans; Hypersensitivity; Immunoglobulin E; Male; N-Formylmethionine Leucyl-Phenylalanine; Pregnancy; Surveys and Questionnaires

Topics: Concanavalin A; Humans; Hypersensitivity; In Vitro Techniques; Lymphocyte Activation; Lymphocytes; Plant Lectins; Pollen; Seasons; Substance P; Trees

The mesenteric and pulmonary mast cells of guinea pigs were obtained by enzymatic dispersion of the tissues with the enzyme collagenase. The guinea pig mast cells obtained by this method were morphologically intact, as judged by light microscopy. The mast cells from lung and mesentery of actively sensitized guinea pigs released histamine in a dose-dependent fashion after challenge with specific antigen. Both pulmonary and mesenteric mast cells of nonsensitized animals were unresponsive to the action of compound 48/80 and concanavalin A. Both populations of mast cells responded to polymyxin B, but the magnitude of histamine release was low. These cells responded strongly to the ionophore A23187; the mesenteric mast cells were markedly more reactive than pulmonary mast cells.

Topics: Animals; Antigens; Cells, Cultured; Concanavalin A; Dose-Response Relationship, Immunologic; Female; Guinea Pigs; Histamine Release; Hypersensitivity; Ionophores; Lung; Mast Cells; Mesentery; Microbial Collagenase; p-Methoxy-N-methylphenethylamine; Polymyxin B

Congenitally athymic nude (nu/nu) mice, immunologically reconstituted by thymus grafting before inoculation with infective larvae, and mice heterozygous for the nu gene (nu/+), mounted potent protective humoral and cellular immune responses to Brugia pahangi. Although responses were not identical, both groups of mice produced IgM, IgG and IgE antibodies specific for adult worm antigen (S-Ag) present in a crude aqueous extract, made immediate and delayed hypersensitivity footpad swelling responses when challenged with S-Ag and eliminated their infection in the early larval stages. Heterozygotes also exhibited a marked eosinophilia which peaked coincident with larval killing. In contrast, thymus grafting of patent nudes had no effect upon microfilaraemias or adult worm burdens and did not completely protect against a challenge larval inoculum although antibodies specific for S-Ag were produced. With the occasional exceptions of moderate immediate footpad swelling and very low titres of IgM specific for S-Ag, no specific immune responses to B. pahangi were found in ungrafted nude mice which allowed full development of adult worms and supported patent infections.

Topics: Animals; Antibody Formation; Brugia; Concanavalin A; Crosses, Genetic; Enzyme-Linked Immunosorbent Assay; Female; Filariasis; Heterozygote; Hypersensitivity; Immunoglobulin G; Immunoglobulin M; Leukocyte Count; Lymphocyte Activation; Lymphocytes; Male; Mice; Mice, Nude; Species Specificity

There has been unjustified neglect of dicotyledonous (dicot; 'weed') pollens in research directed at isolating pure allergens, since dicot pollens are widespread and frequently important in provoking immediate allergic reactions. Sera from patients who showed positive skin prick test reactions to plantain pollen generally also reacted in the radioallergosorbent test (RAST) with at least one other species of dicot pollen. Fractionation of plantain pollen extracts by ultrafiltration and molecular sieving and examination of the fractions by the RAST revealed a spread of allergenic activity. Using crossed immunoelectrophoresis, at least 16 different antigens were detected in plantain pollen and at least 6 of these antigens may be allergenic. Allergenic glycoproteins that react with concanavalin A were isolated and their complexity examined by electrophoresis and electro-focusing. IgE-binding components were found widely distributed in plantain plants and not confined to the pollen.

Topics: Allergens; Chromatography, Gel; Concanavalin A; Humans; Hypersensitivity; Immunoelectrophoresis, Two-Dimensional; Plant Extracts; Plant Lectins; Plantago; Plants, Medicinal; Poaceae; Pollen; Radioallergosorbent Test; Receptors, IgE; Receptors, Immunologic; Ultrafiltration

To detect a potential defect in immunoregulatory function in atopic subjects, we studied histamine-induced suppressor-T-cell activity and histamine Type 1 and Type 2 receptors on T cells. Peripheral-blood mononuclear cells from 16 atopic subjects generated less histamine-induced suppressor activity than did those from 20 nonatopic normal controls (P less than 0.005). The percentage of T lymphocytes bearing histamine Type 2 receptors was lower in the atopic group than in the control group (P less than 0.001), but the percentage of cells with Type 1 receptors was the same in both groups. In the atopic subjects, the functional suppressor-cell abnormality positively correlated with the decreased phenotypic expression of histamine Type 2 receptors. No abnormality in concanavalin A-induced suppressor activity was detected in these subjects. Nonatopic control subjects with systemic mastocytosis had normal functional and phenotypic data, suggesting that chronic activation of atopic T cells in vivo by circulating histamine does not explain the abnormal histamine-induced suppressor response.

Topics: Adolescent; Adult; Cells, Cultured; Concanavalin A; Female; Histamine; Humans; Hypersensitivity; Male; Middle Aged; Receptors, Histamine H1; Receptors, Histamine H2; T-Lymphocytes; T-Lymphocytes, Regulatory

Basophil-rich infiltrates in regional lymph nodes of guinea-pigs were demonstrated by electron microscopy after the intradermal injection of T cell mitogens (PHA and Con A). Basophils infiltrated the stroma of the lymph node via the postcapillary venules (PCV) and migrated to the paracortex. Prior to infiltration of the lymph nodes a cutaneous basophil hypersensitivity reaction was seen in the mitogen-injected skin. B cell mitogen (LPS) injection did not induce this response.

Topics: Animals; Basophils; Concanavalin A; Female; Guinea Pigs; Hypersensitivity; Lymph Nodes; Microscopy, Electron; Phytohemagglutinins; Skin; T-Lymphocytes

Topics: Animals; Ascitic Fluid; Chromatography, Affinity; Concanavalin A; Dose-Response Relationship, Immunologic; Humans; Hypersensitivity; Immunoglobulin E; Immunosuppression Therapy; Lymphocyte Culture Test, Mixed; Lymphocytes; Mice; Mice, Inbred A; Mice, Inbred BALB C; Mice, Inbred C57BL; Organic Chemicals; Species Specificity; X-Rays

Topics: Concanavalin A; Humans; Hypersensitivity; Immunoglobulin E; Immunoglobulin G; Lymphocyte Activation; T-Lymphocytes, Regulatory

Quantiative immunoelectrophoresis used for the analysis of a dialysed, centrifuged and freeze-dried extract from cow hair and dander revealed 17 antigens. Five of these were identified as serum proteins. Partial identity to antigens of serum and extract from hair and dander of goat, sheep, swine, horse, dog, cat and guinea pig, and to antigens of house dust was demonstrated. Sera from 36 patients with manifest allergy to cow hair and dander selected on the basis of case history, RAST, skin and provocation test, were examined in crossed radioimmunoelectrophoresis (CRIE); sera from five persons with high serum IgE, but without allergy to cow hair and dander, and sera from five normal individuals were controls. 31/36 of the sera contained IgE with specific affinity for two of the antigens of the extract. Further, two major and six minor allergens were identified. The control sera showed no specific IgE binding. A significant positive correlation was found between RAST and CRIE for the first group of patients. The approximate molecular weights of the four major allergens obtained by means of gel chromatography were: 2.4 x 10(4), 2 x 10(4), 2 x 10(5) dalton, respectively. Using Con-A and Con-A Sepharose in crossed immunoaffinoelectrophoresis, eight of the antigens were revealed to contain groups with affinity for Con-A.

Topics: Adult; Allergens; Animals; Autoradiography; Child; Chromatography, Gel; Concanavalin A; Electrophoresis, Agar Gel; Hair; Humans; Hypersensitivity; Immunoelectrophoresis; Immunoelectrophoresis, Two-Dimensional; Immunotherapy; Molecular Weight; Radioallergosorbent Test; Radioimmunosorbent Test; Skin Tests

Tridacnin, a lectin from the clam Tridacna maxima was found to precipitate with crude extracts from the house dust mites Dermatophagoides farinae and Dermatophagoides pteronyssinus. Using tridacnin in direct precipitation and affinity chromatography studies, a carbohydrate-rich preparation of high molecular weight was isolated from D. farinae extracts. The isolated preparation gave one precipitin line when used with tridacnin in gel diffusion and immunoelectrophoresis experiments but two bands were seen on polyacrylamide disc gels after electrophoresis at pH 8.9. Radioallergosorbent test (RAST) studies demonstrated that the isolated material reacted strongly with sera from human subjects allergic to house dust mites and accounted for a significant proportion of the IgE binding capacity of the crude D. farinae extracts. Only one out of fifteen mite-allergic subjects gave a positive response when prick tested with the isolated preparation at a concentration of 0.2 mg/ml. A possible explanation for the discrepancy observed between RAST and skin test results is discussed. Concanavalin A also precipitated with D. farinae extracts but the material isolated with this lectin did not react with tridacnin and reacted weakly in the RAST with sera from mite-allergic subjects. We suggest that the high molecular weight component(s) which react with tridacnin may be useful for immunotherapy of house dust mite allergy.

Topics: Allergens; Concanavalin A; Humans; Hypersensitivity; Immunotherapy; In Vitro Techniques; Lectins; Mites; Molecular Weight; Radioallergosorbent Test; Skin Tests

Systemic treatment with a heterologous anti-T cell serum of guinea pigs immunized with EA in IFA markedly suppressed CBH reactivity to specific antigen and T cell mitogens, as judged by gross reactivity, histology, and skin histamine. The antiserum produced a marked drop in circulating lymphocytes, mainly at the expense of T cells, as indicated by the ability of surviving lymphocytes to rosette with rabbit RBC. It was postulated that the suppression of CBH reactivity is due to the depletion of T cells, which would have released a factor chemotactic for basophils. The data therefore provide further evidence that cutaneous reactions rich in basophils are primarily dependent on a population of T cells.

Topics: Animals; Antilymphocyte Serum; Basophils; Concanavalin A; Female; Guinea Pigs; Histamine Release; Hypersensitivity; Immune Adherence Reaction; Lectins; Leukocyte Count; Lipopolysaccharides; Mitogens; Ovalbumin; Skin Tests; T-Lymphocytes

Topics: Allergens; Antibodies; Basophils; Concanavalin A; Histamine Release; Humans; Hypersensitivity; Immunoglobulin E; Lectins; Leukocytes; Plant Extracts; Plant Lectins; Pollen

Topics: Antigens; Cell Division; Concanavalin A; DNA; Humans; Hypersensitivity; Immunity, Cellular; Leukocytes; Liver Abscess, Amebic; Stimulation, Chemical; Thymidine

Topics: Animals; Basophils; Biopsy; Chemotaxis; Concanavalin A; Escherichia coli; Female; Guinea Pigs; Hypersensitivity; Immunity, Cellular; Lectins; Lipopolysaccharides; Mitogens; Polysaccharides, Bacterial; Skin; Skin Tests; T-Lymphocytes