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Results for “Immunity, Humoral”

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At least 415 records · Page 23Linked to original sources

PubMed2005

Effect of hepatitis C virus coinfection on humoral immune alterations in naïve HIV-infected adults on HAART: a three year follow-up study.

Whether HAART allows complete recovery of humoral immune function in HIV-infected individuals is still controversial. Our objective was to study the effect of HAART on both B cell repopulation and hypergammaglobulinemia in 72 naïve patients, including 35 HCV-coinfected individuals, during 156 weeks on HAART. The possible role of HCV coinfection on the recovery of the humoral immune system was also investigated. At baseline, HCV-coinfected patients had greater circulant IgG levels than HIV-only-infected patients, while B cell count and CD21(low) B cell subpopulation were similar in both groups. During HAART, HIV-only-infected patients reached normal B cell counts and circulant IgG levels, while HCV-coinfected individuals did not. CD21(low) B cell subpopulation significantly decreased in both groups of patients at week 48 after the initiation of HAART compared to baseline. Thus, B cells remained continuously stimulated in HCV-coinfected patients and this stimulation seemed to be through a CD21-independent pathway.

Adult↗

PubMed1989

Correlation of humoral immune response with clinical presentation, pulmonary lesions and mortality patterns of goats experimentally infected with peste des petits ruminants virus.

The patterns of humoral immune response, measured by enzyme-linked immunosorbent assay and the development of clinical signs, pulmonary lesions and mortality patterns were studied in goats experimentally infected with peste des petits ruminants virus (PPRV) or Kata virus. It was possible to classify the animals into high and low responders according to the pattern of humoral immune response. The high responders had a prolonged, chronic infection characterized by a giant cell pneumonia which was sometimes complicated by bronchopneumonia. Such animals survived beyond 1 month. The low immune responders had a subacute or acute clinical presentation. In the former case, the animals developed an uncomplicated giant cell pneumonia and died within 1 month of infection. Those with the acute symptoms developed pulmonary congestion and oedema and succumbed to the infection in 1 week. The clinical and pathological response of goats to PPRV infection, and ultimately the outcome of the infection correlated well with the ability of the goats to mount specific antibodies to PPRV.

Animals↗

PubMed2004

Assessment of humoral immunity to poliomyelitis, tetanus, hepatitis B, measles, rubella, and mumps in children after chemotherapy.

BACKGROUND: To evaluate the effect of chemotherapy on humoral immunity to vaccine-preventable disease, the authors investigated the persistence of protective antibody titers in a group of patients who were alive and well after they were treated for pediatric malignancies. METHODS: Serum antibody levels were evaluated for polio, tetanus, hepatitis B, rubella, mumps, and measles in 192 children. The terms lack of immunity and loss of immunity, respectively, were used to describe the absence of immunity in patients who were tested only after chemotherapy and in patients who were tested both before and after chemotherapy and determined to have immunity before chemotherapy. RESULTS: Overall, the absence of a protective serum antibody titer for hepatitis B, measles, mumps, rubella, tetanus, and polio was detected in 46%, 25%, 26%, 24%, 14%, and 7% of patients, respectively. On univariate analysis, loss of antibodies against rubella, mumps, and tetanus was associated significantly with younger age (P < 0.001, P = 0.02, and P = 0.001, respectively), and loss of antibodies against measles was significantly associated with younger age and female gender (P = 0.0003 and P = 0.008, respectively). The administration of 59 booster vaccinations to 51 patients who had lost > or = 1 protective antibody titer resulted in an overall response rate of 93%. CONCLUSIONS: Chemotherapy induced different rates of loss of protective antibody titers depending on the type of vaccination administered. This finding may be responsible for the failure of vaccination programs for patients who have undergone chemotherapy. The administration of a booster dose after the completion of chemotherapy is a simple and cost-effective way to restore humoral immunity against most vaccine-preventable diseases.

Antibody Formation↗

PubMed2004

Potential role of humoral immunity in cardiac dysfunction of patients suffering from dilated cardiomyopathy.

OBJECTIVES: This research was conducted to evaluate the role played by the humoral immune system in cardiac dysfunction among dilated cardiomyopathy (DCM) patients, as enabled by immunoadsorption therapy (IA) that effectively removes functionally active cardiac autoantibodies from plasma. BACKGROUND: Various circulating autoantibodies have been detected among patients suffering from DCM. METHODS: Before IA, antibodies were purified from plasma of 45 DCM patients (left ventricular ejection fraction [LVEF] <30%). We analyzed the functional effects of antibodies (300 mg/l) on calcium transients and on systolic cell shortening in adult rat cardiomyocytes. After this in vitro analysis, IA was performed in four courses at one-month intervals until month 3. RESULTS: Antibodies from 29 patients induced a reduction (>10%) in calcium transients (mean reduction: -16.5 +/- 1.9%) and a simultaneous reduction (>10%) of cell shortening (mean reduction: -21.2 +/- 1.8%) on cardiomyocytes (p < 0.001) (cardiodepressant group). Antibodies from 16 patients did not significantly influence calcium transients and cell shortening (<10%) (non-cardiodepressant group). During the first IA course, the cardiodepressant group demonstrated an acute increase in cardiac index (CI) from 2.2 +/- 0.1 l/min/m(2) to 2.9 +/- 0.1 l/min/m(2) (p < 0.001). In the non-cardiodepressant group, hemodynamics did not significantly change throughout three months. After three months before the final IA course (prolonged effects), the CI was 2.1 +/- 0.1 l/min/m(2) in the non-cardiodepressant group and 2.9 +/- 0.1 l/min/m(2) in the cardiodepressant group (p < 0.001). After three months LVEF increased only in the cardiodepressant group: from 20.8 +/- 1% to 30.5 +/- 1% (p < 0.01). CONCLUSIONS: In the majority of DCM patients, disturbances of humoral immunity with production of cardiodepressant antibodies may play a functional role in cardiac dysfunction. Evidence of cardiodepressant antibodies predicts hemodynamic benefits during IA.

Animals↗

PubMed1994

[Suppressive effects of adenosine on nonspecific and humoral immunities in mice].

Adenosine (Ade) 1.3, 13, 130 mg.kg-1 ip inhibited the ability of peripheral leukocytes and peritoneal macrophages in phagocytosing the Staphylococcus albus with [3H]TdR incorporation in mice, declined the hemolytic ability of plaque-forming cells and the production of antibody in mice immunized by sheep erythrocytes. Ade 13, 130 mg.kg-1 ip decreased the mouse serum muramidase (lysozyme) concentration. Dipyridamole (Dip) 10 mg.kg-1 ip attenuated the effects of Ade 130 mg.kg-1 on humoral immunity reaction, but the nonspecific immunity was not attenuated. These results showed that the uptake of Ade may play an important role in the effects of Ade on humoral immunity reaction. Aminophylline (Ami) 100 mg.kg-1 ip attenuated the effects of Ade 130 mg.kg-1 on hemolytic ability of plaque-forming cells and the ability of peripheral leukocytes in phagocytosing Staphylococcus albus. These results suggested that the effects of Ade on murine humoral and nonspecific immunity reaction were mediated by Ade A2 receptor (A2DR).

Adenosine↗

PubMedDate not supplied

[Seasonal dynamics of the indices of humoral immunity in children aged 3 months to 1 year in relation to nutrition in an arid zone].

The paper reports seasonal data on humoral immunity of 245 Turkmen and 240 European infants aged 3-12 months. Allowances were made for climatic conditions of the arid zone and essential feeding. In summer there were reduced levels of IgM, IgG in the serum and insufficient supply with thiamine and ascorbic acid. IgA serum level was the lowest in spring. IgA strongly correlated (r = 0.7-0.8) with thiamine and ascorbic acid intake in spring, IgM and IgG with retinol and thiamine in summer. The above changes in humoral immunity in summer are associated with growing incidence of intestinal diseases and lower body mass in the infants in the condition of arid zone.

Asian People↗

PubMed1985

Humoral immunity in normal and complicated pregnancy.

To evaluate the role of some immunological phenomena involved in the pathogenesis of preeclamptic toxaemia, we studied the humoral immune reactivity in patients with preeclamptic toxaemia during the third trimester of pregnancy, and three days and six weeks after delivery. The results were compared with those of patients with intrauterine growth retardation and with uneventful pregnancy. During the third trimester, patients with complicated preeclamptic toxaemia had significantly lower IgG, CH50, C4 and C3 levels than normal pregnants. Post-partum levels of IgM were significantly higher than in all other groups of patients. Circulating immune complexes were not detectable by a C1q binding assay in patients and controls. However, with a conglutinin binding assay and a granulocyte phagocytosis test complexes were demonstrable in patients with complicated preeclampsia (incidence 44% and 33%, respectively). In addition, 66% of these patients showed deposits of immunoglobulins and complement components in superficial blood vessels of the skin biopsy, suggestive of the presence of tissue deposits of immune complexes. This was found in about 30% of the other patient groups and in none of control pregnants. Allo-antibodies to lymphocytes were present in 63% of complicated preeclamptic toxaemia patients and 22% of normal pregnants. Our data show several changes in humoral immune reactivity in preeclamptic toxaemia which may contribute to the pathogenesis of this disorder.

Adult↗

PubMed1996

Suppression of cell-mediated and humoral immune responses by an interleukin-2-immunoglobulin fusion protein in mice.

Interleukin-2 (IL-2) plays a pivotal role in the cellular and humoral immune responses directed against foreign antigens. We characterized the in vitro and in vivo properties of a chimeric protein consisting of mouse IL-2 fused to the mouse IgG2b Fc domains. This fusion protein binds to IL-2 and Fc receptors and supports IL-2-dependent cell proliferation but does not mediate lysis of IL-2 receptor-positive cells in the presence of murine complement in vitro. However, in vivo the IL2-IgG2b fusion protein suppresses both cellular and humoral immune responses after immunization with sheep erythrocytes. Surprisingly, delayed hypersensitivity is inhibited despite a dramatic increase of splenic CD3+ and NK1.1+ lymphocytes, indicating that altered homing of IL2-IgG2b-activated lymphocytes rather than cytolysis prevents these cells from accumulating in areas of inflammation. Although in vitro the IL2-IgG2b fusion protein does not alter proliferation of B cells in response to mitogenic stimulation, IgM production in response to sheep erythrocytes is profoundly inhibited in mice treated with the IL2-IgG2b fusion protein. Since no side effects are observed, the IL2-IgG2b fusion protein may expand the therapeutic repertoire of reagents used for the treatment of allograft rejection and autoimmune diseases.

Animals↗

PubMed1997

Effect of hemoglobin status on humoral immune response of weanling pigs differing in coping styles.

The effects of hemoglobin (Hb) status and coping style of pigs on performance and humoral immune response were studied. Twenty-four, 4-wk-old crossbred barrows were assigned to groups of three pigs based on weight and litter origin. Groups were allotted according to a 2 x 2 factorial treatment arrangement: two blood Hb concentration classes (low vs high) and two immunization procedures (control vs immunized). Immunized pigs received an antigen cocktail containing keyhole limpet hemocyanin (KLH), ovalbumin (OA), and tetanus toxoid (TT) at weaning. Additionally, pigs were stratified according to behavioral coping style in response to exposure to a stressor. During 41 d after weaning (approximate time of immunization), blood Hb concentration, ADG, and ADFI were measured weekly and serum antibody titers to KLH, OA, and TT twice weekly. Average Hb concentration differed between low and high Hb pigs (P < .001; 10.0 vs 12.0 g/dL), but this difference declined with time after weaning. Neither immunization procedure nor coping style affected Hb concentrations. In addition, ADG and ADFI were unaffected by any of the treatments. However, ADG was slightly greater in high Hb status pigs (586 vs 633 g/d) and was paralleled by a slightly greater ADFI in high Hb status pigs (812 vs 899 g/d). Antibody responses were negatively or not related to Hb status at weaning. Antibody responses (depending on isotype and antigen) were or tended to be lower in pigs with high blood Hb concentrations. Behavioral coping style strongly affected humoral immune responsiveness; enhanced or accelerated antibody responses were found in pigs that had a passive coping style.

Adaptation, Psychological↗

PubMed2001

[Selected parameters of the cellular and humoral immunity in atopic dermatitis. Relationship to the severity of the disease].

UNLABELLED: Despite the great progress, our understanding of the pathogenesis of atopic dermatitis (AD) is still incomplete. In particular, the clinical importance of various changes of the immune system parameters is unclear. Accordingly we have undertaken the study to compare selected parameters of cellular and humoral immunity between AD subjects (n = 26) and healthy controls (n = 10). These parameters included immunoglobulin levels (IgE in particular), neutrophil respiratory, oxygen burst, peripheral blood lymphocyte phenotype and response to mitogens. We also analysed the relationship between these parameters and clinical severity of skin lesions. RESULTS: Mean total immunoglobulin E levels were very significantly increased in the AD group (1563 +/- 459 vs 35.5 +/- 12.1 IU/ml; p = 0.001). Simultaneously total serum IgE levels varied extensively between individual subjects with AD and were significantly correlated to clinical severity of the disease (Rs = 0.44; p = 0.02). Atopic dermatitis was also associated with the increase in the number of CD4+ and simultaneous decrease in the CD8+ lymphocytes causing statistically significant difference in CD4:CD8 ratio compared to the control group. We also observed changes of proliferation indices to phytohaemagglutinin (decrease) and increase of responses to anti CD3 mAb (OKT-3) and staphylococcal enterotoxin B. None of these immune parameters however, appeared to be statistically correlated to clinical status. CONCLUSIONS: We find that atopic dermatitis is associated with significant changes of several important indices of cellular and humoral immunity including increased IgE levels and altered peripheral lymphocyte proliferation capacity and phenotype. Change of total IgE levels appears to be the most important from clinical point of view.

Antigens, CD↗

PubMed1992

[Pasting acupoints with Chinese herbs applying in infant acute bronchitis and effect on humoral immune substances].

This report described the clinical observation of pasting acupuncture with Chinese herbs applying in 72 infant acute bronchitis cases and regarding to the humoral immune substances such as IgA, IgM, IgG, Complement C3 The result shows high cure and improve rate. The curative effect of infantile group is higher than that of childhood one (x2 = 6.501, 0.05 > p > 0.025). All indexes of humoral immune substances, especially IgA, were increased after treatment (t = 10.50, p < 0.01).

Acupuncture Points↗

PubMed1989

Interference with the humoral immune response in diverse genetic lines of chickens. II. The effect of colloidal carbon.

Two experiments were conducted to study the difference in humoral immune responses between lines of chickens selected for high (H) or low (L) antibody production to sheep red blood cells (SRBC). Prior to i.v. immunization with SRBC or Brucella abortus (BA), chicks of both lines were injected with either 2, 3 or 4 ml carbon suspension (59 mg carbon/ml) per kg body weight; controls were not injected. In both the H and L line, a higher dose of carbon showed a more progressive depression of the total antibody titer to SRBC during the initial stage of the primary response. The 2ME-resistant antibody titers to SRBC showed the same tendency during the latter phase of the primary response. However, chicks treated with 3 ml carbon had lower 2ME-resistant antibody titers than any other group. Following i.m. reimmunization with SRBC, the previous treatment with carbon doses enhanced total antibody titers throughout the secondary response, when compared to the controls. The 3 ml carbon-treated chicks had the highest total anti-SRBC titers in the secondary response. The secondary 2ME-resistant anti-SRBC titers were not affected by the carbon doses. Carbon treatment did not affect the antibody titers to BA. No differences between the H and L line were found in the effects of carbon on the humoral immune responses to SRBC or BA.

Animals↗

PubMed2002

Rituximab treatment results in impaired secondary humoral immune responsiveness.

In lymphoma patients, treatment with chimeric CD20 monoclonal antibodies (rituximab) results in a depletion of normal and malignant B cells, persisting for 6 to 9 months. This B-cell depletion leads neither to a decrease in immunoglobulin levels nor an increase in the number of infectious complications. However, the effect of rituximab treatment on the immune responsiveness is unknown. In 11 patients with relapsed, low-grade lymphoma, we investigated the effect of rituximab treatment on the humoral immune response to 2 primary antigens and 2 recall antigens. After rituximab treatment, the humoral immune response to the recall antigens was significantly decreased when compared with the response before treatment. Already before rituximab treatment, none of these patients was able to mount a response to the primary antigens. These findings are relevant regarding the feasibility of rituximab in maintenance treatment and may also offer a rationale for the treatment of antibody-mediated autoimmune diseases with rituximab.

Adult↗

PubMedDate not supplied

Delta 9-tetrahydrocannabinol selectively inhibits T-cell dependent humoral immune responses through direct inhibition of accessory T-cell function.

The major psychoactive and immunosuppressive component of marihuana, delta 9-tetrahydrocannabinol (delta 9-THC), was investigated for its effects on primary humoral immune responses in the B6C3F1 mouse strain. Oral administration of 50-200 mg/kg delta 9-THC produced a selective and dose related inhibition of primary humoral immune responses to the T-cell dependent antigen, sRBC, as measured by the antibody forming cell (AFC) response with no inhibitory effect on humoral responses to the T-cell independent antigen, DNP-Ficoll. A similar profile of immune inhibition was observed following in vitro direct addition of delta 9-THC to naive spleen cell cultures sensitized with defined antigens. delta 9-THC produced a marked and dose related inhibition of the in vitro sRBC AFC response while having no inhibitory effects on T-cell independent responses to either DNP-Ficoll or the polyclonal B-cell activator, lipopolysaccharide. This selective inhibition of the sRBC response was not due to a shift in the peak day of response or a direct cytotoxic effect on spleen cells. In vivo kinetic studies demonstrated that inhibition by delta 9-THC of the sRBC response was most pronounced when drug administration occurred at times surrounding antigen sensitization. To further evaluate the direct effect of delta 9-THC on T-cell function, T-cell proliferative responses to stimulation by anti-CD3 monoclonal antibodies were measured. delta 9-THC was found to produce a marked and dose related inhibition of anti-CD3 mAb-induced T-cell proliferation which was cell density dependent.(ABSTRACT TRUNCATED AT 250 WORDS)

Administration, Oral↗

PubMed2021

OCT2 pre-positioning facilitates cell fate transition and chromatin architecture changes in humoral immunity.

During the germinal center (GC) reaction, B cells undergo profound transcriptional, epigenetic and genomic architectural changes. How such changes are established remains unknown. Mapping chromatin accessibility during the humoral immune response, we show that OCT2 was the dominant transcription factor linked to differential accessibility of GC regulatory elements. Silent chromatin regions destined to become GC-specific super-enhancers (SEs) contained pre-positioned OCT2-binding sites in naive B cells (NBs). These preloaded SE 'seeds' featured spatial clustering of regulatory elements enriched in OCT2 DNA-binding motifs that became heavily loaded with OCT2 and its GC-specific coactivator OCAB in GC B cells (GCBs). SEs with high abundance of pre-positioned OCT2 binding preferentially formed long-range chromatin contacts in GCs, to support expression of GC-specifying factors. Gain in accessibility and architectural interactivity of these regions were dependent on recruitment of OCAB. Pre-positioning key regulators at SEs may represent a broadly used strategy for facilitating rapid cell fate transitions.

Animals↗

PubMed1982

Corticosteroid action on lymphocyte subpopulations and humoral immune response of axolotl (urodele amphibian).

The effect of in vivo hydrocortisone (HC) treatment on thymocytes, splenic and blood lymphocytes and on allogeneic and humoral immune responses were investigated in the axolotl (urodele amphibian). HC induces a profound lymphocytopenia in the thymus (83% HC sensitive) and the spleen (50% HC sensitive) but not in the blood. The density gradient analysis of HC-treated axolotls showed that thymic cell populations of light density were more sensitive than populations of high density. The timing of HC administration in relation to the antigenic challenge is crucial for the humoral immune response. If HC injection is given 8 days before or on the same day as injection of horse red blood cells (HRBC), the antibody response is markedly enhanced. If HC injection occurs 8 days after injection of HRBC or on the day of the maximum anti-HRBC response, the antibody response is unchanged. The allograft immune response is not affected by HC treatment. The parallelism of the enhanced anti-HRBC response after HC treatment, with the same enhanced response obtained in adult thymectomized (ATx) animals, as well as in ATx-HC-treated axolotl, may be explained by the presence of a corticosensitive, T-like population of suppressor cells in axolotl.

Ambystoma↗

PubMed1983

The effect of environmental temperature on immune response and metabolism of the young chicken. 5. Effect of low environmental temperature on the humoral immune response to sheep red blood cells in relation to energy metabolism.

The effect of low environmental temperature on the humoral immune response to sheep red blood cells (SRBC) was investigated in relation to energy metabolism. Two experiments were done with 3- to 6-week-old pullets using two climate respiration chambers. During both experiments a standard temperature regimen of constant 25 C was maintained in one chamber, whereas the temperature in the other chamber was constant 10 C (Experiment 1) or fluctuated between 5 to 15 C (Experiment 2). The relative humidity was held at 70% at all temperature regimens. Feed allowance was such that growth rates at the two temperatures within experiment were expected to be similar. Indeed, growth rate and body weight were not significantly (P greater than .05) influenced by temperature in Experiment 1. Feed consumption at 10 C was 32.7% above that at 25 C. At 5 to 15 C feed consumption was 34.1% higher than at 25 C, whereas growth rate was reduced (P less than .05) by 8%. At 0 and 10 days after injection, differences in hemagglutinin anti-SRBC antibody titers (log2) between temperatures within each experiment were not significant. The 2-mercaptoethanol resistant (2-MEr) antibody titers 5 days after injection were increased by 26% (P less than .05) at 10 C compared to 25 C. The fluctuating low temperature reduced 2-MER antibody titers 5 days after injection by 19% (P less than .05). Differences in total antibody titers 5 days after injection between temperatures were not significant, but they tended to be reduced by low temperatures. No significant thermal effects on plaque forming cell counts and relative weights (percent of body weight) of spleen and bursa of Fabricius were found. Fat gain during the period between day of injection (Day 0) and peak antibody titers (Day 5) was significantly increased at the low temperatures. Thermal effects on protein gain were not significant, but more protein was deposited at 25 C than at the other temperature regimens during this period after injection.

Animals↗

PubMed1992

Appearance of T lymphocyte-derived proteins specific for the immunizing antigen in serum during a humoral immune response.

Some T lymphocytes produce extracellular proteins that bind nominal antigen specifically (TABM), and these proteins exhibit potent immunoregulatory activity. We have utilized an ELISA for Ag binding by Ag-specific TABM to detect and quantitate the appearance of Ag-specific TABM in murine serum during a humoral Ir to protein Ag. The TABM response was specific for the inducing Ag, stronger and more rapid during a secondary response, and temporally distinct from the appearance of Ig. The non-Ig serum TABM were bound by mAb specific for TCR-alpha chains and isolated by affinity for Ag were Mr 110,000 polypeptides. The TABM response did not occur in scid/scid mice unless the mice were reconstituted with thymocytes and thymocyte-reconstituted scid/scid mice produced TABM, but did not produce Ig. The results suggest that soluble TABM are an Ag-specific humoral manifestation of the Ir of some T lymphocytes.

Animals↗