Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “ANTIBODY FORMATION”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 253 records · Page 14Linked to original sources

Antibody formation and insulin requirements in diabetic children during treatment with purified commercial pork insulins.

40 diabetic children (20 female, 20 male, mean age 8.5 ys, ranging from 0.8 to 14.3 ys), were treated with either of two purified porcine insulin preparations, Komb-Insulin CS (Hoechst) "CS": n = 21, and Semilente MC (Novo) "MC": n = 19, the latter being further purified by ion exchange chromatography. Circulating IgG-antibodies formed in 39 out of 40 subjects during the observation period of more than 2 years. Insulin binding-capacities below 2 mU/ml (mean value after 12 months: 0.45 mU/ml) were found following MC and considerably higher concentrations (mean value after 12 months: 5.16 mU/ml) following CS administration. However, only 52% of the CS-group (n = 11) showed high individual responses (subgroup II), many of which exceeded 5 mU/ml, while the other half (subgroup I) exhibited values as low as those in the MC-subjects. The ratio of girls to boys was high (8 vs 3) in subgroup II, and low (2 vs 8) in subgroup I. Despite great differences in antibody formation, no differences in insulin requirements were noted between the MC- and the CS-groups. Within the CS-group, however, some positive relationship between these parameters was found 6 months and 12 months after the start of therapy, but this did not necessarily apply to individual subjects. Short-term (metabolic control) and long-term effects of therapy (growth) were not different in the MC- and CS-subjects. From these results it may be concluded that antibody formation does not affect insulin requirements or metabolic control during relatively short-term treatment. Provided that antibodies have no direct relation to future vascular changes, both insulin preparations used in this study are equally well-situated for long-term treatment in children and adolescents.

Adolescent↗

Comparison between multilamellar and unilamellar liposomes in enhancing antibody formation.

The effectiveness of two liposomal preparations, multilamellar vesicles (MLV) and unilamellar vesicles (ULV), in enhancing specific antibody formation was compared in this study. The MLV and ULV, prepared in the presence of bovine serum albumin (BSA), were composed of dimyristoyl-lecithin, cholesterol and dicetyl phosphate in a molar ratio of 7:2:1. Excess free BSA was separated from liposome-associated BSA by Blue Sepharose CL-6B column chromatography. The presence of appropriate lamellar structures for each liposome preparation was demonstrated by electron microscopy. The simultaneous injection of control mice with free BSA and 'empty' MLV or ULV failed to elicit a BSA-specific plaque-forming cell (PFC) response. In contrast, animals injected with liposome-associated BSA (MLV-BSA or ULV-BSA) generated a vigorous PFC response; the magnitude of the response induced by BSA entrapped in unilamellar vesicles was significantly higher than that in multilamellar vesicles. These results suggest that the lamellar arrangement of liposomal vesicles may play a role in affecting the magnitude of the potentiated antibody response.

Adjuvants, Immunologic↗

[The effect of high-dosage prednisolone administration on antibody formation and graft survival time following allogenic rat kidney transplantation].

The dose and time dependence of the immunosuppressive effect of prednisolone on renal allograft survival and antibody formation was studied in inbred rats. A single injection of 50 - 300 mg prednisolone/kg body wt. on the day of transplantation resulted in a dose-dependent prolongation of mean graft survival to 12.8 days as compared to 7.8 days for untreated controls. The daily postoperative administration of 10 and 30 mg prednisolone/kg prolonged the mean survival time to a lesser extent. A single bolus injection of 300 mg prednisolone/kg at different times after transplantatin resulted in a significant prolongation of graft survival and suppression of cytotoxic antibody only when given no later than 2 days postoperatively or following antigen injection.

Animals↗

Prefertile vas lesion as a cause of sperm antibody formation: an experimental and clinical study.

It is well known that vasectomy in adult men can induce formation of sperm antibody (SPA) and that the presence of such antibodies can be correlated to decreased fertility. Operations close to the vas, e.g. herniorrhaphy, are common in childhood, implying a potential risk of a vas lesion. However, very little is known about the consequences of a vas lesion at prefertile age with respect to SPA formation in adulthood. The aim of this study was to determine whether a vas lesion at prefertile age can induce SPA formation after puberty; if so, is it possible to prevent the occurrence of such antibodies by microsurgical reconstruction of the vas lumen before puberty? Prefertile rats (aged 3-6 weeks) were subjected to uni- and bilateral vasectomy, uni- and bilateral crush injury to the vas and bilateral injury to the ductal artery. SPA could be demonstrated in all groups of animals at the age of 18-20 weeks by means of indirect immunofluorescence technique. Prefertile uni- and bilateral vasectomy caused SPA formation to the same extent as did adult bilateral vasectomy (90% of the animals SPA-positive), whereas the prefertile vas appeared more sensitive to crush injury than the adult vas (70% and 11% SPA-positive, respectively). In rats subjected to vasectomy at the age of 3-4 weeks, it was possible to prevent SPA formation in adulthood by vas reconstruction before puberty. It was further shown that the vas repair did not have to be performed immediately after injury but could be delayed several weeks postvasectomy provided it was still performed before puberty. By using a tissue glueing agent (fibrin glue) it was found possible to improve the anastomosis healing in vasovasostomies. This was probably due to the fact that the fibrin glue minimises sperm leakage at the site of anastomosis in animals with an ongoing sperm flow through the vas at the time of vasovasostomy procedure. With this vasovasostomy technique, it was also possible to delay the vas reconstruction after prefertile vasectomy until puberty, still preventing the formation of SPA. The clinical implications of these experimental findings were underlined by the findings in a review of 31 postpubertal boys (mean age 17 years) operated upon for inguinal hernia in childhood. In this group, there was 100% accordance between the occurrence of SPA in the blood and vas obstruction. The findings in this clinical study further indicated that there may be a significant risk of acquiring an accidental, unknown vas lesion during herniorrhaphy in childhood.(ABSTRACT TRUNCATED AT 400 WORDS)

Adolescent↗

Effect of the chemical structure of N-(2-hydroxypropyl)methacrylamide copolymers on their ability to induce antibody formation in inbred strains of mice.

The homopolymer of N-(2-hydroxypropyl)methacrylamide (HPMA) and copolymers of HPMA differing in oligopeptide side chains (-Gly-Gly-OH; -Acap-Phe-OH; -Acap-Leu-HMDA and -Gly-Phe-Tyr-OH) or in their content (1%, 3.5% and 8.4% mole of -Gly-Gly-OH side chains) were investigated with respect to their ability to induce antibody formation and mitogenic reaction in inbred strains of mice. The dependence on the antigen dose, on composition of the side chain and on the genetic background of the immunized organism was defined. It was demonstrated that the specificity of the antibody formed is predominantly directed against oligopeptide side chains, though some part of the antibody is also produced against hydroxypropyl chains. Neither the homopolymer nor the copolymers behave in the tissue culture as mitogens.

Acrylamides↗

Detection of antibody formation in mice, rats and rabbits immunized with different Pneumocystis carinii antigens.

Antibody formation to P. carinii of human origin was determined by an indirect immunofluorescence antibody assay (IFA) after immunization of mice, rats and rabbits with pronase-treated whole cysts and soluble antigen in order to obtain more detailed data about the production of polyclonal antibodies. Antibody titre profiles over defined periods have shown that noticeable differences between the immunoreactions to whole cysts and soluble antigen occur. The soluble antigen produced an earlier and stronger titre rise (peak titres of up to 1:2560 2 to 4 weeks after immunization). In contrast to this, whole cysts produced equally high, although retarded, antibody titre peaks only in normal mice and rats and when the dose had been doubled. Nu/nu mice failed to demonstrate any reaction to these P. carinii immunogens. Cross-reactivity of the antibodies with P. carinii antigen from rat lungs was demonstrated. Possible reasons for different immunoreactions to these antigens, the importance of proteolytic digestion for the results obtained and the potential applicability of these polyclonal antibodies to a histochemical demonstration of the parasite are discussed.

Animals↗

[Proliferation of type II collagen specific T cell response and antibody formation in rheumatoid arthritis and their relations to HLA-DR4].

OBJECTIVE: To investigate the proliferation of type II collagen specific T cell response and antibody formation in rheumatoid arthritis (RA) and their relations to HLA-DR4 subtype. METHODS: Peripheral blood mononuclear cells and serum were obtained from 62 RA patients, 14 males and 48 females, aged 43 +/- 29. CII263-272 decapeptide and the peripheral blood mononuclear cells (PBMCs) from 62 RA patients were co-incubated for 5 approximately 7 days. MTT method was used to examine the T cell proliferation. The serum antibodies specific to CII 263-272 were examined by ELISA. HLA-DR typing was detected in 40 patients by SSP-PCR. RESULTS: Positive T cell response challenged by CII 263-272 decapeptide was observed in 38 (61.3%) RA patients. The positive rate of CII 263-272 antibody was 66.7% in the T cell response positive group, significantly higher than that of the T cell response negative group (34.6%, P < 0.05). The T cell response rate of the CII 263-272 antibody positive group was 69.7%, significant higher than that of the negative group (42.1%, P < 0.05). In all patients, the stimulation index (SI) of T cell proliferation to CII263-272 peptide was positively correlated with the level of antibody (r = 0.68, P < 0.01). HLA-DR4 allele was detected in 16 out of the 40 patients. Positive T cell response and presence of antibody to CII 263-272 were not associated with HLA-DR4 phenotype. CONCLUSION: The formation of CII antibody may be related to B cell activation mediated by CII specific T cell.

Adolescent↗

Lack of antibody formation during long-term subcutaneous treatment with the somatostatin analogue octreotide in acromegaly.

Serum samples from 13 patients with active acromegaly on long-term sc treatment with octreotide (SMS 201-995, 1-36 months, mean daily dose 285 micrograms) were taken 12 h after the injection of their regular evening doses. Octreotide assay was performed using 125I-Tyr-SMS and a polyclonal rabbit anti-serum. For assessment of antibody formation both serum coated charcoal adsorption (adsorption of free octreotide) and polyethylene glycol precipitation (precipitation of IgG complexes) were used. The mean binding percentage in the patients proved to be similar to that of 5 healthy volunteers (p greater than 0.10). No specific binding was detected, whatever method used. No correlation was found between the binding percentages and octreotide serum levels, duration of octreotide treatment or daily octreotide dose (p greater than 0.10). These results strongly suggest that clinically relevant endogenous antibody formation is not a frequent event during long-term sc treatment of acromegalic patients with octreotide.

Acromegaly↗

Modulation by malaria infection of the induction of T lymphocyte-dependent delayed-type hypersensitivity and antibody formation to sheep erythrocytes in mice.

A profound alteration of the inductive phase of delayed-type hypersensitivity and antibody formation to SRBC was found in malaria infected mice when sensitization with this antigen was performed intravenously at a critical time of the disease, but not after subcutaneous immunization, suggesting a major role for the spleen in the mechanism of immunodepression.

Animals↗

Stimulation of cAMP levels and modulation of antibody formation in mice immunized with cholera toxin.

Injection of mice with 1.0 mu g of a purified exotoxin derived from Vitro cholerae together with a challenge injection of sheep erythrocytes (SRBC)P OR E. coli LPS markedly influenced the immune response to these antigens. Simultaneous injection of the toxin with antigen resulted in a delayed appearance of antibody-forming cells during the first few days after immunization, followed by a marked enhancement of the peak numbers of antibody-forming cells. In the case of the immune response to SRBC, both 19S and 7S plaque-forming cells (PFC) were enhanced on the peak day of response after simulataneous immunization of toxin-injected mice. The secondary immune response to SRBC was also similarly affected when cholera toxin was given along with a second injection of erythrocytes: i.e. a delay in appearance of the first antibody-forming cells followed by a marked enhancement of the peak 19S and 7S PFC response. Injection of cholera toxin 103 days prior to SRBC or LPS was immunosuppressive. The effect of cholera toxin on the level of splenic cyclic AMP appeared related to the effects on antibody formation.

Animals↗

The nature of the immunologic inadequacy of neonatal rabbits. II. Antibody formation by neonatal splenic cells transferred to adult recipients.

It has been shown that cells from neonatal rabbits are capable of producing considerable amounts of antibody after exposure to antigen in vitro and transfer to x-radiated adult recipients. This suggests that the immunological inadequacy of these neonates is not dependent primarily upon the lack of cells capable of antibody formation. Both in vitro sensitized neonatal lymphoid cells and in vivo sensitized adult lymphoid cells made much more antibody after transfer to x-rayed adult recipients than to neonatal recipients. Possible reasons for and significance of these observations are pointed out in the discussion.

Animals↗

[Effect of stimulating antibody formation under the influence of bone marrow cells in vivo].

Injection of intact bone marrow cells to mice at the peak of the secondary immune response results in a 2.4-fold increase of the number of antibody-forming cells in the regional lymph node. Preliminary injection of bone marrow cells to donors of the immune lymph node cells decreases the stimulation effect of antibody formation when the lymph node cells are subsequently cultivated with the intact bone marrow cells. The data obtained demonstrate the cell interaction at the level of mature antibody producers in vivo.

Animals↗