scholarly journals THE RELATION BETWEEN ANTIANAPHYLAXIS AND ANTIBODY BALANCE

1936 ◽  
Vol 64 (4) ◽  
pp. 657-672 ◽  
Author(s):  
Marion C. Morris
Keyword(s):  
Guinea Pigs ◽  
Horse Serum ◽  
Type Ii ◽  
Partial Saturation ◽  
Type B ◽  
True Nature ◽  
Humoral Antibodies ◽  
Antigen Antibody ◽  
Circulating Antibody

It has been shown that antianaphylaxis is not caused by a partial saturation of cellular or humoral antibodies by the following facts. 1. Guinea pigs passively sensitized with anti-horse or antipneumococcus serum and specifically desensitized do not manifest as great a reactivity upon resensitization with the same antiserum as upon the original sensitization. 2. Guinea pigs passively sensitized with anti-Friedländer Type B serum or antipneumococcus Type II serum and specifically desensitized do not attain the same degree of reactivity as normal animals when passively sensitized with anti-horse serum. 3. Guinea pigs passively sensitized with anti-Friedländer Type B serum and desensitized with the specific carbohydrate remain as resistant to infection with Friedlander's bacillus Type B as undesensitized guinea pigs. Since in this case, at least, it is agreed that type-specific immunity and type-specific hypersensitiveness are due to the same type-specific antibody, a change in anaphylactic response should be accompanied by a change in immune response, provided this change depends on antibody balance. 4. A determination of the antibody content of the serum of sensitized as well as of desensitized guinea pigs by mouse protection tests indicates that a loss of reactivity in desensitized animals cannot be adequately accounted for on the basis of depletion of circulating antibody. These experiments suggest that hypersensitiveness and resistance are different manifestations of the same antigen-antibody reaction while antianaphylaxis is a state of refractoriness which is due neither to excess of circulating antibody nor to antibody depletion, but is the result of secondary changes the true nature of which is still not definitely established.

scholarly journals ANAPHYLAXIS WITH THE TYPE-SPECIFIC CARBOHYDRATES OF PNEUMOCOCCUS

1929 ◽  
Vol 49 (2) ◽  
pp. 251-266 ◽  
Author(s):  
Oswald T. Avery ◽  
William S. Tillett
Keyword(s):  
Guinea Pigs ◽  
Anaphylactic Shock ◽  
Horse Serum ◽  
Free Form ◽  
Rabbit Serum ◽  
Type Ii ◽  
Type Iii ◽  
Positive Results ◽  
Anaphylactic Response ◽  
Immune Rabbit

1. The type-specific carbohydrates (haptens) of Pneumococcus Types I, II and III, when isolated in protein-free form, are devoid of the property of inducing active anaphylactic sensitization in guinea pigs. 2. The bacterial carbohydrates of Pneumococcus, of which the Type II and Type III substances are nitrogen-free, produce rapid and fatal anaphylactic shock in guinea pigs passively sensitized with the precipitating serum of rabbits immunized with pneumococci of the homologous type; the reactions induced are type-specific. 3. In contrast to the positive results with immune rabbit serum, there is a complete absence of anaphylactic response to pneumococcus carbohydrate in guinea pigs passively sensitized with antipneumococcus horse serum.

scholarly journals DELAYED HYPERSENSITIVITY

1958 ◽  
Vol 108 (6) ◽  
pp. 891-904 ◽  
Author(s):  
Jonathan W. Uhr ◽  
A. M. Pappenheimer ◽  
Keyword(s):  
Guinea Pigs ◽  
Single Injection ◽  
Skin Testing ◽  
Specific Antigen ◽  
Delayed Hypersensitivity ◽  
Skin Reactions ◽  
Antibody Complex ◽  
Antigen Antibody ◽  
Free Antigen ◽  
Circulating Antibody

Guinea pigs rendered hypersensitive (delayed-type) to protein antigen can be completely and specifically desensitized by a single injection containing a sufficient amount of the corresponding antigen. Although 1 to 2 mg. of specific antigen are required for complete desensitization, as little as 20 µg. suffices to decrease the size of specific skin reactions in sensitized animals. The duration of non-reactivity lengthens as the amount of antigen in the desensitizing injection is increased, but skin reactivity eventually returns and is accompanied by the appearance of excess circulating antibody. Desensitization can be accomplished with the antigen-antibody complex as well as by "free" antigen. The appearance of delayed skin reactions can be prevented in fully sensitized animals by intravenous desensitization 2 or more hours after intradermal challenge or by simply skin testing with a desensitizing dose of specific antigen. Injection of a desensitizing dose of antigen into specifically sensitized animals also results in a transient anergic state, the implications of which are discussed.

Human Umbilical Cord Mesenchymal Stem Cells Induce into Chondrocytes in 3D Cultured System

2013 ◽  
Vol 749 ◽  
pp. 198-205
Author(s):  
Li Yu ◽  
Jing Liu ◽  
Chao Xu ◽  
Er Mei Luo ◽  
Ming Qiao Tang
Keyword(s):  
Real Time ◽  
Alcian Blue ◽  
Culture System ◽  
Type Ii Collagen ◽  
Human Umbilical Cord ◽  
Type Ii ◽  
Pellet Culture ◽  
Hla Dr

Objective: To investigate a better method of inducing hUC-MSCs into chondrocytes in different culture system in vitro. Method: hUC-MSCs were isolated and cultured by tissue block culture, and the cells surface antigens were identified by flow cytometry, hUC-MSCs were cultured with chondrogenic media and stained with Alcian Blue. The production of matrix was estimated from the determination of hydroxyproline content and Alcian Blue method. Expressions of glycosaminoglycan (GAG), type II collagen and Sox-9 were assayed by real-time fluorescence quantitative PCR. Results: The cultured hUC-MSCs phenotype was CD105+/CD29+/CD44+/ CD31-/CD34-/ CD40-/CD45-/HLA-DR-. hUC-MSCs weakly expressed chondrocyte marker, which strongly expressed GAG and type II collagen after chondrogenic induction, and the cells were incubated in pellet culture with higher expression. Real-time PCR results demonstrated that chondrogenic induction cells were expressed GAG, type II collagen and Sox-9, and the cells were incubated in pellet culture with higher expression. Conclusion: hUC-MSCs incubated in pellet culture is more conducive to differentiate into chondrocytes than those cultured in monolayer culture system.

scholarly journals Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy

2020 ◽  
Vol 29 (8) ◽  
pp. 1253-1273
Author(s):  
Jorge A Pereira ◽  
Joanne Gerber ◽  
Monica Ghidinelli ◽  
Daniel Gerber ◽  
Luigi Tortola ◽  
...  
Keyword(s):  
Mouse Model ◽  
Treatment Strategies ◽  
Underlying Disease ◽  
Potential Treatment ◽  
Type B ◽  
Disease Mechanism ◽  
Demyelinating Neuropathy ◽  
Charcot Marie Tooth ◽  
Dynamin 2

Abstract Some mutations affecting dynamin 2 (DNM2) can cause dominantly inherited Charcot–Marie–Tooth (CMT) neuropathy. Here, we describe the analysis of mice carrying the DNM2 K562E mutation which has been associated with dominant-intermediate CMT type B (CMTDIB). Contrary to our expectations, heterozygous DNM2 K562E mutant mice did not develop definitive signs of an axonal or demyelinating neuropathy. Rather, we found a primary myopathy-like phenotype in these mice. A likely interpretation of these results is that the lack of a neuropathy in this mouse model has allowed the unmasking of a primary myopathy due to the DNM2 K562E mutation which might be overshadowed by the neuropathy in humans. Consequently, we hypothesize that a primary myopathy may also contribute to the disease mechanism in some CMTDIB patients. We propose that these findings should be considered in the evaluation of patients, the determination of the underlying disease processes and the development of tailored potential treatment strategies.

Concluding remarks

1956 ◽  
Vol 146 (922) ◽  
pp. 90-92 ◽  
Keyword(s):  
Guinea Pigs ◽  
Current Trend ◽  
Distinct Type ◽  
Single Species ◽  
Immunological Tolerance ◽  
The Body ◽  
Immunological Reaction ◽  
Picryl Chloride ◽  
Purified Antigen ◽  
Circulating Antibody

In many ways immunological tolerance is an ideal subject for discussion at the present time. Experimental work has gone far enough to allow us to claim that the principle of immunological tolerance is soundly established and that we can see more or less clearly some of its implications. But obviously very much remains to be learnt of the part played by tolerance in the various fields that have been discussed. It is by no means certain that we are dealing with a single topic when we compare tolerance to homografts with inhibition of antibody production against soluble protein in a rabbit. Such a situation provides much for discussion but does not make it easy to condense or interpret that discussion. One might begin by reiterating that immunology is concerned with much more than the production and properties of typical circulating antibody. There are at least four different types of immunological reaction and there are hints of many minor differences within the main types. Pappenheimer’s recent work on the variety of responses given by a single species, man, to a single purified antigen, diphtheria toxoid, offers a characteristic example of the current trend. Chase’s experiments on the response of guinea pigs to simple allergens like picryl chloride, have been only incidentally mentioned in today’s discussion, but their importance is obvious. A form of tolerance very similar to that produced by prenatal treatment of mice can be produced by administering the allergen to adult guinea-pigs by mouth. The animals are resistant to sensitization by skin treatment and the inhibition is general and unrelated to any persistence of allergen in the body. The question immediately arises whether all forms of tolerance are basically similar or whether for each of the qualitatively distinct types of positive immunological reaction, a correspondingly distinct type of inhibition or tolerance must be sought.

scholarly journals Determination of oxidative stress and activities of antioxidant enzymes in guinea pigs treated with haloperidol

2012 ◽  
Vol 5 (2) ◽  
pp. 479-484 ◽  
Author(s):  
JAROMIR GUMULEC ◽  
MARTINA RAUDENSKA ◽  
MARIAN HLAVNA ◽  
TIBOR STRACINA ◽  
MARKETA SZTALMACHOVA ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Antioxidant Enzymes ◽  
Guinea Pigs

scholarly journals Determination of free L-carnitine levels in type II diabetic women with and without complications

2007 ◽  
Vol 61 (7) ◽  
pp. 892-895 ◽  
Author(s):  
A Poorabbas ◽  
F Fallah ◽  
J Bagdadchi ◽  
R Mahdavi ◽  
A Aliasgarzadeh ◽  
...  
Keyword(s):  
Type Ii

Development of Rheumatoid Factors and Anti-F(ab′)2 Antibodies in Guinea Pigs Immunized with Type II Bovine Collagen

1986 ◽  
Vol 80 (2) ◽  
pp. 214-220 ◽  
Author(s):  
Benjamin Wolf ◽  
Reza I. Bashey ◽  
Charles D. Newton ◽  
Sergio A. Jimenez
Keyword(s):  
Guinea Pigs ◽  
Type Ii ◽  
Rheumatoid Factors ◽  
Bovine Collagen

scholarly journals QUANTITATIVE STUDIES OF THE PHOTOCHEMICAL DESPECIATION OF HORSE SERUM

1942 ◽  
Vol 76 (5) ◽  
pp. 451-476 ◽  
Author(s):  
J. P. Henry
Keyword(s):  
Visible Light ◽  
Guinea Pigs ◽  
Phosphotungstic Acid ◽  
Horse Serum ◽  
Wave Length ◽  
Thin Layers ◽  
Antigenic Specificity ◽  
Residual Content ◽  
Quantitative Studies ◽  
Normal Horse Serum

1. Normal horse serum was irradiated for periods of 3 to 4 days, with visible light or with ultraviolet light of known intensity and wave length. The photosensitizer hematoporphyrin was employed in some instances. The serum was exposed to the air in thin layers, and thoroughly agitated throughout irradiation. 2. The irradiated sera were unchanged in color, and over 90 per cent of the original protein content remained precipitable by phosphotungstic acid. 3. Studies of the antigenicity of the sera were carried out on guinea pigs and rabbits. Fresh antigenicities of deviated specificity and of an activity of the order of 1/50th, 1/1,000th, and less than 1/20,000th that of normal horse serum were obtained. The residual content of material having the same antigenic specificity as normal horse serum was estimated as approximately equivalent in activity to dilutions of normal horse serum of 1 cc., 1/10 cc., and less than 1/100 cc. per litre respectively.

Sign in / Sign up

Export Citation Format

Share Document