A NON-SPECIFIC COMPLEMENT FIXATION REACTION DUE TO ION ANTAGONISM

1932 ◽  
Vol 7 (6) ◽  
pp. 585-595
Author(s):  
A. Hambleton

The complement fixation test for tuberculosis gives a non-specific or falsely positive reaction if a balanced physiological saline, akin to Tyrode's solution, replaces the plain saline used in the test. The balanced saline must contain both calcium and magnesium in appropriate concentration. The non-specific reaction is given most strongly by Petroff's whole bacillus antigen, and not at all by "fat-free" tubercle bacillus antigens. The main features of the reaction, and its relation to antagonistic effects of sodium and calcium ions, are indicated.

2021 ◽  
Vol 25 (11) ◽  
pp. 1237-1238
Author(s):  
A. Dmitriev

Alf. Cohn (Derm. Ztschr. Bd. 55, H. 2) gives detailed instructions for the preparation of a specific antigen, patient serum, and also describes in detail the technique of the Bordet-Gengou reaction itself. The author received as a result of his observations with acute gonorrhea in men 40% pos. responses, for chronic 60% and for complicated 80-100%. The results are especially demonstrative in gonorrhoid arthritis (100%). It is important to use the reaction in doubtful cases, when microscopic and bacteriological examinations do not give the necessary answer for making a diagnosis. If people who do not have gonorrhea are vaccinated, the reaction may be positive. If a positive reaction persists for months or years, you need to look for a focus with gonococci. According to the author, the complement fixation reaction cannot replace the previously tested diagnostic methods, but it complements them. Together with bacteriological and clinical research methods, the reaction sometimes helps to understand the diagnosis of difficult cases.


1928 ◽  
Vol 28 (2) ◽  
pp. 172-197 ◽  
Author(s):  
T. J. Mackie ◽  
M. H. Finkelstein

1. When a solution of commercial peptone is substituted for antigen in a complement-fixation test with the unheated normal serum of certain species (man, ox, sheep, horse, rabbit, white rat), a definite fixation reaction occurs both at 37° C. and at 0° C. In the ox, sheep, horse and rabbit this property of serum is partially stable at 55° C., but normal human serum and the serum of the white rat are inactive after heating at this temperature. The property is resident mainly in the carbonic-acid-insoluble globulins of the serum.2. The same results are obtained when ethyl alcohol diluted with several volumes of normal saline solution is substituted for antigen in a complement-fixation test with normal serum.3. Analysis of these reactions shows a close correspondence with complement-fixation by the sera of normal animals plus the Wassermann “antigen”—the Wassermann reaction of normal animals.4. Marked complement-fixation effects are also obtained with heated normal serum of the rabbit, ox, sheep, horse plus cholesterol suspension, and particularly cholesterolised-peptone, these effects occurring in parallel with those produced by serum plus alcohol-saline, peptone solutions and the Wassermann “antigen.” The heated normal serum of the pig, white rat and guinea-pig do not exhibit these reactions, and the same applies to heated normal human serum. Unheated pig serum fails to react. Such results also elicit a close relationship between these non-specific reactions and the Wassermann reactions of normal animals.5. The reacting property is absent from the serum (heated and unheated) of young rabbits during the first 2 to 3 weeks of life, but appears soon after this (e.g. by the 37th day) and is progressive in development. Its development in early life runs parallel to that of the natural haemolytic property of the serum for sheep's blood (due to a natural antibody-like substance). The two properties are, however, independent as illustrated by absorption tests.6. Besides the agents referred to above as capable of fixing complement along with normal sera, other substances possess a similar property, e.g. certain alcohols, sodium oleate, tissue proteins, certain amino-acids and sodium nucleate. Commercial peptone purified by precipitation with alcohol is equally active with the original material. Cholesterolisation of these agents may yield a product whose activity is greater than that due to summation of effects.7. Wassermann-positive and -negative human sera have been tested in the complement-fixation reaction with certain of these “pseudo-antigens,” viz. alcohol-saline, peptone, cholesterol, and cholesterolised-peptone, but a uniform parallelism has not been demonstrated between the reactions with these agents and the Wassermann effect. Some Wassermann-positive sera react also with alcohol-saline, peptone, cholesterol and cholesterolised-peptone, while sera from selected normal persons are quite inactive. A considerable proportion of Wassermann-positive sera yields definite complement-fixation with cholesterol and cholesterolised-peptone; a small proportion of Wassermann-negative sera reacts with these agents.8. The thermolability of the serum principles acting with various “pseudoantigens” has been studied by testing unheated serum and serum heated at temperatures ranging from 46° to 60° C. Two types of thermolability curve have been demonstrated with different specimens of rabbit serum: (1) a more or less progressive weakening of the various reactions with inactivation at 60° C.; (2) inactivation of the effects with Wassermann “antigen,” alcoholsaline and cholesterol at 50–52° C., activation of the effects with the Wassermann “antigen” and cholesterol at 54–56°C. and inactivation again above 60° C.; in this case the curves for peptone and cholesterolised-peptone do not show such double inactivation. Unheated normal human serum yields reactions with the various agents (including the Wassermann “antigen”) but inactivation occurs at 50° to 54° C. whereas certain syphilitic sera yield thermolability curves somewhat similar to type (1) of rabbit serum, with inactivation at 60° C. or over.


1935 ◽  
Vol 13 (1) ◽  
pp. 25-40
Author(s):  
Mary N. Andrews

1. The preparation of a cercarial antigen from infected livers of Oncomelania hupensis the intermediate host of Schistosoma japonicum in China is described.2. The sera of 49 human beings and five dogs have been investigated for the Schistosome complement fixation reaction, using as antigens Bilharzial cercarial antigen, and an alcoholic extract of the livers of Oncomelania hupensis infected with cercariae of S. japonicum.3. Thirty-seven of the 49 sera examined were from cases of Schistosomiasis, and of these 24 gave a positive complement fixation reaction, and 2 others a weak reaction.4. Of the five dogs examined three were infected with Schistosoma japonicum. These gave positive reactions.5. In 24 cases both antigens were used, and the results obtained were almost identical.6. The Bilharzial antigen was used in 33 cases including 25 cases of Schistosomiasis, of which 19 gave a positive reaction.7. In 40 cases the Oncomelania antigen was used. This series included 32 cases of Schistosomiasis of which 23 gave a positive reaction and 3 a weak positive reaction.8. Negative results were obtained with 50 strongly positive Wasserman sera, and with 2 cases of infection with Fasciolopsis buski, and two cases of Clonorchis sinensis. Ascaris and hookworm infestations also gave negative results.


1914 ◽  
Vol 14 (1) ◽  
pp. 52-71 ◽  
Author(s):  
Leonard S. Dudgeon

Experience gained from a previous enquiry on this subject in human tuberculosis led to the belief that much information might be derived from an investigation of the complement fixation reaction in animals experimentally infected with tubercle bacilli. Accurate dosage can be measured and the true path of infection is definitely known. Various enquiries were suggested and investigated by the detailed examination of rabbits and guinea-pigs; the latter class of rodents were used in batches of six to twelve in number, as otherwise the individual differences between animals in the same group of experiments are entirely overlooked. My cultures of the human tubercle bacillus were obtained by inoculating guinea-pigs with the sputum from typical cases of pulmonary tuberculosis at the Brompton Hospital Sanatorium at Frimley. Pure cultures of the bacillus were obtained from the infected guinea-pigs and cultivated on Dorset's egg medium, so that within a period varying from 14 to 21 days an abundant growth was obtained. The culture of the bovine bacillus was supplied to me by Professor Delépine who obtained it directly from the tissues of an infected cow, and subcultures were kept going on Dorset's egg medium. In every experiment without exception the animals were infected with definitely known quantities of the human or bovine bacillus. These were obtained by carefully scraping the growth off the surface of the egg medium and weighing it on sterile platinum foil, while in some cases (for comparison) a portion of the growth was dried in a desiccator before it was weighed. The untreated or dried bacilli were then shaken in a known quantity of sterile saline, so that a perfect emulsion free from clumps was obtained. The bacilli were kept in the dark in brown stoppered bottles and were always employed within a few days of their preparation.


1927 ◽  
Vol 45 (4) ◽  
pp. 701-726
Author(s):  
Paul A. Lewis

The prolonged extraction of the tubercle bacillus with boiling ethyl alcohol, followed by one or more reprecipitations by chilling the hot alcoholic solution, easily yields a preparation very active as antigen in the complement fixation reaction. This preparation gives a precipitation reaction with high dilution of the normal blood serum of a number of species. The precipitation reaction presents as a peculiar feature a very long pro-zone and is further dependent on a preceding heat treatment of the serum for its demonstration. Occurring as a reaction of normal serum, the reaction is apparently not influenced by immunization sufficient to develop moderate specific complement fixation reactions.


Parasitology ◽  
1915 ◽  
Vol 8 (2) ◽  
pp. 156-183 ◽  
Author(s):  
E. A. Watson

This paper is written with the purpose of drawing further attention to the value of the complement fixation reaction as a diagnostic test in dourine and of recommending a method of procedure and technique arrived at with an experience of 15,000 tests for dourine made at the Veterinary Research Laboratory, Lethbridge.


1952 ◽  
Vol 21 (3) ◽  
pp. 391-399 ◽  
Author(s):  
Elwood Buchman ◽  
Harold J. Kullman ◽  
George F. Margonis

1969 ◽  
Vol 62 (1_Suppl) ◽  
pp. S113-S133 ◽  
Author(s):  
Sam Brody

ABSTRACT This report is a summary of 10 years of experience with the complement fixation test as adopted for the immunoassay of HCG in serum. It is based on published as well as unpublished material. The discussion centers mainly around methodological problems, criteria of reliability, and clinical observations. It is our impression that the complement fixation test is a reasonably rapid and simple technical procedure. It is standard practice in every bacteriological and virological laboratory. The precision of the HCG assay is high. Its accuracy is good. The complement fixation assay, as reported here, fulfils the criteria of specificity. It has been evaluated by means of serological techniques and through comparison between biopotency and immunopotency of HCG in serum with reference to a common standard. Its application for routine as well as research work is illustrated.


2014 ◽  
Vol 17 (2) ◽  
pp. 367-369 ◽  
Author(s):  
K. Rypula ◽  
A. Kumala ◽  
P. Lis ◽  
K. Niemczuk ◽  
K. Płoneczka-Janeczko ◽  
...  

Abstract The study was carried out in seven reproductive herds of pigs. In three of them reproductive disorders were observed. Three herds consisted of 10-50 and four consisted of 120-500 adult sows and they were called small and medium, respectively. Fifty-seven adult sows were randomly selected from herds. Serum samples were tested using the complement fixation test and swabs from both eyes and from the vaginal vestibule were examined using real-time PCR. All serum samples were negative. Infected sows were present in each of the study herds. In total, there were 28 positive samples (53%, 28/48) in real-time PCR in sows with reproductive disorders and 35 (53%, 35/66) in sows selected from herds without problems in reproduction. One isolate proved to be Chlamydophila pecorum, whereas all the remaining were Chamydia suis


1950 ◽  
Vol 5 (5) ◽  
pp. 243-247
Author(s):  
Minoru MATSUMOTO ◽  
Saburo IWASA ◽  
Motosige ENDO

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