scholarly journals STUDIES ON COMPLEMENT FIXATION IN TUBERCULOSIS. III

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.

1914 ◽  
Vol 14 (1) ◽  
pp. 76-82 ◽  
Author(s):  
W. O. Meek

The object of this portion of the investigation was to determine(a) Whether the amount of immune-body present in the sera of cases of pulmonary tuberculosis, bore any constant relation to the stage of the disease and the condition of the patient.(b) Whether well-marked clinical phenomena, e.g. periods of fever, attacks of pleurisy etc., were associated in any definite manner with variations in the amount of immune-body in the serum.(c) Whether gradual definite and sustained improvement or deterioration in a patient's condition was accompanied by increase or decrease of the specific immune-body in the serum.


1923 ◽  
Vol 38 (2) ◽  
pp. 219-232 ◽  
Author(s):  
Paul A. Lewis ◽  
Joseph D. Aronson

By means of a method differing in important details from those of previous investigators it has been determined that the blood serum of cases of leprosy exhibits the ability to fix complement with a wide variety of antigens including to a greater or less extent those derived from any culture of the acid-fast group of bacteria available to us. This property of multiple fixation may sufficiently characterize the disease to be of diagnostic significance, although our experience is hardly sufficient to enable us to speak with complete assurance on this point. Certainly, control sera from normal individuals, from cases of tuberculosis, or from cases of syphilis as obtained in our locality have entirely failed to react with certain antigens, whereas serum from cases of leprosy have so reacted to the extent of over 93 per cent. The most characteristic fixation given by the leprosy sera is that with Bacillus lepræ (Clegg) used as antigen, either in the form of a bacterial emulsion or of an alcoholic extract of the dried culture. Antibody absorption may be demonstrated in the acid-fast group if the absorbing bacteria are removed by filtration. Otherwise the resulting fluid is strongly anticomplementary. Leper serum is not deprived of the complement-fixing body when so treated with either Bacillus tuberculosis or Bacillus lepræ (Clegg).


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.


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.


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.


1998 ◽  
Vol XXX (1-2) ◽  
pp. 47-50
Author(s):  
V. I. Guzeva ◽  
N. Р. Taranova ◽  
I. В. Mikhailov

The results of autoantibodies determination to glycolipid antigens of brain cells - galactocerebrosides in blood serum of healthy neonates and their mothers, healthy children up to three y.o. and healthy women are presented. The results were obtained with the help of micromodification of complement fixation reaction. It was determind that in healthy women at intergeneric period these antibodies are absent or are present in vestige quantities. For the first time presence of counter - galactocerebroside antibodies was determined in neonates and their mothers in high titers up to 1:512. It was also established, that counter - galactocerebroside antibodies circulate in healthy neonates blood for not less than 3 months, then their level begins to descrease, and in 5-12 months it approximates to the adults norm border.


1973 ◽  
Vol 30 (01) ◽  
pp. 093-105 ◽  
Author(s):  
C.H.J Sear ◽  
L Poller ◽  
F.R.C Path

SummaryThe antiheparin activity of normal serum has been studied by comparing the antiheparin activities of sera obtained from normal whole blood, platelet-rich plasma and platelet-’free’ plasma with a purified platelet extract during differential isoelectric precipitation and by gel filtration chromatography.The mean values for the activity of PRP-serum and PFP-serum were 106% (S.D. 11) and 10% (S.D. 3) of untreated whole blood respectively. The activity of whole blood serum, PRP serum and whole blood serum plus platelet extract precipitated under identical physical conditions, i.e. pH 7.0, I =0.008, indicating that the activities of the three samples are probably associated with PF4. PF4 precipitated from human platelet extract at pH 4.0, but this is probably due to the difference in the two biochemical environments investigated, i.e. serum and platelet extract.The gel filtration experiments revealed striking similarities between the major antiheparin activities of serum and platelet extract. At physiological pH and ionic strength both activities were associated with high molecular weight material, but at physiological pH and elevated ionic strength both activities behaved as much smaller entities of molecular weight between 25,000 and 30,000 daltons and it seems very likely that both activities are associated with the same molecule, i.e. PF4.


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

1942 ◽  
Vol 76 (6) ◽  
pp. 543-556 ◽  
Author(s):  
John G. Kidd ◽  
William F. Friedewald

The foregoing experiments have shown that complement fixation takes place when the blood serum of normal adult rabbits is mixed with fresh saline extracts of normal rabbit tissues under controlled conditions. A natural antibody, which reacts in vitro with a sedimentable constituent of normal tissue cells, is responsible for the phenomenon.


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