ANTIBODY RESPONSES TO NATURALLY OCCURRING POLIOMYELITIS INFECTIONS IN CHILDREN

PEDIATRICS ◽  
1955 ◽  
Vol 15 (4) ◽  
pp. 392-401
Author(s):  
C. Arden Miller ◽  
Jacqueline Baumeister

Serums collected over an 18-month period from children with a clinical diagnosis of poliomyelitis were studied by means of the complement fixation test. Test antigens were prepared from the nutrient fluid of tissue cultures infected with each of the 3 known types of poliomyelitis viruses. Results were compared with those obtained from neutralization tests on the same serums. The complement fixation test was of little diagnostic help in these patients; a high titer, a rise in titer, and a fall in titer were all inconstant findings. A complement fixing antibody titer persisting beyond 100 days was more indicative of the immunologic type of the infecting virus than any other feature of the complement fixing antibody response. The multitypic nature of the complement fixing antibody response was discussed in relation to the complex antigenic structure of poliomyelitis viruses.

1955 ◽  
Vol 102 (2) ◽  
pp. 133-150 ◽  
Author(s):  
Nathalie J. Schmidt ◽  
Edwin H. Lennette ◽  

A macroscopic (tube) complement fixation test for poliomyelitis, using infected tissue culture fluids, is described. The test was applied to 27 individuals with a clinical diagnosis of poliomyelitis. In 18 patients it was possible to make a laboratory diagnosis of poliomyelitis on the basis of a rise in complement-fixing antibody titer and in 4 others on the basis of a high stationary antibody titer. One individual gave a high and equal antibody response to two virus types, 3 others had no detectable antibody, and 1 appeared not to have poliomyelitis. Heterotypic reactions were encountered, but gave little difficulty in interpreting homologous responses. In those patients from whom a virus had been recovered, the serologic findings corresponded to the virus type recovered. The possible occurrence of dual infections with the viruses of poliomyelitis and Western equine and St. Louis encephalitis is discussed.


1961 ◽  
Vol 59 (4) ◽  
pp. 401-412 ◽  
Author(s):  
Ruth M. Lemcke

By means of a complement-fixation test of the sera of laboratory rats and mice, the immunological response of these animals to both naturally occurring and induced PPLO infections was determined, and the presence and extent of infection in the animals determined by culture.PPLO antibodies specific for the infecting strain were demonstrable in rats and mice from which PPLO were isolated.The amount of serum antibody rises with the extent and severity of the infection. Thus, young rats with PPLO infections confined to the nasopharynx had little or no antibody whereas the oldest rats with consolidated lungs had the highest titres. In mice too, the sera of those with pneumonia had the highest titres.The comparatively low titres found in rat bronchiectasis together with the failure to isolate PPLO from the spleen and other organs, suggest that the chronic form of the disease remains localized. This is in contrast to infections with rat polyarthritis and related PPLO in which the organisms can be isolated from the lymph nodes and other organs and in which antibody is present in high titre.In view of the high degree of correlation between the presence of antibodies to PPLO in the blood and the presence of PPLO in the tissue of rats and mice, it is suggested that specific antibody found in man is a significant indicator of PPLO infection.


1960 ◽  
Vol 15 (6) ◽  
pp. 375-378
Author(s):  
Arno Geissler ◽  
Wolfgang Müller-Ruchholtz ◽  
Else Knake

The immunization of highly inbred Wistar rats with a Benzpyrene-Sarcoma produced in this strain did not stimulate the formation of circulating tumor-specific antibodies. In these studies the complement fixation test, the colloid-complement fixation test, the ring precipitin test, the agar-gel-diffusion technic of Ouchterlony and tissue cultures for the study of cytotoxic antibodies were used.


1960 ◽  
Vol 58 (3) ◽  
pp. 321-330 ◽  
Author(s):  
Golda Selzer

A complement-fixation test for acute poliomyelitis using unheated antigens derived from suckling mouse brain infected with poliovirus Type 1 or Type 2 is described.The results of tests in 62 patients clinically diagnosed as cases of acute poliomyelitis in a recent epidemic and in 26 controls are recorded.The CF tests were positive in 100% of 53 cases with poliovirus Type 1 and/or Type 2 in stool. A positive result was obtained in 23 (76%) of 30 cases whose sera were examined in the first 7 days of illness.Negative tests of the initial serum samples were found in 15 (28·5%) of 53 cases, but all these became positive in titres of 40 or 80 on testing of convalescent serum.In 31 (69%) of 45 cases whose sera were re-tested between the 3rd and 4th weeks of illness the CF antibody levels rose, reaching titres of 80 or 160 in most instances. Of the remaining 14 cases only one dropped in insignificant degree (from titre 320 to 160) and the 13 stationary results had been positive in titres of 40–160 on initial tests most of which were performed in the 2nd week of illness.Homotypic CF antibody response without crossing was found in 37 (71%) of 52 cases with Type 1 or Type 2 virus in stool. In the cases of crossing the heterotypic antibody response was either transient, diminishing or stationary in all and in only low titre in most instances.In 26 control cases there were seven positive CF tests, but one of these was nonspecific, five were in lowest titres, and one case appeared to have had recent poliomyelitis infection.Heating the antigens did not broaden the reaction. It caused only slight loss of potency except in two cases in which the CF titre increased substantially.The antigenic preparation described appears to be superior to antigens of other origin in the diagnosis of acute poliomyelitis by complement-fixation tests, as positive tests are recognized earlier in the illness and the titres are higher. Homotypic results were obtained in all cases and no instance of false negative occurred in this series.I would like to thank the medical staff of the Cape Town City Hospital for Infectious Diseases for the trouble taken in collecting stools and paired sera, and Prof. Kipps for his interest in this work. I am indebted to Miss Karin Larssen for valuable technical assistance.


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


1984 ◽  
Vol 61 (7) ◽  
pp. 216-218
Author(s):  
L. C. LLOYD ◽  
R. T. BADMAN ◽  
J. R. ETHERIDGE ◽  
K. McKECHNIE ◽  
H. IYER

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