1,720,986 research outputs found
Antibody response to ATPC+ascites tumour in mice rendered resistant by intravenous inoculation of liver cells.
No full text
Determination of immunity against tetanus infection by passive haemagglutination assay.
No full textEvaluation of anti-tetanus antibody level in human sera is of primary importance for a prophylaxis of tetanus infection. Many efforts have been made to develop simple, sensitive and reproducible in vitro methods for detecting and quantifying antibodies to tetanus toxin. We have recently developed an HA assay using lyophilized turkey red blood cells (TRBC-HA). In this paper we demonstrated that the TRBC-HA test is more sensitive than the most widely used sheep red blood cell assay (SRBC-HA) and that TRBC-HA assay shows a high correlation with the neutralization test (NT). Furthermore, comparisons of TRBC-HA assay with enzyme-linked immunosorbent assay (ELISA) and counterimmunoelectrophoresis (CIE) indicate that TRBC-HA and ELISA assays detected the same antibody level with a sensitivity up to 400-fold higher than that determined by CIE. However, TRBC-HA also offers many advantages over the ELISA test, because TRBC-HA can be performed in only 40 minutes instead of the 24 hrs. needed for the ELISA, it is less expensive than ELISA and requires no special equipment. Therefore, the overall results suggest that the TRBC-HA is the most appropriate method for rapid and sensitive determination of tetanus antibody levels
Hypertonic salt solution of superficial membrane proteins from ATPc+ mouse ascites tumour which retain tumour specific antigenic properties.
No full textAntigen specificity and immunogenic capacity of 3m KCl cell extracts from ascites tumour ATPCplus.
No full text[Microbiological diagnosis of tetanus and serological verification of the immunological status. Serological monitoring in the course of therapy and prophylaxis].
No full textAnti-candida antibodies in human serum. Detection and definition of Ig classes by a new elution technique.
No full text[Behavior of cell lines transformed by polyoma virus maintained at high incubation temperature (+41 degrees C)].
No full text[The use of passive hemagglutination with turkey erythrocytes for the effective prevention of tetanus in wounded patients].
No full textThe passive haemagglutination assay is at present the most common method available for evaluating tetanus antibody levels. We recently developed a modification of the technique of HA by Mai and Rosin using turkey red blood cells (TRBC-HA) instead of sheep red blood cells (SRBC-HA). TRBC-HA assay seems to offer the advantages of being more sensitive and easier to perform than the SRBC-HA method. More important, with the TRBC-HA assay, we found that the HA values greater than 0.5 H.U./ml always correspond to NT values greater than 0.01 IU/ml. Therefore this value (0.5 H.U./ml) was chosen as a discriminating level between protected and non protected persons. On this rationale base we have tested sera from injured persons in order to individualize a single prophylactic treatment under a rationale guideline against the alternative of a blind intervention under anamnestic basis. Among 437 persons tested 248 did not remember if they had been vaccinated or not. According to the anamnestic basis all these persons should require injection of human antitetanus Ig plus a basic course of vaccination. On the contrary antitetanus antibody levels monitored by TRBC-HA assay indicate that 132 were protected and did not require any treatment; 79 were partially protected and required a boosting of tetanus toxoid and only 37 were not protected and needed human antitetanus IgG plus a complete course of vaccination. These results underline the necessity of monitoring a single person for antitetanus antibodies in order to prevent both under or over evaluation of their tetanus immune status
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