Assessment of quantitative serum Antibody titre in patients with aggressive periodontitis to actinobacillusactinomycetemocomitans and serum antibody titre to porphyromonasgingivalis in chronic periodontitis patients

2018 ◽  
Vol 5 (20) ◽  
pp. 57-63
1983 ◽  
Vol 90 (1) ◽  
pp. 107-115 ◽  
Author(s):  
A. Goodeve ◽  
C. W. Potter ◽  
A. Clark ◽  
R. Jennings ◽  
G. C. Schild ◽  
...  

SUMMARYOne hundred and nineteen volunteers were divided into five groups, and each volunteer inoculated subcutaneously with an aqueous subunit B/Hong Kong/73 vaccine containing 40, 20, 10, or 5 μg of HA or saline alone in a 0·5 ml volume. The incidence of reactions was recorded 24 h after inoculation. One month following immunization the serum HI antibody to B/Hong Kong/73 virus was measured; each volunteer was inoculated intranasally with live, attenuated influenza B (RB77) virus; and the incidence of infection by the challenge virus was determined by HI antibody response.The results showed that the incidence of reactions to all doses of vaccine were relatively low, the severity mild, and the duration short. However, the incidence of reactions was highest for those given 40 μg HA and least for those given 5 μg HA. The serum HI antibody responses to vaccine showed a dose-response relationship. For volunteers given 40 μg HA, 22 (96%) showed a fourfold rise in antibody titre and all volunteers had antibody titres of > 40 following immunization: for volunteers given 5 μg HA the g.m.t. increased from 16·6 to 86·1; and for those given 10 and 20 μg HA the response was intermediate. Following challenge, the lowest incidence of infection was seen in volunteers given the highest dose of vaccine. However, all doses of vaccine induced some protection against challenge virus infection, and the incidence of infection was directly related to the serum antibody titre at the time of challenge. The 50% protection titre of serum HI antibody was estimated as 15 to 20.


1995 ◽  
Vol 4 (6) ◽  
pp. 372-376 ◽  
Author(s):  
Hendri H. Pas ◽  
Marcelus C. J. M. Jong ◽  
Marcel E Jonkman ◽  
Klaas Heeres ◽  
Ida J. Slijper-Pal ◽  
...  

1964 ◽  
Vol 38 (1-2) ◽  
pp. 159-170 ◽  
Author(s):  
L. F. Taffs

Following the oral administration of third- and fourth-stage A. suum larvae, which had previously completed nine or ten days somatic migration in guineapigs, rabbits or a pig, six out of eight pigs showed a rise of serum antibody titre, as measured by the conglutinating complement absorption test using a saline extract of Ascaris worm as antigen. Four of these pigs had negative titres before infection, and in these animals antibodies were first detected between the 14th and 20th days. Maximum serum antibody concentration was reached between the 14th and 34th days of infection, and antibodies were detected for at least as long as 68 days.Larvae were recovered from the faeces on the 23rd and 29th days of infection, and in two pigs out of eight the larvae reached maturity, eggs first being seen in the faeces on the 42nd day.The results suggest that (1) Ascaris larvae, on their return to the intestine, release antigenic substances which are then absorbed by the gut wall to stimulate the production of antibodies; (2) the secondary antibody rise, which occurs about the sixth or seventh week of an infection with Ascaris eggs, is due to the absorption of this larval antigen; and (3) the moulting process (fourth moult) is not only an important stage for stimulating this further antibody production, but is also the time when maturing larvae are affected by the immune mechanisms of the host.On reinfection with Ascaris eggs the phenomenon of “self-cure” was noticed. A fall in the faecal egg count, which became negative on the 21st day, was accompanied by a sharp rise in antibody titre. An increase in the number of infertile eggs in the faeces, rising from 11% on the day of reinfection to 100% on the 14th day, was also observed.


1947 ◽  
Vol 45 (4) ◽  
pp. 497-503 ◽  
Author(s):  
N. H. Hole ◽  
R. R. A. Coombs

1. Observations on the sera of ponies, taken at frequent intervals for 321 days after oral administration of P. mallei, are described.2. It was found that the conglutinating complement absorption test was more sensitive than the haemolytic complement fixation test as a means of diagnosis. It detected the antibodies earlier in the course of the disease and demonstrated their presence over a longer period of time.3. The possibility of another practical use of this reaction as an adjunct to the allergic test is considered. Ten days after an intradermo-palpebral test a pony, which had been previously sensitized and whose serum antibody titre at that time was below 10, developed a serum titre of over 160 as demonstrated by the conglutinating complement absorption test. Under similar circumstances 11 unsensitized ponies developed no detectable serum antibodies.


1979 ◽  
Vol 13 (2) ◽  
pp. 143-148 ◽  
Author(s):  
A. Schaich Fries

Summary The correlation between serum antibody titre and resistance to challenge infection with Bacillus piliformis was studied in naturally infected mice, in experimentally infected but recovered mice, and in mice treated with antigen prepared from infected livers. Irrespective of the way in which the antibodies were acquired resistance to infection was found to be related to the immunofluorescence antibody titre found. Experimentally infected but recovered mice, as well as rats with persistent antibodies to Bacillus piliformis, were given prednisolone in order to activate a possible persistent infection. Bacillus piliformis was detected in the rats, but not in the mice.


1992 ◽  
Vol 11 (1) ◽  
pp. 11-16 ◽  
Author(s):  
L. Institóris ◽  
Olga Siroki ◽  
S. Tóth ◽  
I. Dési

The effects of a single large and repeated small doses of MPT-IP (the industrial product used to produce Wofatox EC 50) containing 60% methylparathion, on the humoral and cellular immunoreactivity of CFLP mice were investigated. Administration of a single LD50/2 dose 3 d prior to immunization caused a 40% increase in the number of splenic PFC on the 5th day but no significant increase in serum antibody titre on the 7th day after immunization. Treatment for 4 weeks with an LD50/40 dose resulted in a 100% increase in splenic PFC, also not associated with a change in serum antibody titre. Under the same conditions and LD50/20 dose had no effect on these parameters. Neither the single large nor the repeated small doses had any effect on the intensity or time course of a DTH reaction. The results show that MPT-IP has an immunotoxic potential in mice under certain experimental conditions.


2018 ◽  
Vol 32 (0) ◽  
Author(s):  
Alexandre Hugo LLANOS ◽  
Carlos Guillermo Benítez SILVA ◽  
Karina Tamie ICHIMURA ◽  
Estela Sanches REBEIS ◽  
Marcela GIUDICISSI ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-5
Author(s):  
Mahdi Kdkhodazadeh ◽  
Mehrdad Hajilooi ◽  
Behzad Houshmand ◽  
Sara Khazaei ◽  
Leila Gholami ◽  
...  

Objective. Our aim in this paper was to investigate the possible genetic association between three Ser563Asn, Leu125Val and Arg670Gly polymorphisms of the PECAM-1 gene and periodontitis. Methods. Genomic DNA was isolated from whole blood of 105 periodontal patient (52 with chronic periodontitis and 53 with aggressive periodontitis) and 101 healthy individuals. Samples were genotyped and analyzed for the three single-nucleotide polymorphisms (SNPs) of PECAM-1 using polymerase chain reaction with sequence-specific primers (PCR-SSPs). Results. A statistically significant difference was found between the genotypic distribution of the Ser563Asn polymorphism in patients with periodontitis compared to controls (P=0.02). But there were no statistically significant difference between the allele frequencies in the different groups (P=0.05). The other two polymorphisms did not show a statistically significant difference in their allele and genotype frequencies between the groups. There was no statistically significant difference found for any of the polymorphisms allele and genotype distribution in aggressive and chronic periodontitis either. Conclusions. No significant association was found between the polymorphism tested and the subgroups of periodontitis, further research is still necessary to determine whether this polymorphism can be used as a genetic marker of periodontitis.


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