EFFECT OF DOSAGE ON ANTIBODY RESPONSE TO POLYVALENT INFLUENZA VIRUS VACCINE IN AN AGED POPULATION

1964 ◽  
Vol 248 (3) ◽  
pp. 273-284 ◽  
Author(s):  
Samuel Saslaw ◽  
Harold N. Carlisle ◽  
Joann Sparks
1955 ◽  
Vol 1 (4) ◽  
pp. 249-255
Author(s):  
Barbara K. Buchner ◽  
D. B. W. Reid ◽  
G. Dempster

The antibody response to the subcutaneous inoculation of a single 1 ml. dose of a quadrivalent formalin-killed influenza virus egg vaccine has been measured. The vaccine used contained two A prime components and an A and a B component. Satisfactory responses were obtained two weeks after inoculation to the A and B components and to one of the A prime strains (FM1). A poor antibody response was noted to the other A prime strain incorporated in the vaccine (FW50). The highest levels were obtained with the Lee strain (Type B) which also stimulated an antibody rise to a recently isolated Type B strain. Antibody levels were maintained for at least 12 weeks. Treatment of the sera with RDE was found to influence the results obtained with the FM1 strain used.


1981 ◽  
Vol 86 (1) ◽  
pp. 1-16 ◽  
Author(s):  
R. Jennings ◽  
C. W. Potter ◽  
P. M. O. Massey ◽  
B. I. Duerden ◽  
J. Martin ◽  
...  

SUMMARYThree different types of bivalent influenza virus vaccine, a whole virus, an aqueous-surface-antigen vaccine and an adsorbed-surface-antigen vaccine were tested at three dosage levels in volunteers primed with respect to only one of the haemagglutinin antigens present in the vaccines.The local and systemic reactions to all three vaccine types were mild in nature and, following first immunization, the aqueous-surface-antigen vaccine was the least reactogenic. The serum haemagglutination-inhibiting antibody response to the A/Victoria/75 component of the vaccines, to which the volunteer population was primed, was greatest following immunization with the aqueous-surface-antigen vaccine; the greatest antibody response to the A/New Jersey/76 component of the vaccines was observed following immunization with whole virus vaccine.


PEDIATRICS ◽  
1959 ◽  
Vol 23 (1) ◽  
pp. 54-62
Author(s):  
Calvin M. Kunin ◽  
Robert Schwartz ◽  
Sumner Yaffe ◽  
John Knapp ◽  
Francis X. Fellers ◽  
...  

Polyvalent influenza-virus vaccine was administered to 55 children; 44 of these children were in various stages of nephrotic syndrome, including 17 under treatment with adrenocortical hormones; 5 were children with the adrenogenital syndrome receiving replacement cortisone therapy, and 6 were normal controls. Antibody response, as measured by the hemagglutination-inhibition test 2 weeks following a single subcutaneous dose of vaccine, was not significantly different in children with active or inactive disease, and appeared to be similar in those receiving hormone therapy and in those who were not. The serum levels of gamma-globulin were lower in children with active nephrotic syndrome, but this did not affect either the prevaccination levels of influenza A prime antibody or the response to the vaccine. No change in the status of activity of nephrosis occurred during the period of immunization or immediately thereafter, even in patients who had moderate febrile reactions to the vaccine. The failure of any of the groups to respond serologically to the Asian strain component of the vaccine is discussed.


BMJ ◽  
1985 ◽  
Vol 291 (6505) ◽  
pp. 1348-1349 ◽  
Author(s):  
M Chavance ◽  
B Herbeth ◽  
T Mikstacki ◽  
C Fournier ◽  
G Vernhes ◽  
...  

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