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Parametry biochemiczne oraz odpornosci nieswoistej u indykow uodpornionych wirusem ND po podaniu KLP-602 lub Mycobacterium chelonae

100%

Wojcik R. , Swiecicka-Grabowska G.

tom 62

nr 07

830-833

The aim of the study was to compare KLP-602 or M. chelonae on some biochemical and nonspecific immunity parameters in turkeys immunized with the virus antigen. Research was carried out on 30 turkeys (3 groups, 10 birds in each), who were given one of the two immunity stimulators: KLP-602 or M. chelonae at the age of 29 days. The control group was comprised of birds receiving no stimulators. All the birds received an active mesogenic Roakin strain of ND virus after 7 days and again after 100 days and the biochemical parameters (total proteins, gammaglobulin, ceruloplasmin level), humoral defense parameters (level of lysozyme), cellular parameters (potential killing activity, respiratory burst activity and proliferation activity) were determined. The obtained results demonstrated that M. chelonae had a more significant stimulatory effect on biochemical and humeral immunity parameters than KLP-602.

Wplyw KLP-602 i Mycobacterium chelonae na odpornosc swoista u indykow szczepionych wirusem ND

80%

Wojcik R. , Swiecicka-Grabowska G.

tom 62

nr 08

922-924

The aim of the study was to evaluate the stimulating effect of KLP-602 and M. chelonae on some parameters of specific cellular and humoral immunity in turkeys vaccinated with ND virus. The research was carried out on 30 turkeys in three groups. Two groups were given one stimulator and one group was control. After 7 and 100 days birds were immunized against the mesogenic Roakin strain of ND virus. Cellular immunity in the blastic transformation and humoral inhibition were determined in the blood. The results shows that KLP-602 and M. chelonae were better stimulators of humoral immunity than cellular immunity. In the case of KLP-602 group gammaglobulin level was higher than in M. chelonae and the control group.

Informacja o wynikach przedklinicznych badan KLP-602 [dimer lizozymu]

80%

Klein P. , Kiczka W.

Życie Weterynaryjne

1994

tom 69

nr 04a

142-145