IMMUNOGLOBULINS:
The
immunoglobulins are a complex group of proteins that make a significant
contribution to the protein content as well as exerting an important
immunological function, especially in colostrum. The structure and general function of bovine immunoglobulins has been reviewed by
Larson (1992) and Buttler ( 1973,1983).
The
immunoglobulins found in bovine whey and colostral whey include:
IgA and secretory IgA
IgG1, IgG2 and IgG fragments
IgM
IgE
J-chain or component
free secretory component
The
nomenclature of the immunoglobulins is based
on their immunological cross reaction with reference proteins,
preferably of human origin and proposed by the World Health Organisation (Buttler, etal.,
1971).
All the
immunoglobulins are glycoproteins that are monomers or polymers of made up of two light chains (~20,000 Dal) and two
heavy chains (~50,000 - 70,000 Dal) linked together with sulphide bonds
(Buttler, 1974, Lascelles, 1979). In the
molecules of a class or subclass, the two have chains are identical -- with a constant and a variable
region. The light chains are also
identical with constant and variable regions.
The variable N-terminal regions of both the heavy and light chains
provide the antigen binding sites, whereas, the complement fixation, membrane
transport, species specific and class specific antigenic determinants are
related to the constant region of the heavy chains (Buttler, 1974, Lascessels,
1979).
The variable
carbohydrate moiety bound to the heavy
chain is considered to be important in the specificity of the Igs.
Biological
Activity:
Immunoglobulins
are well recognized to provide disease protection to new-born through passive
immunity and there is evidence that the immunoglobulins may also have a role in
disease control in adults. Relatively
few studies have been made concerning the incidence and specificity of
immunoglobulins in commercial milk supplies.
Chan, et.al. (1994) reported on the IgG concentration of 254 raw milk
samples collected from the Province of British Columbia over a two year
period. The IgG values varies from 0.03
to 0.71 mg/ml, with media values of
about ~.25mg/ml. There were
significant values in the levels of IgG among the milks from the 14 different
dairies and the IgG values from the same dairy varied from one year to the
next. These findings suggest that milk
from a large number of cows, as would be found in the milk from commercial
dairies, will have activity against a
wide range of different bacteria, although the level of activity may vary from
year to year and with geographical location.
However, using
ELISA testing, all of the milks showed measurable antibody binding activity
against the lipopolysaccharide (LPS) fraction of 5 different bacteria (Shigella flexneri 1A, Escherichia coli
0111:B4, Escherichia coli 0128:B12; Salmonella typhonerium and Salmonella
enteritidis. Immunization of cows with
the 5 organisms gave a significant increase in the LPS activity only for the S. enteritidis in relation
to any of the commercial raw milk samples.
The activities for the other four organisms were about the same.
The
number of specific immunoglobulins in
the whey from commercial milk supplies
is not known, but will reflect the exposure of the cows to antigens in their
natural environment. Where a given milk
supply represents milks from thousands of individual cows, it is to be expected
that there will be a wide range of different immunoglobulins present -- the type of levels of which would be
expected to vary widely. It is known that
whey protein concentrates, treated to avoid denaturation, from mixed milk supplies generally contain
sufficient antibody to E. coli K-99
to meet the requirements of the USDA to serve as a colostrum supplement.
Hyper-immune milk/whey:
Immunization
of cows with specific antibodies has been practiced for a number of years on a
limited basis, with the resulting milk being characterised as “hyper-immune
milk”. Some ‘immune milk has been
produced and marketed in Asian countries (Rider, S., 1992; Hilpert, 1980). However, the extent in the increase in
specific activity of the antibodies appears to be dependend up the specific
organism and agent used for vaccination.
Chan, etal. (1994) found increased ELISA activity for only one of five
bacterial antigen in immunized cows in comparison to the levels of activity in
milk from commercial dairies. Tomita,
et.al. (1995) vaccinated cows with a lipopolysaccharide-protein conjugate
derive from E. coli J5. Immunization
did enhance serum antibody titer to J5, but did not
enhance whey IgG titers.
Ormrod and
Miller (1991) reported the isolation of a low molecular weight fraction of the
milk of dairy cows immunized with a multivariate bacterial vaccine which was
shown to have anti-inflammatory activity in the rat hind-paw oedema assay.
Kobayashi,
et.al (1991) and Ishida, et al (1992) showed that ‘immune’ milk, obtained from
cows immunized with a mix bacteria flora, showed a higher survival rate for
mice given lethal doses of irradiation as compared to control mice not
receiving the ‘immune’ milk.
Concentration of IgA in a cell culture derived from Peyer’s patches,
mesenteric lymph node and spleen was higher from mice given the ‘immune’ milk
than for the control mice.
Several
studies have suggested that feeding immune milk increases antibodies against
the immunizing bacteria and may reduce disease (Murosaki, etal. (1991); Chernokhvostova, et. al, 1990; Boedeker, etal., 1987). In one study reducing the level of free
energy intake by 60% appeared to eliminated the differences between B/W mice
fed immune and control skim milk.
Whey Biological references
up to 1998