V. Rusch et al., Results of an open, non-placebo controlled pilot study investigating the immunomodulatory potential of autovaccine, ARZNEI-FOR, 51(8), 2001, pp. 690-697
Autovaccines are prepared from autologous, human, non-pathogenic, "rough" v
ariants of E. coli derived from the stool flora of individuals according to
a highly standardized procedure. As a fundamental concept within microbiol
ogical therapy, these autovaccines are mainly used to treat chronic inflamm
atory disorders associated with Impaired Immune reactions resistant to stan
dard therapeutic treatments. Generally, Immunomodulatory effects of outer m
embrane components or cell wall fragments of gram-negative bacteria on Inna
te or adaptive immunity are widely accepted but nevertheless mechanisms of
actions of these autovaccines remained obscure, despite some recent publica
tions about other autovaccine preparations of different origin. Hence, immu
nomodulating properties of autovaccine were investigated In a pilot study w
ith 78 outpatients with variable disorders ranging from recurrent respirato
ry infections to diffuse gastrointestinal complaints. Patients received the
ir autologous bacteria parenterally In increasing doses. Before application
and 4 to 6 weeks after application of autovaccine, blood samples of the pa
tients were taken to investigate a range of immunological parameters such a
s acute phase proteins, serum antibodies and cytokines. The results reveale
d that autovaccines were able to modulate significantly the release of thre
e potent immunoregulatory cytokines e.g. interferon-gamma, granulocyte-macr
ophage-colony stimulating factor and interleukin-1 beta, whereas specific h
umoral immunity remained largely unaffected. From these results It may be c
oncluded that the autovaccine mainly act antigen non-specifically on the cy
tokine level rather than Inducing a specific vaccination. Further studies w
ith more detailed kinetic measurements of cytokines will have to verify the
se results.