As surprising as it may seem, bee venom has therapeutic value not only with this study using BV injections, but a new trend in Germany provides asthmatics the ability to inhale bee hive air. There individuals sit behind a beehive and via a tube, inhale air coming out of the beehive. They have identified minute doses of phenolic compounds found in honey, beeswax and propolis but this air also contains bee venom...
These results indicate that BV efficiently
diminishes bronchial inflammation in an OVA-induced allergic asthma murine model,
and that this effect might correlate with Tregs, which play an important role
in maintaining immune homeostasis and suppressing the function of other T cells
to limit the immune response. These results also suggest that BV has potential
therapeutic value for controlling allergic asthma responses.
Bee Venom
Ameliorates Ovalbumin Induced Allergic Asthma Via Modulating CD4(+)CD25(+)
Regulatory T Cells in Mice
Cytokine,
2012 Oct 30
Asthma is a
potentially life-threatening inflammatory disease of the lung characterized by
the presence of large numbers of CD4(+) T cells. These cells produce the Th2
and Th17 cytokines that are thought to orchestrate the inflammation associated
with asthma.
Bee venom
(BV) has traditionally been used to relieve pain and to treat chronic
inflammatory diseases. Recent reports have suggested that BV might be an
effective treatment for allergic diseases. However, there are still unanswered
questions related to the efficacy of BV therapy in treating asthma and its
therapeutic mechanism.
In this
study, we evaluated whether BV could inhibit asthma and whether BV inhibition
of asthma could be correlated with regulatory T cells (Treg) activity. We found
that BV treatment increased Treg populations and suppressed the production of
Th1, Th2 and Th17-related cytokines in an in vitro culture system, including
IL2, IL4, and IL17. Interestingly, production of IL10, an anti-inflammatory
cytokine secreted by Tregs, was significantly augmented by BV treatment. We
next evaluated the effects of BV treatment on allergic asthma in an ovalbumin
(OVA)-induced mouse model of allergic asthma. Cellular profiling of the
bronchoalveolar lavage (BAL) and histopathologic analysis demonstrated that
peribronchial and perivascular inflammatory cell infiltrates were significantly
lowered following BV treatment. BV also ameliorated airway hyperresponsiveness,
a hallmark symptom of asthma. In addition, IL4 and IL13 levels in the BAL fluid
were decreased in the BV treated group.
Surprisingly,
the beneficial effects of BV treatment on asthma were eradicated following Treg
depletion by anti-CD25 antibody injection, suggesting that the major
therapeutic targets of BV were Tregs.