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Important : Citations of scientific journal and other
references found in this web page, and on this website are for
journalistic and educational purposes only, presented as a free
exchange of ideas. They do not represent a recommendation, endorsement,
diagnosis, nor prescription for any health disorder or remedy
by the authors, or their publishers.
Always consult your physician for recognized medical
treatments.
MELISA® is the registered trademark of MELISA MEDICA
FOUNDATION
MELISA stands for "Memory Lymphocyte
Immunostimulation Assay", an "in vitro" test for
metal allergy.
What MELISA provides is a reliable, objective means for determining
individual immune system sensitivity to specific metals, and
metal compounds.
Early work with MELISA indicates a subset of the general human
population, at least 14%, form a memory lymphocyte mediated immune
response specific to commonly used dental metals, at the concentrations
they are leaching from dental restorations into the digestive
system, tissues, and blood stream.
This knowledge is a critical missing piece in understanding
a likely pathology for "amalgam disease", CFIDS , and
various autoimmune conditions. Visit our page Proposed
Immune-Metal Pathology to read our understanding of how
all this fits together for chronic illness.
Below you will find two journal references regarding work
done with the MELISA test. We have created graphs from the authors'
published data to better visualize the study results.
In the case of oral lichens, a causal relationship between
dental mercury and precancerous cells was demonstrated. MELISA
showed a positive result in 72% of the patients against inorganic
mercury. After removal of the mercury fillings, the patients
oral lichens went away.
The second study demonstrates a direct correlation between
brain lesions visible under MRI and a positive MELISA response
to dental metal in the mouth of patients meeting the strictest
definition of chronic fatigue syndrome.
For contact information and other important information concerning
MELISA® test for metal allergy, visit the web site:
Title
Mercury-specific lymphocytes: an indication of mercury allergy
in man.
Author
Stejskal VD; Forsbeck M; Cederbrant KE; Asteman O
Source
Journal of Clinical Immunology, 16(1):31-40 1996 Jan
Abstract
In this study, 18 patients with oral lichen planus (OLP), adjacent
to amalgam fillings, were tested in vitro with an optimized lymphocyte
proliferation test, MELISA (memory lymphocyte immunostimulation
assay) and with a patch test. Twenty subjects with amalgam fillings
but without oral discomfort and 12 amalgam-free subjects served
as controls. The results show that patients with OLP have significantly
higher lymphocyte reactivity to inorganic mercury, a corrosion
product of amalgam, compared to control groups. Removal of amalgam
fillings resulted in the disappearance of oral mucosal changes,
thus indicating a causal relationship. Positive responses to
phenylmercury (phenyl-Hg), a bactericidal agent in root fillings
and in pharmaceutical preparations, were also noted in the oral
lichen group but not in the control groups. Thus, low-grade chronic
exposure to mercury may induce a state of systemic sensitization
as verified by Hg-specific lymphocyte reactivity in vitro.

Title
Immunological and Brain MRI Changes in Patients with Suspected
Metal Intoxication
Author
Tibbling L; Thuomas KA; Lenkei R; Stejskal VD;
Source
International Journal of Occupational Medicine and Toxicology,
Vol. 4, No. 2, 1995
Abstract
Thirty-four patients with central nervous system (CNS) and systemic
symptoms suggestive of intoxication from dental amalgam were
examined with magnetic resonance imaging (MRI) of the brain (n=32)
and with a Memory Lymphocyte Immuno Stimulation Assay (MELISA)
(n=17). Lymphocyte phenotype was analyzed with flow cytometry
(FC) in 22 of the patients. One hundred twenty age-matched patients
without CNS symptoms served as controls for the MRI study, seventy-seven
healthy subjects with dental amalgam fillings served as controls
for the MELISA test, and seventy-five clinically healthy subjects
were controls for the lymphocyte phenotype determination. Pathological
MRI findings were present in 81% of the patients, most of them
with signs of degeneration in the basal ganglia, but none in
the controls. The lymphocyte phenotype determination was pathological
in 58%. The MELISA showed pathological findings in 88%, of which
60% showed an immune reaction to mercuric chloride, 62% of the
patients had some kind of atopic disease, and 35% suffered from
levothyroxine-treated hypothyreosis. A high rate of immunopathologies
and objective signs of immunological reactions in the majority
of the patients with MRI changes in the brain suggests that immunological
mechanisms may play an important role in the development of the
lesions.
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